Daily Archives: April 22, 2022

As with other medical conditions, the understanding of psoriasis has changed over time. Psoriasis likely affected the earliest humans, but it was not until the 1800s that doctors recognized psoriasis as its own condition.

Through the ages, psoriasis has gone from being a feared condition to one that people can treat to control most, if not all, of their symptoms effectively.

Several philosophers both well-known and less prominent from ancient civilizations described psoriasis-like lesions on the skin.

In Ancient Greece, Hippocrates (460377 B.C.E.) described inflammatory skin conditions, including psoriasis, using two words: psora, meaning itch, and lopoi, describing dry, scaly skin.

Centuries later, in the Roman Empire, a nobleman named Cornelius Celsus (25 B.C.E.50 C.E.) described a skin condition that affects the skin and nails.

Starting in ancient times and persisting through the Middle Ages, people did not write much about skin conditions. When they did, they tended to lump them together.

The grouping of skin conditions did not end for several centuries. During the Middle Ages, people living with psoriasis shared the same treatment essentially being cast out from society as people living with leprosy.

During the Renaissance, an Italian named Girolamo Mercuriale (15301606) wrote a book called De Morbis Cutaneis (Diseases of the Skin). This book, which became one of the more important works on skin diseases, described psoriasis as a skin condition called lepra grecorum.

In 1809, an English doctor named Robert Willan (17571812) produced a simple diagnostic description of several skin conditions, including psoriasis. He also defined some psoriasis types, including guttate, scalp, and palmar psoriasis. However, in his description, he used the term lepra vulgaris.

Many consider Willan to be the founder of dermatology as a medical practice.

Doctors continued to group leprosy and psoriasis until the 1800s, when an Austrian physician named Ferdinand Ritter von Hebra (18161880) wrote the book Atlas der Hautkrankeiten (Atlas of Skin Diseases). Unlike many before him, von Hebra separated leprosy from psoriasis in his works.

Many look to von Hebra as the father of modern dermatology and still see his book as one of the most influential books on skin diseases of all time. In 1841, he named psoriasis.

Then, in 1860, Ernest Bazin connected psoriasis to a form of arthritis, calling it arthritic psoriasis.

Also in the 1800s, Dr. Heinrich Kbner noted that psoriasis plaques appear in uncommon areas due to skin abrasion, burns, bruises, and other injuries. This is now known as the Kbner phenomenon, but scientists still do not understand why it occurs.

Throughout the rest of the 1800s into the 1900s, doctors continued to describe and refine what they knew about psoriasis.

As the 20th century progressed, doctors and researchers learned more about the disease and developed detailed descriptions of various subtypes.

In 1973, John M. Moll and Verna Wright made a milestone discovery. They published a paper describing how psoriasis and psoriatic arthritis form part of the same unique disease, explaining that it is different than rheumatoid arthritis.

Researchers today understand that psoriasis is more than just a skin disease. It is a chronic autoimmune disorder that causes systemic inflammation. This newer understanding has helped shape modern medical treatments, including the use of biologics.

Advances in knowledge about psoriasis through the years have led to changes in the treatment landscape. In more recent years, the quality of available treatment has improved dramatically.

Early treatments focused mostly on internal medication. The rationale for this stemmed from the belief that applying a topical treatment to a skin lesion would drive the infection inward, leading to infection of the organs.

Beginning in the 1700s and persisting into the 19th century, early psoriasis treatments often included options such as mercury and arsenic. Little is known about what effect they had on psoriasis or the person, but these treatments can be toxic. As recently as 1956, medical literature mentioned the use of mercury in topical ointments for psoriasis.

As the years progressed, so did psoriasis treatment options:

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Psoriasis: A brief history plus what we know now - Medical News Today

Clinicians should be aware of differences between male and female patients with psoriasis, how the disease manifests and how treatment should be approached.

With psoriasis, differences in disease manifestation and treatment outlook and goals exist between male and female patients using systemic agents, including conventional system agents (CSA) and tumor necrosis factor inhibitors or ustekinumab (TNFi/UST). However, few studies have addressed sex differences as they pertain to systemic agent use, such as CSA discontinuation and switch from CSA to TNFi/UST.

Past research has shown that female patients have higher expectations for achieving treatment goals than male patients. Female patients anticipate faster skin improvement and a return to normal life, even though male patients may present with more severe psoriasis. These differences in psoriasis severity and treatment goals between male and female patients may determine how clinicians manage their treatment. Female patients, for example, may discontinue treatment prematurely or request a treatment change if their skin clearance is slower than expected.

For a paper published in Frontiers in Pharmacology, my colleagues and I utilized a health administrative database to examine sex differences in patterns of CSA use and determine factors linked with switching to (or adding) a TNFi/UST. Our retrospective cohort study included 1,644 patients with psoriasis (mean age, 61; 55.7% female) who started a CSA between 2002 and 2015. The study team used Cox regression models with the Least Absolute Shrinkage and Selecting Operator (LASSO) to identify socioeconomic and clinical characteristics that predicted switch/add-on TNFi/UST.

We observed similar rates for switch and add-on of TNFi/UST between male and female patients with psoriasis. However, most predictors of switch/add-on were sex-specific. For example, among males, we found an increased risk for longer psoriasis disease duration and obesity by at least 2.3-fold. Among female patients, prior use of NSAIDs and the presence of certain mental health disorders increased the risk for switch/add-on by 2.7-fold. Interestingly, female patients with rheumatoid arthritis (RA) as a comorbidity had a 60% reduced risk for switch/add-on (Table).

Our findings may help clinicians improve the management of male and female patients with moderate-to-severe psoriasis in need of systemic agent treatment. Since most countries with a universal healthcare system reimburse biologic agents only for patients who do not respond well to CSA or among whom CSA are contraindicated, a need exists to improve access to biologic agents. For male patients with obesity and for those who have lived with psoriasis for an extended time, and for female patients who experience pain or mental health symptoms, treatment with biologic agents may save them the burden of going through a failed treatment experience and help improve their psoriasis outcomes faster, especially since biologic agents are known for being more effective than CSA.

My colleagues and I also included variables related to psoriasis treatments such as the type of initial CSA received, the specialty of the prescriber, and prior use of topical agents and phototherapy. However, none of these variables were selected by our model, thus possibly indicating that the decision of the healthcare professional to prescribe a biologic agent among male and female patients with psoriasis was mostly based on patients clinical profiles and not on these factors.

We were surprised to find that psoriatic arthritis (PsA) was not associated with a risk for switch in both male and female patients, while RA was linked with a decreased risk for switch among female patients. Since PsA and RA are immune-mediated conditions for which biologic agents can also be prescribed, additional research is warranted to better understand the reduced risk for switch/add-on of TNFi/UST among female patients with both psoriasis and RA.

Additionally, larger studies, specifically those focused on psoriasis severity, are needed to confirm our findings and their impact on clinical practice and provincial drug policy. Larger studies will also allow comparisons between individual CSAs and the assessment of predictors of switch to TNFi/UST and those for receiving these agents as add-on, separately.

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Examining Sex Differences in the Management of Psoriasis - Physician's Weekly

Pediatric patients with psoriasis exhibited significant improvements in self-reported outcomes and objective measures of complete skin clearance when treated with ixekizumab vs placebo, with no new safety findings identified.

Ixekizumab showed results including long-term improvement in patient-reported outcomes and objective measures of complete skin clearance among pediatric patients with psoriasis, according to study findings published in JAMA Dermatology.

Affecting approximately 1% of children and adolescents, psoriasis has a significant impact on the quality of life of pediatric patients and their parents.

Moreover, disease manifestations in certain locations, such as the face, scalp, palms and soles, nails, and genital region, could have a disproportionately greater effect on a patients quality of life, because of its high visibility or challenge in treating given the involvement of more sensitive areas that may be more recalcitrant to topical agents, noted researchers.

Among the several biologic agents approved for first-line treatment of moderate to severe psoriasis in children aged 6 to 18 years, ixekizumab has been shown to be superior to placebo after 12 weeks of treatment in the phase 3 multicenter randomized IXORA-PEDS clinical trial (NCT03073200), with responses sustained through week 48.

The extension period of the IXORA-PEDS trial lasting through week 108 was evaluated by researchers to determine long-term efficacy and safety of ixekizumab for pediatric patients with moderate to severe psoriasis, defined as Psoriasis Area and Severity Index (PASI) of 12 or higher, static Physicians Global Assessment (sPGA) score of 3 or higher, and psoriasis-affected body surface area of 10% or greater at screening and baseline.

A total of 171 patients (mean [SD] age, 13.5 [3.04] years; 99 female children [57.9%]) were randomized to either ixekizumab (n = 115) or placebo (n = 56). Of 166 patients who entered the maintenance period, 139 (83.7%) completed week 108 of the trial, the study authors wrote. Data analysis, which followed the intention-to-treat principle, was conducted from May to October 2021.

Several primary/secondary efficacy and safety outcomes at week 108 were evaluated:

Findings showed that primary and gated secondary end points that were achieved by week 12 were sustained through week 108, with patients achieving PASI 75 (91.7%), PASI 90 (79.0%), PASI 100 (55.1%), sPGA 0 or 1 (78.3%), and sPGA 0 (52.4%). Moreover, 55 patients (78.5%) reported an Itch NRS improvement of 4 points or higher.

Regarding treatment efficacy on more sensitive affected areas, clearance of nail psoriasis was reported in 68.1%, clearance of palmoplantar psoriasis was reported in 90.0%, clearance of scalp psoriasis was reported in 76.2%, and clearance of genital psoriasis was reported in 87.5% of patients who received ixekizumab through 108 weeks.

No new safety findings during weeks 48 to 108 of the trial were identified, including no new cases of inflammatory bowel disease or candida infection.

Additional studies are warranted to address lingering questions, such as the effect of ixekizumab on additional patient-reported outcomes and the effectiveness and safety of ixekizumab for children with psoriasis in the real world, concluded researchers.

Reference

Paller AS, Seyger MMB, Magarios GA, et al. Long-term efficacy and safety of up to 108 weeks of ixekizumab in pediatric patients with moderate to severe plaque psoriasis: the IXORA-PEDS randomized clinical trial. JAMA Dermatol. Published online April 13, 2022. doi:10.1001/jamadermatol.2022.0655

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Ixekizumab Effective Long-term for Treatment of Psoriasis in Pediatric Patients - AJMC.com Managed Markets Network

Introduction

Psoriasis is an inflammatory skin disease triggered by the immune system. Only a few studies have been conducted on the incidence and prevalence of psoriasis worldwide. According to a systematic review, the prevalence in adults ranged from 0.91% (the United States) to 8.5% (Norway). In adults, it varied from 78.9/100,000 person-years (the United States) to 230/100,000 person-years (Italy).1 The disease burden of psoriasis should not be underestimated. The global report on psoriasis by WHO (World Health Organization) showed that global average DALY (disability-adjusted life year) for psoriasis was estimated at 1,050,660 in 2010, which is twice as much as for acute hepatitis C.2 The continued development of effective therapies for patients with psoriasis is urgently needed. It has long been recognized that patient preferences support the principle of patient-centeredness in clinical decisions.3 During past decades, a growing number of patient preferences are now being measured using elicitation methods that quantify them in the clinical setting, such as standard gamble, time trade-off, person trade-off and discrete choice experiment (DCE).4 Several methods have more recently also been used for psoriasis treatment.57 In recent years, the study of quantifying psoriasis patients treatment preferences is expanding to include regulatory marketing authorization decisions of new biologic treatments.810 To adjust decision-making for patient opinion on the meaning and significance of treatment attributes, such as the balance between estimated effects and adverse reactions, quantitative assessments of patient preferences may be helpful in regulatory marketing approvals.11,12 Adherence to a treatment program could be improved by better tailoring it to patient preferences.12

Patients with psoriasis are often treated with multiple disease-modifying anti-psoriasis drugs. Each of these drugs has its own characteristic and method of action, as well as a different frequency of administration and chance for adverse events and monitoring requirements. Patients with mild disease (PASI 10) and mild or moderate quality-of-life impairment (DLQI 10) may only need topical therapy.13 Patients with severe or moderate psoriasis (PASI >10) or significant quality-of-life restrictions (DLQI >10) has several options for treatment. These include phototherapies, conventional systemic immunosuppressive medications, or modern small molecules or biologic agents. Individual risk factors, associated diseases, national guidelines, and approval criteria (which might consider economic aspects) can impact the choice of treatment.13 Clinicians should therefore inform patients of the extent of and probability of experiencing side effects associated with these treatments. Although treatment costs can be an important determinant of preference, they are less relevant in countries with universal health-care systems, as is the case for most of developing regions. Despite the fact that treatment costs can be a determinant of preference, in regions with universal health-care systems, as is the case for the majority of developing regions, treatment costs are less relevant in determining preference.

As professionals, clinicians should get to know our patients perspectives and preferences when discussing potential treatments. This will allow patients to participate in decisions about their treatment, aligning with their preferences.12 Quantitative assessments of patient preferences have the potential to support both clinicians and regulators when they consider patient perspectives. In considering patient perspectives, both clinicians and regulators can benefit from quantitative assessments. Presently, numerous studies have investigated preference associated with psoriasis. A systematic review summarized 23 studies identified 4 areas of preferences related to psoriasis, which covered preferences for treatment options (eg, state preferences with regard to two different ointments or a cream vs an ointment), preferences for attributes of treatment (eg, frequency of drug administration, treatment benefits or avoidance of potential adverse effects), preferences for different health states (eg, health state utility), preferences for different health state domains (eg, interquartile range).4 For treatment attributes, efficacy (eg, duration of benefit, coverage, lesion severity, etc.) and safety (eg, risk of infection, unspecified adverse events, etc.) were selected in most studies.14 Additionally, the global report on psoriasis pointed out that onset speed (get better skin quickly) and complete removal of skin lesions (recover from all skin lesions) are the top two importance of patient needs related to treatment of psoriasis, which accounted for more than 90%.2 However, few studies have evaluated the onset speed, complete removal of skin lesions, and cost-related indicators. Lack of evidence concerning the extent to which patients feel that biologic treatments would be cost-effective and acceptable in a middle-income country, especially in the context of China. The present study examines the preferences of psoriasis patients in China with moderate-to-severe psoriasis regarding biologic therapies and the heterogeneity within these perceptions. It is based on these preferences that one can estimate the relative importance of different treatment characteristics, as well as calculate patients willingness to pay (WTP) for biologic treatments in China with primarily out-of-pocket payment markets.

A study invitation was sent to the members of the Chinese online psoriasis community via email, social media and mobile application. During the study, each participant was informed about the research procedure and provided their informed consent before completing the survey. The survey was distributed online by a consulting and marketing research company (Adelphi FocusRx). For inclusion, there were the following criteria: established moderate-to-severe diagnosis psoriasis (BSA 3%, PASI 3, DLQI 6, based on the guideline for psoriasis in China), over 18years of age, the experience of receiving biologic treatments, and the ability to properly understand and answer the raised questions. The sample size for the DCE was calculated using the Johnson and Orme methodology that the sample size required for the main effects depends on the number of choice tasks (t), the number of alternatives (a), and the number of analysis cells (c) according to the following equation: N > 500c/(t a).15 Data were collected from October 2020 to January 2021.

A DCE method was used to determine treatment preferences for patients with moderate-to-severe psoriasis, which is a cross-sectional survey method used for quantitative assessment of patient preferences for health-care policies, services, and interventions.16,17 Based on the random utility theory (RUT), DCE quantifies the relative importance of one treatment characteristic versus another. In RUT-based approach, the utility (U) of alternative j for individual i in the choice set k was specified as: Uijk=Xijk+ijk, where Uijk is the utility function of individual i from choosing alternative j in choice set k. Xijk represents a linear specification of the DCE attributes. It is assumed that the utility of a product can be determined by the value of the characteristics of that product (ie, attributes) and their levels. In a DCE, respondents are given a choice of hypothetical scenarios with different attributes and levels. Respondents are asked to choose their preferred option for each question and select the option that yields the maximum utility. By modeling the choices respondents make between alternative treatments described by different choice questions, the utility of each treatment can be estimated. Also, DCEs can be used to measure and explain the heterogeneity among the preferences of patients. When out-of-pocket costs are taken into account in a DCE, the results can be used to calculate the value of or WTP for improvements in medication attributes.18,19

To determine attributes and levels to include in the DCE, we followed a stepwise process. The first step was to review previous literature on patient preferences for treatment in psoriasis and to identify 13 potential treatment characteristics.8,10,20 The second step was to consult 5 dermatologists to make sure the attributes and levels described reflected current clinical practice in China.21 Thirdly, a nominal group technique was used for two focus groups with patients with moderate-to-severe psoriasis (n = 11) and these patients were asked to identify new attributes and rank all potential attributes from the most to the least important. The focus groups were audio recorded and conducted using an interview guide, which lasted approximately 60 minutes. Furthermore, five dermatologists, the research team, and eleven patient research partners reviewed and discussed the results from the focus groups during several validation meetings. These meetings revealed four attributes: the average time for achieving 50% reduction after initiation of treatment, proportion of achieving 100% reduction after 3-months treatment, proportion of maintaining 100% reduction after 5-years treatment and monthly average cost on medication. Each attribute was revealed to have four levels based on current clinical knowledge of existing therapies. All attributes and levels included in the DCE are displayed in Table 1.

Table 1 Attributes and Levels in Discrete Choice Experiment

Based on the recommendations of experimental designs for discrete-choice experiments released by the ISPOR task force,22 the current study adopted a fractional factorial design to lighten respondent burden by reducing the number of choice sets. We used R Package choiceDes for a D-efficient experimental design. Designing using the D-efficient method results in orthogonality, level balance, minimum balance, and overlap, all favorable features. Then, 13 choice-set questions were generated from the design. Each choice set included two hypothetical treatment options: alternative of medication A and alternative of medication B. Figure 1 presents an example of a choice question (the questionnaire can be found in the following website: http://qs.focusrxonline.com/limesurvey/index.php/441618?lang=zh-Hans). The participants accessed an online survey website and answered the questionnaire. Prior to entering the DCE, the survey began with information about psoriasis, demographics, and disease-related questions. Thus, the study was designed to make it possible to complete the survey in approximately 30 minutes.

Figure 1 Example of presented discrete choice experiment question.

Before statistical analysis, we checked the quality of the collected questionnaires. If respondents chose either Medicine A or Medicine B for all choices, it indicated that they were inattentive to the choice questions. Therefore, the questionnaire results of the respondents will not be included. The rest of the questionnaire results are retained for statistical analysis. Then, statistical analysis was conducted based on the recommendations of statistical methods for the analysis of discrete choice experiments released by the ISPOR task force.23 Demographic data were analyzed using descriptive statistics. Using conditional logit models, we estimated preference weights for respondents choices among pairs of treatment alternatives, where the different treatment and cost aspects were entered as separate categorical variables (effects-coded). When coding effects, zero indicates the mean of all attribute levels rather than the omitted level as in dummy coding. With this procedure, each attribute level has a parameter estimate, where the parameter on the omitted level of each attribute is the negative sum of the parameters on the other levels of that attribute. The resulting log-odds estimates can be interpreted as preference weights. The relative importance (%) was calculated by dividing the distance between the highest and lowest preference weights for each attribute divided by the sum of all preference weight differences. Patient preference was assessed based on preference weights and relative importance.

The preference weights were used to estimate WTP for improvements in treatment efficacy. WTP is the mean maximum monetary equivalent that an individual is willing to pay for a given improvement in treatment efficacy. WTP represents the variation in out-of-pocket costs that yield a decrease in estimated utility that exactly balances the increase in utility yielded by an improved treatment efficacy. For example, WTP for an improvement in the average time for achieving 50% reduction after initiation of treatment from 5-weeks (WEEK5) to 4-weeks (WEEK4) is calculated as the level of cost (X) that satisfies following equation: COST(X) = WEEK4 WEEK5. represents the coefficients for each attribute level. X may fall between two cost levels since the cost levels are categorical. Interpolating linearly was used between the preferences for the surrounding cost levels to determine the value of X.24

This study was conducted in accordance with the Declaration of Helsinki. The survey was approved by the medical ethics committee of the Renji Hospital, Shanghai, China (no. KY2020-110).

Totally, 613 individuals responded to the invitation, of which 456 consented and completed the survey. There were 437 patients who completed the questionnaire, among whom 201 had no variation in their responses and were excluded from the analysis.

The characteristics of the remaining 236 patients are summarized in Table 2. Most of the patients were male (approximately 62.3%), were 2635 years old (approximately 46.2%), and had at least some college education (47%). Median monthly household income was between RMB 4000 and RMB 5999. The main psoriasis characteristics of these respondents were light red and partly scaly (approximately 40.3%). Most of these respondents whose psoriasis surface area was equal to the size of 35 hands (approximately 22.5%) and mainly distributed in the legs or hips (approximately 59.3%) and scalp (approximately 56.4%).

Among the participants, preference weights derived from the attribute levels indicated that the participants preferred lower costs of biologic treatments and a higher likelihood of retaining PASI 100 after three-month treatment. Preference weights derived from the attribute levels showed that the participants favored the lower cost of biologic treatments and higher probability of keeping PASI 100 at 3 months (Figure 2 and Supplementary Table 1). The distance score of the reduction of monthly costs from RMB 7000 to 1000 is 0.711, whereas improvements from 20% to 50% in the probability of keeping PASI 100 at 5-years is 0.164, improvements from 10% to 40% in the probability of achieving PASI100 at 3 months is 0.221, and improvements from 8 weeks to 2 weeks in the time to achieve PASI50 after initiation the biologic treatment is 0.101, respectively.

Figure 2 Preference weights for attribute levels and Relative importance of attributes (overall results, n = 236). Preference weights are showed on the vertical scale, describing how much each level was selected within one attribute. Non-overlapping error bars indicate statistically significant differences across levels within attributes; Relative importance is relatively described values calculated by the distance between the highest and the lowest attribute levels.

Across all participants, the attribute regarded as the most important was monthly cost (relative importance [RI]: 59.4%), probability of achieving PASI100 at 3 months (RI: 18.5%), probability of keeping PASI100 at 5-years (RI: 13.6%) and time to achieve PASI50 after initiation the biologic treatment (RI: 8.5%).

According to the monthly income, entire cohort is divided into low-income subgroup and high-income subgroup based on the monthly income of less than 8000 and more than 8000.

Preference weights derived from the attribute levels showed that the high-income subgroup preferred the lower cost of biologic treatments and the time to achieve PASI50 after initiation of the biologic treatment (Figure 3). The distance score of the reduction of monthly costs from RMB 7000 to 1000 is 0.370, whereas improvements from 20% to 50% in the probability of keeping PASI 100 at 5-years is 0.110, improvements from 10% to 40% in the probability of achieving PASI100 at 3 months is 0.327, and improvements from 8 weeks to 2 weeks in the time to achieve PASI50 after initiation the biologic treatment is 0.223, respectively. Across all participants, the attribute regarded as most important was monthly cost (RI: 35.9%), probability of achieving PASI100 at 3-month (RI: 31.7%), probability of keeping PASI100 at 5-years (RI: 21.7%) and time to achieve PASI50 after initiation the biologic treatment (RI: 10.7%).

Figure 3 Preference weights for attribute levels and Relative importance of attributes. Orange represents thehigh-income subgroup (monthly income more than RMB 8000, n = 52); Blue representsthe low-income subgroup (monthly income less than RMB 8000, n = 184). Preference weights are showed on the vertical scale, describing how much each level was selected within one attribute. Non-overlapping error bars indicate statistically significant differences across levels within attributes; Relative importance is relatively described values calculated by the distance between the highest and the lowest attribute levels.

Preference weights derived from the attribute levels showed that the low-income subgroup favored the lower cost of biologic treatments, probability of keeping PASI100 at 5-years and the probability of achieving PASI100 at 3 months (Figure 3). The distance score of the reduction of monthly costs from RMB 7000 to 1000 is 0.83, whereas improvements from 20% to 50% in the probability of keeping PASI 100 at 5-years is 0.19, improvements from 10% to 40% in the probability of achieving PASI100 at 3 months is 0.22, and improvements from 8 weeks to 2 weeks in the time to achieve PASI50 after initiation the biologic treatment is 0.20, respectively. Among this subgroup participants, the attribute regarded as most important was monthly cost (relative importance [RI]: 57.6%), probability of achieving PASI100 at 3 months (RI: 15.4%), time to achieve PASI50 after initiation the biologic treatment (RI: 14%) and probability of keeping PASI100 at 5-years (RI: 13.0%).

According to the matching degree between the psoriasis and the picture features, the patients were divided into five subgroups: Mild, Moderate, Severe, Very Severe, Clear disease.

Preference weights derived from the attribute levels showed that the Mild disease subgroup preferred the lower cost of biologic treatments (RI: 34.9%), the probability of keeping PASI100 at 5-years (RI: 34.5%), the probability of achieving PASI100 at 3 months (RI: 24.6%) and the time to achieve PASI50 after initiation the biologic treatment (RI: 6.0%); Across the Moderate disease subgroup, the attribute regarded as the most important was the monthly cost (RI: 36.0%), and the time to achieve PASI50 after initiation the biologic treatment (RI: 25.8%), probability of achieving PASI100 at 3 months (RI: 20.2%), probability of keeping PASI100 at 5-years (RI: 17.9%), respectively; Preference weights showed that the Severe disease subgroup favored the lower cost of biologic treatments (RI: 39.6%), the probability of achieving PASI100 at 3 months (RI: 32.3%), the probability of keeping PASI100 at 5-years (RI: 19.2%) and the time to achieve PASI50 after initiation the biologic treatment (RI: 8.8%); And in very severe disease subgroup, the attribute regarded as the most important was the monthly cost (RI: 49.6%), probability of keeping PASI100 at 5-years (RI: 22.3%), probability of achieving PASI100 at 3 months (RI: 18.0%), and the time to achieve PASI50 after initiation the biologic treatment (RI: 10.1%); Across the Clear disease subgroup, the attribute regarded as the most important was the monthly cost (RI: 62.7%), and the time to achieve PASI50 after initiation the biologic treatment (RI: 25.9%), probability of achieving PASI100 at 3 months (RI: 10.4%), probability of keeping PASI100 at 5-years (RI: 1.0%), respectively. The distance scores of each attribute are summarized in Figure 4.

Figure 4 Preference weights for attribute levels (results in disease condition subgroup n =191). (A) Mild disease subgroup (n = 40); (B) moderate disease subgroup (n = 95); (C) severe disease subgroup (n = 53); (D) very severe disease subgroup (n = 31); (E) clear disease subgroup (n = 17). Preference weights are showed on the vertical scale, describing how much each level was selected within one attribute. Non-overlapping error bars indicate statistically significant differences across levels within attributes.

According to the disease location distributed in body, the entire cohort was divided into the following subgroups: Legs or hips, Toes and feet, Buttocks, Groin or genital area, Stomach, chest, or back, Arms, Fingers or hands, Nails, Neck, Face or ears, Scalp. Across the foot and toe subgroup, the attribute regarded as the most important was probability of keeping PASI100 at 5-years (RI: 37.3%), the monthly cost (RI: 34.1%), probability of achieving PASI100 at 3 months (RI: 22.8%), and the time to achieve PASI50 after initiation the biologic treatment (RI: 5.8%), respectively. And in leg and hip subgroup, the attribute regarded as the most important was the monthly cost (RI: 66.8%), probability of keeping PASI100 at 5-years (RI: 15.2%), probability of achieving PASI100 at 3 months (RI: 12.7%), and the time to achieve PASI50 after initiation of the biologic treatment (RI: 5.3%), respectively. Additionally, preference weights and relative importance of attributes in other disease location subgroups are displayed in Supplementary Figure 1-22.

As expected, all patients were willing to pay more for improvement in probability of keeping PASI100 at 5-years (from RMB 666 to 1379), probability of achieving PASI100 at 3-month (from RMB -15 to 1867) and time to achieve PASI50 after initiation of the biologic treatment (from RMB 376 to 858). The WTP estimates for improving treatment efficacy in other subgroups (monthly income subgroup, disease condition subgroup, disease location subgroup) are summarized in Table 3.

Table 3 Willingness to Pay for Improvements in Treatment Efficacy in Overall Cohort and Subgroup

Our study was designed to quantify and explore psoriasis patients preference among different biological agents from a Chinese perspective and estimated the WTP for different attributes. Among patients with psoriasis, non-adherence rates are high partly due to a disagreement between recommended treatments and individual preferences.25 Compliance can be greatly improved by following patients preference. To our knowledge, there are no relevant studies conducted in China, which to a large extent provide references for future research on psoriasis from the perspective of geographical location. All four attributes (the average time for achieving 50% reduction after initiation of treatment, proportion of achieving 100% reduction after 3-months treatment, proportion of maintaining 100% reduction after 5-years treatment and monthly average cost on medication) were consistent with a prior expectation in terms of the direction and magnitude of the estimated coefficients. Among them, the average time for achieving 50% reduction after initiation of treatment and proportion of achieving 100% reduction after 3-months treatment represented quick response, proportion of maintaining 100% reduction after 5-years treatment was related to the long-term, sustained efficacy.

Overall cohort and most subgroups, regardless of their individual characteristics, attached the highest importance to monthly cost. The probability of achieving PASI100 after 3-months treatment was the second preferred attribute by patients in the entire cohort. Additionally, in the monthly income subgroup, most of patients prioritized quick response (achieving PASI100 at 3-month) compared with long-term, sustained efficacy (achieving PASI100 at 5-year). Moreover, results showed high-income subgroup favored more about onset speed of efficacy than low-income subgroup. In contrast, low-income subgroup only attached the greatest interest to the monthly cost. A systematic review about psoriasis showed that many preference studies conducted previously focused on the efficacy and safety, especially from the perspective of physicians.26 However, from the patients point of view, several studies included the attribute of cost. For instance, a German study included the treatment expenditure per month in the process attributes and calculated the relative importance score (RIS) of participants stratified based on disease duration, number of previous therapies, etc.27 Another study conducted in German showed compared with other attributes, the attribute of cost is not given as much attention.28 Italian studies on biologics for psoriasis included the cost attribute and illustrated that treatment costs and expected therapeutic response concurrently can provide valuable insights which complement and improve the traditional risk-benefit profile and drive treatment decisions.29,30 Probably this depends on different health systems and medicine reimbursement policies in Europe. However, in the process of choosing treatment strategies, medical expenditure has gradually become an important factor for patients in the context of China. It may be due to the income gap between patients in developing and developed countries. With the progress of health insurance negotiations in China during recent two years, the price of biological agents has dropped significantly, to a certain extent, which met the needs of some patients who tend to use biological agents. But the price of biologic agents was still high compared with other types of therapy and became a factor affecting the patients choice when considering the cost. This finding indicated the expenditure should be raised extensive attention, especially in China. And one strategy, called reduced doses, can be used well for clinical setting to control the expenditure, which seek for the minimal doses necessary to reach a good response while achieving a potential reduction of adverse effects. Many studies on optimal dosing strategy using biologic agents for psoriasis involved advantages in terms of drug-exposure risk and cost saving.3133 Regarding efficacy attribute, several DCE researches adopted PASI90 response for testing patients preferences on efficacy. For instance, Schaarschmidts finding indicated both patients and physicians considered PASI90 response is more important (RIS 21.4 and 20.8, respectively) than other attributes.34 But we chose PASI50 and PASI100 in our study, which were common endpoint of clinical trials. First, 50% and 100% reduction are easier to understand for participants than PASI 75 or PASI 90 response. Second, 50% reduction can roughly test participants the response to the concern about quick efficacy. Third, to determine whether or not the PASI50 response is still important for patients. Likewise, we found that quick response may be concerned as the secondary factor. It could indicate that psoriasis as facial skin disease has influences on patients appearance and impression, which are related to physiological and psychosocial function of patients.35 A higher incidence of anxiety and depression, along with lower quality of life, may be attributed to psoriasis. So, quick response may help patients with psoriasis get rid of the troubles caused by the disease.36 As for onset speed of efficacy, several studies on psoriasis-related treatment found that patients preferred differently. For instance, a research about patients with psoriasis preferred durability over onset speed of efficacy in psoriasis treatment in Japan.37 It is noteworthy that the most preferred element was sustained efficacy after drug withdrawal even though those drugs are not currently available in the clinical setting. In addition, for WTP, we can find from the results that patients are willing to spend higher costs for better efficacy. Especially in the high-income subgroup, the values of WTP for efficacy improving are higher than that in the low-income subgroup, which is consistent with our prior expectation. Clearly, the efficacy of biologic agents is still an unmet need for patients.

Several limitations exist in this study. Discrete choice experiment is a theoretical method, which that can be cognitively challenging. It means that actual patients might choose actual medications differently and participants are required to choose one of the two scenarios regardless of whether they like either. A direct conclusion based on individual preferences cannot be made from average preferences. Obviously, the treatment decisions made for each patient are based on their individual preferences. In order to better advise patients about their treatment options, physicians should be aware of what the majority of patients are concerned about and what their preferences are influenced by sociodemographic and disease-related characteristics. To optimize treatment satisfaction, adherence, and outcomes, physicians should incorporate their knowledge of each patients preferences, needs, and concerns into their therapeutic decisions. Some results of subgroup analyses are not consistent with our expectations due to the limited number of participants in the study. Subgroups with different demographic characteristics may differ significantly in their preferences, but a large sample size study is still required to verify this in the future. It is possible that some deviations will occur since the study was only conducted online. Several elderly patients may not be familiar with using digital devices, which limits the distribution of socio-demographic characteristics of participants in this survey. Additionally, the research questionnaire did not include a safety attribute. The safety profile is an important attribute among biologic agents, non-biologic systemic agents and topical compounds in the management of psoriasis.38,39 For example, the risk of infections caused by biologics is also a key safety profile.40 And during the COVID-19 pandemic, clinical management of patients with psoriasis is challenging due to their impaired immune status, especially for those using biologics inhibiting key pathogenic cytokines such as TNF-a and IL-17.41 In our study, the preferences were evaluated in patients with psoriasis using the biologic agents, and the risk of adverse events was similar among biologic agents. Some studies indicated that, despite individual risk tolerances, responders were willing to accept risks above likely clinical exposures to improve psoriasis symptoms or compatible with their personal and professional lifestyle.28,42 Considering that some biologic agents have just been listed in China, the efficacy and cost of biologic agents were primarily considered in order to estimate the economic burden, so this attribute was not included in our research questionnaire.

In conclusion, people are concerned about treatment cost when making decisions regarding the biological treatment regardless of incomes. In the efficacy attribute, the probability of achieving PASI100 at 3-month was the most sensitive factor. Clinicians might change their perceptions of what aspects of treatment plans need to be discussed with patients and their families during consultations based on our findings. It is necessary to conduct future studies using larger and more representative samples to enforce our current findings and to facilitate the measurement of potential preference heterogeneity among individuals.

Ethical approval was obtained from the Renji Hospital (no. KY2020-110).

All authors made substantial contributions to conception and design, acquisition of data, or analysis and interpretation of data; All authors took part in drafting the article or revising it critically for important intellectual content and agreed to submit to the current journal; All authors gave final approval of the version to be published and agree to be accountable for all aspects of the work.

This study was funded by Lilly Suzhou Pharmaceutical Co. Ltd.

Erjia Ye and Guanshen Dou are employees of Eli Lilly and Company. The other authors have no conflicts of interest.

1. Parisi R, Symmons DPM, Griffiths CEM, Ashcroft DM. Global epidemiology of psoriasis: a systematic review of incidence and prevalence. J Investigative Dermatol. 2013;133(2):377385. doi:10.1038/jid.2012.339

2. World Health Organization (WHO). Global report on psoriasis. Published online October 26; 2016. Available from: https://www.who.int/publications/i/item/global-report-on-psoriasis. Accessed April 14, 2022.

3. Charles C, Gafni A. The vexing problem of defining the meaning, role and measurement of values in treatment decision-making. J Comp Eff Res. 2014;3(2):197209. doi:10.2217/cer.13.91

4. Umar N, Yamamoto S, Loerbroks A, Terris D. Elicitation and use of patients preferences in the treatment of psoriasis: a systematic review. Acta Derm Venerol. 2012;92(4):341346. doi:10.2340/00015555-1304

5. Ontario Health (Quality). Home narrowband ultraviolet B phototherapy for photoresponsive skin conditions: a health technology assessment. Ont Health Technol Assess Ser. 2020;20(12):1134.

6. Thai D, de la Cueva P, Pink AE, et al. General practice recommendations for the topical treatment of psoriasis: a modified-Delphi approach. BJGP Open. 2020;4(5):34. doi:10.3399/bjgpopen20X101108

7. Sacristn JA, Dilla T, Daz-Cerezo S, Gabs-Rivera C, Aceituno S, Lizn L. Patient-physician discrepancy in the perception of immune-mediated inflammatory diseases: rheumatoid arthritis, psoriatic arthritis and psoriasis. A qualitative systematic review of the literature. PLoS One. 2020;15(6):e0234705. doi:10.1371/journal.pone.0234705

8. Feldman SR, Regnier SA, Chirilov A, Hey F, Gilloteau I, Cella D. Patient-reported outcomes are important elements of psoriasis treatment decision making: a discrete choice experiment survey of dermatologists in the United States. J Am Acad Dermatol. 2019;80(6):16501657. doi:10.1016/j.jaad.2019.01.039

9. Zhang M, Carter C, Olson WH, et al. Patient preference for dosing frequency based on prior biologic experience. J Drugs Dermatol. 2017;16(3):220226.

10. Tada Y, Ishii K, Kimura J, Hanada K, Kawaguchi I. Patient preference for biologic treatments of psoriasis in Japan. J Dermatol. 2019;46(6):466477. doi:10.1111/1346-8138.14870

11. Mhlbacher AC, Juhnke C, Beyer AR, Garner S. Patient-focused benefit-risk analysis to inform regulatory decisions: the European Union perspective. Value Health. 2016;19(6):734740. doi:10.1016/j.jval.2016.04.006

12. Ho M, Saha A, McCleary KK, et al. A framework for incorporating patient preferences regarding benefits and risks into regulatory assessment of medical technologies. Value Health. 2016;19(6):746750. doi:10.1016/j.jval.2016.02.019

13. Ghoreschi K, Balato A, Enerbck C, Sabat R. Therapeutics targeting the IL-23 and IL-17 pathway in psoriasis. Lancet. 2021;397(10275):754766. doi:10.1016/S0140-6736(21

14. Gonzalez JM. Evaluating risk tolerance from a systematic review of preferences: the case of patients with psoriasis. Patient. 2018;11(3):285300. doi:10.1007/s40271-017-0295-z

15. de Bekker-grob EW, Donkers B, Jonker MF, Stolk EA. Sample size requirements for discrete-choice experiments in healthcare: a practical guide. Patient. 2015;8(5):373384. doi:10.1007/s40271-015-0118-z

16. Goossens LMA, Jonker MF, Rutten-van Mlken MPMH, et al. The fold-in, fold-out design for DCE choice tasks: application to burden of disease. Med Decis Making. 2019;39(4):450460. doi:10.1177/0272989X19849461

17. Vass C, Rigby D, Payne K. The role of qualitative research methods in discrete choice experiments. Med Decis Making. 2017;37(3):298313. doi:10.1177/0272989X16683934

18. Johnson FR, Banzhaf MR, Desvousges WH. Willingness to pay for improved respiratory and cardiovascular health: a multiple-format, stated-preference approach. Health Econ. 2000;9(4):295317. doi:10.1002/1099-1050(200006)9:4<295::

19. Johnson FR, Mohamed AF, Zdemir S, Marshall DA, Phillips KA. How does cost matter in health-care discrete-choice experiments? Health Econ. 2011;20(3):323330. doi:10.1002/hec.1591

20. Fairchild AO, Reed SD, Johnson FR, Anglin G, Wolka AM, Noel RA. What is clearance worth? Patients stated risk tolerance for psoriasis treatments. J Dermatolog Treat. 2017;28(8):709715. doi:10.1080/09546634.2017.1329499

21. Goh SSL, Lai PSM, Liew SM, Tan KM, Chung WW, Chua SS. Development of a PATIENT-Medication Adherence Instrument (P-MAI) and a HEALTHCARE PROFESSIONAL-Medication Adherence Instrument (H-MAI) using the nominal group technique. PLoS One. 2020;15(11):e0242051. doi:10.1371/journal.pone.0242051

22. Reed Johnson F, Lancsar E, Marshall D, et al. Constructing experimental designs for discrete-choice experiments: report of the ISPOR Conjoint Analysis Experimental Design Good Research Practices Task Force. Value Health. 2013;16(1):313. doi:10.1016/j.jval.2012.08.2223

23. Hauber AB, Gonzlez JM, Groothuis-Oudshoorn CGM, et al. Statistical Methods for the Analysis of Discrete Choice Experiments: a Report of the ISPOR Conjoint Analysis Good Research Practices Task Force. Value Health. 2016;19(4):300315. doi:10.1016/j.jval.2016.04.004

24. Hauber AB, Han S, Yang JC, et al. Effect of pill burden on dosing preferences, willingness to pay, and likely adherence among patients with type 2 diabetes. Patient Prefer Adherence. 2013;7:937949. doi:10.2147/PPA.S43465

25. Schmieder A, Schaarschmidt ML, Umar N, et al. Comorbidities significantly impact patients preferences for psoriasis treatments. J Am Acad Dermatol. 2012;67(3):363372. doi:10.1016/j.jaad.2011.08.023

26. Sain N, Willems D, Charokopou M, Hiligsmann M. The importance of understanding patient and physician preferences for psoriasis treatment characteristics: a systematic review of discrete-choice experiments. Curr Med Res Opin. 2020;36(8):12571275.

27. Schaarschmidt ML, Umar N, Schmieder A, et al. Patient preferences for psoriasis treatments: impact of treatment experience: treatment experience impacts patient preferences. J Eur Acad Dermatol Venereol. 2013;27(2):187198. doi:10.1111/j.1468-3083.2011.04440.x

28. Schaarschmidt ML. Patient preferences for psoriasis treatments: process characteristics can outweigh outcome attributes. Arch Dermatol. 2011;147(11):1285. doi:10.1001/archdermatol.2011.309

29. Zagni E, Bianchi L, Fabbrocini G, et al. A real-world economic analysis of biologic therapies for moderate-to-severe plaque psoriasis in Italy: results of the CANOVA observational longitudinal study. BMC Health Serv Res. 2021;21(1):924. doi:10.1186/s12913-021-06866-7

30. Torbica A, Fattore G, Ayala F. Eliciting preferences to inform patient-centred policies: the case of psoriasis. PharmacoEconomics. 2014;32(2):209223. doi:10.1007/s40273-013-0126-6

31. Llamas-Velasco M, Daudn E. Reduced doses of biological therapies in psoriasis may increase efficiency without decreasing drug survival. Dermatol Ther. 2020;33(6):e14134. doi:10.1111/dth.14134

32. Hansel K, Bianchi L, Lanza F, Bini V, Stingeni L. Adalimumab dose tapering in psoriasis: predictive factors for maintenance of complete clearance. Acta Derm Venereol. 2017;97(3):346350. doi:10.2340/00015555-2571

33. Piaserico S, Gisondi P, De Simone C, et al. Down-titration of adalimumab and etanercept in psoriatic patients: a multicentre observational study. Acta Derm Venereol. 2016;96(2):251252. doi:10.2340/00015555-2209

34. Schaarschmidt M, Herr R, Gutknecht M, et al. Patients and physicians preferences for systemic psoriasis treatments: a nationwide comparative discrete choice experiment (PsoCompare). Acta Derm Venerol. 2018;98(2):200205. doi:10.2340/00015555-2834

35. Kelly A, Ryan C. Genital psoriasis: impact on quality of life and treatment options. Am J Clin Dermatol. 2019;20(5):639646.

36. Martnez-Ortega JM, Nogueras P, Muoz-Negro JE, Gutirrez-Rojas L, Gonzlez-Domenech P, Gurpegui M. Quality of life, anxiety and depressive symptoms in patients with psoriasis: a case-control study. J Psychosom Res. 2019;124:109780.

37. Tada Y, Ishii K, Kimura J, Hanada K, Kawaguchi I. Patient preference for biologic treatments of psoriasis in Japan. J Dermatol. 2019;46(6):466477.

38. Marques E, Paluch Z, Boh P, Slana O, Blek J, Hercogov J. The safety profile of biologic agents in comparison with non-biologic systemic agents, and topical compounds in the management of psoriasis-A 30-month prospective, observational cohort study. Int J Clin Pract. 2021;75(12):e14915. doi:10.1111/ijcp.14915

39. Campanati A, Ganzetti G, Giuliodori K, Molinelli E, Offidani A. Biologic therapy in psoriasis: safety profile. CDS. 2016;11(1):411. doi:10.2174/1574886310666151014115532

40. De Simone C, Fargnoli MC, Amerio P, et al. Risk of infections in psoriasis: assessment and challenges in daily management. Expert Rev Clin Immunol. 2021;17(11):12111220. doi:10.1080/1744666X.2021.1997592

41. Talamonti M, Galluzzo M, Chiricozzi A, et al. Management of biological therapies for chronic plaque psoriasis during COVID-19 emergency in Italy. J Eur Acad Dermatol Venereol. 2020;34(12):e770e772. doi:10.1111/jdv.16841

42. Kauf TL, Yang JC, Kimball AB, et al. Psoriasis patients willingness to accept side-effect risks for improved treatment efficacy. J Dermatological Treatment. 2015;26(6):507513. doi:10.3109/09546634.2015.1034071

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Patient preference for biologic treatments of psoriasis | PPA - Dove Medical Press

Psoriatic arthritis (PsA) is an inflammatory arthritis of the joints that occurs in some people who have psoriasis. Both PsA and psoriasis are autoimmune diseases, meaning they are caused by a persons own immune system going astray. Its long been known that people who have one autoimmune condition are more prone to developing others.

Its not surprising, then, that some people with PsA also develop an autoimmune thyroid disorder.

The thyroid is a butterfly-shaped gland at the base of the throat. For such a small part of the body, it can wreak a lot of havoc. This is because the thyroid has many crucial functions, including regulating heartbeats and controlling how speedy or sluggish your metabolism is.

Even among the general population, thyroid disease is not rare. According to theAmerican Thyroid Association (ATA), an estimated 20 million Americans have a thyroid condition. But because symptoms can be nonspecific and hard to attribute directly to the thyroid, up to 60 percent of people are unaware they have it, the ATA says.

Like other glands, the thyroid excretes hormones into the body. When it pumps out too little (hypothyroidism) or too much (hyperthyroidism), a person can feel tired or amped up and may gain or lose weight. Other common symptoms of thyroid problems include depression, constipation, and difficulty concentrating from too little of the hormones, and nervousness, palpitations, and insomnia from too much.

Autoimmune conditions that affect the thyroid include Hashimoto's disease, which causeshypothyroidism, and Graves disease, which causes hyperthyroidism.

With some autoimmune diseases, such as rheumatoid arthritis, people develop autoantibodies, which mistakenly target the persons own tissue, as part of the disease. But those with psoriatic arthritis do not develop these autoantibodies, says Andrew Wang, MD, PhD, a rheumatologist at Yale Medicine and an assistant professor of immunology at the Yale School of Medicine in New Haven, Connecticut.

RELATED:Psoriatic Arthritis vs Rheumatoid Arthritis: What's the Difference?

It's more common for people with autoantibody diseases to also develop autoimmune thyroiditis than it is for those with conditions that dont make autoantibodies, Dr. Wang explains. This means that the co-occurrence rate between autoimmune thyroid disease and PsA is not as high as for other autoimmune diseases, like RA, he says.

Nonetheless, even among people with psoriasis, whether or not they also have PsA, rates of thyroid disease are higher than in the general population. A meta-analysis by Chinese researchers published in BMJ Open in January 2022 found that people with psoriasis have a higher prevalence of autoimmune thyroid disease, most commonly hypothyroidism.

Very few studies have examined the rate of thyroid disease specifically in people with PsA. In a review of the two diseases published in Cureus in January 2021, California researchers found just 45 high-quality articles on the topic.

Most of the studies they examined do show a positive association, meaning if someone has one condition they were more likely than the general public to have the other. But six of the studies showed no increased connection.

The researchers found that the coupling was more common in people who are obese. In some studies, young women were also more prone, but in other research this wasnt the case. People who developed psoriasis in midlife or later, known as late-onset disease, were also more likely to have a thyroid condition than those with early onset.

Because of the small number of studies, though, the researchers could not provide a concrete explanation for the concurrence of the two conditions. More prospective and retrospective studies are needed to assess the association between them before any conclusion can be made, they wrote.

The good news is that regardless of what medications a person is taking to control their psoriatic arthritis, they can continue on them while undergoing treatment for any thyroid condition, Dr. Wang says. Among all the drugs, none of them would affect psoriatic arthritis treatment, he says.

Intriguingly, the Cureus review found hints that some thyroid treatments may actually improve PsA symptoms. For example, the drug propylthiouracil, which is used to treat hyperthyroidism, was found in several studies to clear psoriatic lesions. And two studies noted that after a thyroidectomy (a surgical procedure for hyperthyroidism that removes part of the thyroid), there was marked improvement in psoriatic skin lesions.

Because symptoms of thyroid disease may be vague, doctors dont always think to check the thyroid when PsA patients complain of things like fatigue, insomnia, or weight gain, Wang says.

Its important for people with psoriatic arthritis to make sure your doctor is listening to you, he says. If youre experiencing new or unusual symptoms, I would advocate that your doctor consider the thyroid, he says. A simple blood test checking for thyroid hormone levels can reveal whether thats the source of the problem.

The rest is here:
Psoriatic Arthritis and Thyroid Disease Can Appear Together - Everyday Health

A Scots make-up artist (MUA) with a 'zombie-like' skin condition has bravely opened up on feeling 'judged' by people who think she has a 'contagious rash'.

Danielle Robertson, 32, was diagnosed with psoriasis aged 16 and has endured crippling flare-ups ever since.

Psoriasis is believed to be related to the immune system where sufferers produce more skin cells, causing flaky patches of skin which form scales.

'Scunnered' with 'hiding away' and determined to help others feel good in their own skin, Danielle recently exposed her uncomfortable 'patchy and spotty' flare-up to over 80,000 followers on social media.

While the brave beautician joked she looked like 'an apocalyptic zombie', she demonstrated the 'transformative' power of make-up that 'camouflages' her insecurities.

Danielle, from Bishopton, Renfrewshire told the Record: "It's human nature for people to stare at something different but it has really knocked my confidence in the past.

"Psoriasis can be mistaken for lots of things that are contagious, like impetigo, or seen as dirty. Clients worry I have something like that and ask 'what's on your skin?' which makes me self-conscious.

"After Christmas I got a bad flare up and felt so down. I was stuck in the house, hiding away which isn't great for a public-facing job like mine.

"I was scunnered and wanted to embrace my skin condition to show others that it's okay to have it."

So talented Danielle decided to lay bare her condition on YouTube and TikTok.

Lengthy videos explain her psoriasis before showing how products can conceal flare ups.

"I'm no doctor and I don't claim to be," she added.

"I also think people should be free to go barefaced, no matter what their skin issue is.

"But to me, make-up is like camouflage. If showing other people how it has helped me can make a difference to them, then it's worth it."

Going au naturale is a far cry from Danielle's glamorous career in beauty.

The high-flyer has painted faces in Los Angeles and Dubai as a global make-up artist for Urban Decay.

Alongside a constant stream of bridal clients, Danielle's nine-to-five is with beauty giant, L'Oral who own luxury names such as Armani and Yves Saint Laurent.

"I've had a number of pinch me moments," she said.

"But amongst all the highs, I've had times where I felt like I couldn't go into work as my psoriasis was so bad. I would feel so conscious.

"That's why I wanted to break down the stigma with posting about it."

She added: The reaction has been amazing and I feel it's now almost part of my online profile.

"To anyone else suffering from any skin condition; don't be fazed by something that's just a phase. It does get better and there are products out there to help."

You can follow Danielle by heading to her Facebook page Danielle Roberts Make-Up Artist, or at at daniellerobertsmua on Instagram and TikTok as well as her YouTube channel.

Psoriasis affects around two in 100 people in the UK, find more information on the NHS website.

Don't miss the latest news from around Scotland and beyond - Sign up to our daily newsletter here .

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Scots make-up artist with 'zombie' psoriasis helping others to transform problem skin - Daily Record

Rashes can be thought of as a dysfunctional community of skin cells. Your skin harbors dozens of distinct cell types, including those that form blood vessels, nerves and the local immune system of the skin. For decades, clinicians have largely been diagnosing rashes by eye. While examining the physical appearance of a skin sample under a microscope may work for more obvious skin conditions, many rashes can be difficult to distinguish from one another.

At the molecular level, however, the differences between rashes become more clear.

Scientists have long known that molecular abnormalities in skin cells cause the redness and scaliness seen in conditions like psoriasis and eczema. While almost all the various cell types in your skin can release chemicals that worsen inflammation, which ones leads to rash formation remains a mystery and may vary from patient to patient.

But molecular testing of skin rashes isnt a common practice because of technological limitations. Using a new approach, my colleagues and I were able to analyze the genetic profiles of skin rashes and quantitatively diagnose their root causes.

Traditional genetic analyses work by averaging out the activity of thousands of genes across millions of cells.

Genetically testing tissue samples is standard practice for conditions like cancer. Clinicians collect and analyze tumor biopsies from patients to determine a particular cancers unique molecular characteristics. This genetic fingerprint helps oncologists predict whether a cancer will spread or which treatments might work best. Cancer cells lend themselves to this form of testing because they often grow into recognizable masses that make them easy to isolate and analyze.

But skin is a complex mixture of cells. Collapsing these unique cell communities into a single group may obscure genetic signatures essential to diagnosis.

Recent technological advances called single-cell RNA sequencing, however, have enabled scientists to preserve the identity of each type of cell that lives in the skin. Instead of averaging the genetic signatures across all cell types in bulk, single-cell RNA sequencing analyses allow each cell to preserve its unique characteristics.

Using this approach, my colleagues and I isolated over 158,000 immune cells from the skin samples of 31 patients. We measured the activity of about 1,000 genes from each of those cells to create detailed molecular fingerprints for each patient. By analyzing these fingerprints, we were able to pinpoint the genetic abnormalities unique to the immune cells residing in each rash type. This allowed us to quantitatively diagnose otherwise visually ambiguous rashes.

We also observed that some patients had treatment responses consistent with what we expected with our predicted diagnoses. This suggests that our concept could viably be expanded for further testing.

To make our approach available to clinicians and scientists, we developed an open source web database called RashX that contains the genetic fingerprints of different rashes. This database will allow clinicians to compare the genetic profile of their patients rashes to similar profiles in our database. A closely matching genetic fingerprint might yield clues as to what caused their patients rash and lead to potential treatment avenues.

The rapid development of drugs that target the immune system in recent years has inundated doctors with difficult treatment decisions for individual patients. For example, while certain drugs that act on the immune system are known to work well for conditions like psoriasis or eczema, many patients have atypical rashes that cant be precisely diagnosed.

An open source database like ours could help enable clinicians to profile and diagnose these rashes, providing a stepping stone to choose a suitable treatment.

Furthermore, chronic inflammatory diseases that affect organs other than the skin share similar genetic abnormalities. Lab tests that can illuminate the root causes of skin diseases can likely be expanded to many other conditions.

Our RashX project initially focused on just two very common types of rashes, psoriasis and eczema. It is unknown whether other types of rashes will have similar genetic profiles to psoriasis and eczema or instead have their own unique fingerprints. It is also unclear which parts of the fingerprint would best predict drug response.

But RashX is a living web resource that will grow more useful as more scientists collaborate and contribute new data. Our lab is also working to simplify the process of developing genetic profiles of rashes to make participating in this area of research more accessible for clinics around the world. With more data, we believe that projects like RashX will make precision testing for rashes an essential next step in diagnosis and treatment.

This article is republished from The Conversation under a Creative Commons license. Read the original article.

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What is that rash? - ASBMB Today