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Category Archives: Transhuman News
Genome-based cholesterol drug boosts heart health – Nature.com
Posted: March 19, 2017 at 3:58 pm
Juan Gaertner/Science Photo Library
An LDL, or 'bad' cholesterol molecule (round) binds to an LDL receptor protein (pink) in this illustration.
For years, medical researchers have hoped that a burgeoning class of cholesterol drugs targeting a protein called PCSK9 could be the next generation of blockbuster treatments. Now, a large clinical trial has demonstrated that this approach can lower the risk of heart disease. But its still unclear whether these drugs which attempt to mimic a beneficial genetic mutation will be the breakthrough that scientists and pharmaceutical companies had imagined.
The results, published in the New England Journal of Medicine1 and presented at the American College of Cardiology conference in Washington DC on 17 March, show that a drug called evolocumab (Repatha) reduced the risk of cardiovascular death, heart attack and stroke by about 20% in patients who were already taking other cholesterol-controlling drugs called statins. This reduction in risk is roughly the same magnitude as patients might see from taking statins alone. On another measure that also included hospitalizations for conditions that cause reduced blood flow to the heart, evolocumab reduced the risk by 15%.
The US Food and Drug Administration (FDA) approved evolocumab in 2015 for use in some patients with high cholesterol, based on data showing that the drug could lower levels of bad low-density lipoprotein (LDL) cholesterol circulating in the blood by approximately 60%2. But researchers didnt have evidence then that the drug could also protect against heart attacks or strokes.
It is an exceptionally important study, says Harlan Krumholz, a cardiologist at Yale University in New Haven, Connecticut. The promise of these drugs has been very clear. Whether they would deliver on that promise was suspected, but not known.
The new results from a trial with more than 27,500 participants vindicate the concept that inhibiting PCSK9 can control cholesterol and heart-disease risk. The question now is whether physicians and health-care payers will consider that benefit great enough to warrant the annual price tag of roughly US$14,000.
The PCSK9 protein helps to control the amount of bad cholesterol in the blood by regulating the number of LDL receptor proteins on cell surfaces, which take LDL out of circulation. People with naturally occurring mutations in the PCSK9 gene have unusually low levels of bad cholesterol and up to an 88% lower risk of developing heart disease.
Turning that information into a successful treatment, however, has been a challenge. Several drugs that target PCSK9 are either in development or have been approved, but evolocumab is the first to report results from such a large trial.
Pfizer, based in New York City, abandoned a PCSK9-blocking drug called bococizumab last year after running into problems during patient trials. Bococizumab, like evolocumab, is an antibody that binds to the PCSK9 protein. But participants who received bococizumab tended to form an immune response against the drug, which interfered with the treatments3.
And the FDA approved evolocumab, made by Amgen in Thousand Oaks, California, only for certain patients, such as those with a hereditary condition that causes extremely high levels of LDL.
Now that the data on evolocumab are in, some health-care payers such as insurance companies and government programmes might be more willing to shoulder the treatments steep cost. But any new cholesterol drug faces stiff competition from cheaper statins, which have been used to control LDL levels for decades.
Some analysts say that demonstrating a statistically significant heart-health benefit would not be enough to ensure the PCSK9 drugs status as the next big thing. The more important hurdle is the one that payers have imposed restricting access to these medicines, wrote analysts at the investment bank Leerink Partners in New York City, in a report released 15 March.
To cross that threshold, Leerinks analysts estimated that evolocumab would need to reduce cardiovascular risks by 25% or more.
Overall, the risk reduction was less than what might have been expected based on how much evolocumab reduces the amount of LDL cholesterol in the body, says Krumholz. But the evidence of a benefit is strong enough that he will discuss the drug as an option with his patients, he adds.
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Genome-based cholesterol drug boosts heart health - Nature.com
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Genome Programme launches consortium – Gulf Times
Posted: at 3:57 pm
More than 90 genomics researchers attended the recent launch of Qatar Genome Programmes (QGP) Research Consortium at Qatar Foundation headquarters in Education City. The consortium is the latest step in QGPs precision medicine implementation efforts. Participants at the launch represented several institutions in Qatar, including QGP, Qatar Biobank, Sidra Medical and Research Center, Hamad Medical Corporation, Weill Cornell Medicine-Qatar, Qatar Biomedical Research Institute, Qatar Computing Research Institute, and Qatar University. Several of the investigators also have international collaborators. Dr Asmaa al-Thani, chairperson of Qatar Genome Programme Committee and vice chair of Qatar Biobank, said inaugurating the Research Consortium is a critical next step on the path towards precision medicine. By bringing together so many researchers from a variety of institutions, Qatar Genome Programme is helping co-ordinate the nationwide effort to map the Qatari genome. The investigators will work on exploring the extensive genotypic and phenotypic data sets produced by Qatar Biobank and QGP in an effort to identify key features of the Qatari genome. This knowledge will contribute to the development of individualised disease treatment and prevention methods, which in turn will lead to more efficient and effective outcomes. One of the key pillars of the Qatar Genome Programmes strategy is forging research partnerships with institutions in Qatar, as well as fostering international collaborations, said Dr Said Ismail, manager of QGP. This consortium, which involves key stakeholders from across the research spectrum in Qatar, significantly strengthens those relationships. By consolidating genomic research efforts in Qatar, QGP hopes to leverage the widest range of resources and expertise, as well as avoid duplication or contradiction in research. Also, QGPs publication strategy assures that different entities in Qatar get equal opportunities to work with the data gathered through Qatar Biobank. So far, Qatar Biobank has collected samples from more than 6,000 volunteers, including more than 5,000 Qataris. Of that sample group, QGP has sequenced more than 3,000 genomes.
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Genome Programme launches consortium - Gulf Times
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Before humanity looks to stars, it should look to morals for continuity – The Vermilion
Posted: at 3:57 pm
Photo via spacetravel.jp
One of the most visionary leaders in the world today is Elon Musk. He made his fortune by co-founding PayPal, which changed internet commerce and made Musk one of the wealthiest people on the planet.
Musk is currently the CEO of Tesla, which specializes in solar and electric energy sources, such as their successful cars, the Gigafactory, the Powerwall battery and recent plans to solve Australias electricity crisis. His recent passion has been space exploration, so he founded SpaceX, a private corporation whose ultimate goal is Mars colonization. Youve likely heard of SpaceX for their ongoing project of vertically landing rockets on floating platforms.
An ongoing theme of my column is how technological innovation, if used properly, has allowed us to have a quality of life unimaginable to previous generations. Many futurists believe the next step is to leave Earth and begin exploring and settling in other worlds. It will push the limits of our understanding of science and technology, as well as require the bravest men and women we can find (there is a high probability of many of these early trips being one-way).
Physicist Stephen Hawking has been one of the most prominent supporters of space exploration. He believes it is essential for human survival, arguing that, We are entering an increasingly dangerous period of our history, and we must learn to live on other planets to avoid disaster in the next hundred years, let alone the next thousand or million.
Musk himself has a similar view, saying he believes, I really think there are two fundamental paths (for humans): One path is we stay on Earth forever, and some eventual extinction event wipes us outThe alternative is become a spacefaring and multi-planetary species.
On one hand, their arguments are compelling. The earths environment is in crisis, and sustainable off-world habitats will allow humanity to survive beyond whatever happens to our home planet. More cynical people have questioned this, wondering why people need to travel elsewhere when we cannot even take care of this planet why spread our tendency to self-destruct to other places?
The catch to any of this is, of course, cost. None of this is cheap, especially since it is new technology. Prices will not decrease until mass production, which is a long way away. This may result in a further divide between the wealthy and the middle and lower classes. Those who cannot buy their way off the planet will be condemned to remain here. Space travel will not be a viable option for the human race as a whole until it becomes widely affordable.
Money is a limiting factor for so many of these futurist projects. Consider human longevity the ability to extend life beyond what should be naturally possible. Imagine living until 200 years old, or maybe even longer. Enormous amounts of money are being spent on medical research to find the root causes of aging, and so far, 120 years appears to be a limit; only one person has lived beyond that.
I believe these projects are worth it. Humanity needs to continue pushing itself mentally, scientifically and technologically if it wants to survive. Perhaps most importantly, we need to improve morally. All of this progress has the potential for enormous downsides, and hopefully, those who are leading the way can instill their sense of wonder and duty in the rest of us following their path.
humanity morals space
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Before humanity looks to stars, it should look to morals for continuity - The Vermilion
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Warnings after skin creams used to treat eczema linked to dozens of fire deaths – Mirror.co.uk
Posted: at 3:57 pm
Skin creams have been linked to dozens of deaths in fires, leading to new warnings by manufacturers.
Products used to treat conditions like eczema and psoriasis put users at risk because the paraffin in them can soak into their bedding or clothes, making them flammable.
The medicines regulator has updated its guidance and it says all creams containing paraffin should carry a warning.
There have been 37 deaths in England since 2010 linked to the creams, despite warnings going back more than ten years.
Carol Hoes husband Philip died at Doncaster Royal Infirmary in 2006 when sparks from a cigarette ignited his moiturising cream.
She told Radio 5 Live : Philip sneaked off on to a landing for a sneaky cigarette, a gust of wind must have caught the lighter, and it set fire to him.
Within seconds Mr Hoe, who was having treatment for psoriasis, was engulfed in flames and he died shortly after.
He was covered with 90% burns, said Mrs Hoe.There was nothing they could do.
Christopher Holyoake died in a house fire in September 2015, after his skin cream, now known to be flammable, caught fire.
The coroner at the inquest into the death of 63-year-old Christopher Holyoake in Leicester in 2015 heard his bedding was covered in residue from an over-the counter dermatological cream called E45, according to the BBC .
When the flame from his cigarette lighter came into contact with the bedding, the residue acted as an accelerant, giving Mr Holyoake little chance of surviving the fire.
After the inquest the coroner wrote to the manufacturer of E45 - outlining her concerns there were no warnings on the packaging about the product being highly flammable.
At his inquest, the coroner drew attention to the dangers. The Medicines and Health Care Products Regulatory Agency issued two more warnings, but deaths have gone on.
John Smith, Chief Executive of PAGB, (Proprietary Association of Great Britain), the UK trade association for manufacturers of branded over-the-counter medicines, said: We want to reassure people that the normal use of emollients in the home is considered appropriately safe provided the products are used in accordance with the on-pack instructions and accompanying patient information leaflet.
Manufacturers of emollients are not at present required by regulation or statute to include fire safety warnings on packaging.
"Safety is nonetheless of paramount importance to the OTC medicines industry.
"In the light of this investigation, PAGB is looking to explore this issue further with the member companies and relevant bodies to see if in future, safety warnings should be added to on-pack labelling for all paraffin based emollients as standard practice across the industry, a step which some manufacturers have already taken.
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Warnings after skin creams used to treat eczema linked to dozens of fire deaths - Mirror.co.uk
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Eli Lilly chasing psoriasis jackpot with Taltz – Indianapolis Business Journal
Posted: at 3:56 pm
A man and a woman are barefoot on a couch, snuggling and smiling. In the background, a guitar starts strumming.
When youre close to the people you love, the television announcer says, does psoriasis ever get in the way of a touching moment?
The minute-long commercial, featuring lots of bare shoulders, midriffs and swimsuits, promotes a new drug by Eli Lilly and Co. called Taltz that treats red, scaly patches of skin caused by moderate-to-severe plaque psoriasis.
Its a painful, itchy condition that afflicts more than 5 million Americanswho spend an estimated $5 billion a year on drugs and medical treatments to remedy their discomfort.
In the commercial, couples with smooth skin frolic in swimming pools and take dreamy walks in the woods.
Now is your chance for completely clear skin, the announcer says.
The commercial, and several others like it, are part of one of the most closely watched drug campaigns in recent years. Taltz, which hit the market last year, is taking on an armful of older treatments, including creams, lotions, pills and injectables, such as Amgens Enbrel and AbbVies Humira.
Lilly said the drug helped six times as many patients completely clear up their skin irritations as Enbrel, according to data it collected in two large trials dating back to 2006.
In the meantime, Lilly is also working aggressively to catch up to a competing drug called Cosentyx, which hit the market in 2015, beating Lilly to the punch by a year and already ringing up much higher sales.
For Lilly, the stakes are high. The companys traditional portfolio of once-brisk-selling products has slid into decline in recent years amid patent expirations. Sales of cancer drug Alimta tumbled 8 percent last year, while antidepressant Cymbalta fell 9 percent and antipsychotic Zyprexa plunged 23 percent.
Now, its up to new products like Taltz to pick up the slack. Last year, Taltz rang up worldwide sales of $113 million, the bulk of it in the fourth quarter. The Indianapolis drugmaker has spent millions of dollars and nearly a decade to develop and launch the drug.
Some experts say Taltz could become a blockbustera product that generates more than $1 billion a yearwithin a decade. Jami Rubin, a drug analyst at Goldman Sachs, predicts that sales of Taltz could hit $2.5 billion a year by 2025.
Lilly officials say the drug is off to a good start.
We are pleased with early uptake for Taltz, Dave Ricks, who took over as Lillys CEO in January, recently told analysts.
But Lillys efforts to turbocharge Taltz sales are just getting started. Last month, the company released 14 scientific papers on Taltz at the American Academy of Dermatologys annual meeting, touting the drugs benefits. One paper said Taltz outperformed a competing product, Johnson & Johnsons Stelara, in a head-to-head comparison after 24 weeks of treatment.
Lilly also is seeking approval to market the drug to treat joint pain and back stiffness, which could add billions of dollars more to the market opportunity.
The drug works by attacking psoriasis not just as a skin condition, but as a disorder of the bodys immune system. Psoriasis is caused by certain chemicals when they falsely sense the body is being attacked.
When theres a trigger, these chemicals become very excited, said Dr. Olawale Osuntokun, senior medical director for Lilly. Theyre a bit more active than they ought to be. And this results in the skin lesions that you see in plaque psoriasis.
Taltz works by using an antibody to inhibit a protein called interleukin 17, thus interrupting the chemical inflammation, he said.
Lilly says that up to 90 percent of psoriasis patients using Taltz have a significant improvement in their plaque, and about 40 percent achieve completely clear skin.
Its long-term sales prospects might hinge, in part, on whether doctors gravitate toward Taltz or Cosentyx, which also binds to interleukin 17.
Switzerland-based Novartis International AG won FDA approval for Cosentyx in January 2015, giving Novartis bragging rights for first-in-class.
Both drugs are biologicsgenetically engineered proteins derived from human genesand work well, dermatologists say.
Biologics in general have been highly effective and life-changing for many people with psoriasis, said Dr. Scott Fretzin, a dermatologist and partner at Dawes Fretzin Dermatology Group LLC in Indianapolis.
He and his partner, Dr. Ken Dawes, enrolled patients in clinical trials for Taltz. Fretzin said they were amazed by the results and that the drug provided the highest efficacy rate for treatment of psoriasis.
In my clinical practice, it has been shown to be extremely effective and really does work in almost everybody, Fretzin said.
With its big lead, Cosentyx had sales last year of $1.1 billion, and analysts forecast they might reach $2.9 billion a year by 2020.
Some observers think Lilly has more than a fighting chance to catch up. In November, U.S. dermatologists surveyed by research firm Spherix Global Insights reported a significant increase in familiarity with and use of Taltz.
The research firm concluded that current users of Taltz expected to double their use in the next three months, while one-third of non-users intend to try Taltz.
Though Cosentyx benefits from its first-to-market status and dermatologist comfort, Taltz appears to be making headway as a more efficacious option, with slightly more convenient dosing options and a high-quality patient support program, Spherix reported.
Novartis, of course, isnt backing down. This month, it released an analysis concluding that plaque-psoriasis patients treated with Cosentyx rapidly regained clear or almost clear skin following a short relapse caused by a treatment pause.
For patients, completely clear skin could be an expensive proposition. Lilly said the list price for Taltz is about $4,460 a month, or more than $53,000 a year. To make prices affordable, Lilly said, it has instituted a co-pay program for commercially insured patients that will cost $5 to $25 a month for the first two years.
Cosentyx is similarly priced. Its list price is $56,000 for an annual, 13-dose maintenance package. But Novartis said it offers financial assistance, and that patients without third-party insurance might qualify to receive the drug free through a company foundation.
Even so, plaque psoriasis is a chronic condition that needs regular attention, so treatments can last many years. For patients, that could mean years of expensive payments. For Lilly, it could mean a road to financial success.
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New ‘gene silencer’ drug reduce cholesterol by over 50 percent – Science Daily
Posted: at 3:56 pm
The findings come from the largest trial yet to test the safety and effectiveness of this kind of therapy. The technique, known as RNA interference (RNAi) therapy, essentially 'switches off' one of the genes responsible for elevated cholesterol.
Researchers from Imperial College London and their colleagues, who conducted the trial, say the twice-a-year treatment could be safely given with or without statins, depending on individual patient needs. Eventually, inclisiran could help to reduce the risk of heart attacks and stroke related to high cholesterol.
"These initial results are hugely exciting for patients and clinicians," said Professor Kausik Ray, lead author of the study from the School of Public Health at Imperial.
"We appear to have found a versatile, easy-to-take, safe, treatment that provides sustained lowering of cholesterol levels and is therefore likely to reduce the risk of cardiovascular disease, heart attacks, and stroke. These reductions are over and above what can be already be achieved with statins alone or statins plus ezetemibe, another class of cholesterol-lowering drug.
Elevated levels of low-density lipoprotein (LDL) cholesterol can lead to cardiovascular disease and blood vessel blockage, leading to an increased risk heart attacks and stroke in patients.
Statins are currently the standard treatment for high cholesterol, combined with exercise and healthy diet, as they reduce levels in the blood and therefore help to prevent heart attacks and stroke.
However, many patients are unable to tolerate the highest doses and they need to be taken consistently. Forgetting to take them or taking them infrequently reduces the expected benefit from these treatments. Also, in some patients cholesterol levels can remain high despite being given the maximum doses of statins.
Now, this new phase 2 clinical trial has confirmed the effectiveness of injecting inclisiran for reducing cholesterol that can be taken alone or potentially combined with statins for maximum effect.
In the study, researchers gave 497 patients with high cholesterol and at high risk of cardiovascular disease either inclisiran at varying doses, or placebo. Seventy-three per cent of these patients were already taking statins, and 31 per cent were taking ezetimibe. Participants, who were recruited from Canada, USA, Germany, Netherlands, and the UK, were excluded if they were taking monoclonal antibodies for cholesterol lowering.
Patients were given different doses of inclisiran or placebo via subcutaneous injection, either via a single dose, or via a dose on day one and another at three months. They were followed up regularly for a subsequent eight months and tested for blood cholesterol and side effects.
The researchers found that just one month after receiving a single treatment of inclisiran, participants' LDL cholesterol levels had reduced by up to 51 per cent.
In those on a single dose of 300 mg, cholesterol levels were reduced by 42 per cent at six months. In the matched placebo group, cholesterol levels had increased by two per cent within that time frame.
In those on two doses of 300 mg, cholesterol levels were reduced by up to 53 per cent at six months. Moreover, cholesterol levels had gone down for all patients in this group, and 48 per cent of them had achieved cholesterol levels (below 50 mL/dL).
In all patients, cholesterol levels stayed lower for at least eight months. No extra side effects were seen in the study group compared to the placebo group.
The study will now follow up patients for a further four months (one year total follow up). The results from this trial, known as ORION-1, are published in the New England Journal of Medicine, and are presented today at the American College of Cardiology's 66th Annual Scientific Session in Washington.
The authors say the results show the drug acts quickly to reduce cholesterol levels by as early as two weeks post-injection, while also giving a prolonged effect when given in two doses over a year. Therefore, the next step is to conduct an extended study, using more patients and for a longer period of time, to determine whether these reductions in cholesterol translate into a reduction in heart attacks and strokes. Professor Ray said: "We are keen to enter the next phase of development to assess long-term safety and to see how this novel approach might translate into improvements in patient health."
Aside from its effectiveness, the authors point out that because inclisiran acts on a different biological pathway to statins, the two drugs would likely be combined for the best results. Professor Ray said: "Even the single dose of inclisiran appears to lower cholesterol by 35-40% at eight months. We could essentially experiment with how often to give the drug based on levels of cardiovascular risk for each patient. Lower risk patients could in theory have once yearly injections whereas higher risk patients might have two injections a year."
The authors emphasise that because this is an early-phase study, and because this is one of the first clinical studies on this type of drug, more research is needed before it can go to market.
He added: "The effectiveness of statins and other cholesterol-lowering treatments such as monoclonal antibodies relies on patients' ability to take them consistently. Therefore, giving inclisiran up to twice yearly at a GP surgery, much in the same way flu vaccinations are provided, might be more effective."
"We believe that these clinical visits might only be twice a year at most, so ultimately, they are more convenient and more effective for patients and their health."
Inclisiran is being developed by Alnylam Pharmaceuticals and The Medicines Company. This study was funded by The Medicines Company, and performed by the sponsors and World Wide Clinical Trials (Nottingham, UK).
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New 'gene silencer' drug reduce cholesterol by over 50 percent - Science Daily
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New report gives cautious support for embryonic gene editing in humans – PRI
Posted: at 3:56 pm
Last month, the National Academy of Sciences and the National Academy of Medicine released areport about the use of gene editing techniques like CRISPR on human embryos. The new report, coming from two globally respected scientific organizations, suggests the technique could be warranted in certain cases not just in the laboratory, but in real life.
In an article for Sciencemagazine, staff writer Jocelyn Kaiser called the report a yellow light for embryonic gene editing, which has long been off the table in the United States. Thats because when it comes to editing human embryos, there are thorny ethical concerns on both sides of the debate and according to Kaiser, the reports authors proceed cautiously.
So, what the report says, is, there are many reasons why we need to be very careful about editing the human germline that is, making changes to eggs or sperm or embryos that could be passed on to the next generation, Kaiser says.
When might that yellow light turn green?
There are a few rare instances where we may want to do it, she explains, and that is families that have a severe genetic disease that they are going to pass on to their child, but they can't prevent it any other way, that we might want to allow [gene editing] to happen in those cases.
Although genetic editing could protect embryos from devastating medical conditions, Kaiser says that many people worry its application wouldnt end there.
If we do let it happen, then it could sort of open the door to many other changes to embryos that we would not maybe feel so comfortable with, she says. Like modifying an embryo to make it a better athlete, or make it smarter, or have blue eyes, or whatever.
Those potential designer edits bring up issues of access. What about the people who didn't have the ability to do this? Kaiser wonders. Would they be left out? Not only that, the effects of embryonic edits would ripple through generations.
If you change the DNA of an embryo versus an adult or a child, that change will be passed on to that embryos descendants, she says. That's something you couldn't stop once you've done it. It's going to be passed on.
And so that's one reason why people are worried about doing this. Do you want to start tinkering with our genes in that way?
We might not get much choice: Scientists in China have already reported genetically editing embryos. Ultimately, Kaiser says, the national academies report is not binding its just advice. Not only to the United States, but to other countries. And they can decide if they want to follow the advice.
But these are very respected bodies, and when they offer their advice on something, it will it will have a lot of influence.
This article is based on aninterviewthat aired on PRI'sScience Friday.
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New report gives cautious support for embryonic gene editing in humans - PRI
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The Tao of Steve King: Master of the Politically Incorrect – Progressive.org
Posted: at 3:55 pm
It's a federal crime to watch animals fight, but it's not a federal crime to watch people fighting? There's something wrong with the priorities of people that think like thatthat raise animals above people. I will not raise animals above people!
Meet Iowa congressman Steve King, defending the classic American sport of dog fighting back in 2012.
King harkens from Denison, a small town in Western Iowa best known for producing Its a Wonderful Life, actress Donna Reed. I grew up in a small town just two hours from Denison. Unlike the rest of Iowa, where population decline has reduced the states representation in Washington, DC, from eight congressional seats in 1960 to four today, over the same time period Denison has nearly doubled in size, from a population of 4,930 to 8,390. But heres the big difference: Back in the old days, Denison was almost all white.
Today, whites make up only 48.6 percent of the population and Latinos, now 46.9 percent, are on a trajectory to become the majority soon. In fact, 59 percent of students enrolled in Denison's K-12 public school system are of Latino descent.
The demographic changes in King's home town apparently drove him to run for the Iowa state Senate in 1996, where he focused on such pressing issues as English-only bills. He alsounsuccessfullytried to pass a bill he called the "God and Country Bill, which Des Moines Register columnist Chuck Offenburger described as an "attempt to end the requirement that Iowas school children receive a multicultural, non-sexist and global education."
While running for Congress in 2002, King braggedthat he waslabeled by the Des Moines Register as Iowas most politically incorrect state legislator, and Im very proud of that. In early 2004, he made national news by shrugging-off the atrocities of Abu Ghraib as "hazing."
King brags that he's been labeledIowas most politically incorrect state legislator, and Im very proud of that.
That was just the beginning. On nearly every issue, King displays an impressive knack for both bigotry and ignorance.
Here are some beauties:
Last July, King defended the Confederate flag he keeps on his desk in his congressional officean odd racist homage in any circumstance, but especially strange for a Congressman representing a northern Union state that lost more troops, per capita, than any other state during the Civil War. King refused to take the flag down, using the old racist saw that the Civil War was just about states rights and only a "small part of if was about slavery."
A few weeks before that, King tried to have the House vote on an amendment to prevent civil rights hero Harriet Tubman from appearing on the $20 billcalling the removal of white male Andrew Jackson both sexist and racist. In reality, Andrew Jackson was never slated to leave the $20 billhe still will have one side of the bill to himself, with Tubman replacing the image of the White House.
All this was a fitting build-up for his recent racist coup de grace, when he tweeted:
He later added that his goal was "an America that's just so homogenous that we look a lot the same, from that perspective."
This meshes with King's previous comments, including his statement that whites have done their share to "contribute to civilization" and asked, "Where are these contributions that have been made by these other categories of people?"
Ugh.
In the 2012 election, Iowa Democrats believed they had a great shot to finally get rid of King. Iowa lost a congressional seat and the new district King would be in was an area President Obama won 53 percent to 45 percent in 2008. The popular former First Lady of Iowa, Christie Vilsack, was convinced to runthe table was set for King's final dinner.
But there was no Obama bump the second time around: Romney won the district and King emerged victorious with 53 percent of the vote.
In 2014, Democrats got a decorated Iraq war veteran to face-off against King (a hawk on recent wars, although he sought four deferments to get out of going to Vietnam). But 2014 was another wave year for Republicans and King won in a landslide.
In 2016, Kim Weaver ran a spirited campaign against King, but Donald Trump won the district by a breathtaking 61 percent to 34 percent margin on his way to carrying all four of Iowa's districts and winning the state for the GOP for only the second time since 1984.
In other words, King owes his electoral success to a combination of ten years as the incumbent in a deep-red district and three recent elections in which national political headwinds blew away his Democratic opponents.
King owes his electoral success to a combination of ten years as the incumbent in a deep-red district and three recent elections in which national political headwinds blew away his Democratic opponents.
A 2015 poll showed that only 41 percent of registered voters in his district held a favorable view him and 41 percent had an unfavorable view. Not a glowing endorsement even from an electorate far and away the most conservative in the state.
Like many politicians, if King faces the right candidate in the right year, he will be gone. The rather progressive Berkley Bedell, who had to leave office because of Lyme Disease, held onto this same congressional district when it was smaller and more conservative back in the 1970s and 1980s.
Perhaps 2018 will finally be the year when the combination of Kings lunacy and voters feelings about the leader of the Republican party add up to defeat.
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The Tao of Steve King: Master of the Politically Incorrect - Progressive.org
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5 Most Politically Incorrect ‘Seinfeld’ Moments – PJ Media
Posted: at 3:55 pm
NBC's "Seinfeld" did far more than introduce "yada, yada yada" into the lexicon.
The show featured the kind of funny bits that might make Social Justice Warriors' heads explode.Yes, the bulk of the long-running series was pure comedy gold, the kind that few could find offensive. Who hasn't dreaded the "drop in" or wasting an entire night waiting for a restaurant table to open?
Other bits have proven more subversive over time.
Consider the following five comic sequences from the now-legendary show. They didn't seem button-pushing at the time. But who could have predicted a generation of easily offended snowflakes would deconstruct every joke a decade or so later?
It's especially rich given Jerry Seinfeld's later attack on our PC culture.
via GIPHY
The notion of the three main characters abstaining from self-love might rub some SJWs the wrong way. Why not Elaine? Was this simply old-school mansplaining?
Making matters worse? How Kramer ends his time in the contest. He ogles a naked woman from across the street and is soon "out."
How sexist!
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5 Most Politically Incorrect 'Seinfeld' Moments - PJ Media
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Malaysian Censor Says Sought 4+ Minutes of ‘Beauty And The Beast’ Cuts – Deadline
Posted: at 3:55 pm
Deadline | Malaysian Censor Says Sought 4+ Minutes of 'Beauty And The Beast' Cuts Deadline Disney's Beauty And The Beast is enjoying a fantastic run in its offshore and domestic debut this weekend with full numbers to come later today. As reported last week, the film is not screening in Malaysia after the local censor approved it with what ... 'Beauty and the Beast' Malaysia Ban Is Just the Latest Foreign Censorship Sir Ian McKellen slams censorship of Beauty and the Beast over gay character China declines to censor gay kiss in 'Beauty & the Beast' despite objections |
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Malaysian Censor Says Sought 4+ Minutes of 'Beauty And The Beast' Cuts - Deadline
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