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Category Archives: Transhuman News
DOGGY DNA: Unique startup has roots at Cornell – Ithaca Journal
Posted: April 23, 2017 at 12:25 am
Matt Weinstein , mweinstein@ithacajournal.com | @SteinTime44 4:55 p.m. ET April 22, 2017
Embark Dog DNA Test is not the first dog DNA test, but it's the most comprehensive available to consumers. Brothers Ryan and Adam Boyko partnered with Cornell University College of Veterinary Medicine and Spencer Wells, a pioneer in consumer genetics, to found Embark. Wochit
Ryan Boyko traveled all over the world to give DNA tests to village dogs.(Photo: Provided photo)
Brothers Ryan and Adam Boyko always had a family dog growing up, but they never gave much thought to turning their love for dogs into a business.
Even while pursuing higher education Ryan has graduate degrees in public health and ecology from Yale University and the University of California at Davis and Adam has a doctorate in biology from Purdue University the brothers were more focused on human genetics and ecology.
One day a few years ago at the genetics lab at Cornell University, Adam began a project looking at pure-bred dogs and for the first time began to think about dogs as a genetic system.
It kind of bugged me that there are millions of dogs in the world and the vast majority arent pure-bred dogs, and people really didnt know much about them at all, said Adam Boyko, who is now an assistant professor in biomedical sciences at Cornells College of Veterinary Medicine. If they thought about the dogs at all, they just thought they were a random mutt mix.
The brothers later began collecting genetic data of village dogs from all over the world, building a database of valuable information regarding diseases, medical conditions and breeding. As interest in their work began to grow, so did the idea for a consumer business which could help dog owners learn important information about their pets.
Embark Veterinary Inc. the company the brothers founded by partnering with Cornell and consumer genetics pioneer Spencer Wells is the result of nearly a decade of research. The Embark DNA Test, which sells on their website for $199, can trace a canines ancestry and disease risk using the companys huge database of 20,000 samples which was built from testing village dogs and the thousands of samples from the Cornell Veterinary Biobank.
Ryan Boyko traveled all over the world to give DNA tests to village dogs, setting up makeshift labs wherever he was at.(Photo: Provided photo)
The test has been a hit with dog owners and has received glowing reviews since hitting the market last year. Canine Journal gave the test 4.5 out of 5 stars and reviewer Sally Jones said Embarks genetic health screening is, paws down, the best youll find for an at-home dog DNA test (Embark blows other DNA dog tests out of the water). Amazon has given the test a score of 4.8 out of 5 based on 36 consumer reviews.
My husband did not want to spend $200 for a dog DNA test but I convinced him its worth it for our spaniel Jackson, said Erin Groover, who lives in Mission Viejo, Calif, with her husband Jeff and two sons. We were both amazed when we got the results. Jackson has six distinct breeds and although it did reveal a future medical condition, now we know and can brace for it.
It takes a village
Years before Embark was created, Adam Boyko was having lunch with his adviser Carlos Bustamante, who had just returned from Venezuela and made a remark about the small size of the village dogs in the area. Bustamante, who was a biology professor at Cornell University before joining Stanford University, suggested a transect study of village dogs in the Americas. Boyko, who remembered his brother Ryan was taking a honeymoon in Africa later in the year, replied, How about Africa?
Within a couple months the Boykos received seed money from Cornell to do a pilot program in Puerto Rico, and then Ryan set off to Africa with a bunch of butterfly needles and a centrifuge to begin the collecting of data.
They key concept for a village dog is that it is free breeding. Most village dogs are free ranging, but even those tied up are not spayed or neutered. In closed breeding populations which are typically owned as pets every breed has the same type of ears, a consistent coat color and coat type. With the natural breeding of village dogs, there are no fixed traits and lots of variation in shape and color. The village dogs in some areas can be smaller, weighing from 12 to 30 pounds, while village dogs in another part of the world can range from 40 to 80 pounds.
Looking at village dogs, they kind of looked like they were evolved like a natural population, Adam Boyko said.
The study in Africa was published by the Proceedings of National Academy of Sciences and the National Science Foundation provided funding for the brothers to take more samples. They eventually traveled most of the world sampling village dogs, constructing a comprehensive analyses of the geographic and population structure of the dogs and how they fit in compared to wild canids and pure bred dogs. Ryan did much of the travelling collecting samples and Adam mostly spent time in the lab.
Ryan Boyko traveled all over the world to give DNA tests to village dogs.(Photo: Provided photo)
The research showed village dogs are much more diverse than a purebred or mixed breed. Many areas of the world have village dogs descending from European dogs in colonial time (when Europeans traveled new lands, they often brought dogs, chickens and pigs with them), but there are vast areas of the world where they are very instilled in indigenous populations with not much mixture coming from modern dogs. Diversity was particularly high in Asia specifically Mongolia and Nepal which is likely a reflection of the original domestication of dogs, Adam Boyko says. They are working on sampling more central Asian and east Asian dogs to look for patterns.
Embarking on a consumer business
The Cornell College of Veterinary Medicine has an extensive collection of samples from owners donating their dogs DNA for research. Owners eventually began asking for information about their dogs gathered from the samples and the brothers realized they may have an idea for a business.
It was clear there was a demand not being met by commercial dog DNA tests, Adam Boyko said. Most treat them as a commodity to make the cheapest test possible so the consumer doesnt pay a ton of money but still feels they are getting results.
We thought if we did a cutting-edge research, maybe not the cheapest on the market but absolutely the most comprehensive, there is good demand for that. So far its proven to be the case.
The Embark Dog DNA Test provides a wealth of information for owners, and the most important is information about health and diseases. Owners swab the inside of their dogs mouths and mail the results back to Embark.
The MDR1 gene mutation, which causes sensitivity to certain drugs, is common among many breeds and important to identify so a dog can avoid adverse reactions to medications. The test can also find inherited eye disorders and bleeding disorders, which owners would want to know before a dog has any surgical procedure. The test also can spot later onset conditions like degenerative myopathy, so owners can look out for it, reduce the severity and make the dogs livelihood better.
The test also can identify breeds, which has surprised many owners thinking they own a certain breed but testing shows the dog is a completely different breed. Matt Barton, the companys CTO, received a shocking surprise about his adopted dog Aussie, who he had assumed was a Bichon Frise. The dog was actually a Schnoodle with no traces of Bichon Frise.
For Matt this was earth shattering news; he went into hiding for a while, Adam Boyko joked.
Ryan Boyko traveled all over the world to give DNA tests to village dogs.(Photo: Provided photo)
The Embark team recently worked the 2017 Puppy Bowl in February, testing the dogs and supplying statistics for the broadcast on Animal Planet. The teams base of operations is in Austin, Texas, but they also have an office at Cornell.
The future looks bright for Embark, which is hoping to ramp up the number of employees shortly. Embark currently has 14 employees. With a data collection constantly growing, the Boykos hope to keep expanding the depth of information gathered from the testing.
If we can take steps to prevent dogs from suffering or provide information to help owners be prepared for certain conditions to develop, we have to do it, Adam Boyko said.
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Murder of UNCC student from Chapel Hill revisited with new DNA evidence – WRAL.com
Posted: at 12:25 am
Charlotte, N.C. A high profile murder case connected to the Triangle is making headlines once again. The man convicted of killing a UNC Charlotte Student from Chapel Hill is hoping to be exonerated.
Investigators are now focused around DNA evidence on the victim's car. Though he was convicted to life in prison for murder, Mark Carver says he is innocent.
"I didn't do it. I didn't go around the car or near the car," Carver said.
He's talking about this car found near the edge of the Catawba River in 2008. It belonged to 20-year old Ira Yarmolenko, who was found strangled to death nearby.
Carver's DNA was found on the victim's car, but not on her body or any murder weapon.
Chris Mumma, an attorney with the North Carolina Center for Actual Innocence, said she thinks Carver's DNA was accidentally transferred to the vehicle by investigators after they interviewed him. She wants that DNA evidence retested.
"I am expecting to see exactly what our experts have seen. They submitted reports as part of our filing that it would never be reported that Mark Carver's DNA was on that car."
In a hearing, a Gaston County Judge agreed to the re-testing. Mumma then asked for DNA from five investigators who worked the crime scene around the car.
It was decided that attorneys could ask investigators to voluntarily give those samples.
Leaving the courthouse, Carver's family members seemed hopeful after the hearing.
"The truth will come out, he will be found innocent."
Mumma hopes to earn a retrial in Carver's case.
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Adam and the Genome– Part Five – Patheos – Patheos (blog)
Posted: at 12:24 am
Modern evolutionary science, including the science of genetics is based on the hypothesis that most if not all things can be explained in a natural way through empirical research. A theist evolutionist will simply say that evolution is the way God works things. Suppose however that God is not like a watchmaker who creates a watch, winds it up, and leaves it to the empirical parts to do their jobs their after? Suppose God is constantly involved not merely in human history but in all things great and small. Suppose the designer constantly has his hand on the design, and makes changes and modifications? Suppose he designed human beings to be like other higher order creatures so that humans would feel some kinship with them, and take care of them, and be good governors of Gods creation? Evolution is a theory that leave God constantly out of the equation, or alternately simply says this is the natural mechanism God chose to accomplish things.
The same problems arise in applying this sort of information to the historical figures of Adam and Eve as arises in the neuro-scientific discussions about the mind and the brain, where the assumption is that human beings are psychosomatic wholes, and as such, when the body goes the whole person dies. There is no human spirit, human personality that survives death. Of course, no scientist has gone to the other side of death and done an empirical study of whether there might be spirits of the departed in heaven or elsewhere. The assumption again is this world, this life, these natural processes, like evolution are all there is, and so a theory which explains some things, is globalized to explain everything, including ruling out ongoing divine action in the natural and human worlds, never mind ruling out the afterlife.
My point by drawing attention to these two differing attempts at discussing science and the Bible together is that science often has to extrapolate or theorize from the known to the unknown to come up with a purely materialistic and empirical explanation for things.
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This Dingo Has Won the Title of the World’s Most Interesting Genome – ScienceAlert
Posted: at 12:24 am
The winner of the World's Most Interesting Genome competition has been announced and a pure bred dingo called Sandy has ended up on top.
The competition was tough, with Sandy beating a 'solar-powered' sea slug, an explosive beetle, and a deadly Asian snake to take out the top spot.
Sandy and her siblings were found as abandoned three-week old pups in the Australian desert, two years ago.
Barry Eggleton
Being a wild-born pure Australian desert dingo is a pretty big deal most dingos have interbred with wild dogs and domestic dogs, so it makes Sandy rare.
"Sandy is truly a gift to science. As a rare, wild-born pure dingo, she provides a unique case study," said project leader Bill Ballard, from the University of New South Wales (UNSW).
"Pure dingoes are intermediate between wild wolves and domestic dogs, with a range of non-domesticated traits."
"So sequencing Sandy's genome will help pinpoint some of the genes for temperament and behaviour that underlie the transition from wild animals to perfect pets," he added.
Let's take a look at the rest of the finalists:
Elysia timida the "solar-powered" sea slug
Parent Gry/Wikimedia
Elysia timida is a sea slug that can 'steal' and use the chloroplasts of the algae it consumes as food.
Chloroplasts are the parts of plants that undergo photosynthesis a process that takes light and turns it into energy.
Currently scientists don't understand how the slugs maintain chloroplasts typically only used by plants, but it allows them to survive for months without eating.
Nesoenas mayeri, the Pink Pigeon
The pink pigeon is interesting for more than just its colour.
As a species that nearly became extinct in the 1990's (having only 16 wild birds remaining), they managed to bounce back, with records showing there are now more than 400 individuals.
But the pink pigeon isn't out of the woods yet with low genetic diversity, over 60 percent of baby birds dying due to infection, we need to understand as much as we can about these guys to make sure they don't end up like their dodo cousins.
Tropidolaemus waglerithe "sexually dimorphic" Temple Pit Viper
The temple pit viper is pretty badass.
Not only does it have unique toxins in its venom not found anywhere else in the world, but its sexual characteristics also is quite different to most snake species.
Temple pit viper males are small and green, while the females are 10 times the male's size and beautifully coloured.
Plus you can find these vipers in the Snake Temple in Malaysia, which is one of the only temples of its kind in the whole world.
Brachinus elongatulusthe "explosive" bombardier beetle
The bombardier beetle is basically the mad scientist of the bug world.
With explosive chargers of toxic chemicals that explode out of the bug at temperatures over 100 degrees Celsius (212 degrees Fahrenheit) they can definitely hold their own in a fight.
It also doesn't seem to hurt itself in the process.
The beetle itself has been baffling evolutionary geneticists for decades with how such a creature managed to evolve at all. One evolutionary slip-up and the bug itself would explode.
It's totally worth checking out this video below to find out more:
But despite all this notable wildlife, we're excited that Sandy came first.
The company behind the competition, PacBio, will now sequence the DNA with their extremely precise machine to investigate the secrets of Sandy's genome.
We're looking forward to seeing what the UNSW team discovers.
UNSW Science is a sponsor of ScienceAlert. Find out more about their world-leading research.
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CRISPR genome editing and immunotherapy the early adopter … – Cancer Research UK (blog)
Posted: at 12:24 am
Its been a couple of years since the genome editing tool CRISPR first hit the headlines. And talk of its potential to cure all manner of diseases, create superhumans and bring dinosaurs back from the dead has followed.
But among that speculation, one area of medicine has been quick to pick up the technology and is now leading the way in early clinical trials.
In this second post in our series taking a closer look at CRISPR, we explore its potential for new developments in cancer immunotherapy.
Immunotherapy can take a range of forms. Some experimental approaches use viruses that kill cancer cells and alert the immune system to attack. Others involve giving patients drugs that release the brakes on immune cells to target cancer. And some use specially engineered immune cells that when injected into a patient have the potential to hunt out and kill cancer cells.The aim of immunotherapy treatments is to alert the bodys immune system to cancer, so that its better equipped to recognise and fight the disease.
In each of these cases, scientists need to be able to understand and fine-tune the bodys complex immune system. And some are turning to CRISPR for help.
Dr Martin Pule, a clinical senior lecturer in haematology at UCL, says that genome editing techniques such as CRISPR have quickly become part of the tool-kit for researchers like him.
In the past, many of the technical problems around introducing new genes into cells were worked out, but we didnt have an easy way of efficiently and precisely disrupting existing genes, he says. New genome editing technologies changed all that.
By using CRISPR, scientists are able to tweak specific genes in viruses or the bodys own immune cells, and so make them behave differently.
Researchers have been able to do this before using similar techniques, but the excitement around CRISPR is that this can be done much quicker, cheaper and more precisely than ever before.
Genome editing techniques have been used in people to treat cancer and other diseases before.
There was lots of excitement when news broke in 2015 of a 1 year old girl with acute lymphoblastic leukaemia (ALL) being treated with a similar editing technique known as TALENs, after all other treatments had failed.
She received a transplant of cancer-fighting immune T cells from a donor, which had been tweaked in the lab to give them 2 new characteristics.
Normally, the donated cells would see their new environment as foreign and attack the patients healthy cells, but genes that control this process were turned off. The T cells would also be susceptible to attack from the anti-cancer drugs that the baby was receiving, and so modifications were made to protect them.
She responded well to the treatment, and another infant received a similar therapy.
Following in the footsteps of its cousin TALENs, CRISPR itself has moved on from the lab to clinical trials. Late last year, a Chinese group became the first to use CRISPR-edited cells in humans.
Find out more:9 burning questions about CRISPR genome editing answered
The team took immune cells from a patient with an aggressive lung cancer and edited them in the lab. This editing deactivates a gene that allows tumours to put the brakes on these immune cells, preventing them from attacking cancer cells.
By switching off the gene, which produces a molecule on the cells surface called PD-1, the full force of the bodys immune system is released, helping it clear the tumour. Drugs that target PD-1 are among the much-lauded immunotherapy treatments already showing promise in advanced melanoma and lung cancers. So theres a lot of hope that CRISPR may provide another step forward here too.
10 patients will be involved in the early-stage Chinese trial, and it will look at whether the treatment is safe, rather than testing effectiveness.
The scientists are also hoping to start clinical trials using CRISPR to treat bladder,prostateandkidney cancers. Its also positive news that both blood cancers and solid tumours appear to be responding to various immunotherapy approaches, as different challenges are faced in treating these diseases.
One clever immunotherapy trick fuses together 2 components of the immune system with different jobs.
Chimeric antigen receptor (CAR) T cells are a mix of an antibody molecule, which can home in on a specific target on tumour cells, fused to a T cell that provides the knock-out blow to the cancer cell.
Weve blogged before about how these engineered cells work, and small trials in 2011 caused lots of excitement. But one of the latest updates is that using CRISPR instead of older genome editing techniques might supercharge these CAR T-cells even further.
The older technology is less precise and can result in the genes mistakenly being inserted at random locations in the cells DNA. The knock-on effect is that the engineered cells might be less effective or unintended side-effects could be introduced.
But a US-based group found that CRISPR improved the precision with which the modified gene was inserted into T cells. Their research suggests that the cells were then more potent in their fight against leukaemia in mice because they had more stamina. The researchers are now hoping to test these findings in people.
Cancer cells are relentless in their attempt to evade treatment, so we need CAR T cells that can match and outlast them, Dr Michel Sadelain, the researcher leading the study at Memorial Sloan Kettering Cancer Center, said at the time.
Find out more:Engineering a cancer-fighting immune super soldier
Its findings like these that will hopefully make engineered immune cell treatments better and kinder in the future, though they arent yet the Holy Grail.
In one kind of leukaemia called B-ALL, almost 100% of children who received engineered T cells responded, despite having a disease which had become resistant to all standard treatments, says Pule.
This suggests that, in some circumstances, there may not be an upper limit on who may respond to these treatments. But achieving this in other cancers will take further fine-tuning. In other diseases, such as another kind of blood cancer called DLBCL, the response rates are more like 60%.`
This reflects the fact that a good CAR T cell product is hard to make, or that there are factors inside the tumour making the T cells less effective, Pule adds.
Lots of the progress using CAR T cells has so far been in blood cancers rather than solid tumours, which have even tougher conditions.
Because CRISPR allows scientists to do lots of small-scale tinkering, this is a rapidly developing field and researchers are trying to find solutions.
Right now a lot of people are asking why theres this response gap between DLBCL and B-ALL. Can we edit something in the CAR T cell, or put something extra in which will increase the response rates?
One reason might be that the tumour lives in a hostile environment that stops the engineered T-cells ability to attack the cancer cells. One way around this is to delete the molecules on T cells that coordinate the stop messages from the microenvironment.
This strategy looks like it might be quite effective and could increase the number of patients who respond, says Pule.
Some of the research thats taken place since CRISPR burst onto the scene has also raised more questions than answers. The immune system is a powerful and complicated machine, and we dont yet understand how to control it.
Not all of these treatments have been as successful as hoped. As well as varying response rates, they can also cause serious side effects, including, in rare cases, death.
There have been recent reports of patients with bladder cancer whose tumours increased in size after immunotherapy treatment, although this has caused some debate among researchers. Side effects including extreme fever or organ damage have also been well documented in clinical trials.
In the US, a total of 5 patients died following treatment with an experimental CAR T cell therapy for ALL. The clinical trial was paused after 3 people died, and then stopped after 2 more deaths.
While this is very rare, its clear that as well as working to make treatments more effective in more people, researchers also need to look at how they can reduce side effects.
Similar problems were seen in the past in the early days of treatments such as combination chemotherapy, before they were refined.
Pule points to how scientists are already using genome editing to increase safety. For example, in many cases, it isnt possible to engineer a patients own T cells and so cells from a donor are needed.
But this raises some challenges.
The donor T cells might attack the recipient causing graft-versus-host disease, says Pule. Graft-versus-host disease is a condition where the donor cells see their new environment as foreign and attack it. If we remove a specific molecule in the donor T cells using gene-editing technology, we can reduce the chance of this happening.
This is how the two infants with ALL were treated.
Like many new technologies, CRISPR was greeted with excited fanfare in some parts, and a more cautious realism is now settling in.
Its clear that CRISPR opens up so many doors for immunotherapy and lets researchers go further, more easily than ever before. But as the technology is understood better, its limitations and challenges also come into focus.
The third part of our CRISPR series will take a look at what the future might hold for CRISPR and cancer research.
Michael
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Hundreds in Athens join worldwide marches for science – Online Athens
Posted: at 12:24 am
Maybe it wasnt exactly scientifically confirmed, but it was nonetheless clear that Saturdays March for Science in downtown Athens not a march, exactly, as things turned out exceeded the limits of the police-issued permit for the event in front of the federal courthouse on Hancock Avenue.
I think weve broken the law, folks! an exuberant Mark Farmer, a cellular biologist at the University of Georgia, told the crowd jamming the courthouse lawn from the steps into the street.
Because the local March for Science part of hundreds of such marches held around the world on Earth Day coincided with the popular G-Day intrasquad University of Georgia football game that brings thousands of visitors to town, organizers couldnt get a parade permit for downtown Athens, according to Farmer.
Instead, they were granted a permit to rally on the federal courthouse grounds outside the heaviest G-Day traffic from 11 a.m. until noon, with a limit of 400 people. But one glance around the crowded lawn made it clear that the actual number of people was well above that limit, with one estimate placing the crowd at 600 people or more, who waved signs and chanted as a line of speakers extolled the human progress made possible by science.
And, with a little lighthearted civil disobedience in his heart, as the rally was winding down Saturday morning, Farmer looked at the permit and said, I see nothing on here saying you cant all take your signs and walk downtown!
The Athens event and those held worldwide were aimed at promoting an understanding of science and defending science from issues such as proposed federal government budget cuts that could adversely affect scientific research in this country.
Waving signs with slogans like Grab them by the data and Science is not a liberal conspiracy, the hundreds of people who attended the March for Science in downtown Athens heard from a number of speakers including Marilyn Williams, the director of spiritual care at St. Marys Hospital in Athens.
Prior to becoming a chaplain, Williams worked for two decades in cancer research and health care management, and she spoke Saturday about the nexus between science and religion.
Theres no conflict between the two, she said. Both are just different approaches for understanding our world.
And, Williams said, pastoral care work shows the connection between faith and science.
We really do see where science and faith come together, she said. Theyve always been connected.
Also speaking Saturday was Kathy Fowler, a veterinarian and march organizer who suggested to the crowd that without science particularly the medical research that has improved human health and longevity many of the people at Saturdays march might not have been there.
The scientific discoveries of the the last few centuries are what allowed you to be here today, she said.
Human health has also been improved by scientific advancements in water quality and in properly handling wastewater, Fowler continued.
They all came about because of scientific research and discovery, she said.
The local focus on science will continue in neighboring Oconee County on Sunday, where the Oconee County Democrats will host a nonpartisan event called Walk and Talk with a Scientist.
The walk is scheduled for 3 to 5 p.m. at Herman C. Michael Park off Georgia Highway 53 and Elder Road. Scientists will gather at the walking trail, which is paved and about a third of a mile long.
People can choose a scientist and walk the trail with them while talking about that persons scientific investigations or study. Among the scientists participating in the event are a geologist, an expert in water toxicity, a botanist, a specialist in endangered species and an expert on coral reefs.
Across the United States on Saturday, one of the organizers of the first Earth Day, Denis Hayes, said the crowd he saw on the National Mall in Washington appeared energized and magical, almost like what he saw on the first Earth Day 47 years ago.
Hundreds turned out in light rain for a pro-science rally on the Vermont Statehouse lawn in Montpelier. One of the speakers, Rose Paul, director of conservation science for The Nature Conservancy of Vermont, told the crowd that Science is not a partisan issue. She said climate change is happening and scientists are needed to help understand how shifting weather patterns are affecting the world.
In Nashville, Tenn., hundreds of people braved pouring rain, marching through city streets and chanting science, not silence.
President Donald Trump said in an Earth Day statement that his administration is committed to keeping our air and water clean, to preserving our forests, lakes and open spaces and to protecting endangered species.
But that wont be done, he said, in a way that harms working families, and he added that the government is reducing unnecessary burdens on American workers and American companies, while being mindful that our actions must also protect the environment.
The Associated Press contributed to this report.
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At 117, world’s oldest woman works hard and avoids pork – Greensboro News & Record
Posted: at 12:24 am
DUANVALE, Jamaica Violet Brown spent much of her life cutting sugarcane in the fields around her home in western Jamaica. She attended church regularly, avoids pork and chicken and celebrated her 117th birthday last month.
On Saturday, she is believed to have become the world's oldest living person following the death of Emma Morano of Italy, born Nov. 29, 1899.
Brown told The Associated Press she is surprised but grateful to have lived this long.
"This is what God has given me, so I have to take it long life," Brown said in an interview in her home in the town of Duanvale.
Brown is considered to be the oldest person in the world with credible birth documentation, according to Robert Young, director of the supercentenarian research and database division at Gerontology Research Group, a network of volunteer researchers into the world's oldest people. Its website says she was born on March 10, 1900.
Brown has not yet been declared the world's oldest by Guinness World Records, considered to be the official arbiter of the oldest person title but Guinness depends heavily on Young's group. Young said he has met Brown and examined her birth certificate, which was issued by the British authorities who governed Jamaica at the time of her birth.
"She's the oldest person that we have sufficient documentation for at this time," Young said.
Jamaica's prime minister congratulated Brown on Twitter.
Guinness said it was researching a number of candidates for the new world's oldest person title.
"It can be a uniquely complex and sometimes lengthy process," Guinness spokeswoman Elizabeth Montoya said. "There is no confirmation of a new title holder until our thorough processes are complete."
Brown has two caregivers and spends most of the day resting in the home she shares with her 97-year-old son. She is able to sit up by herself and walk short distances. And while she is hard of hearing, she offered swift, complete responses to questions about her life and family.
The secret to long life is hard work, she said.
"I was a cane farmer. I would do every work myself," she said. "I worked, me and my husband, over that hill."
She also credited her Christian faith for her long life.
"I've done nearly everything at the church," she said. "I spent all my time in the church. I like to sing. I spent all my time in the church from a child to right up," to today, she said.
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Human Umbilical Cord Blood Helps Aging Mice Remember, Study Finds – NPR
Posted: at 12:24 am
Researchers found that a protein in human umbilical cord blood plasma improved learning and memory in older mice, but there's no indication it would work in people. Mike Kemp/Rubberball/Getty Images hide caption
Researchers found that a protein in human umbilical cord blood plasma improved learning and memory in older mice, but there's no indication it would work in people.
Decades ago, scientists surgically attached pairs of rats to each other and noticed that old rats tended to live longer if they shared a bloodstream with young rats.
It was the beginning of a peculiar and ambitious scientific endeavor to understand how certain materials from young bodies, when transplanted into older ones, can sometimes improve or rejuvenate them.
From the beginning, the findings were exciting, complex and, sometimes, contradictory. For example, scientists have shown that young blood can restore cell activity in the muscles and livers of aging mice. They've also found that linking old mice to young ones helped reverse heart muscle thickening.
On the other hand, researchers weren't able to replicate some of the most eye-catching findings and another study concluded that, in mice that swapped blood without being connected surgically, the negative effects of being exposed to old blood outweighed the benefits of getting young blood.
What was clear was that, like humans, as mice age their bodies and their behavior change on a fundamental level. For example, older mice stop building nests, and they tend to become forgetful, taking a long time to remember how to escape from a maze.
"We see a pretty dramatic difference between young and aged mice in terms of their performance," says Joe Castellano, a neuroscientist at Stanford University School of Medicine.
Castellano and his colleagues wondered if young human blood might have beneficial effects for aging mice.
Now, they report in the journal Nature that they've found a protein in human umbilical cord blood that improved learning and memory in aging mice. It's an exciting find in the field of regenerative medicine.
But, scientists caution, it does not mean people should start ordering umbilical cord blood online. There is no indication that it would work in humans.
For their study, Castellano and his colleagues collected plasma, which is the watery part of blood, from people of different ages. Some were in their 60s and 70s, others in their 20s. They also collected plasma from human umbilical cords.
Then, they injected human plasma from those different age groups and from umbilical cord blood into mice several times over the course of a couple of weeks.
The mice were 12 and 14 months old, which is approximately the mouse equivalent of being in your late 50s or 60s.
When they dissected the mouse brains and inspected the hippocampi, they found that certain genes linked to making new memories had been turned on in some of the mice.
"So, we had a hint early on that one of these donor groups, specifically the [umbilical] cord plasma, might be having an effect on the brain itself," he says.
Next, they injected more aging mice with human plasma and tested the animals' ability to remember things.
For example, they watched how long it took the mice to escape from a maze the mice had done before, using visual cues to choose an exit that would lead to safety.
Castellano says it's basically like observing a person try to navigate through a crowded garage to locate their parked car.
Before being injected with umbilical cord blood, Castellano says, "their performance wasn't very impressive." It took them a long time to learn and remember the location of the escape hole, and some of them didn't manage at all. "But after cord plasma treatment, both the time [it took to] find it, the rate at which they'd find it and the fact that they do find it was improved and changing," he says.
Similarly, mice treated with human umbilical cord blood performed better on a second memory test. That test involved introducing mice to a chamber and then delivering a little shock to their feet. Mice that remembered the unpleasant experience would, when reintroduced to the chamber, freeze in anticipation of the shock. A forgetful mouse, on the other hand, would go about its usual business.
Castellano says the mice that had received umbilical cord plasma froze more often.
"We were, first of all, surprised and excited that there was something in human plasma, and more specifically there's something exciting about cord plasma," he says.
After a series of other experiments, Castellano and his colleagues concluded that one protein, called TIMP2, in human umbilical cord blood was likely responsible for the improvement.
When they removed TIMP2 from cord plasma and injected the plasma into mice, they didn't observe any improvement on the memory tests. And when they injected plasma containing TIMP2 into elderly mice, they again observed improvement in memory and learning tasks.
"The really exciting thing about this study, and previous studies that have come before it, is that we've sort of tapped into previously unappreciated potential of our blood our plasma and what it can do for reversing the harmful effects of aging on the brain," says Castellano.
It's an intriguing hint at how potential therapies might someday work to prevent age-related illness, including Alzheimer's disease, from developing.
"The desired outcome is overall whole body rejuvenation," says Aubrey de Grey, a biomedical gerontologist who founded the SENS Research Foundation.
The study by Castellano and colleagues, he says, is an "excellent" starting point.
"The only thing, of course, is that it's a mouse experiment and mouse experiments often don't actually translate faithfully into the human setting," he says.
And Castellano agrees that this finding does not mean that people should start sprinkling TIMP2 protein on their cereal or signing up for umbilical cord transfusions.
First off, he says, there's no evidence that elderly humans would experience the same effects as the mice did in this study. It's also unclear what would happen to mice if they received the plasma for more than just a few weeks.
There's also the nagging worry that, while proteins like TIMP2 may be beneficial for developing babies, they could be harmful in older humans.
"Maybe there's a reason that older brains aren't exposed to certain proteins any longer," says Castellano.
And Irina Conboy, who studies aging and degenerative diseases at the University of California, Berkeley, points out that the TIMP2 protein is actually present in higher levels in people with Alzheimer's disease.
That runs counter to the argument made by Castellano and colleagues that TIMP2 is associated with improved memory and learning, and that TIMP2 levels would drop as people age.
"TIMP2 is a very well-known protein," she says. She also notes that one of Castellano's co-authors, Tony Wyss-Coray, is the board chair for a company called Alkahest, which has separately studied plasma injections as a potential treatment for Alzheimer's.
And, Conboy says, there is no indication that the TIMP2 Castellano and colleagues detected in mouse brains actually came from the injections of human plasma. It's unclear, she says, whether a protein in plasma could actually make its way from a mouse's bloodstream into its brain, or that, once there, it could actually impact brain function.
Last year, Conboy published a study in which she and colleagues swapped half of the blood in old mice with that of young mice, and vice versa. They saw signs of regeneration in the muscles and liver.
But, says Conboy, "There was zero positive effect on the brain. The mice were not smarter. They did not learn better."
Such conflicting results reflect two fundamentally different ways of thinking about aging.
From the point of view of Castellano and colleagues, aging involves a loss of beneficial materials; for example, diminishing amounts of proteins that were once present in the plasma.
To Conboy, however, "The problem is not that you run out of positive things, but that you accumulate negative things."
She and others hold that proteins likely accumulate with old age, sometimes inhibiting certain functions, including the growth of new cells.
"We have hundreds of proteins that change with age," she says, and finding a way to reduce the effects of aging will likely require tinkering with a huge bouquet of them.
"If you are looking for miracles, it will not come from [injecting] bodily fluids," she says. "There will not be one silver bullet."
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Human Umbilical Cord Blood Helps Aging Mice Remember, Study Finds - NPR
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Valeant says its plaque psoriasis drug will cost $3500 a month – MarketWatch
Posted: at 12:23 am
Valeant Pharmaceuticals International VRX, -4.17% said early Friday that the company's new plaque psoriasis drug Siliq will cost $3,500 a month. Siliq, an injectable drug that Valeant got the rights for from AstraZeneca AZN, -0.47% is intended for patients with moderate-to-severe iterations of the chronic skin condition, who haven't responded to other medications. Valeant said the $3,500 price tag was "the lowest injectable biologic psoriasis treatment currently on the market" and was evaluated and approved by its Patient Access and Pricing Committee, which was created in May 2016 after a series of scandals, including one about drug pricing, rocked the company. Valeant expects to start selling and marketing Siliq starting in the second half of this year. Siliq's label will contain a "black box warning" about risks for patients with a history of suicidal thoughts or behavior. Valeant shares, which slumped 0.5% in premarket trade on Friday, have dropped 39.7% over the last three months, compared with a 3.7% rise in the S&P 500 SPX, -0.30%
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‘It is not all gloomy if you’ve psoriasis’ – The Standard (press release)
Posted: at 12:23 am
Hellen Wangui ,28 years with a skin condition called Psoriasis she has been having for 13years.19th APRIL 2017 PHOTO DAVID GICHURU
She basked in her rosy glow during pregnancy and wished it could last forever. However, after the birth of her son, a skin condition she has battled since 2008 was back with a vengeance.
Hellen Wangui Gathere, 28, is suffering frompsoriasis, a condition that makes her skin appear dry, scaly and flaky on the legs, hands and back.
The Advocate of the High Court of Kenya is a member of thePsoriasisAssociation of Kenya that seeks to create awareness, champion for improved medical care and research on the disease.
"I choose to speak aboutpsoriasisbecause it is often misunderstood and persons with the condition stigmatised or prevented from participating in social activities," said the mother of a nine-month old boy.
Individuals with the condition are prone to heart disease, diabetes, obesity, heart attack, stroke and liver disease among other lifestyle diseases.
Psoriasisis not contagious, however, if not properly managed, it can lead to heart complications like hardening and narrowing of artery walls, diabetes and arthritis.
These underlying complications worried Wangui when she was pregnant with her first child last year.
Its an unpredictable scenario when a person withpsoriasisis pregnant because it can either improve, worsen or remain unchanged.
Luckily, pregnancy favoured Wangui, the condition was suppressed leaving a flawless youthful skin.
My skin took a different turn.Psoriasisdisappeared leaving me with an even-toned skin. It felt great to have smooth skin that I could rub without the dry and scaly feel, said Wangui in an interview with Saturday Standard.
On the advice of her dermatologist, she discontinued the oral medicines and ointments that had become a daily routine before pregnancy.
For a while, I forgot aboutpsoriasisand concentrated on my pregnancy that was also trouble-free, she added.
But after delivery,psoriasiswas back and she had to start a regime of oral medicines, ointments and phototherapy.
It is not all gloomy because I know how to take care of my skin to prevent flares. I am more concerned about a young lady or man too embarrassed to admit that they have psoriaisis and take an extra step to seek medical assistance, said Wangui.
The World Health Organisation (WHO) describespsoriasisas a chronic, painful, disfiguring, disabling and incurable disease.
Consultant skin specialist Hoseah Waweru describespsoriasisas a build up of new cells in the top layer of the skin, forming a scaly-like appearance.
These skin cells grow faster than your body can shed them off leaving thick red patches, says Dr Waweru. In 2014, he was part of a delegation to the 67th World Health Assembly urging the member states to recognisepsoriasisas a serious non communicable disease.
The resolution was adopted as World Health Assembly resolution WHA67.9 and it highlighted that many people in the world suffer needlessly frompsoriasisdue to incorrect or delayed diagnosis, inadequate treatment options and insufficient access to care, and because of social stigmatisation.
Though there are various types ofpsoriasis, Dr Waweru estimates that about one in every two persons have a type known as scalppsoriasiswhich has a silvery and powdery appearance, but very different from dandruff.
What causes this skin condition?
Though the causes of the condition remain largely unknown, it can be provoked by external and internal triggers, including mild trauma, sunburn, infections, medicines and stress.
Dr Evanson Kamuri, a dermatologist, said that the condition most likely runs in families. However, he advice's one to consult a skin specialist on medicines, both topical and oral, that are best suited for use during pregnancy.
Phototherapy, also known as light therapy uses specific wavelengths of light to help treatpsoriasis.
Wangui said this method is effective but expensive. I need two phototherapy sessions twice a week at Sh3,000 each besides oral medicines that cost Sh36,000 per month, she said.
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'It is not all gloomy if you've psoriasis' - The Standard (press release)
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