Monthly Archives: August 2017

Genetic Engineering with Strict Guidelines? Ha! – Discovery Institute

Posted: August 9, 2017 at 4:47 am

Human genetic engineering is moving forward exponentially and there is still no meaningful societal, regulatory, or legislative conversation about whether, how, and to what extent we should permit the human genome to be altered in ways that flow down the generations.

But dont worry. The Scientists assure us, when that can be done, there will (somehow) be STRICT OVERSIGHT. From the AP story:

And lots more research is needed to tell if its really safe, added Britains [Robin] Lovell-Badge. He and [Johns Hopkins University bioethicist Jeffrey] Kahn were part of a National Academy of Sciences report earlier this year that said if germline editing ever were allowed, it should be only for serious diseases with no good alternatives and done with strict oversight.

Please!No more! When I laugh this hard it makes mystomach hurt.

Heres the problem: Strict guidelines rarely are strict and they almost never offer permanent protection. Theyare ignored, unenforced, or stretched over time until they, essentially, cease to exist.

Thats awful with actions such as euthanasia. But wecant let that kind of pretense rule the day withtechnologies that could prove to be among themost powerful and potentially destructive inventions in human history. Indeed, other than nuclear weapons, I cant think of a technology with more destructive potential.

Strict oversight will have to include legal limitations and clear boundaries, enforced bystiff criminalpenalties, civil remedies, and international protocols.

They wont be easy to craft and it will take significant time to work through all of the scientific and ethical conundrums.But we havent yet made a beginning. If we wait until what may be able to be done actually can be done, it will be too late.

Photo: Genetically engineering mice, via Wikicommons.

Cross-posted at The Corner.

Read the original here:
Genetic Engineering with Strict Guidelines? Ha! - Discovery Institute

Posted in Genetic Engineering | Comments Off on Genetic Engineering with Strict Guidelines? Ha! – Discovery Institute

Genetic Arms Race: A Threat to Human Dignity And National Security? – CNSNews.com

Posted: at 4:47 am


CNSNews.com
Genetic Arms Race: A Threat to Human Dignity And National Security?
CNSNews.com
A new genetic technology is being called a weapon of mass destruction. I'll tell you why that may not be hyperbole. In late July, the MIT Technology Review published news many of us have been dreading: A team of scientists at Oregon Health and Sciences ...

and more »

Read more from the original source:
Genetic Arms Race: A Threat to Human Dignity And National Security? - CNSNews.com

Posted in Human Genetics | Comments Off on Genetic Arms Race: A Threat to Human Dignity And National Security? – CNSNews.com

Grant to compare large-scale genomic sequencing, standard clinical tests for childhood cancer patients – Baylor College of Medicine News (press…

Posted: at 4:47 am

Baylor College of Medicine is one of six U.S. institutions to receive a grant through the National Human Genome Research Institutes Clinical Sequencing Evidence-Generating Research Consortium, or CSER2. The four-year grant, including $2.8 million for fiscal year 2017, co-funded by the National Cancer Institute, will support Baylors new KidsCanSeq program that will compare the results of large-scale genomic testing, such as whole exome sequencing, to targeted clinical tests in childhood cancer patients at five sites across the state that serve a highly diverse patient population, including Texas Childrens Cancer Center.

In addition to Texas Childrens Cancer Center, pediatric patients will be enrolled in KidsCanSeq at the Vannie E. Cook Childrens Cancer Clinic in McAllen, the Childrens Hospital of San Antonio, the University of Texas Health Science Center at San Antonio, and Cook Childrens Health Care System in Fort Worth.

KidsCanSeq follows the Baylor Advancing Sequencing in Childhood Cancer Care(BASIC3) study at Baylor and Texas Childrens Cancer Center, which developed the initial protocols for performing clinical genomic testing of pediatric cancer patients, reporting results and communicating those results to families and oncologists. BASIC3 was part of the NHGRI Clinical Sequencing Exploratory Research program, a precursor to CSER2.

Through BASIC3 we explored broad questions, such as whether we could conduct large-scale genomic testing in a clinical setting, what kind of results it would generate, and how to communicate the results to families and physicians. KidsCanSeq is focused more on generating specific data on what tests are better or worse than standard tests in pediatric cancer patients, said the studys principal investigator Dr. Sharon Plon, professor of pediatrics and of molecular and human genetics at Baylor and director of the Cancer Genetics Clinical and Research Programs at Texas Childrens Hospital.

BASIC3 was essentially a pilot study, and now that we have a better idea of how to implement broad-scale genetic testing in the clinic, we can focus this study more specifically on determining which patients would be most likely to benefit from it or for whom it would be most likely to impact care, said Dr. Will Parsons, co-principal investigator and associate professor of pediatrics at Baylor and Texas Childrens Cancer Center. For example, tumor sequencing of cancer types for which kids are almost always cured at the time of diagnosis is not likely to be as useful as for high-risk and relapsed cancers.

KidsCanSeq will strive to answer questions such as how effective is a germline and tumor panel of approximately 150 to 200 genes at picking up hereditary genetic factors and tumor-specific actionable information compared with larger scale tests, like whole exome sequencing, which evaluates thousands of genes. Specifically, the study will compare the targeted cancer panel to whole exome sequencing of a blood sample of all enrolled childhood cancer patients to find hereditary factors and to whole exome sequencing, transcriptome sequencing and copy number array of tumor samples for the subset of patients with high-risk or relapsed tumors to find mutations that might guide treatment. This comprehensive set of genomic tests will be performed by a unique collaboration between multiple diagnostic facilities with the involvement of Dr. Richard Gibbs, director of the Human Genome Sequencing Center, Drs. Christine Eng and Shashikant Kulkarni, professors of molecular and human genetics, all of Baylor, and Dr. Angshumoy Roy, assistant professor of pathology & immunology at Baylor and Texas Childrens Hospital.

The program, in which about 900 patients are expected to be enrolled over four years, also will include parent and doctor surveys to determine what they found most useful from the testing as well as the development of video and other educational materials in both English and Spanish. Understanding differences among families from different ethnic or racial backgrounds as well as in different healthcare settings, including large academic medical centers versus smaller clinical settings, also is a goal of KidsCanSeq.

Dr. Amy McGuire, Leon Jaworski Professor of Biomedical Ethics and director of the Center for Medical Ethics and Health Policy at Baylor, also is co-principal investigator of the study. She will investigate the ethics and utility of genomic testing for pediatric cancer patients.

It is important to study the clinical and psychosocial risks and benefits of any new technology in order to plan for its responsible use, McGuire said. We also want to make sure the infrastructure is in place so that oncologists in non-academic settings can understand, effectively communicate and appropriately manage the results of germline and tumor whole exome sequencing.

Specific aims of the KidsCanSeq study include:

Assess the clinical utility of large-scale genomic testing by measuring the frequency of diagnostic and/or actionable germline (blood) and tumor findings and the effect on treatment decisions Compare uptake by first-degree relatives for familial genetic testing and recommended cancer surveillance by race, ethnicity and clinical settings. Describe perceived utility of large scale testing by surveying and interviewing parents and participating pediatric oncologists. Work with pediatric cancer stakeholders, including advocates, BASIC3 study parents and national organizations, to create and evaluate the use of culturally sensitive educational materials, including videos in English and Spanish, improved integrated genomic test reports and counseling materials, and compare in-person versus telemedicine exome results disclosure. Provide data to guide future application of clinical genomics through three innovative pilot projects focused on health economics, decision support for cancer surveillance and whole genome sequencing.

Drs. Plon, Parsons and McGuire all are members of the NCI-designated Dan L Duncan Comprehensive Cancer Center at Baylor College of Medicine.

Go here to see the original:
Grant to compare large-scale genomic sequencing, standard clinical tests for childhood cancer patients - Baylor College of Medicine News (press...

Posted in Human Genetics | Comments Off on Grant to compare large-scale genomic sequencing, standard clinical tests for childhood cancer patients – Baylor College of Medicine News (press…

Police: Man left DNA in toilet during burglary – USA TODAY

Posted: at 4:47 am

7

Let friends in your social network know what you are reading about

When you gotta go, you gotta go.

Try Another

Audio CAPTCHA

Image CAPTCHA

Help

CancelSend

A link has been sent to your friend's email address.

A link has been posted to your Facebook feed.

This undated booking photo provided by the Ventura County Sheriff shows Andrew David Jensen, 42, of Ventura, Calif., who was arrested on July 28, 2017 on suspicion of committing a burglary.(Photo: Ventura County Sheriff via AP)

When you gotta go, you gotta go.

A California man accused of burglary left DNA evidence in the toilet of the home he robbed last October, Associated Press reported Tuesday.

Andrew David Jensen, 42, "did his business and didn't flush it,"Detective Tim Lohman of the Ventura County Sheriffs Office told the Associated Press.

When police initially responded to the break-in last year, they "were able to locate items that potentially contained the suspects DNA," according to a statement from the Ventura County Sheriff's Office. Forensic analysts were then able to match the samples from the scene with DNA already in their system.

Lohman told the Associated Press that this is the first case he knows of where fecal evidence collected from a toilet after a burglary had a successful DNA match.

"When people think of DNA evidence, they usually think of hair samples or saliva," Lohman told the Associated Press.

Jensen was arrested July 28 and remains in pre-trial custody, according to the police statement.

Contributing: Associated Press

Read or Share this story: https://usat.ly/2wGoa7r

Read the original post:
Police: Man left DNA in toilet during burglary - USA TODAY

Posted in DNA | Comments Off on Police: Man left DNA in toilet during burglary – USA TODAY

Sampling DNA From a 1000-Year-Old Illuminated Manuscript – The Atlantic

Posted: at 4:47 am

The York Gospels were assembled more than a thousand years ago. Bound in leather, illustrated, and illuminated, the book contains the four gospels of the Bible as well as land records and oaths taken by clergymen who read, rubbed, and kissed its pages over centuries. The Archbishops of York still swear their oaths on this book.

The York Gospels are also, quite literally, a bunch of old cow and sheep skins. Skin has DNA, and DNA has its own story to tell.

A group of archaeologists and geneticists in the United Kingdom have now analyzed the remarkably rich DNA reservoir of the York Gospels. They found DNA from humans who swore oaths on its pages and from bacteria likely originating on the hands and mouths of those humans. Best of all though, they found 1,000-year-old DNA from the cows and sheep whose skin became the parchment on which the book is written.

Remarkably, the authors say they extracted all this DNA without destroying even a tiny piece of parchment. All they needed were the crumbs from rubbing the book with erasers, which conservationists routinely use to clean manuscripts. The authors report their findings in a preprint that has not yet been peer-reviewed, though they plan to submit it to a scientific journal.

If their technique works, it could revolutionize the use of parchment to study history. Every one of these books is a herd of animals. Using DNA, researchers might track how a disease changed the makeup of a herd or how the skin of sheep from one region moved to another medieval trade routes. Its part of a growing movement to bring together scholars in the sciences and humanities to study medieval manuscripts.

Scientists have extracted DNA from parchment before, but this non-destructive technique expands the potential pool of research material. Archivists are loathe to allow researchers to cut off a piece of, say, the York Gospels, but some eraser crumbs? Sure. Thats why its such an exciting breakthrough. It allows a lot of different manuscripts from a lot of different areas to be analyzed together, says Bruce Holsinger, an English professor at the University of Virginia who is writing a book about parchment.

The idea to study parchment came to Matthew Collins, an archaeologist at the University of York, after a failed study in bones. A few years ago, he had a graduate student trying to extract ancient DNA from animal bones at an old Viking settlement. There were thousands of bones on the site, but only six that they tested yielded DNAtoo few for any statistically significant results. You can imagine the frustration, says Collins.

So Collins got to thinking about archives full of old manuscripts. You look at these shelves, and every one of them has a skin of an animal with a date written on it, he says. Suddenly you have thousands of animals. And you didnt even need to go out into the field and dig. When Collins and postdoctoral researcher Sarah Fiddyment first approached archives to collaborate though, they made the mistake of thinking like archaeologists used to routinely pulverizing bone for DNA analysis. They told us we would not be allowed to sample the parchments. Matthew and I didnt think of it, says Fiddyment. She ended up shadowing conservationists for several weeks and learned about their eraser technique. White plastic erasers made by Staedtler turned out to be perfect for cleaning manuscripts and for collecting DNA.

Collins and Fiddyment had previously collaborated with Holsinger to use the eraser technique to study proteins from uterine vellumso named because it is so thin that people thought that they were made from the skin of unborn livestock. Others, however suggested the skin came from different animals entirely, like squirrel or rabbit. The team published a study in 2015 analyzing proteins rubbed off of uterine vellum. They found that uterine vellum is indeed from calves, sheep, and goats, though not necessarily unborn ones.

With the York Gospels, Collins and Fiddyment went one step further to look for DNA with the eraser technique. They analyzed eraser dust from eight pages. Three of the samples yielded enough DNA to compare to modern cattle genomes, and the single most complete parchment genome was similar to modern Norwegian reds and Holsteins.

They also looked at the sex of the calves. Four of the five whose sex they could determine from DNA were female, which they found highly unusual if representative. Females are more valuable if you want to grow your herds, so why would you kill so many females to make parchment? Collins and Fiddyment consulted with Annelise Binois-Roman, a zooarchaeologist, who noted that a cattle plague swept through England in the years before the York Gospels were created. Perhaps those dead calves were salvaged to make parchment. Another colleague who specialized in the Anglo-Saxon era suggested maybe precious female calves were deliberately used because it is such an important book.

The First Book of Selfies

Collins and Fiddyment recognize that scientists alone cant make sense of the DNA from parchment. They need historians and literary scholars and curators to interpret their findings. Since then, Collins has reached out to scholars and archivists far and wide to collect more DNA samples.

Timothy Stinson, an English professor at North Carolina State University, first wrote about studying DNA from parchment seven years ago. I felt like the voice in the wilderness, says Stinson. Thats changed now with the efforts of Collins and others. Stinson is interested in using DNA to study how the production of books changed over time. Early on, he says, manuscripts were likely made up of related animals from the same herd. But as cities like London and Paris grew, guilds sprung up to make books, bringing in parchment from all over.

Collins points out that medievalists studying copying errors in manuscripts have long used the same phylogenetic programs that evolutionary biologists use to study how DNA mutations appear over time. DNA analysis is simply a new way to read the hidden messages in parchment.

View original post here:
Sampling DNA From a 1000-Year-Old Illuminated Manuscript - The Atlantic

Posted in DNA | Comments Off on Sampling DNA From a 1000-Year-Old Illuminated Manuscript – The Atlantic

How a ‘Velcro’ chip that traps alien DNA could improve prenatal testing – STAT

Posted: at 4:47 am

Why fentanyl is deadlier than heroin, in a single

Why fentanyl is deadlier than heroin, in a single photo

Allergan CEO looks smart for pledging to rein in

Allergan CEO looks smart for pledging to rein in prices. But will it make a difference?

The electrifying fitness technique that has doctors worried

The electrifying fitness technique that has doctors worried

Drug treatments didnt work. Can a simple diet help

Drug treatments didnt work. Can a simple diet help change these childrens lives?

After her own complicated delivery, lawmaker aims to address

After her own complicated delivery, lawmaker aims to address Texass alarming maternal death rate

White House rejects appeal to call national emergency over

White House rejects appeal to call national emergency over opioid epidemic

Go here to see the original:
How a 'Velcro' chip that traps alien DNA could improve prenatal testing - STAT

Posted in DNA | Comments Off on How a ‘Velcro’ chip that traps alien DNA could improve prenatal testing – STAT

Sacramento County Sheriff’s Department using new DNA technology for cold case – ABC10

Posted: at 4:47 am

Alexa Renee, KXTV 5:43 PM. PDT August 08, 2017

Investigators say Robin Brooks found dead 37 years ago was sexually assaulted prior to being stabbed to death in her apartment. (Photo: Sacramento County Sheriff's Department)

The Sacramento County Sheriff's Department is taking a crack at a cold case using an advanced DNA technology.

On April 24, 1980, Robin Gisela Brooks, was found stabbed to death in the bedroom of her Rosemont apartment. The 20-year-old had been sexually assaulted prior to her death and investigators found DNA evidence of the suspect at the crime scene but have been unable to identify the killer.

Brooks was scheduled to work at Donut Time on Kiefer Boulevard on the day she was found dead, but never show up for her shift. That's when coworkers came looking for Brooks and made the tragic discovery. Brooks family has a $10,000 reward for information leading to the arrest and conviction of the person responsible for her murder.

Her family may get closer to getting answers because of the sheriff's department new efforts in finding the suspect. The department has a full DNA profile of the suspect but no matches have come up on any federal or state DNA database.

Sacramento County investigators are hoping DNAphenotypingcould paint a picture of who killed Brooks. The DNA service cost the department $4,000 and is charged per case, it's not a flat rate fee. It's the first time the sheriff's department has used DNA phenotypingto try and solve a case.

What is DNA phenotyping?

Phenotyping can also help identify relatives of a person through DNA connections.

The testing cannot determine factors such as age, weight and facial hair since those details are not available in a person's genetic code. Parabonpredicts a person at 25-years-old by default. Forensic artists would have to adjust age, facial hair and weight based on description information provided by police or eye witnesses.

DNA phenotyping helps illustrate what a person may look like when there are no leads on identification or when a DNA profile doesn't match anything in a database. The tool is especially helpful in case like the Brooks murder, where there were no eyewitnesses to the crime to describe a suspect, but traces of DNA were left behind.

The technology was created fordefense, security, justice, and intelligence communities and has been used by numerous agencies to help generate leads. Private citizens have used Snapshot to find ancestry information.

Has DNA phenotyping helped solve cases?

Phenotyping can be a great tool for eliminating suspects and sparking leads.

Police had previously believed the suspect was a Latino male because Bouzigard was last seen with a group of Latino men. However, the Parabonanalysis found the suspect to be a white male.

Parabon led the Rockingham County Sheriff's Office to Jose Alvarez Jr., the brother of couple's daughter's boyfriend at the time of the murder. He was arrested in Aug. 2015 and later pled guilty to two both murders. In July of 2016, he was sentenced to two consecutive life sentences without the possibility of parole.

Phenotyping can also help with unidentified remains when there is no visual on what the person may have looked like.

What are the issues with DNAphenotyping?

Phenotypingrelies on identifying using physical appearance, which is a method that can run into some problems. Parabontechnology cannot positively create a photo ID of a person, it can only help create a visual when there are no other leads.

Also, a person can look like a sibling or relative, or even another completely unrelated person. There's no science available that can confirm a person's DNA through face structure.

The only way to identify someone using DNA phenotypingis if a person of interest is tested for DNA and it comes back as a match with the sample used to create the Parabonsketch. This means, there'd have to be a tip leading to that person. Unfortunately, the actual suspect may not look like the sketch and misleading tips may come in.

Another issue the ACLU touches on is social and racial profiling. When a sketch is that of a person of color it can fuel "existing societal prejudices to further increase the risks to innocent people". Also, police officers with less sophisticated science tools may rely too heavily on the images and pressure DNA tests from innocent people.

Phenotypingshould be used as more of a tool to narrow down or eliminate suspects, rather than as a point of probable cause to "create" a suspect.

In cold cases such as the killing of Brooks, phenotypingcan help jog memories of someone who may have seen something or knows anything about the suspect, since there is nothing else to go on to solve the case but the DNA profile of the suspect.

Below are the Snapshot DNA phenotyping results for the suspect in the Brooks case. Note physical appearance of subject may have changed over the years.

Snapshot prediction of suspect in 1980 murder of Rosemont woman, Robin Grisela Brooks. (Photo: Parabons NanoLabs Inc.)

Snapshot prediction of suspect in 1980 murder of Rosemont woman, Robin Grisela Brooks. (Photo: Parabons NanoLabs Inc.)

2017 KXTV-TV

Read more:
Sacramento County Sheriff's Department using new DNA technology for cold case - ABC10

Posted in DNA | Comments Off on Sacramento County Sheriff’s Department using new DNA technology for cold case – ABC10

NIH accelerates the use of genomics in clinical care – National Institutes of Health (press release)

Posted: at 4:46 am


National Institutes of Health (press release)
NIH accelerates the use of genomics in clinical care
National Institutes of Health (press release)
The National Institutes of Health (NIH) is awarding $18.9 million towards research that aims to accelerate the use of genome sequencing in clinical care. The new awards will generate innovative approaches and best practices to ensure that the ...
NIH accelerates genomics in clinical healthcareUPI.com

all 3 news articles »

See more here:
NIH accelerates the use of genomics in clinical care - National Institutes of Health (press release)

Posted in Genome | Comments Off on NIH accelerates the use of genomics in clinical care – National Institutes of Health (press release)

TOM PURCELL: Too much of a good thing? – The Daily Freeman

Posted: at 4:46 am

A 125-year life expectancy for human beings? I have zero desire to stick around that long.

Ah, yes, you speak of a debate among scientists over human longevity. I read about it at Business Insider. Some scientists argue that the maximum age humans may live is 115 years, whereas others argue that 125 years is possible.

A hundred and twenty-five years of watching Republicans and Democrats going at it? The heck with that.

Living is rife with challenges, to be sure. But living a long life has its upsides. Wouldnt you want to visit your parents and other family members for a lot more years than most of us are able? Wouldnt you like to see them all at a Sunday dinner several more times than most human beings are able?

Advertisement

Maybe with your family. My family has taken years off of my life!

I see, but wouldnt it be awesome if some of our finest human beings could stick around longer? Don Rickles, one of the greatest entertainers ever, died this year at 91. How great would it be to keep him around for two more decades?

True, but if Rickles were to stick around longer, that means annoying celebrities would stick around, too, and keep yapping at us every time a Republican becomes president.

There are other upsides to a longer life. What if we could keep our greatest minds around longer? Where would the world be if Einstein had another 25 years to unlock the mysteries of the universe?

But what if he figured out ways to extend human life even further, which would require me and the wife to have to keep coming up with new things to bicker about? Who has that kind of energy?

The downsides are a fair point. As people live longer, they could overburden government programs, such as Social Security. Where would we get all the money to support them?

How about we especially extend the lives of the rich so we can take them to the cleaners?

And living is expensive. If you live to 125, how will you pay for your housing and food and everyday expenses?

Thank goodness McDonalds is always hiring, but I for one have no desire to flip burgers at the age of 125.

The costs of medical care are too high for millions now. I imagine that at 125 years of age, ones medical bills would be difficult to manage.

Look, as a middle-aged guy, who is already showing signs of fatigue, here is what I know about living. Life is largely made up of colds, bills, speeding tickets and people who let you down. These experiences are connected together by a series of mundane tasks.

Did anyone tell you how cheerful you can be? Go on.

Well, these drudgeries are occasionally interrupted by a wonderful meal, a really good laugh with friends or a romantic evening with a lovely woman. Then the mundane stuff starts all over again. Who wants 125 years of that?

A lot of people do. The human lifespan has improved significantly in the past few generations. Millions are living healthy lives beyond the age of 80 today, and, when they were younger, few of them expected to live that long. Why not live relatively good lives until 125?

Because then Id really worry about my slacker son.

Why?

Hes 35 years old and still living at home. If we drastically extend lifespans, my wife will have to tell him: Son, youre 100 years old! When are you going to move out of the basement and get a job?

Tom Purcell is syndicated by Cagle Cartoons Inc. Readers may write to him via email at Tom@TomPurcell.com.

See the original post:
TOM PURCELL: Too much of a good thing? - The Daily Freeman

Posted in Human Longevity | Comments Off on TOM PURCELL: Too much of a good thing? – The Daily Freeman

An extra dose of this longevity hormone helped make mice smarter … – Popular Science

Posted: at 4:46 am

Klotho, in ancient Greek mythology, is one of the Fates controlling the span of human destiny tasked as she was with cutting the string that determined the length of a persons life. Klotho is also a naturally occurring hormone in the body. More than two decades ago, Japanese researchers discovered that this hormone plays a role in aging. People with more klotho in their body, tend to live longer and to retain more of their facultiesthat is to stay sharpwell into old age.

There are many elderly people who walk around and have completely normal, sharp vibrant brain function despite the fact that they are much older and the fact that they have a lot of disease toxins in the brain, Dr. Dena Dubal a neurobiologist at the University of California, San Franciscos Memory and Aging Center told Popular Science.

Dubal is the author on a study released today in the journal Cell Reports that looks at what happens to brain function when you inject klotho protein into mice.

Aging researchers like Dubal arent interested in extending life for its own sakethey dont have a Methuselah complexbut rather because aging is the biggest factor for disease. If they can find a way to slow aging, or at least its effects, they might find a way to allow us to avoid the cognitive declines, and diseases such as stroke, heart disease, and diabetes that tend to come as we flip through more pages on the calendar.

A few years ago, we discovered in collaboration with several people that in human populations those people that had higher levels of klotho had better cognitive functions in normal aging, says Dual.

Which is great if you happen to be genetically blessed with higher levels of klotho, less great if youre not.

Earlier studies have looked at the impacts of klotho on longevity and health, including brain health, but they tended to rely on genetically modified mice. The genes of these mice had been modified to allow them to produce more klotho or less.

Those studies found that mice modified to produce more klotho lived longer, which is promising. But despite recent advances, genetically modifying humans is still an ethical minefield away in the future, especially if the modifications are being made to improve wellbeing as opposed to preventing disease. And, genetically altering embryos might help future populations, but it doesnt do much for those of us already living. So, Dubal wanted to see is if mice injected with klothoacting essentially a hormonal supplementwould show cognitive improvements.

The answer, seems to be yes.

To get the result, Dubal and her colleagues injected three types of mice with a portion of the protein. They injected young mice, aged mice, and mice genetically altered to have brains similar to that which we would see in Alzheimers or Parkinsons patients in humans.

Within hours they showed better cognitive function, says Dubal.

Since you cant exactly administer a mouse an IQ test, they assessed brain power based on the mices ability to navigate a series of water mazes, in an experiment that sounds on par with human a trip to Wisconsins famed waterslide park, The Dells.

They found that mice that had daily injections and were better able to navigate the maze (as measured by the distance traveled to find a hidden platform) than their control group peers. In a classic example of work smarter, not harder, the klotho mice were just much more efficient seekers.

We tested them two weeks later in a different cognitive test and they were still smarter, says Dubal, which suggested that getting the klotho protein into their bodies combined with brain training and stimulation had a long-lasting effect in their brain. Because the half-life of the protein is only seven and a half hours long, any of the protein should have been long out of their system.

There are a few caveats.

First, this was an experiment in micenot in humans. While its incredibly promising, the study results are short term and they werent looking for side effects. The pace at which a promising scientific study is turned into a supplement of dubious efficacy is stunning these days, so please dont subject yourself to some back-alley klotho injection. Between resveratrol and superfoods weve been there before.

At the same time, we know that klotho levels can be affected not only by genetics - but also by stress. If you want to help your body keep its klotho levels at your own peak you might want to try proven stress reduction techniques like exercise and chilling out about your own impending mortality.

Finally, the researchers arent sure how klotho seems to be generating this effect because the protein is too big to pass from the body into the brain. For a long time, weve studied the brain in isolation from the body with the brain mostly telling the body what to do, and the body acting like a series of censors that give the brain useful data. But this study like our growing understanding of the connection between our microbiome and brain health, and exercise and brain health, this study touches on our growing understanding of how the body connects to the brain to help make the brain more resilient.

Read the original:
An extra dose of this longevity hormone helped make mice smarter ... - Popular Science

Posted in Human Longevity | Comments Off on An extra dose of this longevity hormone helped make mice smarter … – Popular Science