A new study casts doubt on the ‘extreme male brain’ theory, which posits that high levels of testosterone in the womb raise the risk of autism.
Researchers studied 81 children with congenital adrenal hyperplasia (CAH), a condition marked by a prenatal overproduction of testosterone in girls. According to the extreme male brain theory, girls with CAH should have more autism traits than those without CAH. But this isn’t the case. The 43 girls with CAH in the study achieved similar scores on a test for autism traits as those without CAH.
The researchers also looked at amniotic testosterone in 92 children without CAH or autism. Testosterone levels do not track with autism traits in these children either.
The study, published last week in the Journal of Child Psychology and Psychiatry, is small. But it supports the notion that something other than testosterone underlies the overwhelming preponderance of autism among boys relative to girls.
23 and everyone
By pooling genetic data from more than 450,000 people, researchers have uncovered 15 regions of the genome tied to depression. The data came from the popular gene-testing company 23andMe.
The crowdsourcing feat, published Monday in Nature Genetics, shows the power of numbers when probing complex conditions. Previous efforts to unearth the genetic roots of depression, including a 2013 study of 9,000 people, came up short.
“The big story is that 23andMe got us over the inflection point for depression,” Douglas Levinson, professor of psychiatry and behavioral sciences at Stanford University, told MIT Technology Review. “That is exciting. It makes us optimistic that we are finally there.”
A similar approach could help researchers close in on genetic variants tied to autism. A genome-wide association study of about 17,000 people with autism — the largest analysis to date — turned up five segments of DNA tied to the condition.
MIT Technology Review / 01 Aug 2016
More and more researchers are sharing their raw data so that other labs can try to replicate their results. But such openness is still far from the norm, according to a trio of papers published yesterday in The New England Journal of Medicine.
In one of the papers, U.S. Senator Elizabeth Warren urges regulatory agencies and medical journals to make data-sharing a mandatory part of the clinical trial approval and publication process. Obstacles include fears about being scooped, protecting private medical information and finding a secure place for the data to live.
“I appreciate that there are many policy, privacy, and practical issues that need to be addressed in order to make data sharing practical and useful for the research community,” she writes in the report. “But the stakes are too high to step back in the face of that challenge.”
In the past, researchers have held their data close until they’re ready to publish. But almost half of all pediatric clinical trials go unfinished or unreported in the scientific literature, according to a study that appeared yesterday in Pediatrics. As a result, researchers may spend time and money repeating work. Worse, the considerable time and effort families put into these studies may go to waste.
“Thousands of children have participated in these trials, representing considerable inefficiencies and waste of financial and human resources,” the authors write.
The New England Journal of Medicine / 04 Aug 2016
Pediatrics / 02 Aug 2016
How do you feel about the prospect of preventing childhood conditions through gene editing, or easing Alzheimer’s with a brain implant? If you feel good about these fixes, you’re in the minority.
More Americans are wary of these possibilities than are excited about them, according to a Pew Research Center survey of nearly 5,000 people. Some see the high-tech treatments as “meddling with nature,” and many fear they could be put in play before they are fully vetted. There’s also concern that only the wealthy would be able to afford them.
Pew Research Center / 26 Jul 2016
The president of the prestigious Pasteur Institute in Paris must relinquish his post next year not because of his performance, but because of his age, Science reports.
Virologist Christian Bréchot became president of the institute in 2013, starting a four-year term that ends in October 2017. He would like to stay on for a second term. But a long-standing statute of the Pasteur Foundation says that “at the time of his or her nomination or of the renewal of his or her mandate, the president must not have reached the age of 65.”
Bréchot turns 65 next July.
Some researchers say the statute is likely to kill the momentum for plans that Bréchot put into motion his first term. Others say it’s time for him to go, regardless of his age, because they don’t like his leadership. Is 65 too old to be a scientific leader? Tell us what you think in the comments section.
Science / 01 Aug 2016
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