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2024-11-11

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submitted 1 month ago by ooli to c/science
 
 

No psychiatric treatment has attracted quite as much cash and hype as psychedelics have in the past decade. Articles about the drugs’ surprising results—including large improvements on depression scores and inducing smokers to quit after just a few doses—earned positive coverage from countless journalists (present company included). Organizations researching psychedelics raised millions of dollars, and clinicians promoted their potential to be a “new paradigm” in mental-health care. Michael Pollan’s 2018 psychedelics book, How to Change Your Mind, became a best seller and a Netflix documentary. Psychedelics were made out to be a safe solution for society’s most challenging mental-health problems.

But the bubble has started to burst: It’s been a bad year for fans of psychedelics.

A few months ago, two articles appeared, one in The New York Times and another in Business Insider, that portrayed major figures in psychedelics research as evangelists whose enthusiasm for the drugs compromised the integrity of their findings. In August, the FDA rejected the first application for therapy assisted by MDMA, the drug commonly known as ecstasy, saying that it “could not be approved based on data submitted to date,” according to the company that brought the application, Lykos. And five people, including two doctors, were recently charged in the death of the Friends actor Matthew Perry, who was found unconscious in his pool after he took large doses of the psychedelic ketamine. (Three of the five have reached plea agreements; the other two pleaded not guilty.)

These incidents, though unrelated, point to a problem for psychedelic research: Many of the studies underpinning these substances’ healing powers are weak, marred by a true-believer mentality among its researchers and an underreporting of adverse side effects, which threatens to undermine an otherwise bright frontier in mental-health treatment.

Read: Psychedelics open your brain. You might not like what falls in.

Psychedelics are by nature challenging to research because most of them are illegal, and because blinding subjects as to whether they’ve taken the drug itself or a placebo is difficult. (Sugar pills generally do not make you hallucinate.) For years, scientific funding in the space was minimal, and many foundational psychedelic studies have sample sizes of just a few dozen participants.

The field also draws eccentric types who, rather than conducting research with clinical disinterest, tend to want psychedelics to be accepted by society. “There’s been really this cultlike utopian vision that’s been driving things,” Matthew W. Johnson, himself a prominent psychedelic researcher at Sheppard Pratt, a mental-health hospital in Baltimore, told me.

Johnson, who has published many studies on psilocybin, the active compound in magic mushrooms, recently left his lab at Johns Hopkins after a dispute with Roland Griffiths, a senior researcher with whom he worked closely. Griffiths, who died last year, said in talks that psychedelics might be “critical to the survival of the human species.” He also behaved like a “spiritual leader,” according to a complaint by Johnson obtained by The New York Times, ran “his psychedelic studies more like a ‘new-age’ retreat center,” and recommended spiritual literature and meditation classes to study participants. Johnson argued that Griffiths’s emphasis on the metaphysical risked steering study participants toward his desired outcomes.

Albert Garcia-Romeu, the current associate director of the Hopkins psychedelics lab, disputes this description of Griffiths and the lab in general. “I never saw him behave like a ‘spiritual leader,’ or running the lab like a ‘new-age retreat center,’ whatever that means,” Garcia-Romeu told me. He noted that researchers have long used psychedelics to explore spiritual experiences but that “there was no imposition of any particular beliefs going on.”

Still, Griffiths isn’t the only one who zealously promoted psychedelics. Take Rick Doblin, the founder of an organization called the Multidisciplinary Association for Psychedelic Studies, or MAPS. He, too, is prone to grandiose thinking, saying he believed psychedelics could be “an antidote to evil” or might lead to a more “spiritualized humanity.” Doblin also encouraged marijuana use at work, arguing that there are “smokable tasks,” which some people “do better while under the influence of marijuana, such as working on complicated spreadsheets.” (Betty Aldworth, the director of education at MAPS, told me that Doblin was “adamant about the science being valid and proving out the answers to these questions through clinical trials.” Doblin did not reply to a request for comment.)

Neşe Devenot, a Johns Hopkins writing instructor and a former MAPS volunteer, told me that many people in the psychedelics field let their political and spiritual beliefs “influenc[e] the type of data that is being collected. The researchers should have more clinical equipoise and not be so assured of what works.”

Inside Lykos, a MAPS spinoff, many staffers were sold on the presumed benefits of MDMA, according to Stat News. One trial participant said her Lykos therapists told her she was “helping make history” and was “part of a movement.” The company failed to collect data on some of the side effects of MDMA, such as euphoria, that might have revealed the drug’s potential for abuse, Stat reported. (In a statement to Stat News, the company stood by its studies, saying that they were conducted with appropriate checks and balances and that the company did add data on positive side effects to some protocols.)

Last month, The Wall Street Journal reported that several participants in the Lykos studies said they felt pressured to report only good outcomes. Three of them said that their thoughts of suicide worsened after they took the MDMA, but that these deteriorations weren’t captured by the study results. (In response to the Journal, Lykos said it reported any significant increases in suicidality to the FDA.)

The FDA is reportedly now looking into Lykos’s data, and the journal Psychopharmacology retracted three papers stemming from MAPS’ early MDMA trials because of “protocol violations amounting to unethical conduct.” (MAPS’ Aldworth says the studies should have been revised instead of retracted. Lykos did not respond to a request for comment.)

The underreporting of adverse events and overhyping of tepid data appear to be widespread in psychedelic research. One review concluded that in many studies of psychedelics, adverse events “were not systematically assessed” and are therefore probably underreported.

And although esketamine (a ketamine-like nasal spray) was approved by the FDA in 2019, one 2021 review noted that there is “a paucity of data concerning long-term safety” of ketamine and esketamine, and a 2023 review found that esketamine’s negative side effects have been systematically underreported in journal articles. Some researchers overstate ketamine’s benefits and underplay its risks, according to a recent review article.

Many people taking ketamine for mental-health issues use the drug repeatedly for weeks or months, but little long-term safety data on the drug exist, says Boris Heifets, an anesthesiology and psychiatry professor at Stanford. For some, the drug’s dissociative effects can become addictive—Matthew Perry was injecting the drug six to eight times a day, prosecutors said, and he spent $55,000 on it in the month before he died. “You’re giving a drug that most definitely has abuse potential, and you’re giving it out online, without supervision, to anybody who can convince you they’re depressed,” Heifets told me. “It’s honestly a little fucked up.”

Read: A new chapter in the science of psychedelic microdosing

In a recent study conducted by Heifets, surgeons administered ketamine or a saline placebo to patients who were undergoing surgical anesthesia. Unlike patients in many psychedelic studies, these were truly blinded: They were unconscious, so those who got ketamine didn’t have a ketamine trip. It turned out that about half of both groups, ketamine and placebo, felt less depressed afterward. And those who felt less depressed assumed they had gotten ketamine.

In other words, ketamine did work, a little. But so did the placebo. Heifets attributes this effect to the extensive care and attention that all the study participants received before the procedure. The researchers told them that their mental health is important, and listened to them talk about their problems—in some cases, for hours. They told them that ketamine might make them feel better. To Heifets, this shows that rather than jumping to ketamine, doctors would do well to connect depressed people with caring, attentive therapists as a first step. (But “good luck finding one,” he acknowledged.)

These scientific shortcomings don’t seem to be dampening the enthusiasm about psychedelics. Hundreds of ketamine clinics across the country purport to treat conditions as varied as anxiety and chronic pain, and online services will send ketamine to people’s homes. An initiative to legalize psychedelics will be on the ballot in Massachusetts in November. Veterans’ groups and others are clamoring for the legalization of psychedelic therapies. This is understandable, because these drugs do show promise, especially for treating depression, PTSD, and certain types of addiction. The alternatives—bouncing between SSRIs or scrambling to find an in-network therapist—are bleak, and they fail plenty of desperate people. No new PTSD treatments have been approved in two decades. Some people truly have been cured of their ailments with short, monitored courses of psychedelics.

But the intense interest in psychedelics makes it only more important that the science behind them is as rigorous as possible, untainted by the personal views of researchers. Suggesting that people should get off proven medications in order to try MDMA or psilocybin is dangerous unless those drugs are backed by airtight evidence. And when dealing with psychologically vulnerable people, researchers would do well to align expectations with the reality of what psychedelics can actually accomplish.

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Act now and you too can see as well as a bat!

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WTF Iran???

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Feeding a baby born by caesarean section milk containing a tiny bit of their mother’s poo introduces beneficial microbes to their gut, according to a clinical trial. The approach might one day help to prevent diseases during childhood and later in life.

Some studies show that babies born by c-section, rather than vaginal birth, have a higher risk of asthma, inflammation of the digestive system and other diseases associated with a dysfunctional immune system... Experiments have attempted to compensate for that by swabbing babies born by c-section with microbes from their mother’s vagina or giving them these microbes orally, a practice known as ‘vaginal seeding’. But this technique has had limited success, because vaginal microbes, scientists have learnt, cannot effectively colonize infants’ guts...

Helve and his colleagues have been pioneers in testing whether faecal transplants can instead improve the health of a baby’s microbiome. In their latest trial, which recruited women scheduled for a c-section at the Helsinki University Hospital, the researchers mixed a fluid containing 3.5 milligrams of a mother’s poo into milk and gave the concoction to the corresponding baby. They did this for 15 babies during their first feed. Another 16 babies received a placebo.

An important next step in the field, Shao says, would be to pinpoint the specific maternal gut microbes that are most likely to transmit to and colonize their babies’ guts. Shao asks: “If these species do exist across human populations, wouldn’t it be more effective and safer” to give newborns a laboratory-made transplant that’s guaranteed to be pathogen-free?

"This is the shit"

But seriously don't try this at home. Fecal matters can contain pathogens, in fact 54 of the 90 women screened were excluded because of detected pathogens. If this goes well maybe ppl can make some type of lab-made probiotics for C-section babies or stuff

The abstract presented at IDWeek 2024: https://idweek2024.eventscribe.net/index.asp?presTarget=2886841

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A newly described species of tardigrade is giving scientists insights into what makes these tiny eight-legged creatures so resistant to radiation.

Now, scientists have sequenced the genome of a species new to science, and revealed some of the molecular mechanisms that give tardigrades their extraordinary resilience. Their study, published in Science on 24 October, identifies thousands of tardigrade genes that become more active when exposed to radiation. These processes point to a sophisticated defence system that involves protecting DNA from the damage that radiation causes and repairing any breaks that do occur.

The authors hope that their insights could be harnessed to help protect astronauts from radiation during space missions, clean up nuclear pollution or improve cancer treatment.

"Radiation and multi-omics sequencing go brrrr"

Original paper on Science: https://doi.org/10.1126/science.adl0799

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We've all been there – caught outside without an umbrella as the sky opens up. Whether it's a light drizzle or a heavy downpour, instinct tells us that running will minimise how wet we get. But is that really true? Let's take a scientific look at this common dilemma.

You're out and about, and it starts to rain – and naturally you've forgotten your umbrella. Instinctively, you lean forward and quicken your pace. We all tend to believe that moving faster means we'll spend less time getting wet, even if it means getting hit with more rain as we move forward.

But is this instinct actually correct? Can we build a simple model to find out if speeding up really reduces how wet we'll get? More specifically, does the amount of water that hits you depend on your speed? And is there an ideal speed that minimises the total water you encounter on your way from point A to point B?

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The ability of large language models (LLMs) to create text and images almost indistinguishable from those created by humans is disrupting, if not revolutionizing, countless fields of human activity. Yet the potential for misuse is already manifest, from academic plagiarism to the mass generation of misinformation.

This week, Sumanth Dathathri at DeepMind, Google’s AI research lab in London, and his colleagues report their test of a new approach to ‘watermarking’ AI-generated text by embedding a ‘statistical signature’, a form of digital identifier, that can be used to certify the text’s origin. The word watermark comes from the era of paper and print, and describes a variation in paper thickness, not usually immediately obvious to the naked eye, that does not change the printed text. A watermark in digitally generated text or images should be similarly invisible to the user — but immediately evident to specialized software.

Dathathri and his colleagues’ work represents an important milestone for digital-text watermarking. But there is still some way to go before companies and regulators will be able to confidently state whether a piece of text is the product of a human or a machine. Given the imperatives to reduce harm from AI, more researchers need to step up to ensure that watermarking technology fulfils its promise.

This is the official paper and the Nature News report related to the SynthID project. Basically, "watermarking" to make sure the model outputs can be easily recognized computationally... but it's not foolproof. Especially relevant in light of AI regulations. News article itself contains some interesting opinions

Paper: https://doi.org/10.1038/s41586-024-08025-4

GitHub repo: https://github.com/google-deepmind/synthid-text

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I think there needs to be a solution to the racism shown by the research done here.

Note: I know that the article have "what we can do" section, but it does not propose any applicable solution.

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submitted 1 month ago* (last edited 1 month ago) by Sterile_Technique to c/science
 
 

I'm guessing the legal fuzziness is causing a reluctance to report from providers, but I'm having a hell of a time finding much of anything post RvW.

Specifically, I'm wanting to compare rates of IUFDs/stillbirths, speed and effectiveness of care following IUFDs/stillbirths, and maternal complications/deaths - all in states (or countries) that offer access to abortion care vs locations where that's restricted.

Hypothesis is that if someone needs an abortion and can't get one, they're more likely to have a IUFD/stillbirth, and since poor abortion access correlates with poor women's health in general, that they're more susceptible to sepsis or death as a result of delayed or insufficient care following the IUFD/stillbirth.

This is for a presentation that's ready to go as is, but with an election happening RIGHT NOW I'd really like to drive these points home.

Any pointers for sources of info on things like this would be much appreciated - thank you, all!

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Many voters are willing to accept misinformation from political leaders – even when they know it’s factually inaccurate. According to our research, voters often recognize when their parties’ claims are not based on objective evidence. Yet they still respond positively, if they believe these inaccurate statements evoke a deeper, more important “truth.”

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AlphaFold predicted that three sperm proteins work together to form a complex. Two of these proteins were previously known to be important for fertility. Pauli and her colleagues then confirmed that the third is also critical for fertility in both zebrafish and mice, and that the three proteins interact with one another.

The team also found that, in zebrafish, the trio creates a place for an egg protein to bind, providing a mechanism by which the two cells could recognize one another. “It’s a way to say, ‘Sperm, you found an egg’ and ‘Egg, you found a sperm’,” says Andreas Blaha, a biochemist at the Research Institute of Molecular Pathology and co-author of the paper.

The findings might one day yield a way to screen people struggling with infertility, to find out whether problems with this complex could be the cause, says Wright.

And the results highlight a role for AlphaFold in studying fertilisation, he adds. “We’re limited in terms of experiments,” he says. “It might be that these modelling studies have an important role to play in the future.”

In other words, the team used AlphaFold to help with discovering a three-protein complex that allows sperm & egg to bind together. And this complex seems to be conserved between zebrafish and humans (!!). Despite the news title: this study is actually less about AlphaFold and more about using it to help do very important biochemistry

Original paper (open access): A conserved fertilization complex bridges sperm and egg in vertebrates. https://doi.org/10.1016/j.cell.2024.09.035

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"Scientists have designed a new form of insulin that can automatically switch itself on and off depending on glucose levels in the blood. In animals, this ‘smart’ insulin reduced high blood-sugar concentrations effectively while preventing levels from dropping too low... A spokesperson for Novo Nordisk says that although this study is a proof of principle of NNC2215’s glucose-sensitive insulin properties, further research to optimize the molecule is ongoing."

From the research article: "Here we report the design and properties of NNC2215, an insulin conjugate with bioactivity that is reversibly responsive to a glucose range relevant for diabetes, as demonstrated in vitro and in vivo... In animal studies, the glucose-sensitive bioactivity of NNC2215 was demonstrated to lead to protection against hypoglycaemia while partially covering glucose excursions."

Brought to you by a passionate research group from Novo Nordisk, home of the $1,349 per month weight-loss drug Wegovy

This is still fairly early-stage research so the final commercialization might take quite some time

The article itself, open access: https://doi.org/10.1038/s41586-024-08042-3

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#Abstract

Twenty years after the first publication using the term microplastics, we review current understanding, refine definitions and consider future prospects. Microplastics arise from multiple sources including tires, textiles, cosmetics, paint and the fragmentation of larger items. They are widely distributed throughout the natural environment with evidence of harm at multiple levels of biological organization. They are pervasive in food and drink and have been detected throughout the human body, with emerging evidence of negative effects. Environmental contamination could double by 2040 and widescale harm has been predicted. Public concern is increasing and diverse measures to address microplastics pollution are being considered in international negotiations. Clear evidence on the efficacy of potential solutions is now needed to address the issue and to minimize the risks of unintended consequences.

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