Yes, but the future has probably always been bleak, some people have always been corrupt, and yet humans are still here. The same tools used to produce and magnify all that fakery can also be used to increase transparency and increase knowledge, to allow people to inform themselves, better than ever before. There are good people trying to make things better, as ME/CFS Skeptic's blog illustrates.Fake news. Fake research. Fake people. Damn the future is bleak.
Indeed. A general lowering of methodological standards, in particular inadequate control, is the broader picture.but fabrication and falsification of data is only the end of the tip of the iceberg.
Ha, that's interesting. So post-exertional malaise became 'submit-exertional malaise'?Having said that, last year I came across a paper with "tortured phrases", obviously the product of some automated tool, although it wasn't a biomedical paper.
Yup. Looking back at the paper I spotted another one, too - "capability player bias" (probably an automated rephrasing of "participant bias").Ha, that's interesting. So post-exertional malaise became 'submit-exertional malaise'?
That link was to a range of papers for Digoxin in various diseases, all suspiciously similar. This is the link to the ME one.On Twitter Wigglethemouse also suggested this study as problematic:
https://www.ncbi.nlm.nih.gov/pubmed/?term=Kurup+RK%5BAuthor%5D+digoxin%5BTitle%5D
And the Perez study using 23 and ME data:
Genetic Predisposition for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: A Pilot Study 2019 Perez Nathanson Klimas et al | Science for ME
We investigated 172 clinical trials from one group and notified serious integrity concerns to all journals and publishers in July 2019.[3] The concerns were similar for all trials, including evidence that random allocation of participants could not have produced the treatment groups reported, evidence that the distribution of numbers of participants withdrawing from the trials was implausible, frequently contradictory reporting of the size of participant populations, implausibly prolific research activity, unethical conduct, and very frequent discrepancies between trial registration documents and journal publications for study conduct, study location, participant age, and participant number (including wholesale updating of trial registration documents after we notified these concerns to journals and publishers).
LinkMore than five years later, only 22 of the 157 trials covered by Web of Science have been retracted, with to date 289 citations in systematic reviews, clinical guidelines, and consensus statements. The 135 unretracted trials have 1989 citations in systematic reviews, clinical guidelines, and consensus statements. Presumably, some of these currently unretracted trials will eventually be retracted, further compounding the problem.
My impression as a patient is that they don’t care about it and take anything official as «true».It still find it weird that standards are so low in (medical) science. So how do real scientists deal with this: do they simply ignore 90% of the literature and only focus on results from labs/teams they know and trust?
This is a funny one: Book on AI looks to be written by LLM full of made-up stuff https://retractionwatch.com/2025/06...achine-learning-is-full-of-made-up-citations/
At least AI is making it glaringly obvious that the quality control at most journals is terrible..The same day Behrendt replied to our query, Springer Nature published a post on its blog titled, “Research integrity in books: Prevention by balancing human oversight and AI tools.”
“All book manuscripts are initially assessed by an in-house editor who decides whether to forward the submission to further review,” Deidre Hudson Reuss, senior content marketing manager at the company, wrote. “The reviewers – subject matter experts – evaluate the manuscript’s quality and originality, to ensure its validity and that it meets the highest integrity and ethics standards.”
I meant the true scientists, the people who really want to figure things out, discover truth etc, rather than academics making a career.My impression as a patient is that they don’t care about it and take anything official as «true».
From a risk perspective, it makes sense. You won’t suffer consequences from the government by doing what the government told you to do.
Kahneman comes to mind as a Nobel prize winner that failed to do exactly that (and has admitted to doing so):I meant the true scientists, the people who really want to figure things out, discover truth etc, rather than academics making a career.
The people who will win future Nobel prizes. I suspect that they simply ignore most of what gets published.
On one of my first interactions with an ME/CFS researcher they explained to me 95% of research is not replicable. I think the biggest issue they explained was incorrectly controlled methods and sample handling. At the time I think I asked about metabolomics and Seahorse experiments. I was shocked but then discovered from others that the 90-95% was true.So how do real scientists deal with this: do they simply ignore 90% of the literature and only focus on results from labs/teams they know and trust?