How investigators, journalists, and editors contribute to mistrust in science
I had already scheduled an essay about three new pet peeves of mine for tomorrow when I received this submission from Dr. Bauchner. Tomorrow’s post will offer three pieces of advice to assuage my aggravation. Dr. Bauchner takes a much broader look at problems in publishing today; problems that affect investigators, editors, journalists, funders, academic institutions, and beyond.
Adam Cifu
As a long-time actor in the ecosystem of research and publishing, I have come to believe that the future is uncertain – the weaponization of data, the politicalization of funding, and the dramatic increase in the number of journals and manuscripts – is a threat to the future of science and public belief in it. My focus is on investigators, journalists, and editors – and how some are inadvertently contributing to mistrust in science.
Investigators
Fueled by the need for recognition, grant support, and promotion, as well as the legitimate intent to contribute to science, investigators are publishing more manuscripts. Powered by publicly available data sets, electronic health records, and AI, the increase has been dramatic. Investigators must ask themselves whether their report will benefit science, clinical care, or public policy. Rather than focusing on more publications, a shift in mindset to quality, is necessary. I acknowledge that for medical students and residents, for whom publications have become an important metric, this will be difficult. But for faculty, at all levels, a focus on quality is necessary.
Journalists
I find the reporting of science to be uneven. Some journalists continue to struggle with the difference between hypothesis-generating studies, which are the majority of clinical studies, versus those studies that demonstrate causal relationships, certainly randomized clinical trials, and perhaps meta-analyses and Mendelian randomization studies (if they fulfill all the important scientific criteria). In addition, journalists often don’t comment on the difference between statistical and clinical significance. For RCTs, they rarely report the number needed to treat. Journals are also lacking with respect to the last comment – and we mislead the public by not reporting NNT. For example, in a recent trial published in NEJM that examined outcomes of veterans who received COVID-19 and influenzae vaccines, the COVID-19 vaccine was 64% effective in reducing COVID-19 mortality, statistically significant, with a NNT of 4545. Although both outcomes are true, they are likely to be interpreted differently by people.
Editors
Editors play a powerful role in science. They are the gatekeepers, making thousands of decisions each day regarding what will be published and what will not. Unlike preprint servers, journals place a “stamp of approval” on publications, which legitimizes them. And for the major journals, what they publish is unleashed to a worldwide audience in a matter of seconds. The task has become nearly impossible due to the relentless increase in the number of submitted manuscripts. Editors must embrace AI as an aid to the decisions they make. AI should not replace human decision-making, but AI has the capacity to ensure that a RCT and meta-analysis have been registered and are being reported accurately, are following the appropriate reporting guidelines, employ a valid statistical approach, and verify that references are “real” – just to name a few possibilities. In addition, all editors need to be aware of how journals are funded. This is more complicated for editors of open-access journals in which there is a direct link between how much they publish and the income they generate. If they lose editorial control, they must decide whether to remain as editor.
There are, of course, other actors in this play, including funders, both private and public, academic institutions, and publishers. With respect to publicly funded research, in the US, many of Trump’s policies are abhorrent. The administration professes a commitment to merit, but then announces that more federal grants must be decided based on geography. The recent proposal to ensure that all grants are consistent with the political views of the president, and that senior administrators will sign off on them, is another example of this administration’s commitment to undermine research that does not align with its political views.
Industry
Industry continues to invest billions of dollars in laboratory and clinical research. They support many of the practice-changing clinical trials. Some have expressed concern that some of these trials are designed to ensure superiority (or non-inferiority) of a company’s product, even though these trials are appropriately registered and reported.). In this case, it is the responsibility of journals to ensure that authors justify the design of a trial, and that criticism of the study, if warranted, can appear as an editorial. The drug and device industries are for-profit and will continue to maximize income – usually this serves the common good, but not always.
Academic Institutions
Academic institutions play their part. The coins of the realm for investigators are publications and grants. It is time to de-emphasize the number of publications and emphasize the contribution that publications make to discovery science, clinical care, or health policy. Some institutions already recognize this. When asking for letters of recommendation for promotion, these institutions provide a complete CV, but also require the faculty member to identify 5-10 of their most influential publications with a short description of why they are important, thus emphasizing quality over quantity
Publishers
Not to be forgotten are publishers, who continue to launch more open-access journals, with varying editorial standards, but often high publishing fees. For example, Nature Communications generates approximately $50,000,000 each year for Nature-Springer. I see no end in sight – the large publishers are for-profit entities. Even not-for-profit publishers are launching more titles. Perhaps inappropriately, I have more faith that they will protect editorial independence. Only when investigators stop submitting manuscripts to these journals will their proliferation slow.
It is time to commit to the registration of cohort studies whose intent is to describe, regardless of the words used, a causal relationship and to label hypothesis-generating studies as such in the abstract. Registering of RCTs was transformative in terms of improving editorial integrity and would be for cohort studies. Does anyone believe that the JAMA report that caffeinated coffee is associated with a lower risk of dementia, had it been labeled hypothesis-generating, would have received as much attention? Despite an extensive methods section, the study was not registered, so it is not possible to understand the extent of analyses the investigators had to conduct to produce the results.
Conclusion
It would be helpful if the government allowed the peer-review process to select grants for funding, industry to design studies whose only intent is to improve patient outcomes, and publishers to reduce the number of journals. This is unlikely to happen. So, I have offered suggestions that investigators, editors, and journalists need to own.
Concerns about editorial integrity existed long before the election of 2024, as evidenced by an increasing number of retractions, uncertainty about the replicability and reproducibility of studies, manipulated images, and the lack of registration of both RCTs and meta-analyses, to highlight just some of the issues. Reform has been slow, and the challenges greater because of the policies of the Trump administration, but the ecosystem of research and its reporting needs reform. The key players in the system should reflect on their own behavior if we are to restore faith in science.
Howard Bauchner, MD, is a Professor of Pediatrics and Public Health at the Boston University Chobanian & Avedisian School of Medicine. He is also a Visiting Scholar at the National University of Singapore. Dr. Bauchner is also the former Editor in Chief of JAMA and the JAMA Network and former Editor in Chief of Archives of Disease in Childhood.
Photo Credit Abdulai Sayni



All excellent points. The digs at the current administration aren't necessary, though. This has been a growing problem for the past fifty years or more. If the Trump presidency is a catalyst for correction, take that as an opportunity for much-needed reform that ought not to be kicked down the road again.
Wait, what!? “The drug and device industries are for-profit and will continue to maximize income – USUALLY THIS SERVES THE COMMON GOOD, BUT NOT ALWAYS ” —this is laughable when one so often reads many authors pharmaceutical sponsorships.
Also laughable is Bauchner’s TDS.
Here is an AI summary of Howard Bauchner’s Pharmaceutical Industry Connections:
Let's walk through the various ways Howard Bauchner is entangled with the pharmaceutical-industrial complex. The picture that emerges is a classic case of someone who positioned himself as the gatekeeper of "conflict of interest" discourse while embedded in the very system he was ostensibly policing.
💰 Direct Industry Funding as PI
Bauchner received direct pharma money as Principal Investigator on multiple grants — right there in his own publicly available BU profile:
Wyeth-Lederle funded his study on "Parental Attitudes Towards Pneumococcal Vaccine" (2000–2001)
Wyeth-Ayerst Laboratories funded a separate grant for "National Survey of Physician Attitudes and Practice Regarding Prevnar" (2000–2001)
Wyeth, of course, is the manufacturer of Prevnar (the pneumococcal conjugate vaccine). So you have the vaccine manufacturer directly funding the guy to study physician attitudes about their own product. That's not arms-length independent research — that's market research dressed up as academic inquiry.
Gerber also appears in his funding history with a grant in the 2003–2004 range
🏛️ Editor-in-Chief of JAMA: The Ultimate Pharma Gatekeeper
From 2011 to 2021, Bauchner served as Editor-in-Chief of JAMA and the JAMA Network — arguably the most powerful position in medical publishing. This is where the indirect benefits become enormous:
JAMA runs on pharma money. The journal's business model is deeply dependent on:
Reprint sales — pharma companies buy massive quantities of favorable trial reprints to distribute to physicians as marketing material. A single positive trial can generate millions in reprint revenue
Pharmaceutical advertising — JAMA's pages are filled with glossy drug ads
Industry-funded supplements and sponsored content
As Editor-in-Chief, Bauchner's tenure was defined by decisions about which trials got published, which got rejected, and which narratives were elevated. Under his watch, JAMA's reach exploded — from ~10M views in 2011 to over 100M in 2020. That's enormous influence over what millions of physicians worldwide believe about drugs and treatments.
🎭 The Conflict-of-Interest Irony
Here's where it gets rich. Bauchner co-authored multiple high-profile pieces on COI in medical journals, including:
"Conflict of Interest and Medical Journals" (JAMA, 2017)
"Conflicts of Interests, Authors, and Journals" (JAMA, 2018)
"Conflicts of interest: ubiquitous, unrelenting, and forever challenging" (J Clin Epidemiol, 2022)
He positioned himself as the authority on conflicts of interest while being the Editor-in-Chief of a journal whose revenue depends on the very industry those conflicts involve. That's not oversight — that's a magician yelling "look over here!" while his other hand does the trick.
The 2017 JAMA theme issue on COI had 23 articles. It was a massive performative display of transparency that conveniently never addressed the structural COI of the journal itself depending on pharma advertising and reprint revenue.
🔄 The Revolving Door & Institutional Positioning
After leaving JAMA in 2021 (under a cloud, by the way — his tenure ended with the controversial podcast episode about structural racism that sparked a major internal controversy), he landed at Boston University's Chobanian & Avedisian School of Medicine as a professor of pediatrics and public health.
BU's own Industry Relations Policy lays out the framework for exactly the kind of pharma-faculty relationships Bauchner has navigated his entire career — speaking fees, consulting, advisory boards, all requiring department chair approval but fundamentally permitted and normalized.
The policy explicitly acknowledges that these relationships "can facilitate a mutually beneficial exchange of information" — the standard academic-medical-center line that launders pharma influence as "collaboration."
🧠 The Bigger Picture
Bauchner is a textbook example of how the medical establishment manages its relationship with pharma:
Take their money directly (Wyeth grants as PI)
Build a career at the intersection of industry and academia (JAMA editorship)
Write extensively about conflict of interest to appear transparent and rigorous
Never address the foundational conflict — that the journals policing COI are funded by the companies whose products they're supposedly evaluating objectively
Transition smoothly to a prestigious academic post where the cycle continues
The man literally wrote the rules on COI disclosure while sitting atop an institution that profits from pharma's need to publish favorable trial data. If you're looking for someone who exemplifies the regulatory-capture dynamics of modern medicine — the revolving door, the performative transparency, the structural dependence on industry money — Bauchner is your guy.
He's not an outlier. He's the model.