Eating disorder screens predict GLP-1 use
A US survey of 1,309 adults links positive eating disorder screens to higher GLP-1 awareness and telehealth drug-seeking.
Why we wrote this. GLP-1 prescribing is expanding faster than eating disorder screening. This study quantifies the overlap for the first time in a nationally representative sample.
In this article (7 sections)
A cross-sectional study published on 19 June 2026 in the International Journal of Eating Disorders surveyed 1,309 US adults from the nationally representative AmeriSpeak panel[1]. The researchers, led by Jaclyn Siegel at NORC at the University of Chicago, wanted to know whether people who screen positive for eating disorders differ from the general population in their awareness of, interest in, and use of GLP-1 receptor agonists such as semaglutide. The short answer: they are more aware, more interested, and more likely to try to access these drugs outside traditional clinical channels.
What the study measured
Participants completed the Eating Disorder Screen for Primary Care (ESP), a validated five-item tool designed to flag possible eating disorder symptoms. The survey then asked about GLP-1 awareness, personal interest in using GLP-1 medications for weight loss, and whether participants had tried to obtain them. Approximately 10 percent of the sample reported past or current GLP-1 use[1].
Positive screens linked to higher GLP-1 interest
Adults who screened positive on the ESP showed greater awareness of GLP-1 medications and more interest in using them for weight loss than those who screened negative. Women in the sample were also more interested in GLP-1 drugs than men overall. Notably, individuals with positive eating disorder screens were more likely to report trying to access GLP-1 medications through telehealth pharmacies without a full medical consultation[1].
The finding about telehealth access is the most clinically consequential. Direct-to-consumer telehealth platforms that prescribe GLP-1 drugs for weight loss have expanded rapidly in the US. If people with undiagnosed or unmanaged eating disorders are disproportionately seeking these drugs through channels that skip structured screening, the risk of harm increases.
Why this matters for GLP-1 prescribing
GLP-1 receptor agonists such as semaglutide suppress appetite and reduce food-reward signalling. Those mechanisms can help people with binge eating disorder reduce episodes. But the same appetite suppression could reinforce restrictive eating patterns in people with anorexia or atypical anorexia. A separate commentary published in the same journal in June 2026 argued that most GLP-1 prescribing pathways currently lack any eating disorder screening step[2].
A 2026 clinical review in the Psychiatric Clinics of North America reached a similar conclusion: preliminary evidence suggests GLP-1 drugs may reduce weight and binge-eating symptoms in people with binge eating disorder, but these drugs could also cause harm or be misused in other eating disorder populations[3]. The review called for careful individual evaluation before prescribing.
The telehealth prescribing gap
The rapid expansion of telehealth GLP-1 prescribing has created a gap between access and oversight. Many platforms advertise weight-loss prescriptions with minimal evaluation: a brief questionnaire, a short video consultation, and a prescription shipped to the door. The standard screening questions ask about BMI, diabetes history, and thyroid disease. They rarely ask about binge-purge cycles, restriction, or body-image distress[2].
This is not unique to GLP-1 drugs. The broader trend toward direct-to-consumer prescribing has raised similar concerns with testosterone, tirzepatide, and compounded peptide formulations. But the scale of GLP-1 demand makes the eating disorder question particularly urgent. By some estimates, more than 15 million Americans have been prescribed a GLP-1 agonist for weight management since 2021, and a substantial portion of new prescriptions now originate through telehealth channels.
What researchers recommend
The Siegel team's recommendation is direct: clinicians working with patients who have eating disorders or body-image concerns should raise GLP-1 medications proactively rather than waiting for the patient to ask[1]. The reasoning is that patients will seek these drugs regardless, and a clinician-initiated conversation creates space for screening and monitoring.
The Škudar commentary goes further, proposing six priorities: routine eating disorder screening before and during GLP-1 treatment, validated monitoring tools to distinguish normal appetite reduction from emerging eating disorder pathology, and multidisciplinary care models that pair prescribers with mental health clinicians[2]. None of these are standard practice yet.
Limitations worth noting
The study is cross-sectional, so it captures associations, not causes. It cannot tell us whether eating disorder symptoms drive GLP-1 interest or whether the same underlying body-image concerns drive both the screen result and the drug-seeking behaviour. The ESP is a screening tool, not a diagnostic instrument: a positive result flags risk but does not confirm an eating disorder diagnosis. And the 10 percent GLP-1 use rate in the sample was self-reported[1].
The survey also did not distinguish between specific GLP-1 medications. Drugs in this class include semaglutide (marketed as Wegovy for weight management and Ozempic for type 2 diabetes) and tirzepatide (Zepbound for weight management, Mounjaro for diabetes). Each has a different side-effect profile and prescribing context, and the eating disorder implications may differ between them. Future research would need to track outcomes by specific drug and dose.
What we do not yet know
No study has yet tracked what happens when people with positive eating disorder screens start GLP-1 therapy without specialist oversight. Whether the appetite suppression helps, harms, or has no net effect on eating disorder pathology in real-world settings is an open question. The authors of the original study recommend that clinicians working with patients who have eating disorders or body-image concerns should proactively discuss GLP-1 medications and that telehealth prescribing platforms should build in screening safeguards.
Anyone considering a GLP-1 medication should discuss both the potential benefits and risks with a healthcare provider, particularly if they have a history of disordered eating.
Frequently asked
Are people with eating disorders more interested in GLP-1 drugs?
A 2026 nationally representative US survey found that adults who screened positive for eating disorders on the ESP tool showed greater awareness of and interest in GLP-1 medications for weight loss compared with those who screened negative.
Can GLP-1 drugs worsen eating disorders?
It depends on the type. Preliminary evidence suggests GLP-1 drugs may reduce binge-eating episodes in people with binge eating disorder. However, the appetite-suppressing effects could reinforce restrictive eating in people with anorexia-spectrum conditions. More research is needed, and individual clinical evaluation is essential.
Should telehealth platforms screen for eating disorders before prescribing GLP-1s?
Multiple researchers have called for this. The Siegel et al. 2026 study found that people with positive eating disorder screens were more likely to seek GLP-1 drugs through telehealth channels that skip full clinical evaluation, raising concerns about unsupervised use in vulnerable populations.
What is the ESP eating disorder screening tool?
The Eating Disorder Screen for Primary Care (ESP) is a validated five-item questionnaire designed to flag possible eating disorder symptoms in clinical settings. A positive result indicates risk and warrants further evaluation but does not constitute a diagnosis.
Sources
- [1]Siegel et al. (2026): Eating Disorder Screen Results and GLP-1 Awareness, Interest, and Use in a Nationally Representative Sample of Adults in U.S. Households (Int J Eat Disord; PMID 42319160)Tier 1 · primary↩
- [2]Škudar (2026): Eating Disorders in the GLP-1 Era: A Spotlight on Emerging Clinical Risks, Research Gaps, and Practice Priorities (Int J Eat Disord; PMID 42223191)Tier 1 · primary↩
- [3]Schaefer et al. (2026): Use (and Potential for Abuse) of Glucagon-Like Peptide-1 Medications Among Individuals with Eating Disorders: Empirical Review and Clinical Guidance (Psychiatr Clin North Am; PMID 41708263)Tier 1 · primary↩
No revisions yet. First published .