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Association Between Lifetime Hallucinogen Use and Valvular Heart Disease: Findings from the All of Us Research Program

Kevin H. Yang, Miranda Rasmussen, Kush Bhatt, Nora Satybaldiyeva, Wayne Kepner, Alison A. Moore, Jaclyn Bergstrom

Journal of Psychoactive Drugs May 18, 2026 DOI: 10.1080/02791072.2026.2673845 via OpenAlex

Summary

AI-generated from the abstract

Lifetime use of hallucinogens (LSD, psilocybin, MDMA, ketamine, or PCP) is associated with a modest increase in the odds of valvular heart disease after accounting for sociodemographic factors and other health conditions. In a large US adult sample, 13.2% reported lifetime hallucinogen use. The unadjusted prevalence of VHD was lower among users (3.6%) than non-users (4.7%), but after adjustment the odds rose slightly (adjusted odds ratio 1.08). The authors call for longitudinal studies to confirm this exploratory finding.

Study at a glance

Characteristics Cross-sectional study Longitudinal Peer reviewed
Sample size 286,842
Population US adults in the NIH All of Us Research Program with linked electronic health records who completed the Lifestyle survey
Citations 1
Key finding Lifetime hallucinogen use was associated with modestly increased odds of valvular heart disease after adjusting for confounders (aOR = 1.08, 95% CI: 1.01–1.55).

Abstract

Recent literature suggests potential associations between hallucinogen use and valvular heart disease (VHD) due to prolonged activation of serotonin 5-HT2B receptors, which may lead to valvular fibrosis – a condition also linked to drugs including fenfluramine and pergolide. Despite these concerns, epidemiological studies exploring this association are lacking. This exploratory analysis investigated associations between lifetime hallucinogen use and VHD using cross-sectional data from US adults with linked electronic health record data in the NIH All of Us Research Program who completed the Lifestyle survey. This survey included questions about lifetime hallucinogen use (lysergic acid diethylamide [LSD], mushrooms/psilocybin, 3,4-Methylenedioxymethamphetamine [MDMA]/ecstasy, ketamine, phencyclidine [PCP]). Multivariable logistic regression models examined the association between hallucinogen use and VHD, adjusting for sociodemographic factors and other confounding health conditions. Our sample comprised 286,842 adults (mean age 50.8 [SD 16.7], 61.4% female, 60.6% White). Among them, 13.2% reported lifetime hallucinogen use. Individuals with lifetime hallucinogen use had lower unadjusted VHD prevalence compared to those without lifetime hallucinogen use (3.6% vs. 4.7%, p < .001). However, after adjusting for confounders, models revealed modestly increased VHD odds (aOR = 1.08, 95% CI: 1.01–1.55, p = .017). This exploratory study found that hallucinogen use was associated with modestly increased VHD odds after adjustment, requiring confirmation through longitudinal research.

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