# Impact of Cannabis and Cannabis Legalization on US Atrial Septal Defect Rates

**Authors:** Albert Stuart Reece, Gary Kenneth Hulse

PMC · DOI: 10.3390/jox16020043 · 2026-03-01

## TL;DR

This study suggests that cannabis use and legalization may be strongly linked to rising rates of atrial septal defects in US children.

## Contribution

The study identifies cannabis and its legalization as a potential driver of increasing atrial septal defect rates in the US.

## Key findings

- ASD rates increased significantly in states with higher cannabis use and legalization.
- Cannabinoids like Δ9THC, cannabidiol, and cannabigerol are statistically linked to higher ASD rates.
- ASD rates rose supra-exponentially in the US, with the highest rates in Nevada among Non-Hispanic Asians and Pacific Islanders.

## Abstract

Atrial septal defect (ASD) affects 1:11.3 children in some US states; however, the antecedents of these trends are yet to be identified. A total of 1882 ASD rates (ASDRs) for 2003–2020 were sourced from the National Birth Defects Prevention Network reports. A total of 406,893 ASDs are reported. Substance (cigarettes, binge alcohol, cannabis, cannabinoids, analgesics, cocaine) exposure data were taken from the National Survey of Drug Use and Health. Income and ethnicity data were derived from the US Census. Adjustment was performed by mixed effects, survey and generalized additive regression. Causal analysis was by inverse probability weighting and E-values. Data were analyzed in RStudio. The highest ASDR of 884/10,000 live births was amongst Non-Hispanic Asians and Pacific Islanders in Nevada in 2016–2020. The 2005–2018 median ASDR rose >12-fold in Nevada and New Mexico, >6-fold in New York, and 4.2-fold nationally 1989–2020; it doubled in NY from 2012–2016 to 2016–2020. The average state ASDR rose supra-exponentially (p = 0.0075) and was associated with higher cannabis use states (p = Zero, Cohen’s D = 1.24), apparently driven by cannabis legalization (p = Zero). Estimated exposures to Δ9THC, cannabidiol and cannabigerol were implicated (from p = 2.67 × 10–68). Cannabis-legal states were compared with others (mean ASDR (C.I.) 178.15 (131.68, 224.62) vs. 74.28 (70.60, 77.96), p = Zero; O.R. 1.82 (1.81, 1.84), E-values 3.04 (lower C.I. 3.02), Cohen’s D 1.29 (0.96, 1.62)). Overall, 29/39 (74.4%) E-value estimates were >4; 39/39 (100%) were >1.25. Cannabis, cannabinoids and cannabis legalization are strong candidates for driving the US ASDR supra-exponentially. Estimates of many cannabinoids, including cannabidiol, Δ9THC, and cannabigerol, are implicated. The results are consistent with other large epidemiological studies. The importance of the results is magnified by the increasing legalization and penetration of cannabinoids into the US population. Since therapeutic abortion is not practiced for ASD, it may be used as a bellwether index of heritable transgenerational cannabinoid genotoxicity and epigenotoxicity associated with cannabinoid exposure.

## Linked entities

- **Chemicals:** cannabidiol (PubChem CID 644019), cannabigerol (PubChem CID 5315659)
- **Diseases:** atrial septal defect (MONDO:0006664)

## Full-text entities

- **Genes:** RARS1 (arginyl-tRNA synthetase 1) [NCBI Gene 5917] {aka ArgRS, DALRD1, HLD9, RARS}, TMEM107 (transmembrane protein 107) [NCBI Gene 84314] {aka GRVS638, JBTS29, MKS13, PRO1268}, NKX2-2 (NK2 homeobox 2) [NCBI Gene 4821] {aka NKX2.2, NKX2B}, Tbx5 (T-box 5) [NCBI Gene 21388], SHH (sonic hedgehog) [NCBI Gene 395615] {aka ShhNC}, QRSL1 (glutaminyl-tRNA amidotransferase subunit QRSL1) [NCBI Gene 55278] {aka COXPD40, GatA}, MEF2A (myocyte enhancer factor 2A) [NCBI Gene 4205] {aka ADCAD1, RSRFC4, RSRFC9, mef2}, GLI3 (GLI family zinc finger 3) [NCBI Gene 2737] {aka ACLS, GCPS, GLI3-190, GLI3FL, PAP-A, PAPA}, TET1 (tet methylcytosine dioxygenase 1) [NCBI Gene 80312] {aka CXXC6, LCX, bA119F7.1}, MEGF8 (multiple EGF like domains 8) [NCBI Gene 1954] {aka C19orf49, CRPT2, EGFL4, SBP1}, NKX2-5 (NK2 homeobox 5) [NCBI Gene 1482] {aka CHNG5, CSX, CSX1, HLHS2, NKX2.5, NKX2E}, BMP4 (bone morphogenetic protein 4) [NCBI Gene 652] {aka BMP2B, BMP2B1, MCOPS6, OFC11, ZYME}, NR2F2 (nuclear receptor subfamily 2 group F member 2) [NCBI Gene 386585] {aka COUP-TFII, TFCOUP2}, Aldh1a2 (aldehyde dehydrogenase family 1, subfamily A2) [NCBI Gene 19378] {aka Aldh1a7, Raldh1, Raldh2}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 395909] {aka VEGF}
- **Diseases:** lung cancer (MESH:D008175), analgesic abuse (MESH:D051271), cerebral disorders (MESH:D002547), hypoplasia of the heart chambers (MESH:D006331), cardiogenic (MESH:D013575), Legal Status (MESH:D001766), injury to (MESH:D014947), neurodevelopmental disorders (MESH:D002658), congenital cardiac anomalies (MESH:C535853), cocaine abuse (MESH:D019970), ASD (MESH:D006344), Congenital Anomalies (MESH:D000013), atrial hypoplasia (MESH:D064752), Birth Defects (MESH:D000014), seizures (MESH:D012640), CHDs (MESH:D006330), cannabis (MESH:D002189), COVID-19 (MESH:D000086382), cardiac teratogen (MESH:C535542), mental retardation (MESH:D008607), right heart hypoplasia (MESH:D006333), alcohol use disorder (MESH:D000437)
- **Chemicals:** vitamin A (MESH:D014801), cannabigerol (MESH:C037036), cannabinol (MESH:D002187), thalidomide (MESH:D013792), DeltaTHC (-), Delta9THC (MESH:D013759), olivetol (MESH:C016630), RA (MESH:D014212), Cocaine (MESH:D003042), Retinoids (MESH:D012176), Cannabinoid (MESH:D002186), cannabidiol (MESH:D002185), Alcohol (MESH:D000438)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Nicotiana tabacum (American tobacco, species) [taxon 4097], Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13010746/full.md

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Source: https://tomesphere.com/paper/PMC13010746