{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,21]],"date-time":"2026-01-21T16:04:59Z","timestamp":1769011499063,"version":"3.49.0"},"reference-count":86,"publisher":"MDPI AG","issue":"19","license":[{"start":{"date-parts":[[2022,10,5]],"date-time":"2022-10-05T00:00:00Z","timestamp":1664928000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["IJERPH"],"abstract":"<jats:p>Background. The cause of the worldwide doubling-tripling of testicular cancer rates (TCRs) in recent decades is unknown. Previous cohort studies associated cannabis use with TCR including dose\u2013response relationships but the contribution of cannabis to TCRs at the population level is unknown. This relationship was tested by analyzing annual trends across US states and formally assessed causality. Four US datasets were linked at state level: age-adjusted TCRs from Centers for Disease Control Surveillance Epidemiology and End Results database; drug use data from annual National Survey of Drug Use and Health including 74.1% response rate; ethnicity and median household income data from the US Census Bureau; and cannabinoid concentration data from Drug Enforcement Agency reports. Data was processed in R in spatiotemporal and causal inference protocols. Results. Cannabis-use quintile scatterplot-time and boxplots closely paralleled those for TCRs. The highest cannabis-use quintile had a higher TCR than others (3.44 \u00b1 0.05 vs. 2.91 \u00b1 0.2, mean \u00b1 S.E.M., t = 10.68, p = 1.29 \u00d7 10\u221222). A dose\u2013response relationship was seen between TCR and \u03949-tetrahydrocannabinol (THC), cannabinol, cannabigerol, and cannabichromene (6.75 \u00d7 10\u22129 &lt; p &lt; 1.83 \u00d7 10\u2212142). In a multivariate inverse probability-weighted interactive regression including race and ethnic cannabis exposure (ECE), ECE was significantly related to TCR (\u03b2-estimate = 0.89 (95%C.I. 0.36, 2.67), p &lt; 2.2 \u00d7 10\u221216). In an additive geospatiotemporal model controlling for other drugs, cannabis alone was significant (\u03b2-estimate = 0.19 (0.10, 0.28), p = 3.4 \u00d7 10\u22125). In a full geospatial model including drugs, income and ethnicity cannabinoid exposure was significant (cannabigerol: \u03b2-estimate = 1.39 (0.024, 2.53), p = 0.0017); a pattern repeated at two spatial and two temporal lags (cannabigerol: \u03b2-estimate = 0.71 (0.05, 1.37), p = 0.0.0350; THC: \u03b2-estimate = 23.60 (11.92, 35.29), p = 7.5 \u00d7 10\u20135). 40\/41 e-Values &gt; 1.25 ranged up to 1.4 \u00d7 1063 and 10 &gt; 1000 fitting causal relationship criteria. Cannabis liberalization was associated with higher TCRs (ChiSqu. = 312.2, p = 2.64 \u00d7 10\u221211). Rates of TC in cannabis-legal states were elevated (3.36 \u00b1 0.09 vs. 3.01 \u00b1 0.03, t = 4.69, p = 4.86 \u00d7 10\u22125). Conclusions. Cannabis use is closely and causally associated with TCRs across both time and space and higher in States with liberal cannabis legislation. Strong dose\u2013response effects were demonstrated for THC, cannabigerol, cannabinol, cannabichromene and cannabidiol. Cannabinoid genotoxicity replicates all major steps to testicular carcinogenesis including whole-genome doubling, chromosomal arm excision, generalized DNA demethylation and chromosomal translocations thereby accelerating the pathway to testicular carcinogenesis by several decades.<\/jats:p>","DOI":"10.3390\/ijerph191912759","type":"journal-article","created":{"date-parts":[[2022,10,8]],"date-time":"2022-10-08T22:19:27Z","timestamp":1665267567000},"page":"12759","update-policy":"https:\/\/doi.org\/10.3390\/mdpi_crossmark_policy","source":"Crossref","is-referenced-by-count":16,"title":["State Trends of Cannabis Liberalization as a Causal Driver of Increasing Testicular Cancer Rates across the USA"],"prefix":"10.3390","volume":"19","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-3256-720X","authenticated-orcid":false,"given":"Albert","family":"Reece","sequence":"first","affiliation":[{"name":"Division of Psychiatry, University of Western Australia, Crawley, WA 6009, Australia"},{"name":"School of Medical and Health Sciences, Edith Cowan University, Joondalup, WA 6027, Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Gary","family":"Hulse","sequence":"additional","affiliation":[{"name":"Division of Psychiatry, University of Western Australia, Crawley, WA 6009, Australia"},{"name":"School of Medical and Health Sciences, Edith Cowan University, Joondalup, WA 6027, Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"1968","published-online":{"date-parts":[[2022,10,5]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"29","DOI":"10.1038\/s41572-018-0029-0","article-title":"Testicular cancer","volume":"4","author":"Cheng","year":"2018","journal-title":"Nat. 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