{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,31]],"date-time":"2026-10-31T16:33:33Z","timestamp":1793464413860,"version":"4.5.0"},"reference-count":55,"publisher":"Cambridge University Press (CUP)","license":[{"start":{"date-parts":[[2025,3,28]],"date-time":"2025-03-28T00:00:00Z","timestamp":1743120000000},"content-version":"unspecified","delay-in-days":86,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0"}],"content-domain":{"domain":["cambridge.org"],"crossmark-restriction":true},"short-container-title":["Psychol. Med."],"published-print":{"date-parts":[[2025]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec id=\"S0033291725000352_sec1\">\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Preexisting epidemiological studies suggest that early pubertal development in males is associated with externalizing (e.g. conduct problems, risky behavior, and aggression) and internalizing (e.g. depression and anxiety) traits and disorders. However, due to problems inherent to observational studies, especially of residual confounding, it remains unclear whether these associations are causal. Mendelian randomization (MR) studies take advantage of the random allocation of genes at conception and can establish causal relationships.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"S0033291725000352_sec2\" sec-type=\"methods\">\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>In this study, N\u00a0=\u00a076 independent genetic variants for male puberty timing (MPT) were derived from a large genome-wide association study (GWAS) on 205,354 participants and used as an instrumental variable in MR studies on 17 externalizing and internalizing traits and psychopathologies utilizing outcome GWAS with 16,400\u20131,045,957 participants.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"S0033291725000352_sec3\" sec-type=\"results\">\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>In these MR studies, earlier MPT was significantly associated with higher scores for the overarching phenotype of \u2018Externalizing Traits\u2019 (b\u00a0=\u00a0\u22120.03, 95% CI [\u22120.06, \u22120.01]). However, this effect was likely driven by an earlier age at first sexual contact (b\u00a0=\u00a0\u22120.17, 95% CI [\u22120.21, \u22120.13]), without evidence for an effect on further externalizing phenotypes. Regarding internalizing phenotypes, earlier MPT was associated with higher levels of the \u2018Depressed Affect\u2019 subdomain of neuroticism (b\u00a0=\u00a0\u22120.04, 95% CI [\u22120.07, \u22120.01]). Late MPT was related to higher scores of internalizing traits in early life (b\u00a0=\u00a00.04, 95% CI [0.01, 0.08]).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"S0033291725000352_sec4\" sec-type=\"conclusions\">\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>This comprehensive MR study supports a causal effect of MPT on specific traits and behaviors. However, no evidence for an effect of MPT on long-term clinical outcomes (depression, anxiety disorders, alcohol dependency, cannabis abuse) was found.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1017\/s0033291725000352","type":"journal-article","created":{"date-parts":[[2025,3,28]],"date-time":"2025-03-28T04:28:28Z","timestamp":1743136108000},"update-policy":"https:\/\/doi.org\/10.1017\/policypage","source":"Crossref","is-referenced-by-count":9,"title":["The causal role of male pubertal timing for the development of externalizing and internalizing traits: results from Mendelian randomization 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