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Measures of General Intelligence and Risk for Alcohol Use Disorder

队列 酒精使用障碍 全基因组关联研究 孟德尔随机化 医学 队列研究 精神科 优势比 心理学 智商 人口学 认知 内科学 遗传学 单核苷酸多态性 基因型 生物化学 生物 化学 社会学 遗传变异 基因
作者
Andrea Johansson Capusan,Christal N. Davis,Emelie Thern,Jürgen Rehm,Joel Gelernter,Henry R. Kranzler,Markus Heilig
出处
期刊:JAMA Psychiatry [American Medical Association]
标识
DOI:10.1001/jamapsychiatry.2025.2689
摘要

Importance Associations among general intelligence (IQ), educational attainment (EA), and alcohol use disorder (AUD) are not well understood. Objective To examine the relationship between IQ, EA, and AUD risk. Design, Setting, and Participants The association between IQ and AUD risk was examined in a Swedish national conscription cohort. Potential causality was explored using mendelian randomization (MR) analyses, and the association of polygenic scores (PGS) for cognitive performance with AUD diagnosis was assessed. Participant data were obtained from cross-linked Swedish national registers, genome-wide association study (GWAS) summary statistics, and the US Yale-Penn cohort. Exposures IQ and genetic variants associated with cognitive performance. Main Outcomes and Measures Hazard ratios (HRs; time-to-event analyses) or odds ratios (ORs) for AUD. Results Included in this study was a national cohort of 645 488 males, born between 1950 and 1962, from the Swedish Military Conscription Register, of whom 573 855 individuals were included in this analysis. All individuals were aged 18 years at IQ assessment with no substance use disorder diagnosis at conscription, and mean (SD) follow-up time (SD) was 60.5 (7.9) years. Summary statistics from GWAS of cognitive performance (n = 257 481) and AUD (total = 753 248; cases = 113 325) in individuals of European-like genetic ancestry (EUR), with FinnGen AUD GWAS as a replication sample (total = 500 348; cases = 20 597), were used for MR analyses. PGS analyses were conducted using the data of EUR individuals from the Yale-Penn cohort (n = 5424). IQ at age 18 years was inversely associated with AUD risk in Swedish males (adjusted HR, 1.43; 95% CI, 1.40-1.47; P < .001), adjusting for parental substance use disorder, probands’ psychiatric disorders, socioeconomic factors, and birth year strata. MR analyses suggested a causal relationship between lower cognitive performance and AUD risk (β [SE], 0.11 [0.02]; P = 2.6 × 10 −12 ). The mediating role of EA differed between national contexts. Higher cognitive performance PGS were associated with reduced odds of AUD in Yale-Penn participants (OR, 0.83; 95% CI, 0.78-0.89). Conclusions and Relevance IQ and cognitive performance have a significant but context-dependent association with AUD risk, highlighting the need for a better understanding of the interplay among genetic factors, cognitive traits, and sociocultural influences on AUD susceptibility.

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