Ho Ada Man-Choi, Geske Jennifer R, Pazdernik Vanessa K, Waller T Cameron, Batzler Anthony, Winham Stacey J, Karpyak Victor M
Department of Psychiatry and Psychology, Mayo Clinic, Rochester, MN, USA.
Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
Addiction. 2025 Oct;120(10):2107-2117. doi: 10.1111/add.70104. Epub 2025 Jun 16.
Sex-related hormones and proteins may underlie sex differences in alcohol use disorder characteristics and consequences. Previous reports suggest steroid sex hormones may influence alcohol consumption behaviors while proteins that regulate their circulation levels are rarely investigated. Following up on our earlier study of individual sex-related hormones' associations with alcohol dependence (AD), this study measured the associations between the combinations of sex-related hormones and proteins and AD in a larger sample.
Sex-stratified case-control comparison and clustering of plasma sex-related hormone and protein levels, plus a genome-wide association study on the AD-associated hormone and protein combinations.
Addiction treatment programs in the United States.
Four hundred treatment-seeking recently abstained AD patients (median = 24.5 days) and 388 age-and-sex-matched controls from a community biobank (male:female ≈ 2:1).
Plasma levels of total testosterone, estrone (E1), estradiol (E2), follicle-stimulating hormone (FSH), luteinizing hormone (LH), sex hormone binding globulin (SHBG) and albumin.
In males, we found higher E2 [β = 0.13, P < 0.001, false discovery rate (FDR) = 0.005], progesterone (β = 0.01, P = 0.025, FDR = 0.054), LH (β = 0.12, P = 0.017, FDR = 0.044) and albumin (β = 0.09, P < 0.001, FDR = 0.005) in AD patients than controls; in females, we observed lower E1 (β = -0.24, P = 0.024, FDR = 0.113) and progesterone (β = -1.86, P = 0.026, FDR = 0.113) and higher albumin (β = 0.18, P < 0.001, FDR = 0.001) in AD patients than controls. Three principal components (PCs), reflecting hormone signatures, were statistically significantly associated with AD in each sex: PC1 (TT, E2 and SHBG; β = -0.15, P = 0.016), PC3 (E1, progesterone and albumin; β = 0.28, P = 0.007) and PC4 (SHBG and albumin; β = 0.34, P = 0.001) in males; PC3 (progesterone and albumin; β = -0.38, P = 0.009), PC4 (TT and albumin; β = -0.49, P = 0.001) and PC5 (TT and progesterone; β = 0.54, P = 0.004) in females. Statistically significant SNP × group associations were found in females between PC4 and polymorphisms in RP51004I9.1 (top SNP: rs6082693; P = 5.41E-12) and in males between PC3 and a genomic locus that contained SLC35E4, DUSP18 and OSBP2 (top SNP: rs13053277; P = 1.77E-07).
Three sex-related hormone and protein signatures appear to be associated with alcohol dependence in each sex. Peripheral levels of sex-related hormones and proteins, as well as their combinations, could be altered in people with alcohol dependence who have abstained for a few weeks compared with controls, and such differences may be sex-specific.
与性别相关的激素和蛋白质可能是酒精使用障碍特征及后果存在性别差异的基础。既往报告提示,类固醇性激素可能影响酒精消费行为,而调节其循环水平的蛋白质则鲜少被研究。在我们早期关于个体性激素与酒精依赖(AD)关联的研究基础上,本研究在更大样本中测量了性激素与蛋白质组合和AD之间的关联。
按性别分层的病例对照比较以及血浆性激素和蛋白质水平聚类分析,外加一项关于与AD相关的激素和蛋白质组合的全基因组关联研究。
美国的成瘾治疗项目。
400名寻求治疗的近期戒酒的AD患者(中位数 = 24.5天)以及来自社区生物样本库的388名年龄和性别匹配的对照者(男性:女性≈2:1)。
血浆总睾酮、雌酮(E1)、雌二醇(E2)、促卵泡激素(FSH)、促黄体生成素(LH)、性激素结合球蛋白(SHBG)和白蛋白水平。
在男性中,我们发现AD患者的E2(β = 0.13,P < 0.001,错误发现率[FDR] = 0.005)、孕酮(β = 0.01,P = 0.025,FDR = 0.054)、LH(β = 0.12,P = 0.017,FDR = 0.044)和白蛋白(β = 0.09,P < 0.001,FDR = 0.005)水平高于对照者;在女性中,我们观察到AD患者的E1(β = -0.24,P = 0.024,FDR = 0.113)和孕酮(β = -1.86,P = 0.026,FDR = 0.113)水平低于对照者,而白蛋白水平高于对照者(β = 0.18,P < 0.001,FDR = 0.001)。反映激素特征的三个主成分(PCs)在各性别中均与AD存在统计学显著关联:男性中的PC1(总睾酮、E2和SHBG;β = -0.15,P = 0.016)、PC3(E1、孕酮和白蛋白;β = 0.28,P = 0.007)和PC4(SHBG和白蛋白;β = 0.34,P = 0.001);女性中的PC3(孕酮和白蛋白;β = -0.38,P = 0.009)、PC4(总睾酮和白蛋白;β = -0.49,P = 0.001)和PC5(总睾酮和孕酮;β = 0.54,P = 0.004)。在女性中,发现PC与RP51004I9.1中的多态性之间存在统计学显著的单核苷酸多态性(SNP)×组关联(顶级SNP:rs6082693;P = 5.41E - 12),在男性中,PC3与包含SLC35E4、DUSP18和OSBP2的基因组位点之间存在关联(顶级SNP:rs13053277;P = 1.77E - 07)。
三种与性别相关的激素和蛋白质特征似乎在各性别中均与酒精依赖相关。与对照者相比,戒酒几周的酒精依赖者体内与性别相关的激素和蛋白质外周水平及其组合可能发生了改变,且这种差异可能具有性别特异性。