Hildebrand Karlén Malin, Lindqvist Bagge Ann-Sophie, Berggren Ulf, Fahlke Claudia, Andiné Peter, Doering Sabrina, Lundström Sebastian
Centre for Ethics, Law and Mental Health, Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden Department of Forensic Psychiatry, National Board of Forensic Medicine, Gothenburg, Sweden Department of Psychology, University of Gothenburg, Gothenburg, Sweden.
Department of Psychology, University of Gothenburg, Gothenburg, Sweden Centre for Ethics, Law and Mental Health, Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden.
Nordisk Alkohol Nark. 2023 Aug;40(4):391-405. doi: 10.1177/14550725221090383. Epub 2023 May 24.
: Heritability of alcohol use disorders (AUDs) varies widely, with reported estimates of 30-78% in twin studies. This variation might be due to methodological differences (e.g., using different thresholds for AUDs, age differences between samples). : To investigate the heritability of AUDs in a nation-wide sample of male and female twins in late adolescence (18 years). : The study is based on data from 8,330 18-year-old Swedish monozygotic (MZ) and dizygotic (DZ) twins from the Child and Adolescent Twin Study (Sweden). : Univariate sex-limitation twin analyses were performed using (a) total AUDIT score, (b) different AUDIT cut-offs (AUDIT-10: potentially harmful alcohol use and most likely alcohol dependent ; AUDIT-C: potential hazardous alcohol consumption/active alcohol use disorders), and (c) a risk-group classification for alcohol dependence based on AUDIT total score. : Prevalence of potential hazardous alcohol consumption/active alcohol use was 57.1%, and for potentially harmful alcohol use prevalence was 26.5%. Prevalence was higher among females (59.0% and 31.1% respectively) than males (54.4% and 20.0% respectively). Overall, the results of the univariate model fitting indicated that there were qualitative sex differences in the genetic and environmental influences on AUDs, with generally moderate heritability estimates ranging between 0.37 and 0.50. : At odds with previous research, a harmful/hazardous drinking pattern was more common in this age group among females than a low-risk drinking pattern (where males were overrepresented). Heritability estimates were moderate throughout all measures and cut-offs, with equally high contributions from shared and non-shared environment. Sex-limitation models revealed qualitative sex differences for AUDs, suggesting that different genetic and/or environmental factors influence variation in AUDs in males and females.
酒精使用障碍(AUDs)的遗传度差异很大,双生子研究报告的估计值在30%至78%之间。这种差异可能是由于方法学差异(例如,对AUDs使用不同的阈值、样本之间的年龄差异)。:调查全国范围内处于青春期末期(18岁)的男性和女性双生子中AUDs的遗传度。:该研究基于来自瑞典儿童和青少年双生子研究的8330名18岁瑞典同卵(MZ)和异卵(DZ)双生子的数据。:使用(a)酒精使用障碍鉴定测试(AUDIT)总分、(b)不同的AUDIT临界值(AUDIT-10:潜在有害饮酒且很可能酒精依赖;AUDIT-C:潜在危险饮酒/活跃酒精使用障碍)以及(c)基于AUDIT总分的酒精依赖风险组分类进行单变量性别限制双生子分析。:潜在危险饮酒/活跃酒精使用的患病率为57.1%,潜在有害饮酒的患病率为26.5%。女性中的患病率(分别为59.0%和31.1%)高于男性(分别为54.4%和20.0%)。总体而言,单变量模型拟合结果表明,在对AUDs的遗传和环境影响方面存在质性性别差异,遗传度估计值一般在0.37至0.50之间。:与先前的研究不同,在这个年龄组中,有害/危险饮酒模式在女性中比低风险饮酒模式更常见(男性在低风险饮酒模式中占比过高)。在所有测量和临界值中,遗传度估计值均为中等,共享环境和非共享环境的贡献同样高。性别限制模型揭示了AUDs的质性性别差异,表明不同的遗传和/或环境因素影响男性和女性AUDs的变异。