Department of Psychiatry, University of Oxford, Oxford, UK.
Neuropsychopharmacology. 2012 Jul;37(8):1808-15. doi: 10.1038/npp.2012.45. Epub 2012 Apr 11.
Elevated lifetime prevalence rates of alcohol use disorders (AUDs) are a feature of bipolar disorder (BD). Individuals at-risk for AUDs exhibit blunted subjective responses to alcohol (low levels of response), which may represent a biomarker for AUDs. Thus, individuals at-risk for BD may exhibit low responses to alcohol. Participants were 20 unmedicated adult males who reported high rates of hypomanic experiences (bipolar phenotype participants; BPPs), aged 18 to 21 years, and 20 healthy controls matched on age, gender, IQ, BMI, and weekly alcohol intake. Subjective and pharmacokinetic responses to acute alcohol (0.8 g/kg) vs placebo administration were collected in a randomized, double-blind, cross-over, placebo-controlled, within-subjects design. BPP participants reported significantly lower subjective intoxication effects ('feel high': F=14.2, p=0.001; 'feel effects': F=8.1, p=0.008) across time, but did not differ in their pharmacokinetic, stimulant, or sedative responses. Paradoxically, however, the BPP participants reported significantly higher expectations of the positive effects of alcohol than controls. Our results suggest that unmedicated young males with previous hypomanic experiences exhibit diminished subjective responses to alcohol. These blunted alcohol responses are not attributable to differences in weekly alcohol intake, pharmacokinetic effects (eg, absorption rates), or familial risk of AUDs. These observations suggest that the dampened intoxication may contribute to the increased rates of alcohol misuse in young people at-risk for BD, and suggest possible shared etiological factors in the development of AUDs and BD.
终生酒精使用障碍 (AUD) 的发生率升高是双相情感障碍 (BD) 的一个特征。有 AUD 风险的个体对酒精的主观反应迟钝 (反应水平低),这可能是 AUD 的生物标志物。因此,有 BD 风险的个体可能对酒精的反应较低。参与者为 20 名未接受药物治疗的成年男性,他们报告了较高的轻躁狂体验发生率 (双相情感障碍表型参与者;BPPs),年龄在 18 至 21 岁之间,以及 20 名年龄、性别、智商、BMI 和每周酒精摄入量相匹配的健康对照者。在一项随机、双盲、交叉、安慰剂对照、自身对照设计中,收集了他们对急性酒精 (0.8g/kg) 与安慰剂给药的主观和药代动力学反应。BPP 参与者报告在整个时间内主观醉酒效应 ('感觉兴奋':F=14.2,p=0.001;'感觉效应':F=8.1,p=0.008) 显著降低,但他们的药代动力学、兴奋剂或镇静剂反应没有差异。然而,具有讽刺意味的是,BPP 参与者报告的对酒精积极影响的期望明显高于对照组。我们的研究结果表明,有先前轻躁狂经历的未接受药物治疗的年轻男性对酒精的主观反应减弱。这些迟钝的酒精反应不能归因于每周酒精摄入量、药代动力学效应(例如吸收速率)或 AUD 的家族风险的差异。这些观察结果表明,在有 BD 风险的年轻人中,醉酒程度的降低可能导致酒精滥用率的增加,并表明 AUD 和 BD 的发展可能存在共同的病因因素。