Topiwala Anya, Allan Charlotte L, Valkanova Vyara, Zsoldos Enikő, Filippini Nicola, Sexton Claire, Mahmood Abda, Fooks Peggy, Singh-Manoux Archana, Mackay Clare E, Kivimäki Mika, Ebmeier Klaus P
Department of Psychiatry, University of Oxford, Warneford Hospital, Oxford OX3 7JX, UK
Department of Psychiatry, University of Oxford, Warneford Hospital, Oxford OX3 7JX, UK.
BMJ. 2017 Jun 6;357:j2353. doi: 10.1136/bmj.j2353.
To investigate whether moderate alcohol consumption has a favourable or adverse association or no association with brain structure and function. Observational cohort study with weekly alcohol intake and cognitive performance measured repeatedly over 30 years (1985-2015). Multimodal magnetic resonance imaging (MRI) was performed at study endpoint (2012-15). Community dwelling adults enrolled in the Whitehall II cohort based in the UK (the Whitehall II imaging substudy). 550 men and women with mean age 43.0 (SD 5.4) at study baseline, none were "alcohol dependent" according to the CAGE screening questionnaire, and all safe to undergo MRI of the brain at follow-up. Twenty three were excluded because of incomplete or poor quality imaging data or gross structural abnormality (such as a brain cyst) or incomplete alcohol use, sociodemographic, health, or cognitive data. Structural brain measures included hippocampal atrophy, grey matter density, and white matter microstructure. Functional measures included cognitive decline over the study and cross sectional cognitive performance at the time of scanning. Higher alcohol consumption over the 30 year follow-up was associated with increased odds of hippocampal atrophy in a dose dependent fashion. While those consuming over 30 units a week were at the highest risk compared with abstainers (odds ratio 5.8, 95% confidence interval 1.8 to 18.6; P≤0.001), even those drinking moderately (14-21 units/week) had three times the odds of right sided hippocampal atrophy (3.4, 1.4 to 8.1; P=0.007). There was no protective effect of light drinking (1-<7 units/week) over abstinence. Higher alcohol use was also associated with differences in corpus callosum microstructure and faster decline in lexical fluency. No association was found with cross sectional cognitive performance or longitudinal changes in semantic fluency or word recall. Alcohol consumption, even at moderate levels, is associated with adverse brain outcomes including hippocampal atrophy. These results support the recent reduction in alcohol guidance in the UK and question the current limits recommended in the US.
为了研究适度饮酒与脑结构和功能之间是存在有益关联、有害关联还是无关联。进行观察性队列研究,对30年(1985 - 2015年)期间的每周酒精摄入量和认知表现进行反复测量。在研究终点(2012 - 2015年)进行多模态磁共振成像(MRI)检查。研究对象为英国白厅II队列中的社区居住成年人(白厅II成像子研究)。研究基线时,550名男性和女性的平均年龄为43.0岁(标准差5.4),根据CAGE筛查问卷,没有人“酒精依赖”,且所有人在随访时都适合接受脑部MRI检查。23人因成像数据不完整或质量差、存在明显结构异常(如脑囊肿)或酒精使用、社会人口统计学、健康或认知数据不完整而被排除。脑结构测量包括海马萎缩、灰质密度和白质微结构。功能测量包括研究期间的认知衰退和扫描时的横断面认知表现。在30年的随访中,较高的酒精摄入量与海马萎缩几率增加呈剂量依赖性相关。与戒酒者相比,每周饮酒超过30单位的人风险最高(比值比5.8,95%置信区间1.8至18.6;P≤0.001),即使是适度饮酒者(14 - 21单位/周)右侧海马萎缩的几率也高出三倍(3.4,1.4至8.1;P = 0.007)。轻度饮酒(1 - <7单位/周)相较于戒酒没有保护作用。较高的酒精摄入量还与胼胝体微结构差异和词汇流畅性更快下降有关。未发现与横断面认知表现或语义流畅性或单词回忆的纵向变化存在关联。即使是适度饮酒,酒精消费也与包括海马萎缩在内的不良脑部后果相关。这些结果支持了英国近期对酒精指南的修订,并对美国目前推荐的限量提出质疑。