Institute of Psychiatry, Psychology and Neuroscience, Centre for Population Neuroscience and Stratified Medicine (PONS), King's College London, London, United Kingdom.
Behavior and Basal Ganglia Unit (EA-4712), University of Rennes 1, Rennes, France.
JAMA Psychiatry. 2020 Apr 1;77(4):409-419. doi: 10.1001/jamapsychiatry.2019.4063.
Alcohol abuse correlates with gray matter development in adolescents, but the directionality of this association remains unknown.
To investigate the directionality of the association between gray matter development and increase in frequency of drunkenness among adolescents.
DESIGN, SETTING, AND PARTICIPANTS: This cohort study analyzed participants of IMAGEN, a multicenter brain imaging study of healthy adolescents in 8 European sites in Germany (Mannheim, Dresden, Berlin, and Hamburg), the United Kingdom (London and Nottingham), Ireland (Dublin), and France (Paris). Data from the second follow-up used in the present study were acquired from January 1, 2013, to December 31, 2016, and these data were analyzed from January 1, 2016, to March 31, 2018. Analyses were controlled for sex, site, socioeconomic status, family history of alcohol dependency, puberty score, negative life events, personality, cognition, and polygenic risk scores. Personality and frequency of drunkenness were assessed at age 14 years (baseline), 16 years (first follow-up), and 19 years (second follow-up). Structural brain imaging scans were acquired at baseline and second follow-up time points.
Increases in drunkenness frequency were measured by latent growth modeling, a voxelwise hierarchical linear model was used to observe gray matter volume, and tensor-based morphometry was used for gray matter development. The hypotheses were formulated before the data analyses.
A total of 726 adolescents (mean [SD] age at baseline, 14.4 [0.38] years; 418 [58%] female) were included. The increase in drunkenness frequency was associated with accelerated gray matter atrophy in the left posterior temporal cortex (peak: t1,710 = -5.8; familywise error (FWE)-corrected P = 7.2 × 10-5; cluster: 6297 voxels; P = 2.7 × 10-5), right posterior temporal cortex (cluster: 2070 voxels; FWE-corrected P = .01), and left prefrontal cortex (peak: t1,710 = -5.2; FWE-corrected P = 2 × 10-3; cluster: 10 624 voxels; P = 1.9 × 10-7). According to causal bayesian network analyses, 73% of the networks showed directionality from gray matter development to drunkenness increase as confirmed by accelerated gray matter atrophy in late bingers compared with sober controls (n = 20 vs 60; β = 1.25; 95% CI, -2.15 to -0.46; t1,70 = 0.3; P = .004), the association of drunkenness increase with gray matter volume at age 14 years (β = 0.23; 95% CI, 0.01-0.46; t1,584 = 2; P = .04), the association between gray matter atrophy and alcohol drinking units (β = -0.0033; 95% CI, -6 × 10-3 to -5 × 10-4; t1,509 = -2.4; P = .02) and drunkenness frequency at age 23 years (β = -0.16; 95% CI, -0.28 to -0.03; t1,533 = -2.5; P = .01), and the linear exposure-response curve stratified by gray matter atrophy and not by increase in frequency of drunkenness.
This study found that gray matter development and impulsivity were associated with increased frequency of drunkenness by sex. These results suggest that neurotoxicity-related gray matter atrophy should be interpreted with caution.
酗酒与青少年的灰质发育相关,但这种关联的方向性尚不清楚。
研究青少年中酗酒频率增加与灰质发育之间的关联的方向性。
设计、地点和参与者:本队列研究分析了 IMAGEN 的参与者,这是一项在德国 8 个欧洲站点(曼海姆、德累斯顿、柏林和汉堡)、英国(伦敦和诺丁汉)、爱尔兰(都柏林)和法国(巴黎)进行的健康青少年多中心脑成像研究。本研究中使用的第二次随访数据于 2013 年 1 月 1 日至 2016 年 12 月 31 日获得,这些数据于 2016 年 1 月 1 日至 2018 年 3 月 31 日进行分析。分析控制了性别、地点、社会经济地位、酒精依赖家族史、青春期评分、负面生活事件、人格、认知和多基因风险评分。人格和酗酒频率在 14 岁(基线)、16 岁(第一次随访)和 19 岁(第二次随访)进行评估。在基线和第二次随访时间点进行结构脑成像扫描。
通过潜在增长模型测量酗酒频率的增加,使用体素层次线性模型观察灰质体积,使用张量基形态测量学测量灰质发育。假设在数据分析之前提出。
共纳入 726 名青少年(基线时的平均[标准差]年龄,14.4[0.38]岁;418[58%]为女性)。酗酒频率的增加与左侧后颞叶皮质(峰值:t1,710=-5.8;家族性错误(FWE)校正 P=7.2×10-5;簇:6297 个体素;P=2.7×10-5)、右侧后颞叶皮质(簇:2070 个体素;FWE 校正 P=0.01)和左侧前额叶皮质(峰值:t1,710=-5.2;FWE 校正 P=2×10-3;簇:10624 个体素;P=1.9×10-7)的灰质萎缩加速有关。根据因果贝叶斯网络分析,73%的网络显示从灰质发育到酗酒增加的方向,这与晚期酗酒者与清醒对照组相比的灰质萎缩加速一致(n=20 与 60;β=1.25;95%置信区间,-2.15 至-0.46;t1,70=0.3;P=0.004),酗酒增加与 14 岁时的灰质体积之间的关联(β=0.23;95%置信区间,0.01-0.46;t1,584=2;P=0.04),灰质萎缩与酒精饮酒单位(β=-0.0033;95%置信区间,-6×10-3 至-5×10-4;t1,509=-2.4;P=0.02)和 23 岁时的酗酒频率(β=-0.16;95%置信区间,-0.28 至-0.03;t1,533=-2.5;P=0.01)之间的关联,以及按灰质萎缩分层而不是按酗酒频率增加分层的线性暴露-反应曲线。
本研究发现,灰质发育和冲动性与酗酒频率的增加有关,这与性别有关。这些结果表明,应谨慎解释与神经毒性相关的灰质萎缩。