Department of Psychiatry, Oregon Health & Science University, Portland, OR, USA.
Department of Behavioral Neuroscience, Oregon Health & Science University, Portland, OR, USA.
Neuropsychopharmacology. 2019 May;44(6):1076-1083. doi: 10.1038/s41386-019-0315-x. Epub 2019 Jan 12.
Adolescence is a time of significant neurobiological development, including changes in white matter microstructure. Familial alcoholism and adolescent binge-drinking have both been associated with altered white matter microstructure; however, the temporal nature of these effects, and their interaction, is unclear. Using diffusion-weighted imaging and voxel-wise multilevel modeling, the effects of familial alcoholism and future binge-drinking on white matter microstructural development were assessed in 45 adolescents, who went on to binge-drink (but were alcohol-naive at baseline), and 68 adolescents, who remained largely alcohol-naive, all with varying degrees of familial alcoholism. Both future binge-drinking and familial alcoholism were associated with altered frontostriatal white matter microstructure early in adolescence, prior to alcohol use. While several binge-drinking-related effects persisted throughout adolescence (in the posterior limb of the internal capsule, superior corona radiata, and cerebellar peduncles), the association between familial alcoholism and altered white matter microstructure dissipated across adolescence in all regions. There were no white matter regions identified where future binge-drinking or familial alcoholism were significantly associated with emergent or exacerbated alterations in white matter microstructure. Altogether, these findings suggest that alterations in frontostiatal white matter microstructure, some of which are associated with familial alcoholism, may be used to predict which adolescents are more likely to go on and engage in alcohol use. Meanwhile, a reduction in family history-related associations with altered white matter microstructure by late-adolescence is encouraging for future prevention work targeted at at-risk youth.
青春期是神经生物学发育的重要时期,包括白质微观结构的变化。家族性酗酒和青少年 binge-drinking 都与白质微观结构的改变有关;然而,这些影响的时间性质及其相互作用尚不清楚。使用扩散加权成像和体素水平多层次建模,评估了家族性酗酒和未来 binge-drinking 对 45 名青少年(在基线时仍为酒精未接触者,但后来 binge-drinking)和 68 名青少年(大部分仍为酒精未接触者)的白质微观结构发育的影响,所有这些青少年都有不同程度的家族性酗酒。未来 binge-drinking 和家族性酗酒都与青少年早期(在额纹状体白质和内囊后肢、上辐射冠和小脑脚)之前的额纹状体白质微观结构改变有关。虽然一些与 binge-drinking 相关的影响在整个青春期都持续存在(在内囊后肢、上辐射冠和小脑脚),但家族性酗酒与白质微观结构改变之间的关联在青春期所有区域都逐渐消失。没有发现与未来 binge-drinking 或家族性酗酒显著相关的白质区域,有新出现或加剧的白质微观结构改变。总之,这些发现表明,额纹状体白质微观结构的改变,其中一些与家族性酗酒有关,可能被用来预测哪些青少年更有可能继续饮酒。与此同时,青少年晚期家族史相关的白质微观结构改变的关联减少,这对于针对高危青少年的未来预防工作是令人鼓舞的。