不良童年经历与酒精使用障碍成人脑容量和皮层厚度变化之间的关系

IF 3.1 3区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Cagdas Türkmen, Haoye Tan, Sarah Gerhardt, Emilie Bougelet, Maria Bernardo, Noah Machunze, Yasmin Grauduszus, Maurizio Sicorello, Traute Demirakca, Falk Kiefer, Sabine Vollstädt-Klein
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引用次数: 0

摘要

研究背景 以前的研究已经证实了不良童年经历(ACE)与酒精使用障碍(AUD)之间的联系,这两者都与灰质体积(GMV)和皮质厚度(CT)的改变有关。本研究旨在评估ACE对AUD的神经生物学影响,以及虐待类型(即虐待或忽视)和时间的作用。 方法 收集了 35 名患有 AUD 的成人(平均年龄:40 岁;31% 为女性)和 28 名健康对照者(平均年龄:36 岁;61% 为女性)的结构磁共振成像数据。使用童年创伤问卷和虐待与受虐年表访谈对 ACE 进行回顾性评估。使用基于体素和表面的形态计量学方法估算全球和区域GMV和CT。 结果 与健康对照组相比,AUD 组的左额叶下回、脑岛左环沟、中央下回和脑沟(C1 组)以及中央沟和中央前回(C2 组)的 CT 明显减少。在 AUD 组中,C1 群 CT 的减少与 ACE 和 AUD 的严重程度显著相关。类型和时间分析表明,13 至 15 岁时遭受虐待的程度较高与 AUD 组中 C1 群 CT 减少之间存在显著关联。 结论 在患有 AUD 的成年人中,青春期早期遭受的虐待与抑制控制区域的 CT 值降低有关,这表明认知途径在 ACE 与 AUD 之间的关联中可能具有相关性。需要进行纵向研究来证实和扩展目前的研究结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The association between adverse childhood experiences and alterations in brain volume and cortical thickness in adults with alcohol use disorder

The association between adverse childhood experiences and alterations in brain volume and cortical thickness in adults with alcohol use disorder

Background

Previous studies have established a connection between adverse childhood experiences (ACE) and alcohol use disorder (AUD), both of which are associated with alterations in grey matter volume (GMV) and cortical thickness (CT). The current study aimed to assess the neurobiological impact of ACE specifically in the context of AUD, as well as the role of maltreatment type (i.e., abuse or neglect) and timing.

Methods

Structural MRI data were collected from 35 adults with AUD (mean age: 40; 31% female) and 28 healthy controls (mean age: 36; 61% female). ACE were assessed retrospectively using the Childhood Trauma Questionnaire, and the Maltreatment and Abuse Chronology interview. Global and regional GMV and CT were estimated using voxel- and surface-based morphometry.

Results

Relative to the healthy controls, the AUD group had significantly reduced CT in the left inferior frontal gyrus, left circular sulcus of the insula and subcentral gyrus and sulci (cluster C1), and in the central sulcus and precentral gyrus (cluster C2). Within the AUD group, a reduction of CT in cluster C1 was significantly associated with higher severity of ACE and AUD. Type and timing analyses revealed a significant association between higher levels of abuse at ages 13 to 15 and reduced CT in cluster C1 within the AUD group.

Conclusions

In adults with AUD, abuse experienced during early adolescence is associated with reduced CT in regions involved in inhibitory control, indicating the potential relevance of cognitive pathways in the association between ACE and AUD. Longitudinal studies are needed to confirm and expand upon current findings.

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来源期刊
Addiction Biology
Addiction Biology 生物-生化与分子生物学
CiteScore
8.10
自引率
2.90%
发文量
118
审稿时长
6-12 weeks
期刊介绍: Addiction Biology is focused on neuroscience contributions and it aims to advance our understanding of the action of drugs of abuse and addictive processes. Papers are accepted in both animal experimentation or clinical research. The content is geared towards behavioral, molecular, genetic, biochemical, neuro-biological and pharmacology aspects of these fields. Addiction Biology includes peer-reviewed original research reports and reviews. Addiction Biology is published on behalf of the Society for the Study of Addiction to Alcohol and other Drugs (SSA). Members of the Society for the Study of Addiction receive the Journal as part of their annual membership subscription.
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