Family History of Substance Use and Stressful Life Events Impact Adolescent Maturation of Cerebral White Matter

IF 2.6 3区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yizhou Ma, Ashley Acheson, Corneliu Bolbocean, Mustafa N. Mithaiwala, Si Gao, Neda Jahanshad, Paul M. Thompson, Bhim M. Adhikari, Xiaoming Du, A. Ankeeta, Alia Warner, Antonio F. Pagán, L. Elliot Hong, Peter Kochunov
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引用次数: 0

Abstract

Family history (FH) of substance use disorders (SUDs) and stressful life events (SLEs) are known risk factors for SUDs in adolescents and young adults. Cross-sectional studies suggest that FH and SLEs affect adolescent white matter (WM) development and form abnormal WM patterns. Here, we examined the effects of FH, SLEs and their interaction on WM integrity in youths in the Adolescent Cognitive Brain Development (ABCD) study at baseline and 2- and 4-year follow-ups. ABCD youths (N = 8939, age ± SD = 9.9 ± 0.6 years, 4302 female) completed baseline diffusion tensor imaging, of which 5661 repeated the scan at 2-year follow-up (age ± SD = 12.0 ± 0.7 years, 2634 female) and 2177 at 4-year follow-up (age ± SD = 14.1 ± 0.7 years, 1007 female). FH was measured as the weighted sum of biological parents and grandparents with alcohol and/or drug problems. SLEs were measured with parental report of life events. WM integrity was measured with fractional anisotropy (FA) of 23 WM tracts. Linear mixed effect models were used to examine the effects of FH, SLEs and their interaction on FA at baseline and longitudinally, modelling family and study site as random intercepts and correcting for multiple comparisons with false discovery rate (FDR) q = 0.05. At baseline, there were no significant effects of FH, SLEs and their interaction on FA after multiple comparison correction when controlling for race, family income and parental education. From baseline to 4-year follow-up, FH significantly negatively interacted with newly occurred SLEs on FA in 19 out of 23 tracts, so that FA at 4-year was lower in youths with both FH and newly occurred SLEs when controlling for baseline FA (βinteraction = −0.049 − −0.018, pFDR = 6.2 × 10−5 − 4.7 × 10−2). These negative interactions were not significant with shorter time spans (baseline to 2-year follow-up and 2- to 4-year follow-up). In conclusion, we replicated findings from cross-sectional cohorts of the effects of FH and SLEs on lower WM integrity in youths. The study utilized Big Data longitudinal design to show that FH-by-SLE interaction, rather than their independent effects was responsible for developmental WM changes associated with FH of SUDs and life stressors.

Abstract Image

物质使用家族史和应激性生活事件影响青少年脑白质成熟
物质使用障碍(SUDs)家族史和应激性生活事件(SLEs)是青少年和年轻人发生SUDs的已知危险因素。横断面研究表明,FH和SLEs影响青少年白质(WM)发育并形成异常的WM模式。在这里,我们在青少年认知脑发育(ABCD)研究中,在基线和2年和4年的随访中,研究了FH、SLEs及其相互作用对青少年WM完整性的影响。ABCD青年(N = 8939,年龄±SD = 9.9±0.6岁,女性4302人)完成基线弥散张量成像,其中5661人在2年随访时重复扫描(年龄±SD = 12.0±0.7岁,女性2634人),2177人在4年随访时重复扫描(年龄±SD = 14.1±0.7岁,女性1007人)。FH测量为有酒精和/或药物问题的亲生父母和祖父母的加权和。通过父母对生活事件的报告来测量SLEs。用分数各向异性(FA)测量23个WM束的WM完整性。采用线性混合效应模型检验FH、SLEs及其相互作用在基线和纵向上对FA的影响,将家族和研究地点建模为随机截点,并以错误发现率(FDR) q = 0.05对多重比较进行校正。在基线时,在控制种族、家庭收入和父母教育程度的多重比较校正后,FH、SLEs及其相互作用对FA无显著影响。从基线到4年的随访,在23个区中有19个区FH与FA新发生的SLEs显著负相互作用,因此在控制基线FA的情况下,FH和新发生的SLEs在4年的FA较低(β相互作用= - 0.049 - - 0.018,pFDR = 6.2 × 10−5 - 4.7 × 10−2)。这些负相互作用在较短的时间跨度(基线至2年随访和2至4年随访)中不显著。总之,我们重复了横断面队列中FH和SLEs对青少年低WM完整性影响的研究结果。该研究利用大数据纵向设计表明,FH与sle的相互作用,而不是它们的独立影响,是导致与sud和生活压力源的FH相关的发育性WM变化的原因。
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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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