Examining the interaction between prenatal stress and polygenic risk for attention-deficit/hyperactivity disorder on brain growth in childhood: Findings from the DREAM BIG consortium

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Mónica López-Vicente, Eszter Szekely, Marie-Elyse Lafaille-Magnan, J. Bruce Morton, Tim F. Oberlander, Celia M. T. Greenwood, Ryan L. Muetzel, Henning Tiemeier, Anqi Qiu, Ashley Wazana, Tonya White
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Abstract

This study explored the interactions among prenatal stress, child sex, and polygenic risk scores (PGS) for attention-deficit/hyperactivity disorder (ADHD) on structural developmental changes of brain regions implicated in ADHD. We used data from two population-based birth cohorts: Growing Up in Singapore Towards healthy Outcomes (GUSTO) from Singapore (n = 113) and Generation R from Rotterdam, the Netherlands (n = 433). Prenatal stress was assessed using questionnaires. We obtained latent constructs of prenatal adversity and prenatal mood problems using confirmatory factor analyses. The participants were genotyped using genome-wide single nucleotide polymorphism arrays, and ADHD PGSs were computed. Magnetic resonance imaging scans were acquired at 4.5 and 6 years (GUSTO), and at 10 and 14 years (Generation R). We estimated the age-related rate of change for brain outcomes related to ADHD and performed (1) prenatal stress by sex interaction models, (2) prenatal stress by ADHD PGS interaction models, and (3) 3-way interaction models, including prenatal stress, sex, and ADHD PGS. We observed an interaction between prenatal stress and ADHD PGS on mean cortical thickness annual rate of change in Generation R (i.e., in individuals with higher ADHD PGS, higher prenatal stress was associated with a lower rate of cortical thinning, whereas in individuals with lower ADHD PGS, higher prenatal stress was associated with a higher rate of cortical thinning). None of the other tested interactions were statistically significant. Higher prenatal stress may promote a slower brain developmental rate during adolescence in individuals with higher ADHD genetic vulnerability, whereas it may promote a faster brain developmental rate in individuals with lower ADHD genetic vulnerability.

Abstract Image

研究产前压力和注意力缺陷/多动症多基因风险对儿童期大脑发育的相互作用:DREAM BIG联合会的研究结果。
本研究探讨了产前压力、儿童性别和注意力缺陷/多动障碍(ADHD)多基因风险评分(PGS)之间的相互作用,以及与 ADHD 相关的脑区结构发育变化。我们使用了两个基于人口的出生队列的数据:我们使用了两个基于人口的出生队列的数据:新加坡的 "在新加坡成长,走向健康结果"(GUSTO)(n = 113)和荷兰鹿特丹的 "R一代"(n = 433)。产前压力通过问卷进行评估。我们通过确证因子分析获得了产前逆境和产前情绪问题的潜在结构。我们使用全基因组单核苷酸多态性阵列对参与者进行了基因分型,并计算了多动症的PGS。在 4.5 岁和 6 岁(GUSTO)以及 10 岁和 14 岁(Generation R)时进行了磁共振成像扫描。我们估算了与多动症相关的大脑结果的年龄相关变化率,并建立了(1)产前压力与性别的交互模型;(2)产前压力与多动症 PGS 的交互模型;以及(3)3 向交互模型,包括产前压力、性别和多动症 PGS。我们观察到产前压力和 ADHD PGS 对 R 代平均皮层厚度年变化率的交互作用(即在 ADHD PGS 较高的个体中,较高的产前压力与较低的皮层变薄率相关,而在 ADHD PGS 较低的个体中,较高的产前压力与较高的皮层变薄率相关)。其他测试的交互作用均无统计学意义。对于遗传易感性较高的多动症患者,较高的产前压力可能会导致其青春期大脑发育速度减慢,而对于遗传易感性较低的多动症患者,较高的产前压力可能会导致其大脑发育速度加快。
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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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