The contribution of attention-deficit/hyperactivity disorder polygenic load to metabolic and cardiovascular health outcomes: a large-scale population and sibling study.

IF 5.8 1区 医学 Q1 PSYCHIATRY Translational Psychiatry Pub Date : 2024-11-13 DOI:10.1038/s41398-024-03178-2
Ebba Du Rietz, Tian Xie, Rujia Wang, Rosa Cheesman, Miguel Garcia-Argibay, Zihan Dong, Jia Zhang, Jacobien Niebuur, Melissa Vos, Harold Snieder, Henrik Larsson, Catharina A Hartman
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Abstract

Emerging evidence suggests that ADHD is associated with increased risk for metabolic and cardiovascular (cardiometabolic) diseases. However, an understanding of the mechanisms underlying these associations is still limited. In this study we estimated the associations of polygenic scores (PGS) for ADHD with several cardiometabolic diseases and biomarkers. Furthermore, we investigated to what extent the PGS effect was influenced by direct and indirect genetic effects (i.e., shared familial effects). We derived ADHD-PGS in 50,768 individuals aged 18-90 years from the Dutch Lifelines Cohort study. Using generalised estimating equations, we estimated the association of PGS with cardiometabolic diseases, derived from self-report and several biomarkers measured during a physical examination. We additionally ran within-sibling PGS analyses, using fixed effects models, to disentangle direct effects of individuals' own ADHD genetic risk from confounding due to indirect genetic effects of relatives, as well as population stratification. We found that higher ADHD-PGS were statistically significantly associated with several cardiometabolic diseases (R-squared [R2] range = 0.03-0.50%) and biomarkers (related to inflammation, blood pressure, lipid metabolism, amongst others) (R2 range = 0.01-0.16%) (P < 0.05). Adjustment for shared familial factors attenuated the associations between ADHD-PGS and cardiometabolic outcomes (on average 56% effect size reduction), and significant associations only remained for metabolic disease. Overall our findings suggest that increased genetic liability for ADHD confers a small but significant risk increase for cardiometabolic health outcomes in adulthood. These associations were observable in the general population, even in individuals without ADHD diagnosis, and were partly explained by familial factors shared among siblings.

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注意缺陷/多动障碍多基因负荷对代谢和心血管健康结果的影响:大规模人群和同胞研究。
新的证据表明,多动症与代谢和心血管(心血管代谢)疾病风险的增加有关。然而,人们对这些关联的机制了解仍然有限。在这项研究中,我们估算了多动症的多基因评分(PGS)与几种心血管代谢疾病和生物标志物的关联。此外,我们还研究了 PGS 效应在多大程度上受到直接和间接遗传效应(即共同的家族效应)的影响。我们从荷兰生命线队列研究(Dutch Lifelines Cohort study)中 50,768 名 18-90 岁的个体中得出了 ADHD-PGS。通过使用广义估计方程,我们估计了 PGS 与心脏代谢疾病的关系,该关系来自自我报告和体检中测量的几种生物标志物。此外,我们还使用固定效应模型进行了同胞内部的 PGS 分析,以将个体自身多动症遗传风险的直接影响与亲属的间接遗传效应以及人群分层造成的混淆区分开来。我们发现,在统计学上,较高的 ADHD-PGS 与多种心脏代谢疾病(R 平方 [R2] 范围 = 0.03-0.50%)和生物标志物(与炎症、血压、脂代谢等有关)(R2 范围 = 0.01-0.16%)显著相关(P<0.05)。
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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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