Polygenic risk for schizophrenia and bipolar disorder in relation to cardiovascular biomarkers.

IF 3.5 3区 医学 Q1 CLINICAL NEUROLOGY European Archives of Psychiatry and Clinical Neuroscience Pub Date : 2024-08-01 Epub Date: 2023-05-05 DOI:10.1007/s00406-023-01591-0
Elina J Reponen, Thor Ueland, Jaroslav Rokicki, Francesco Bettella, Monica Aas, Maren C F Werner, Ingrid Dieset, Nils E Steen, Ole A Andreassen, Martin Tesli
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Abstract

Individuals with schizophrenia and bipolar disorder are at an increased risk of cardiovascular disease (CVD), and a range of biomarkers related to CVD risk have been found to be abnormal in these patients. Common genetic factors are a putative underlying mechanism, alongside lifestyle factors and antipsychotic medication. However, the extent to which the altered CVD biomarkers are related to genetic factors involved in schizophrenia and bipolar disorder is unknown. In a sample including 699 patients with schizophrenia, 391 with bipolar disorder, and 822 healthy controls, we evaluated 8 CVD risk biomarkers, including BMI, and fasting plasma levels of CVD biomarkers from a subsample. Polygenic risk scores (PGRS) were obtained from genome-wide associations studies (GWAS) of schizophrenia and bipolar disorder from the Psychiatric Genomics Consortium. The CVD biomarkers were used as outcome variables in linear regression models including schizophrenia and bipolar disorder PGRS as predictors, age, sex, diagnostic category, batch and 10 principal components as covariates, controlling for multiple testing by Bonferroni correction for the number of independent tests. Bipolar disorder PGRS was significantly (p = 0.03) negatively associated with BMI after multiple testing correction, and schizophrenia PGRS was nominally negatively associated with BMI. There were no other significant associations between bipolar or schizophrenia PGRS, and other investigated CVD biomarkers. Despite a range of abnormal CVD risk biomarkers in psychotic disorders, we only found a significant negative association between bipolar disorder PGRS and BMI. This has previously been shown for schizophrenia PGRS and BMI, and warrants further exploration.

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精神分裂症和双相情感障碍的多基因风险与心血管生物标志物的关系。
精神分裂症和躁郁症患者罹患心血管疾病(CVD)的风险增加,而且在这些患者中发现了一系列与心血管疾病风险相关的生物标志物异常。除生活方式因素和抗精神病药物外,共同的遗传因素也是一种潜在的机制。然而,心血管疾病生物标志物的改变在多大程度上与精神分裂症和躁狂症的遗传因素有关尚不清楚。在一个包括 699 名精神分裂症患者、391 名躁郁症患者和 822 名健康对照者的样本中,我们评估了包括体重指数在内的 8 种心血管疾病风险生物标志物,以及子样本中心血管疾病生物标志物的空腹血浆水平。多基因风险评分(PGRS)来自精神病基因组学联盟(Psychiatric Genomics Consortium)的精神分裂症和双相情感障碍全基因组关联研究(GWAS)。将心血管疾病生物标志物作为线性回归模型的结果变量,包括精神分裂症和双相情感障碍的 PGRS 作为预测因子,年龄、性别、诊断类别、批次和 10 个主成分作为协变量,并通过 Bonferroni 校正独立测试的次数来控制多重测试。经多重检验校正后,躁郁症 PGRS 与体重指数呈显著负相关(p = 0.03),精神分裂症 PGRS 与体重指数呈名义负相关。双相情感障碍或精神分裂症 PGRS 与其他已调查的心血管疾病生物标志物之间没有其他明显的关联。尽管精神障碍患者存在一系列异常的心血管疾病风险生物标志物,但我们只发现双相情感障碍 PGRS 与体重指数之间存在显著的负相关。精神分裂症的 PGRS 和体重指数也曾出现过这种情况,因此值得进一步探讨。
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来源期刊
CiteScore
8.80
自引率
4.30%
发文量
154
审稿时长
6-12 weeks
期刊介绍: The original papers published in the European Archives of Psychiatry and Clinical Neuroscience deal with all aspects of psychiatry and related clinical neuroscience. Clinical psychiatry, psychopathology, epidemiology as well as brain imaging, neuropathological, neurophysiological, neurochemical and moleculargenetic studies of psychiatric disorders are among the topics covered. Thus both the clinician and the neuroscientist are provided with a handy source of information on important scientific developments.
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