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脑源性神经营养因子(BDNF)水平可作为双相情感障碍高低风险健康双胞胎精神病理学的预测因子。

Brain Derived Neurotrophic Factor (BDNF) levels as a possible predictor of psychopathology in healthy twins at high and low risk for affective disorder.

机构信息

Psychiatric Centre Copenhagen, Rigshospitalet, University Hospital of Copenhagen, Blegdamsvej 9, DK-2100 Copenhagen, Denmark.

出版信息

Psychoneuroendocrinology. 2014 Jan;39:179-183. doi: 10.1016/j.psyneuen.2013.09.007. Epub 2013 Sep 17.

Abstract

Brain Derived Neurotrophic Factor (BDNF) is a potential biomarker of affective disorder. However, longitudinal studies evaluating a potential predictive role of BDNF on subsequent psychopathology are lacking. The aim of this study was to investigate whether BDNF alone or in interaction with the BDNF Val66Met polymorphism predict onset of affective disorder in healthy individuals at heritable risk for affective disorder. In a high-risk study, we assessed whole blood levels of BDNF in 234 healthy monozygotic and dizygotic twins with or without a co-twin history of affective disorder (high and low risk twins, respectively). Participants were followed up longitudinally with questionnaires at 6-month intervals for mean seven years and then reassessed with a personal interview to obtain information about whether they had developed psychiatric illness. At follow-up 36 participants (15.4%) had developed psychiatric disorder. Cox regression analysis revealed that BDNF levels at baseline were not associated with onset of illness in this explorative study. Further, two-way interactions between BDNF levels and the Val66Met polymorphism or between familial risk and the Val66Met polymorphism did not predict illness onset.

摘要

脑源性神经营养因子(BDNF)是情感障碍的一个潜在生物标志物。然而,缺乏评估 BDNF 对随后精神病理学的潜在预测作用的纵向研究。本研究的目的是调查 BDNF 本身或与 BDNF Val66Met 多态性的相互作用是否可以预测具有情感障碍遗传风险的健康个体中情感障碍的发病。在一项高危研究中,我们评估了 234 名健康的同卵和异卵双胞胎的全血 BDNF 水平,这些双胞胎中有或没有同卵双胞胎的情感障碍病史(分别为高风险和低风险双胞胎)。参与者接受了长达 7 年的平均 6 个月一次的纵向问卷调查,然后进行个人访谈,以获取有关他们是否患有精神疾病的信息。在随访中,36 名参与者(15.4%)患有精神疾病。Cox 回归分析显示,在这项探索性研究中,基线时的 BDNF 水平与疾病发作无关。此外,BDNF 水平与 Val66Met 多态性之间或家族风险与 Val66Met 多态性之间的双向相互作用均不能预测疾病发作。

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