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Meta-analysis of paternal age and schizophrenia risk in male versus female offspring.

机译:对男性和女性后代的父亲年龄和精神分裂症风险的荟萃分析。

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INTRODUCTION: Advanced paternal age (APA) is a reported risk factor for schizophrenia in the offspring. We performed a meta-analysis of this association, considering the effect of gender and study design. METHODS: We identified articles by searching Pub Med, PsychInfo, ISI, and EMBASE, and the reference lists of identified studies. Previously unpublished data from the Northern Finland 1966 Birth Cohort (NFBC 1966) study were also included. RESULTS: There were 6 cohort studies and 6 case-control studies that met the inclusion criteria. In both study designs, there was a significant increase in risk of schizophrenia in the offspring of older fathers (>/=30) compared to a reference paternal age of 25-29, with no gender differences. The relative risk (RR) in the oldest fathers (>/=50) was 1.66 [95% confidence interval (95% CI): 1.46-1.89, P < 0.01]. A significant increase in risk was also found for younger fathers (<25) in males (RR = 1.08, 95% CI: 1.02-1.14, P = 0.01) but not females (RR = 1.04, 95% CI: 0.97-1.14, P = 0.28). The population attributable risk percentage (PAR%) was 10% for paternal age >/=30 and 5% for paternal age <25. DISCUSSION: Both APA (>/=30) and younger paternal age (<25) increase the risk of schizophrenia; younger paternal age may be associated with an increased risk in males but not females. This risk factor increases the risk of schizophrenia as much as any single candidate gene of risk. The mechanism of these associations is not known and may differ for older and younger fathers.
机译:简介:较高的父亲年龄(APA)是后代精神分裂症的危险因素。考虑到性别和研究设计的影响,我们对该关联进行了荟萃分析。方法:我们通过搜索Pub Med,PsychInfo,ISI和EMBASE以及已鉴定研究的参考文献列表来鉴定文章。还包括以前未发表的1966年芬兰北部出生队列研究(NFBC 1966)的数据。结果:有6项队列研究和6项病例对照研究符合纳入标准。在两种研究设计中,与参考父亲的年龄为25-29岁相比,老年父亲的后代(> / = 30)患精神分裂症的风险均显着增加,而没有性别差异。大龄父亲(> / = 50)的相对风险(RR)为1.66 [95%置信区间(95%CI):1.46-1.89,P <0.01]。男性(RR = 1.08,95%CI:1.02-1.14,P = 0.01)的年轻父亲(<25)的风险也显着增加,而女性(RR = 1.04,95%CI:0.97-1.14, P = 0.28)。父本年龄> / = 30的人群归因风险百分比(PAR%)为10%,父本年龄<25为5%。讨论:APA(> / = 30)和较年轻的父亲年龄(<25)都增加了精神分裂症的风险。父亲年龄偏低可能与男性患病风险增加有关,而与女性无关。该危险因素与任何单个候选危险基因一样,增加了精神分裂症的危险。这些关联的机制尚不清楚,对于年龄较大的父亲和年龄较小的父亲可能有所不同。

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