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父亲年龄与精神分裂症风险的荟萃分析:子女性别差异。

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

机构信息

Department of Psychiatry, Medical College of Georgia, Augusta, GA 30912, USA.

出版信息

Schizophr Bull. 2011 Sep;37(5):1039-47. doi: 10.1093/schbul/sbq011. Epub 2010 Feb 25.

Abstract

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 Previously unpublished data from the Northern Finland 1966 Birth Cohort (NFBC 1966) study were also included.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.

摘要

介绍

高龄父亲(APA)被报道是后代精神分裂症的一个风险因素。我们进行了一项荟萃分析,考虑了性别和研究设计的影响。

方法

我们通过搜索 Pub Med、PsychInfo、ISI 和 EMBASE 以及已确定研究的参考文献列表来确定文章。还包括来自芬兰北部 1966 年出生队列(NFBC 1966)研究的先前未发表的数据。

结果

有 6 项队列研究和 6 项病例对照研究符合纳入标准。在这两种研究设计中,与参考父亲年龄 25-29 岁相比,高龄父亲(≥30 岁)的后代患精神分裂症的风险显著增加,且无性别差异。最年长父亲(≥50 岁)的相对风险(RR)为 1.66[95%置信区间(95%CI):1.46-1.89,P < 0.01]。在男性中,也发现年轻父亲(<25 岁)的风险增加(RR = 1.08,95%CI:1.02-1.14,P = 0.01),但在女性中没有(RR = 1.04,95%CI:0.97-1.14,P = 0.28)。父亲年龄≥30 时的人群归因风险百分比(PAR%)为 10%,父亲年龄<25 时为 5%。

讨论

APA(≥30)和年轻的父亲年龄(<25)都增加了精神分裂症的风险;年轻的父亲年龄可能与男性的风险增加有关,但与女性无关。这种风险因素增加了精神分裂症的风险,与任何单一的风险候选基因一样多。这些关联的机制尚不清楚,并且可能因年长和年轻的父亲而异。

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