Department of Psychological and Brain Sciences, Indiana University, Bloomington.
Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
JAMA Psychiatry. 2014 Apr;71(4):432-8. doi: 10.1001/jamapsychiatry.2013.4525.
Advancing paternal age is associated with increased genetic mutations during spermatogenesis, which research suggests may cause psychiatric morbidity in the offspring. The effects of advancing paternal age at childbearing on offspring morbidity remain unclear, however, because of inconsistent epidemiologic findings and the inability of previous studies to rigorously rule out confounding factors.
To examine the associations between advancing paternal age at childbearing and numerous indexes of offspring morbidity.
DESIGN, SETTING, AND PARTICIPANTS: We performed a population-based cohort study of all individuals born in Sweden in 1973-2001 (N = 2,615,081), with subsets of the data used to predict childhood or adolescent morbidity. We estimated the risk of psychiatric and academic morbidity associated with advancing paternal age using several quasi-experimental designs, including the comparison of differentially exposed siblings, cousins, and first-born cousins.
Paternal age at childbearing.
Psychiatric (autism, attention-deficit/hyperactivity disorder, psychosis, bipolar disorder, suicide attempt, and substance use problem) and academic (failing grades and low educational attainment) morbidity.
In the study population, advancing paternal age was associated with increased risk of some psychiatric disorders (eg, autism, psychosis, and bipolar disorders) but decreased risk of the other indexes of morbidity. In contrast, the sibling-comparison analyses indicated that advancing paternal age had a dose-response relationship with every index of morbidity, with the magnitude of the associations being as large or larger than the estimates in the entire population. Compared with offspring born to fathers 20 to 24 years old, offspring of fathers 45 years and older were at heightened risk of autism (hazard ratio [HR] = 3.45; 95% CI, 1.62-7.33), attention-deficit/hyperactivity disorder (HR = 13.13; 95% CI, 6.85-25.16), psychosis (HR = 2.07; 95% CI, 1.35-3.20), bipolar disorder (HR = 24.70; 95% CI, 12.12-50.31), suicide attempts (HR = 2.72; 95% CI, 2.08-3.56), substance use problems (HR = 2.44; 95% CI, 1.98-2.99), failing a grade (odds ratio [OR] = 1.59; 95% CI, 1.37-1.85), and low educational attainment (OR = 1.70; 95% CI, 1.50-1.93) in within-sibling comparisons. Additional analyses using several quasi-experimental designs obtained commensurate results, further strengthening the internal and external validity of the findings.
Advancing paternal age is associated with increased risk of psychiatric and academic morbidity, with the magnitude of the risks being as large or larger than previous estimates. These findings are consistent with the hypothesis that new genetic mutations that occur during spermatogenesis are causally related to offspring morbidity.
随着精子发生过程中遗传突变的增加,父亲年龄的增长与精神疾病发病风险增加有关。然而,由于流行病学研究结果不一致,以及先前的研究无法严格排除混杂因素,父亲在生育时的年龄对后代发病的影响仍不清楚。
研究父亲在生育时的年龄增长与后代多种发病指标之间的关系。
设计、地点和参与者:我们对 1973-2001 年在瑞典出生的所有个体(N=2615081)进行了基于人群的队列研究,使用部分数据来预测儿童或青少年的发病情况。我们使用几种准实验设计来估计与父亲年龄增长相关的精神和学术发病风险,包括比较不同暴露的兄弟姐妹、表亲以及第一代表亲。
父亲的生育年龄。
精神疾病(自闭症、注意缺陷多动障碍、精神病、双相情感障碍、自杀未遂和物质使用问题)和学术(成绩不及格和教育程度低)发病情况。
在研究人群中,父亲年龄的增长与某些精神疾病(如自闭症、精神病和双相情感障碍)的发病风险增加有关,但与其他发病指标的风险降低有关。相比之下,兄弟姐妹比较分析表明,父亲年龄的增长与每个发病指标都呈剂量反应关系,其关联的大小与整个人群的估计值一样大或更大。与父亲年龄在 20 至 24 岁的子女相比,父亲年龄在 45 岁及以上的子女患自闭症的风险更高(风险比[HR] =3.45;95%可信区间,1.62-7.33)、注意力缺陷多动障碍(HR=13.13;95%可信区间,6.85-25.16)、精神病(HR=2.07;95%可信区间,1.35-3.20)、双相情感障碍(HR=24.70;95%可信区间,12.12-50.31)、自杀未遂(HR=2.72;95%可信区间,2.08-3.56)、物质使用问题(HR=2.44;95%可信区间,1.98-2.99)、成绩不及格(比值比[OR] =1.59;95%可信区间,1.37-1.85)和教育程度低(OR=1.70;95%可信区间,1.50-1.93)。在兄弟姐妹内比较中使用几种准实验设计进行的额外分析得出了类似的结果,进一步增强了研究结果的内部和外部有效性。
父亲年龄的增长与精神和学术发病风险增加有关,其风险的大小与以往的估计值一样大或更大。这些发现与精子发生过程中发生的新遗传突变与后代发病有关的假设一致。