...
首页> 外文期刊>Biological psychiatry >Delineation of Two Genetic Pathways to Major Depression
【24h】

Delineation of Two Genetic Pathways to Major Depression

机译:描绘抑郁症的两种遗传途径

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Background: We sought to identify two sets of familial/genetic riskfactors for major depression (MD): 1) high familial loading for MD, which we predicted would be most prominent in cases of MD with an early age at onset (AAO), and 2) high familial loading for vascular disease (VD), which should be strongest in MD cases with a late AAO.Methods: We examined 4785 twin pairs from the Swedish Twin Registry, assessed at a mean age of 54.0 (SD = 7.4), where both members of the pair were evaluated by interview and at least one member reported a lifetime history of modified DSM-IV MD. Riskfor VD was assessed from hospital discharge information and death certificates.Results: Using Cox proportional hazard models and controlling for zygosity, age, and sex, early AAO in depressed twins predicted risk for MD in their cotwins, whereas late AAO predicted cotwin risk for VD. Using piecewise regression, the hazard ratio (HR) relating AAO per decade to risk for MD in cotwin was much stronger for AAO from 13-23 years (HR = .62) than for AAO 24-65 years (HR = 0.94). The HR relating AAO of MD in twin and riskfor VD in cotwin was twice as strong for AAO from 47-65 years (HR = 1.17) as for AA013-46 years (1.08).Conclusions: From a familial/genetic perspective, MD is etiologically heterogeneous. Early and late onset MD are indexed, respectively, by the riskfor MD and VD in relatives.
机译:背景:我们试图确定两组严重抑郁症(MD)的家族/遗传危险因素:1)MD的家族负荷高,我们预计这在发病年龄较早的MD病例中最为突出(AAO),以及2)家族性血管疾病(VD)的高负荷,这在AAO晚期的MD患者中应该最强。方法:我们检查了来自瑞典Twin Registry的4785对双胞胎,评估的平均年龄为54.0(SD = 7.4),该对中的两名成员均接受了访谈评估,并且至少一名成员报告了DSM-IV MD改良版的生命史。通过出院信息和死亡证明书评估了VD风险。结果:使用Cox比例风险模型并控制同卵性,年龄和性别,抑郁双胞胎的早期AAO预测其双子的MD风险,而后期AAO则预测双子的VD风险。 。使用分段回归,在13至23岁的AAO(HR = .62)中,每十年AAO与cotwin的MD风险相关的危险比(HR)比AAO 24-65岁(HR = 0.94)要强得多。从双胞胎的MD的AAO和在考特温的VD风险相关的HR在47-65岁(HR = 1.17)时是AA013-46(1.08)的两倍。结论:从家族/遗传的角度来看,MD是病因异质。发病的早期和晚期MD分别通过亲属的MD和VD风险进行索引。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号