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首页> 外文期刊>Biological psychiatry >Familial Liability to Epilepsy and Attention-Deficit/Hyperactivity Disorder: A Nationwide Cohort Study
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Familial Liability to Epilepsy and Attention-Deficit/Hyperactivity Disorder: A Nationwide Cohort Study

机译:癫痫和注意力缺陷/多动障碍的家族责任:全国范围内的队列研究

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摘要

Abstract Background Epilepsy and attention-deficit/hyperactivity disorder (ADHD) are strongly associated; however, the underlying factors contributing to their co-occurrence remain unclear. A shared genetic liability has been proposed as one possible mechanism. Therefore, our goal in this study was to investigate the familial coaggregation of epilepsy and ADHD and to estimate the contribution of genetic and environmental risk factors to their co-occurrence. Methods We identified 1,899,654 individuals born between 1987 and 2006 via national Swedish registers and linked each individual to his or her biological relatives. We used logistic regression to estimate the association between epilepsy and ADHD within individual and across relatives. Quantitative genetic modeling was used to decompose the cross-disorder covariance into genetic and environmental factors. Results Individuals with epilepsy had a statistically significant increased risk of ADHD (odds ratio [OR]?= 3.47, 95% confidence interval [CI]?= 3.33–3.62). This risk increase extended to children whose mothers had epilepsy (OR?= 1.85, 95% CI?= 1.75–1.96), children whose fathers had epilepsy (OR?= 1.64, 95% CI?= 1.54–1.74), full siblings (OR?= 1.56, 95% CI?= 1.46–1.67), maternal half siblings (OR?= 1.28, 95% CI?= 1.14–1.43), paternal half siblings (OR?= 1.10, 95% CI?= 0.96–1.25), and cousins (OR?= 1.15, 95% CI?= 1.10–1.20). The genetic correlation was 0.21 (95% CI?= 0.02–0.40) and explained 40% of the phenotypic correlation between epilepsy and ADHD, with the remaining variance largely explained by nonshared environmental factors (49%, nonshared environmental correlation?= 0.36, 95% CI?= 0.23–0.49). The contribution of shared environmental factors to the cross-disorder overlap was not statistically significant (11%, shared environmental correlation?= 0.32, 95% CI?=??0.16–0.79). Conclusions This study demonstrates a strong and etiologically complex association between epilepsy and ADHD, with shared familial factors and risk factors unique to the individual contributing to co-occurrence of the disorders. Our findings suggest that epilepsy and ADHD may share less genetic risk as compared with other neurodevelopmental disorders.
机译:摘要背景癫痫和注意力缺陷/多动障碍(ADHD)强烈关联;然而,有助于他们的共同发生的潜在因素仍然不清楚。已提出共同的遗传责任作为一种可能的机制。因此,我们在本研究中的目标是调查癫痫和ADHD的家庭共gggregation,并估算遗传和环境风险因素对其共同发生的贡献。方法我们确定了1987年至2006年间出生的1,899,654人,通过国家瑞典登记册,并将每个个人与其生物学亲属联系起来。我们使用Logistic回归来估计个人和亲属内的癫痫和ADHD之间的关联。定量遗传建模用于将跨无序协方差分解为遗传和环境因素。结果具有癫痫的个体具有统计学上显着增加的ADHD风险(差距[或]?= 3.47,95%置信区间[CI]?= 3.33-3.62)。这种风险增长扩展到母亲癫痫的儿童(或?= 1.85,95%ci?= 1.75-1.96),父亲癫痫的儿童(或?= 1.64,95%ci?= 1.54-1.74),全兄弟姐妹(或?= 1.56,95%CI?= 1.46-1.67),母体半兄弟姐妹(或?= 1.28,95%CI?= 1.14-1.43),父亲半兄弟(或?= 1.10,95%CI?= 0.96- 1.25)和表兄弟(或?= 1.15,95%CI?= 1.10-1.20)。遗传相关是0.21(95%CI = 0.02-0.40),并解释了癫痫和ADHD之间的表型相关性的40%,其剩余的差异很大程度上解释了Nonshared环境因素(49%,非正日的环境相关性?= 0.36,95 %ci?= 0.23-0.49)。共享环境因素对跨紊乱重叠的贡献在统计学上没有统计学意义(11%,共享环境相关性?= 0.32,95%CI?= ?? 0.16-0.79)。结论本研究展示了癫痫和ADHD之间的强大和病因综合症,具有共同的家庭因素和危险因素,这些因素具有促成疾病的共同发生的个人。我们的研究结果表明,与其他神经发育障碍相比,癫痫和ADHD可能与遗传风险相比。

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