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研究综述:ADHD 与其他精神症状之间遗传重叠的强度——系统综述和荟萃分析。

Research Review: The strength of the genetic overlap between ADHD and other psychiatric symptoms - a systematic review and meta-analysis.

机构信息

School of Medical Sciences, Örebro University, Örebro, Sweden.

School of Psychology, Law and Social Work, Örebro University, Örebro, Sweden.

出版信息

J Child Psychol Psychiatry. 2020 Nov;61(11):1173-1183. doi: 10.1111/jcpp.13233. Epub 2020 Mar 10.

Abstract

BACKGROUND

Attention-deficit/hyperactivity disorder (ADHD) frequently co-occurs with other psychiatric disorders. Twin studies have established that these co-occurrences are in part due to shared genetic risks. However, the strength of these genetic overlaps and the potential heterogeneity accounted for by type of psychiatric symptoms, age, and methods of assessment remain unclear. We conducted a systematic review to fill this gap.

METHODS

We searched PubMed, PsycINFO, Embase, and Web of Science until March 07, 2019. Genetic correlations (r ) were used as effect size measures.

RESULTS

A total of 31 independent studies fulfilled the inclusion criteria. The pooled estimates showed that the associations between ADHD and other psychiatric symptoms were partly explained by shared genetic factors, with a pooled genetic correlation of 0.50, 95% confidence interval: 0.46-0.60. The genetic correlations (r ) between ADHD and externalizing (r  = .49 [0.37-0.61]), internalizing (r  = .50 [0.39-0.69]), and neurodevelopmental (r  = .56 [0.47-0.66]) symptoms were similar in magnitude. The genetic correlations in childhood and adulthood were r  = .53 (0.43-0.63) and r  = .51 (0.44-0.56), respectively. For methods of assessment, the genetic correlations were also similar in strength, self-reports r  = .52 (0.47-0.58), other informants r  = .55 (0.41-0.69), and combined raters r  = .50 (0.33-0.65).

CONCLUSIONS

These findings indicate that the co-occurrence of externalizing, internalizing, and neurodevelopmental disorder symptoms in individuals with ADHD symptoms in part is due to a shared genetic risk.

摘要

背景

注意力缺陷多动障碍(ADHD)常与其他精神疾病共病。双胞胎研究已经证实,这些共病部分归因于共同的遗传风险。然而,这些遗传重叠的强度以及由精神症状类型、年龄和评估方法引起的潜在异质性尚不清楚。我们进行了一项系统综述来填补这一空白。

方法

我们检索了 PubMed、PsycINFO、Embase 和 Web of Science,检索时间截至 2019 年 3 月 07 日。遗传相关系数(r)用作效应量指标。

结果

共有 31 项独立研究符合纳入标准。汇总估计表明,ADHD 与其他精神症状之间的关联部分由共同的遗传因素解释,其遗传相关系数为 0.50,95%置信区间为 0.46-0.60。ADHD 与外向性(r=0.49[0.37-0.61])、内向性(r=0.50[0.39-0.69])和神经发育(r=0.56[0.47-0.66])症状之间的遗传相关性相似。儿童期和成年期的遗传相关性分别为 r=0.53(0.43-0.63)和 r=0.51(0.44-0.56)。在评估方法方面,遗传相关性的强度也相似,自我报告 r=0.52(0.47-0.58),其他信息来源 r=0.55(0.41-0.69),和综合评估者 r=0.50(0.33-0.65)。

结论

这些发现表明,ADHD 患者的外向性、内向性和神经发育障碍症状共病部分归因于共同的遗传风险。

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