Suppr超能文献

普通人群中亚阈下自闭症特征的代际传递。

Intergenerational transmission of subthreshold autistic traits in the general population.

作者信息

Constantino John N, Todd Richard D

机构信息

Department of Psychiatry, Washington University School of Medicine, St. Louis, MO 63110, USA.

出版信息

Biol Psychiatry. 2005 Mar 15;57(6):655-60. doi: 10.1016/j.biopsych.2004.12.014.

Abstract

BACKGROUND

Autistic disorder (AD) is a disabling oligogenic condition characterized by severe social impairment. Subthreshold autistic social impairments are known to aggregate in the family members of autistic probands; therefore, we conducted this study to examine the intergenerational transmission of such traits in the general population.

METHODS

The Social Responsiveness Scale (SRS), a quantitative measure of autistic traits, was completed on 285 pairs of twins (by maternal report) and on their parents (by spouse report).

RESULTS

Correlation for social impairment or competence between parents and their children and between spouses was on the order of .4. In families in which both parents scored in the upper quartile for social impairment on the SRS, mean SRS score of offspring was significantly elevated (effect size 1.5). Estimated assortative mating explained approximately 30% of the variation in parent SRS scores.

CONCLUSIONS

Children from families in which both parents manifest subthreshold autistic traits exhibit a substantial shift in the distribution of their scores for impairment in reciprocal social behavior, toward the pathological end. As has been previously demonstrated in children, heritable subthreshold autistic impairments are measurable in adults and appear continuously distributed in the general population.

摘要

背景

孤独症谱系障碍(AD)是一种以严重社交障碍为特征的致残性寡基因疾病。已知阈下孤独症社交障碍在孤独症先证者的家庭成员中聚集;因此,我们开展了这项研究,以检验此类特征在普通人群中的代际传递情况。

方法

采用社交反应量表(SRS),这是一种对孤独症特征的定量测量工具,对285对双胞胎(由母亲报告)及其父母(由配偶报告)进行了测评。

结果

父母与子女之间以及配偶之间社交障碍或社交能力的相关性约为0.4。在父母双方在SRS社交障碍得分处于上四分位数的家庭中,后代的平均SRS得分显著升高(效应量为1.5)。估计的选型交配解释了父母SRS得分变异的约30%。

结论

父母双方均表现出阈下孤独症特征的家庭中的孩子,其在相互社交行为障碍得分的分布上出现了显著变化,朝着病理端偏移。正如之前在儿童中所证明的那样,可遗传的阈下孤独症障碍在成年人中是可测量的,并且在普通人群中呈连续分布。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验