Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center, Utrecht, the Netherlands.
Biol Psychiatry. 2010 Dec 15;68(12):1156-62. doi: 10.1016/j.biopsych.2010.08.034. Epub 2010 Oct 29.
Several genetic mechanisms have been proposed for the variability of the Klinefelter syndrome (KS) phenotype such as the parent-of-origin of the extra X chromosome. Parent-of-origin effects on behavior in KS can possibly provide insights into X-linked imprinting effects on psychopathology that may be extrapolated to other populations. Here, we investigated whether the parent-of-origin of the supernumerary X chromosome influences autistic and schizotypal symptom profiles in KS.
Parent-of-origin of the X chromosome was determined through analysis of the polymorphic CAG tandem repeat of the androgen receptor gene. Autistic traits (Autism Diagnostic Interview-Revised) were measured in a younger KS sample (n = 33) with KS and schizotypal traits (Schizotypal Personality Questionnaire) were assessed in an older KS sample (n = 43). Scale scores on these questionnaires were entered in statistical analyses to test parent-of-origin effects.
The results show that parent-of-origin of the X chromosome is reflected in autistic and schizotypal symptomatology. Differences were shown in the degree of both schizotypal and autistic symptoms between the parent-of-origin groups. Furthermore, the parent-of-origin could be correctly discriminated in more than 90% of subjects through Autism Diagnostic Interview-Revised scales and in around 80% of subjects through Schizotypal Personality Questionnaire scales.
These findings point to parent-of-origin effects on psychopathology in KS and indicate that imprinted X chromosomal genes may have differential effects on autistic and schizotypal traits. Further exploration of imprinting effects on psychopathology in KS is needed to confirm and expand on our findings.
已经提出了几种遗传机制来解释克氏综合征(KS)表型的变异性,例如额外 X 染色体的亲本来源。KS 中行为的亲本来源效应可能为 X 连锁印迹对精神病理学的影响提供见解,这些影响可能会推广到其他人群。在这里,我们研究了额外 X 染色体的亲本来源是否会影响 KS 中的自闭症和精神分裂症样症状特征。
通过雄激素受体基因的多态性 CAG 串联重复分析来确定 X 染色体的亲本来源。在年轻的 KS 样本(n = 33)中测量自闭症特征(自闭症诊断访谈修订版),在较年长的 KS 样本(n = 43)中评估精神分裂症样特征(精神分裂症人格问卷)。将这些问卷的量表评分输入统计分析中,以测试亲本来源效应。
结果表明,X 染色体的亲本来源反映在自闭症和精神分裂症样症状中。在亲本来源组之间,精神分裂症样和自闭症症状的严重程度都存在差异。此外,通过自闭症诊断访谈修订版量表,可正确区分 90%以上的受试者的亲本来源,通过精神分裂症人格问卷量表,可正确区分约 80%的受试者的亲本来源。
这些发现指向 KS 中精神病理学的亲本来源效应,并表明印迹 X 染色体基因可能对自闭症和精神分裂症样特征有不同的影响。需要进一步探索 KS 中印迹对精神病理学的影响,以证实和扩展我们的发现。