Roybal Melissa R, Liu Siyuan, Larsen Isabella G, Wass Anastasia, Schaffer Lukas, Ajumobi Tiffany, Whitman Ethan T, Warling Allysa, Clasen Liv, Blumenthal Jonathan, Rau Srishti, Raznahan Armin
Section on Developmental Neurogenomics, National Institute of Mental Health, National Institutes of Health, Bethesda, MD, USA.
Georgetown University School of Medicine, Washington, DC, USA.
Eur Child Adolesc Psychiatry. 2025 May 23. doi: 10.1007/s00787-025-02743-4.
Sex chromosome trisomies (SCTs) are a group of genetic disorders characterized by presence of a supernumerary sex chromosome, resulting in karyotypes other than XX or XY. These include XXX (Trisomy X), XXY (Klinefelter syndrome), and XYY (Jacobs syndrome). SCTs have been linked to increased risk for psychopathology; however, this relationship warrants additional research. Specifically, little is known regarding potential age-related variation in risk for psychopathology and how this may differ across karyotypes and subdomains of psychopathology. This has important implications for psychoeducation (e.g., informing carriers of the likelihood for varying manifestations with age), personalized care, and research into the mechanisms of pathophysiology. Thus, we used the Child Behavior Checklist (CBCL) to estimate age-related variation in psychopathology in a large cross-sectional sample of SCT carriers (n = 201) and euploidic controls (n = 304) spanning the age range of 5-18 years. We found that elevations of psychopathology in carriers were significantly associated with age in a manner that varied as a combined function of the karyotype and CBCL scale being considered. Post hoc tests revealed there is a uniquely pronounced age-associated increase in severity of social problems in the XYY karyotype, alongside a lack of statistical evidence for age-related variation in the severity of psychopathology for other CBCL domains and SCT karyotypes. Our findings are relevant for advancing the personalization of clinical assessment and monitoring in SCT carriers. They also highlight potential windows of dynamic risk emergence for closer clinical and biological study, as well as opportunities to provide intervention to mitigate future risk.
性染色体三体综合征(SCTs)是一组遗传性疾病,其特征是存在一条额外的性染色体,导致核型不同于XX或XY。这些包括XXX(三体X综合征)、XXY(克兰费尔特综合征)和XYY(雅各布斯综合征)。SCTs与精神病理学风险增加有关;然而,这种关系值得进一步研究。具体而言,关于精神病理学风险中潜在的年龄相关差异以及这种差异在不同核型和精神病理学亚领域中可能如何不同,人们知之甚少。这对心理教育(例如告知携带者随着年龄增长出现不同表现的可能性)、个性化护理以及病理生理学机制的研究具有重要意义。因此,我们使用儿童行为检查表(CBCL)来估计一大组5至18岁的SCT携带者(n = 201)和整倍体对照(n = 304)样本中精神病理学的年龄相关差异。我们发现携带者中精神病理学的升高与年龄显著相关,其方式因所考虑的核型和CBCL量表的综合作用而有所不同。事后检验显示XYY核型中社会问题严重程度存在独特且明显与年龄相关的增加趋势,而对于其他CBCL领域和SCT核型,精神病理学严重程度缺乏与年龄相关差异的统计学证据。我们的研究结果对于推进SCT携带者临床评估和监测的个性化具有重要意义。它们还突出了动态风险出现的潜在窗口期以供更深入的临床和生物学研究,并提供了进行干预以减轻未来风险的机会。