Kumra S, Wiggs E, Krasnewich D, Meck J, Smith A C, Bedwell J, Fernandez T, Jacobsen L K, Lenane M, Rapoport J L
Child Psychiatry Branch, NIMH, Bethesda, MD 20892, USA.
J Am Acad Child Adolesc Psychiatry. 1998 Mar;37(3):292-6. doi: 10.1097/00004583-199803000-00014.
An apparent excess of sex chromosome aneuploidies (XXY, XXX, and possibly XYY) has been reported in patients with adult-onset schizophrenia and with unspecified psychoses. This study describes the results of cytogenetic screening carried out for pediatric patients meeting DMS-III-R criteria for childhood-onset schizophrenia (COS) and a subgroup of patients with childhood-onset psychotic disorder not otherwise specified, provisionally labeled by the authors as multidimensionally impaired (MDI).
From August 1990 to July 1997, karyotypes were determined for 66 neuroleptic-nonresponsive pediatric patients (28 MDI, 38 COS), referred to the National Institute of Mental Health for an inpatient treatment trial of clozapine.
Four (6.1%) of 66 patients (3 MDI, 1 COS) were found to have sex chromosome anomalies (mosaic 47,XXY; 47,XXY; 47,XYY; mosaic 45,XO, respectively), which is higher than the expected rate of 1 per 426 children or 2.34 per 1,000 in the general population (4/66 versus 1/426, chi 2 = 19.2, df = 1, p = .00001). All cases had been previously undiagnosed.
These findings lend support to a hypothesis that a loss of balance of gene products on the sex chromosomes may predispose affected individuals to susceptibility to additional genetic and environmental insults that result in childhood-onset psychotic disorders. Karyotyping of children with psychotic disorders should be routine.
据报道,成年期精神分裂症患者及未明确诊断的精神病患者中性染色体非整倍体(XXY、XXX,可能还有XYY)明显过多。本研究描述了对符合美国精神障碍诊断与统计手册第三版修订版(DMS-III-R)儿童期起病精神分裂症(COS)标准的儿科患者以及一组未另作说明的儿童期起病精神障碍患者(作者暂将其标记为多维受损[MDI])进行细胞遗传学筛查的结果。
1990年8月至1997年7月,对66名对神经阻滞剂无反应的儿科患者(28名MDI,38名COS)进行了核型分析,这些患者被转至美国国立精神卫生研究所接受氯氮平住院治疗试验。
66名患者中有4名(6.1%)(3名MDI,1名COS)被发现存在性染色体异常(分别为嵌合型47,XXY;47,XXY;47,XYY;嵌合型45,XO),高于普通人群中每426名儿童1例或每1000名儿童2.34例的预期发生率(4/66对1/426,卡方 = 19.2,自由度 = 1,p = 0.00001)。所有病例此前均未被诊断出。
这些发现支持了一种假说,即性染色体上基因产物平衡的丧失可能使受影响个体易受额外的遗传和环境损伤,从而导致儿童期起病的精神障碍。对患有精神障碍的儿童进行核型分析应成为常规检查。