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诊断为腭心面综合征患者的双相谱系障碍:22q11染色体半合子缺失会导致双相情感障碍吗?

Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?

作者信息

Papolos D F, Faedda G L, Veit S, Goldberg R, Morrow B, Kucherlapati R, Shprintzen R J

机构信息

Department of Psychiatry, Albert Einstein College of Medicine, Yeshiva University, Bronx, NY 10461, USA.

出版信息

Am J Psychiatry. 1996 Dec;153(12):1541-7. doi: 10.1176/ajp.153.12.1541.

Abstract

OBJECTIVE

The purpose of this study was to conduct a systematic assessment of psychiatric illness in patients diagnosed with velo-cardio-facial syndrome, a genetic syndrome that involves over 40 somatic anomalies, learning disabilities, and behavioral disorders and is associated with a microdeletion on chromosome 22q11.

METHOD

Subjects were referred for psychiatric diagnostic evaluation without regard to age or previous psychiatric history. In order to establish DSM-III-R consensus clinical diagnoses for patients who ranged in age from 5 to 34 years, the Diagnostic Interview for Children and Adolescents--Revised or the Structured Clinical Interview for DSM-III-R (SCID) was used. A review of available medical and psychiatric records and a clinical interview performed by two research psychiatrists to validate specific symptoms and syndromes reported in the Diagnostic Interview for Children and Adolescents--Revised and the SCID were used to elucidate the chronological appearance and duration of symptoms.

RESULTS

Sixty-four percent (N = 16 of 25) of this unselected series of patients with velo-cardio-facial syndrome met DSM-III-R criteria for a spectrum of bipolar disorders with full syndromal onset in late childhood or early adolescence (mean age at onset = 12 years, SD = 3). In addition, 20% (N = 5) met DSM-III-R criteria for attention deficit hyperactivity disorder (ADHD), while 16% (N = 4) met criteria for attention deficit disorder without hyperactivity. In contrast to previous reports of a high prevalence of schizophrenia, none of the patients was diagnosed with schizophrenia, and only four had psychotic symptoms during a phase of their illness, all in their 20s or 30s.

CONCLUSIONS

Given that the prevalence of bipolar disorder in the general population is estimated to be 1.5% and that the average age at onset is 24, these findings support an unusually strong association between velo-cardio-facial syndrome and early-onset bipolar disorder and suggest that a gene deleted at the 22q11 chromosomal locus may be involved in its pathogenesis. If confirmed, these findings may provide a new and fruitful line of investigation into the molecular basis of bipolar spectrum disorders.

摘要

目的

本研究旨在对被诊断患有腭心面综合征的患者的精神疾病进行系统评估。腭心面综合征是一种遗传性综合征,涉及40多种躯体异常、学习障碍和行为障碍,与22q11染色体微缺失相关。

方法

受试者被转介进行精神科诊断评估,不考虑年龄或既往精神病史。为了对年龄在5至34岁之间的患者建立DSM-III-R共识临床诊断,使用了修订版儿童及青少年诊断访谈或DSM-III-R结构化临床访谈(SCID)。通过查阅现有的医学和精神科记录以及由两位研究精神科医生进行的临床访谈,以验证修订版儿童及青少年诊断访谈和SCID中报告的特定症状和综合征,从而阐明症状的出现时间和持续时间。

结果

在这个未经筛选的腭心面综合征患者系列中,64%(25例中的16例)符合DSM-III-R中一系列双相情感障碍的标准,在儿童晚期或青春期早期出现完全综合征发作(平均发病年龄 = 12岁,标准差 = 3)。此外,20%(5例)符合DSM-III-R中注意力缺陷多动障碍(ADHD)的标准,而16%(4例)符合无多动的注意力缺陷障碍的标准。与先前关于精神分裂症高患病率的报告不同,没有患者被诊断为精神分裂症,只有4例在疾病的某个阶段出现精神病性症状,均在20多岁或30多岁。

结论

鉴于一般人群中双相情感障碍的患病率估计为1.5%,平均发病年龄为24岁,这些发现支持腭心面综合征与早发性双相情感障碍之间存在异常强烈的关联,并表明在22q11染色体位点缺失的基因可能参与其发病机制。如果得到证实,这些发现可能为双相情感障碍谱系障碍的分子基础提供一条新的、富有成果的研究途径。

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