Kendler K S, McGuire M, Gruenberg A M, O'Hare A, Spellman M, Walsh D
Department of Psychiatry, Medical College of Virginia, Virginia Commonwealth University, Richmond.
Arch Gen Psychiatry. 1993 Jul;50(7):527-40. doi: 10.1001/archpsyc.1993.01820190029004.
We sought to examine, in a rural county in the West of Ireland, the degree of familial relationship between schizophrenia and other nonaffective psychoses and affective illness (AI).
A case-controlled epidemiologic family study using DSM-III-R criteria.
This study included three proband groups: (1) all cases with a clinical diagnosis of schizophrenia from the Roscommon County Case Register born from 1930 onward (n = 285); (2) a random sample of cases from the register with a clinical diagnosis of severe AI (n = 99); and (3) a matched, random sample of Roscommon residents ascertained from the electoral register (n = 150). Face-to-face structured interviews were conducted with 86% of traceable, living relatives (n = 1, 753) and 88% of traceable, living probands (n = 415).
In interviewed relatives, the lifetime risks (+/- SE) for schizophrenia, as a function of the "blind" proband diagnosis, were as follows: schizophrenia, 6.5% +/- 1.6%; schizoaffective disorder, 6.8% +/- 2.5%; schizotypal personality disorder, 6.9% +/- 3.9%; other nonaffective psychoses, 5.1% +/- 2.4%; psychotic AI, 2.8% +/- 1.2%; nonpsychotic AI, 0.6% +/- 0.6%; and control, 0.5% +/- 0.3%. Individuals with schizophrenia reproduced at a rate about one quarter that of controls and the risk for schizophrenia in parents of probands was much less than that found in siblings.
These results support the following hypotheses: (1) in the West of Ireland, as in other populations, schizophrenia is a strongly familial disorder; (2) schizophrenia shares a familial predisposition with a spectrum of clinical syndromes that includes schizoaffective disorder, other nonaffective psychoses, schizotypal personality disorder, and probably psychotic AI, but not nonpsychotic AI; and (3) the diminished reproductive rates associated with schizophrenia have a large impact on the pattern of risk of illness in relatives.
我们试图在爱尔兰西部的一个乡村县,研究精神分裂症与其他非情感性精神病和情感性疾病(AI)之间的家族关系程度。
一项采用《精神疾病诊断与统计手册》第三版修订版(DSM-III-R)标准的病例对照流行病学家族研究。
本研究包括三个先证者组:(1)罗斯康芒县病例登记册中自1930年起临床诊断为精神分裂症的所有病例(n = 285);(2)登记册中临床诊断为重度AI的病例的随机样本(n = 99);(3)从选民登记册中确定的罗斯康芒居民的匹配随机样本(n = 150)。对86%可追踪的在世亲属(n = 1753)和88%可追踪的在世先证者(n = 415)进行了面对面的结构化访谈。
在接受访谈的亲属中,根据“盲法”先证者诊断,精神分裂症的终生风险(±标准误)如下:精神分裂症,6.5%±1.6%;分裂情感性障碍,6.8%±2.5%;分裂型人格障碍,6.9%±3.9%;其他非情感性精神病,5.1%±2.4%;伴有精神病性症状的情感性疾病,2.8%±1.2%;不伴有精神病性症状的情感性疾病,0.6%±0.6%;以及对照组,0.5%±0.3%。精神分裂症患者的生育率约为对照组的四分之一,先证者父母患精神分裂症的风险远低于其兄弟姐妹。
这些结果支持以下假设:(1)在爱尔兰西部,与其他人群一样,精神分裂症是一种家族性很强的疾病;(2)精神分裂症与一系列临床综合征具有家族易感性,这些综合征包括分裂情感性障碍、其他非情感性精神病、分裂型人格障碍,可能还包括伴有精神病性症状的情感性疾病,但不包括不伴有精神病性症状的情感性疾病;(3)与精神分裂症相关的生育率下降对亲属的患病风险模式有很大影响。