抑郁症的基因。单极和神经性反应性抑郁症患者的家庭研究。

C Perris, H Perris, U Ericsson, L von Knorring
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引用次数: 16

摘要

60名患有神经反应性抑郁症的单极患者(23名男性和37名女性)和67名患者(25名男性和42名女性)连续住进尤梅夫大学精神学系,参加了一项旨在确定一级亲属中精神疾病发病率风险的家庭研究(n = 437)。除了用于研究目的的情感障碍分类外,根据ICD-9, DSM-III,发病年龄(低于或高于40岁)和Winokur的原发性情感障碍分类,对患者进行了分类。然而,本文只给出了有关umedef分类和Winokur分类的研究结果。在调查时,90%的患者符合肯德尔抑郁症的标准,而其他人在研究时处于缓解阶段。继发性病例的诊断是在不了解先证者诊断的情况下做出的。在单极先证者的亲属中,仅发现了两个继发性双相情感障碍病例——一个在父母中,一个在兄弟姐妹中(MR%分别为1.1和0.6)。情感性障碍的总体发病风险(父母中MR% 22.8,兄弟姐妹中MR% 15.5)比以前的研究高。在神经反应性患者的家庭中,双相情感障碍的发病率风险也非常低(父母的MR%为1.0,兄弟姐妹的MR%为0.7),而情感障碍的总体MR%却惊人地高(父母的MR%为12.1,兄弟姐妹的MR%为6.7)。在两组的亲属中都没有发现精神分裂症或酒精中毒的风险增加。当亲属按性别划分时,父亲和兄弟与母亲和姐妹在发病风险上没有明显的差异,但酗酒在男性亲属中更常见。在二级亲属中的初步发现表明,根据Winokur的分类,被归类为“散发性抑郁症”的患者的二级亲属中可能发生继发性情感障碍病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The genetics of depression. A family study of unipolar and neurotic-reactive depressed patients.

Sixty unipolar (23 male and 37 female) patients and 67 patients (25 male and 42 female) suffering from a neurotic-reactive depressive disorder, consecutively admitted to the Department of Psychiatry of Umeå University have participated in a family study aimed at identifying morbidity risks for psychiatric illnesses among first degree relatives (n = 437). Besides the classification of affective disorders used in Umeå for research purposes the patients have been classified, according to the ICD-9, DSM-III, age at onset (below or above 40 years), and the Winokur's classification of primary affective disorders. However, only the findings regarding the Umeå classification and the Winokur's classification are given in the present article. Of the patients 90% fulfilled Kendell's criteria for depression at the time of the investigation whereas the others were in a phase of remission when studied. The diagnosis of secondary cases were made without knowledge of the diagnoses of the probands. Among relatives of unipolar probands only two secondary cases of bipolar affective disorder were found--one among parents, and one among siblings (MR% 1.1 and 0.6 respectively). The overall morbidity risk for affective disorders (MR% 22.8 among parents and 15.5 among siblings) proved to be higher than in previous studies. In the families of neurotic-reactive patients the morbidity risk for bipolar affective disorders was also very low (MR% 1.0 among parents and 0.7 among siblings), whereas the overall MR% for affective disorders proved to be surprisingly high (12.1 among parents and 6.7 among siblings). No increased risk for schizophrenia or alcoholism was found among the relatives of either group. When the relatives were divided according to their sex no clear-cut difference in morbidity risk emerged when fathers and brothers were compared with mothers and sisters but alcoholisms occurred more frequently in male relatives. Preliminary findings in second degree relatives suggest that secondary cases of affective disorders might occur among second degree relatives of patients classified as suffering from "sporadic depression" according to Winokur's classification.

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