Tényi Tamás, Trixler Mátyás, Csábi Györgyi, Jeges Sára
Department of Psychiatry and Medical Psychology, University of Pécs, Faculty of Medicine, Rét u. 2, 7623 Pécs, Hungary.
J Affect Disord. 2004 Apr;79(1-3):259-62. doi: 10.1016/S0165-0327(02)00360-9.
The prevalence of minor physical anomalies (MPAs) was evaluated in patients with unipolar recurrent major depression to get indirect data on the possible role of aberrant neurodevelopment in the aetiology of major depression. One published study [Lohr et al., Am. J. Geriatr. Psychiatry 5 (1997) 318] on the MPA prevalence in unipolar depression, evaluated by the recently widely criticized Waldrop-scale, reports on a significantly higher MPA rate among patients.
A scale developed by Méhes [Prog. Clin. Biol. Res. 163 (1985) 45] was used to detect the presence or absence of 57 MPAs in 30 patients with major depression and in 30 matched controls.
The depressive sample did not differ significantly from the control group (P=0.200). By comparing each MPA individually we could not find any significant differences between the depressive and the control sample.
Patients and control subjects had a negative family history in connection with affective disorders; a high-risk population should give significant positive results.
The results do not support the role of an 'early neurodevelopmental origin' in unipolar depression.
对单相复发性重度抑郁症患者的轻微身体异常(MPA)患病率进行评估,以获取关于异常神经发育在重度抑郁症病因中可能作用的间接数据。一项已发表的关于单相抑郁症中MPA患病率的研究[洛尔等人,《美国老年精神病学杂志》5(1997)318],采用最近受到广泛批评的沃尔德罗普量表进行评估,报告称患者中的MPA发生率显著更高。
使用由梅赫斯开发的量表[《临床生物学研究进展》163(1985)45],检测30例重度抑郁症患者和30例匹配对照中57种MPA的存在与否。
抑郁症样本与对照组无显著差异(P = 0.200)。通过单独比较每种MPA,我们在抑郁症样本和对照样本之间未发现任何显著差异。
患者和对照受试者在情感障碍方面有阴性家族史;高危人群应得出显著的阳性结果。
结果不支持“早期神经发育起源”在单相抑郁症中的作用。