Biological risk factors for late life depression

被引:2
作者
Henning Tiemeier
机构
[1] Dept. of Epidemiology/Biostatistics, Erasmus Medical Centre, Rotterdam
[2] Dept. of Epidemiology/Biostatist., Erasmus Medical Centre, 3000 DR Rotterdam
关键词
Depression; Elderly; Hormones; Inflammation; Nutrition; Vascular pathology;
D O I
10.1023/A:1025388203548
中图分类号
学科分类号
摘要
Depression in late life is a recognised public health problem. After establishing socio-demographic and psychological risk factors for depression, epidemiological research has focused on biological factors. This review summarises the evidence on the associations of cerebrovascular pathology, inflammation, and endocrine and nutritional status with depression in the elderly. The most consistent finding in biological psychiatry is the disturbance of the hypothalamic-pituary-adrenal axis in depressed persons. About half of the patients with severe depression have a disturbed glucocorticoid feedback mechanism and many exhibit hypercortisolism. Longitudinal studies show that this endocrine dysfunction increases the risk of relapse. More recently, silent brain infarcts and cerebral white matter lesions on MRI were found to be more frequent in the depressed elderly than in controls. Cerebral small vessel disease has been rediscovered as a potential cause of depression. Furthermore, there is evidence of immune activation in depressed persons. However, it remains unclear as to whether inflammation contributes to the pathological process as longitudinal studies are lacking. Clinical studies have also related many nutrients to psychological symptoms, but the evidence in elderly persons is consistent only for some vitamin deficiencies. In conclusion, despite a substantial body of literature on biological correlates of late life depression, little is known about causal relations. Prospective population-based studies are warranted.
引用
收藏
页码:745 / 750
页数:5
相关论文
共 90 条
  • [21] Olff M., Stress, depression, and immunity: The role of defense and coping styles, Psychiatry Res, 85, pp. 7-15, (1999)
  • [22] Zorrilla E.P., Luborsky L., McKay J.R., Et al., The relationship of depression and stressors to immunological assays: A meta-analytic review, Brain Behav Immun, 15, pp. 199-226, (2001)
  • [23] Ormel J., Neeleman J., Towards a dynamic stress-vulnerability model of depression. The role of neuroticism, life events, and gender, Where Inner and Outer World Meet, pp. 151-169, (2000)
  • [24] Stahl S.M., Peripheral models for the study of neuro-transmitter receptors in man, Psychopharmacol Bull, 21, pp. 663-671, (1985)
  • [25] Elliott J.M., Peripheral markers in anxiety and depression, Mol Aspects Med, 13, pp. 173-190, (1992)
  • [26] Alexopoulos G.S., Meyers B.S., Young R.C., Et al., Vascular depression' hypothesis, Arch Gen Psychiatry, 54, pp. 915-922, (1997)
  • [27] Gaupp R.E., Die depressionszustände des höheren lebensalters, Med Wschr, 52, pp. 1531-1537, (1905)
  • [28] Krishnan K.R., McDonald W.M., Arteriosclerotic depression, Med Hypotheses, 44, pp. 111-115, (1995)
  • [29] Krishnan K.R., Hays J.C., Blazer D.G., MRI-defined vascular depression, Am J Psychiatry, 154, pp. 497-501, (1997)
  • [30] Andersen G., Vestergaard K., Riis J., Et al., Incidence of post-stroke depression during the first year in a large unselected stroke population determined using a valid standardized rating scale, Acta Psychiatr Scand, 90, pp. 190-195, (1994)