Foley Debra L, Morley Katherine I, Madden Pamela A F, Heath Andrew C, Whitfield John B, Martin Nicholas G
Biostatistics Unit, Orygen Youth Health Research Centre & Centre for Youth Mental Health, The University of Melbourne, Australia.
Twin Res Hum Genet. 2010 Aug;13(4):347-58. doi: 10.1375/twin.13.4.347.
The aim of this study is to characterize the relationship between major depression and the metabolic syndrome in a large community based sample of Australian men and women aged 26-90 years. A lifetime history of major depression was assessed by telephone interview following the DSM-III-R. A current history of metabolic syndrome was assessed following the United States National Cholesterol Education Program Adult Treatment Panel III (NCEP AP-III) guidelines 1 to 3 years later. Logistic regression was used to estimate the association between depression and the metabolic syndrome, and its component criteria, controlling for age, sex and alcohol dependence. There was no association between a lifetime history of major depression and the presence of the metabolic syndrome. There was a weak association between depression and low high-density lipoprotein cholesterol but not with other component criteria of the metabolic syndrome. Despite calls for interventions directed at depression to reduce the onset of the metabolic syndrome there are important failures to replicate in large samples such as this, no consensus regarding the threshold at which depression may pose a significant risk even allowing for heterogeneity across populations, and no consensus regarding confounders that may explain inter-study differences. The absence of any dosage effect of depression on the associated risk for the metabolic syndrome in other unselected samples does not support a direct causal relationship. The call for intervention studies on the basis of the currently published evidence base is unwarranted.
本研究旨在描述澳大利亚26至90岁社区男女大样本中重度抑郁症与代谢综合征之间的关系。根据《精神疾病诊断与统计手册》第三版修订本(DSM-III-R),通过电话访谈评估重度抑郁症的终生病史。1至3年后,按照美国国家胆固醇教育计划成人治疗小组第三次报告(NCEP AP-III)指南评估代谢综合征的当前病史。采用逻辑回归估计抑郁症与代谢综合征及其组成标准之间的关联,并对年龄、性别和酒精依赖进行控制。重度抑郁症的终生病史与代谢综合征的存在之间没有关联。抑郁症与低高密度脂蛋白胆固醇之间存在微弱关联,但与代谢综合征的其他组成标准无关。尽管有人呼吁针对抑郁症进行干预以减少代谢综合征的发生,但在这样的大样本中仍存在重要的无法重复的情况,对于抑郁症在何种阈值下可能构成重大风险(即使考虑到人群间的异质性)没有共识,对于可能解释研究间差异的混杂因素也没有共识。在其他未选择的样本中,抑郁症对代谢综合征相关风险没有任何剂量效应,这不支持直接的因果关系。基于目前已发表的证据基础呼吁进行干预研究是没有道理的。