Association of major depressive disorder with serum myeloperoxidase and other markers of inflammation: A twin study

被引:117
作者
Vaccarino, Viola [1 ,2 ]
Brennan, Marie-Luise [5 ,6 ]
Miller, Andrew H. [3 ]
Bremner, J. Douglas [3 ]
Ritchie, James C. [3 ,4 ]
Linclau, Frauke [1 ,3 ]
Veleclar, Emir [1 ]
Su, Shaoyong [1 ]
Murrah, Nancy V. [1 ]
Jones, Linda [1 ]
Jawed, Farhan
Dai, Jun [1 ]
Goldberg, Jack [8 ]
Hazen, Stanley L. [5 ,6 ,7 ,9 ]
机构
[1] Emory Univ, Sch Med, Dept Med, Div Cardiol, Atlanta, GA 30306 USA
[2] Emory Univ, Rollins Sch Publ Hlth, Dept Epidemiol, Atlanta, GA 30306 USA
[3] Emory Univ, Sch Med, Dept Psychiat & Behav Sci, Atlanta, GA 30306 USA
[4] Emory Univ, Sch Med, Emory Univ Hosp, Dept Pathol & Lab Med, Atlanta, GA 30306 USA
[5] Cleveland Clin Fdn, Ctr Cardiovasc Diagnost & Prevent, Cleveland, OH 44195 USA
[6] Cleveland Clin Fdn, Dept Cell Biol, Cleveland, OH 44195 USA
[7] Cleveland Clin Fdn, Dept Cardiovasc Med, Cleveland, OH 44195 USA
[8] Univ Washington, Sch Publ Hlth & Community Med, Seattle, WA 98195 USA
[9] Vietnam Era Twin Registry, Seattle, WA USA
基金
美国国家卫生研究院;
关键词
biomarkers; cardiovascular disease; depression; genetic factors; inflammation; twins;
D O I
10.1016/j.biopsych.2008.04.023
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Major depressive disorder (MDD) has been linked to inflammation, but this association maybe due to common precursors to both depression and inflammation. Myeloperoxidase (MPO) is an inflammatory enzyme produced by activated leukocytes that predicts risk of coronary heart disease. We sought to examine whether MPO and other markers of inflammation are associated with MDD and whether the association is confounded by genetic or other shared familial factors. Methods: We examined 178 monozygotic and dizygotic middle-aged male twin pairs. We assessed MDD with the Structured Clinical Interview for DSM-IV. Blood markers of inflammation included MPO, interleukin-6, white blood cell count, C-reactive protein, tumor necrosis factor (TNF)-alpha, the TNF-alpha soluble receptor II, and fibrinogen. Analyses were conducted in the overall sample and among 67 twin pairs discordant for MDD using mixed effects regression. Results: Twins with a history of MDD had 32% higher levels of MPO (p <.0001); this difference persisted after adjusting for other risk factors. Among dizygotic MDD-discordant twin pairs, twins with MDD had 77% higher MPO than their brothers without MDD, after adjusting for other factors (p <.0001). In contrast, no significant association was found in monozygotic twins (p =.13). Similar, but weaker, associations were found between MDD and other inflammatory biomarkers. Conclusions: Myeloperoxidase is a useful biomarker of immune activation in MDD. However, the association between inflammation and MDD is largely due to common genetic liability. Our results are consistent with the hypothesis that genes promoting inflammation are involved in the pathogenesis of MDD.
引用
收藏
页码:476 / 483
页数:8
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