Depression and oxidative damage to lipids

被引:105
作者
Yager, Sarah [1 ]
Forlenza, Michael J. [2 ]
Miller, Gregory E. [1 ]
机构
[1] Univ British Columbia, Dept Psychol, Vancouver, BC V6T 1Z4, Canada
[2] Duquesne Univ, Sch Leadership & Profess Advancement, Pittsburgh, PA 15282 USA
关键词
Depression; Oxidative damage; Lipid damage; Atherosclerosis; 8-Isoprostaglandin-F-2; alpha; Comorbidity; CORONARY-HEART-DISEASE; C-REACTIVE PROTEIN; 8-ISO-PROSTAGLANDIN F2-ALPHA; CARDIOVASCULAR-DISEASE; PSYCHOSOCIAL FACTORS; MAJOR DEPRESSION; DNA-DAMAGE; RISK; MARKERS; STRESS;
D O I
10.1016/j.psyneuen.2010.03.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Depression is associated with increased morbidity and mortality from cardiovascular and cerebrovascular diseases. Oxidative damage to lipids is one of the key early events in the etiology of atherosclerosis, the pathologic condition that underlies these diseases. The current study examines the pathophysiological consequences of depression by comparing serum levels of F-2 alpha-isoprostanes (8-iso-PGF(2 alpha)), a biomarker of oxidative damage to lipids, in a group of depressed individuals (n = 73) and a matched comparison group (n = 72). The depressed group had significantly higher levels of serum 8-iso-PGF(2 alpha), while controlling for age, gender, race, years of education, daily smoking, number of alcoholic drinks per week, average amount of physical activity per week, and body mass index. Analyses using interviewer ratings on the Hamilton Scale revealed that, within the depressed cohort, there was no significant association between the severity of symptoms and levels of 8-iso-PGF(2 alpha), suggesting this is a threshold rather than a dose response relationship. Results extend on our knowledge of depression and oxidative damage to lipids. In conclusion, oxidative damage to lipid molecules may represent a common pathophysiological mechanism by which depressed individuals become more vulnerable to atherosclerosis and its clinical sequelae. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1356 / 1362
页数:7
相关论文
共 38 条
[1]   Phagocytes and oxidative stress [J].
Babior, BM .
AMERICAN JOURNAL OF MEDICINE, 2000, 109 (01) :33-44
[2]   Depression as a risk factor for mortality in patients with coronary heart disease: A meta-analysis [J].
Barth, J ;
Schumacher, M ;
Herrmann-Lingen, C .
PSYCHOSOMATIC MEDICINE, 2004, 66 (06) :802-813
[3]  
BHATTACHARYYA G, 1998, PATHOPHYSIOLOGY HEAR, P101
[4]   Antioxidative enzyme activities and lipid peroxidation in major depression:: alterations by antidepressant treatments [J].
Bilici, M ;
Efe, H ;
Köroglu, MA ;
Uydu, HA ;
Bekaroglu, M ;
Deger, O .
JOURNAL OF AFFECTIVE DISORDERS, 2001, 64 (01) :43-51
[5]   Depression as a risk factor for cardiac mortality and morbidity - A review of potential mechanisms [J].
Carney, RM ;
Freedland, KE ;
Miller, GE ;
Jaffe, AS .
JOURNAL OF PSYCHOSOMATIC RESEARCH, 2002, 53 (04) :897-902
[6]   Determinants of F2-isoprostane biosynthesis and inhibition in man [J].
Davì, G ;
Falco, A ;
Patrono, C .
CHEMISTRY AND PHYSICS OF LIPIDS, 2004, 128 (1-2) :149-163
[7]   Increased plasma levels of 8-iso-PGF2α and IL-6 in an elderly population with depression [J].
Dimopoulos, Nikolaos ;
Piperi, Christina ;
Psarra, Vassiliki ;
Lea, Robert W. ;
Kalofoutis, Anastasios .
PSYCHIATRY RESEARCH, 2008, 161 (01) :59-66
[8]   Plasma 8-iso-prostaglandin F2α , a marker of oxidative stress, is increased in patients with acute myocardial infarction [J].
Elesber, AA ;
Best, PJ ;
Lennon, RJ ;
Mathew, V ;
Rihal, CS ;
Lerman, LO ;
Lerman, A .
FREE RADICAL RESEARCH, 2006, 40 (04) :385-391
[9]   Increased serum levels of 8-hydroxy-2′-deoxyguanosine in clinical depression [J].
Forlenza, MJ ;
Miller, GE .
PSYCHOSOMATIC MEDICINE, 2006, 68 (01) :1-7
[10]   The Depression Interview and Structured Hamilton (DISH): Rationale, development, characteristics, and clinical validity [J].
Freedland, KE ;
Skala, JA ;
Carney, RM ;
Raczynski, JM ;
Taylor, CB ;
de Leon, CFM ;
Ironson, G ;
Youngblood, ME ;
Krishnan, KRR ;
Veith, RC .
PSYCHOSOMATIC MEDICINE, 2002, 64 (06) :897-905