Association of Oxidative Stress, Iron, and Centralized Fat Mass in Healthy Postmenopausal Women

被引:36
作者
Crist, Betsy L. [1 ]
Alekel, D. Lee [1 ,2 ]
Ritland, Laura M. [1 ]
Hanson, Laura N. [1 ]
Genschel, Ulrike [3 ]
Reddy, Manju B. [1 ]
机构
[1] Iowa State Univ, Dept Food Sci & Human Nutr, Ames, IA 50011 USA
[2] Iowa State Univ, Nutr & Wellness Res Ctr, Ames, IA 50011 USA
[3] Iowa State Univ, Dept Stat, Ames, IA 50011 USA
基金
美国国家卫生研究院;
关键词
CARDIOVASCULAR-DISEASE RISK; INSULIN-RESISTANCE SYNDROME; CORONARY-HEART-DISEASE; SERUM FERRITIN; MYOCARDIAL-INFARCTION; METABOLIC SYNDROME; OXIDANT STRESS; MEN; OBESITY; INFLAMMATION;
D O I
10.1089/jwh.2008.0988
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Objective: Centralized adiposity, insulin resistance, excess iron, and elevated oxidative stress place postmenopausal women at risk for atherosclerotic cardiovascular disease (CVD). The objective of this study was to determine the relationship among excess iron, oxidative stress, and centralized fat mass in healthy postmenopausal women. Methods: The parent project recruited healthy women for a randomized, double-blind, clinical trial designed to examine the effect of soy isoflavones on bone. At baseline (n=122), we measured three antioxidant enzymes, iron status indices (serum ferritin among others), oxidative stress indices (oxidized low-density lipoprotein [oxLDL], urinary isoprostanes [PGF(2 alpha)], protein carbonyls, DNA damage), and waist, hip, and thigh fat mass using dual-energy x-ray absorptiometry (DXA). We calculated insulin resistance using the homeostasis model assessment (HOMA). Multiple regression analysis was used to determine the CVD risk factors that contributed to oxidative stress and centralized fat mass (waist+hip=thigh AndGynFM ratio). Results: Almost 14% (p<0.0005) of the variability in oxLDL was accounted for by AndGynFM ratio (6.1%, p<0.0005), age (4.0%, p=0.012), and serum iron (2.8%, p=0.053). Similarly, 16% (p<0.0001) of the variability in PGF2a was accounted for by the AndGynFM ratio (4.8%, p=0.011), HOMA (3.9%, p=0.021), and serum iron (2.7%, p=0.054). We accounted for 33% (p <= 0.0001) of the variability in AndGynFM ratio by high-density lipoprotein cholesterol (HDL-C) (4.3%, p=0.008), ferritin (4.9%, p=0.005), HOMA (4.5%, p=0.006), oxLDL (2.6%, p=0.04), and PGF(2 alpha) (3.0%, p=0.025). Conclusions: Our study suggests that reducing centralized fat mass and maintaining a favorable lipid profile, antioxidant status, and iron status all may be important in protecting postmenopausal women from atherosclerotic CVD.
引用
收藏
页码:795 / 801
页数:7
相关论文
共 40 条
[1]   SERUM FERRITIN, SEX-HORMONES, AND CARDIOVASCULAR RISK-FACTORS IN HEALTHY WOMEN [J].
BERGE, LN ;
BONAA, KH ;
NORDOY, A .
ARTERIOSCLEROSIS AND THROMBOSIS, 1994, 14 (06) :857-861
[2]   Iron supplementation does not affect the susceptibility of LDL to oxidative modification in women with low iron status [J].
Binkoski, AE ;
Kris-Etherton, PM ;
Beard, JL .
JOURNAL OF NUTRITION, 2004, 134 (01) :99-103
[3]   Serum lipid concentration in relation to anthropometric indices of central and peripheral fat distribution in 20,021 British men and women: Results from the EPIC-Norfolk population-based cohort study [J].
Canoy, Dexter ;
Wareham, Nicholas ;
Luben, Robert ;
Welch, Ailsa ;
Bingham, Sheila ;
Day, Nicholas ;
Khaw, Kay-Tee .
ATHEROSCLEROSIS, 2006, 189 (02) :420-427
[4]   Iron status and risk of cardiovascular disease [J].
Corti, MC ;
Gaziano, M ;
Hennekens, CH .
ANNALS OF EPIDEMIOLOGY, 1997, 7 (01) :62-68
[5]   Vascular biology of the isoprostanes [J].
Cracowski, JL ;
Devillier, P ;
Durand, T ;
Stanke-Labesque, F ;
Bessard, G .
JOURNAL OF VASCULAR RESEARCH, 2001, 38 (02) :93-103
[6]   Coronary heart disease and iron status - Meta-analyses of prospective studies [J].
Danesh, J ;
Appleby, P .
CIRCULATION, 1999, 99 (07) :852-854
[7]   Platelet activation in obese women -: Role of inflammation and oxidant stress [J].
Davì, G ;
Guagnano, MT ;
Ciabattoni, G ;
Basili, S ;
Falco, A ;
Marinopiccoli, M ;
Nutini, M ;
Sensi, S ;
Patrono, C .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 288 (16) :2008-2014
[8]   Iron status in association with cardiovascular disease risk in 3 controlled feeding studies [J].
Derstine, JL ;
Murray-Kolb, LE ;
Yu-Poth, S ;
Hargrove, RL ;
Kris-Etherton, PM ;
Beard, JL .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2003, 77 (01) :56-62
[9]   Iron measures in coronary angiography patients [J].
Eichner, JE ;
Qi, H ;
Moore, WE ;
Schechter, E .
ATHEROSCLEROSIS, 1998, 136 (02) :241-245
[10]   Serum ferritin as a component of the insulin resistance syndrome [J].
Fernández-Real, JM ;
Ricart-Engel, W ;
Arroyo, E ;
Balançá, R ;
Casamitjana-Abella, R ;
Cabrero, D ;
Fernández-Castañer, M ;
Soler, J .
DIABETES CARE, 1998, 21 (01) :62-68