Iron Status Is Associated with Carotid Atherosclerotic Plaques in Middle-Aged Adults

被引:52
作者
Ahluwalia, Namanjeet [1 ]
Genoux, Annelise [4 ]
Ferrieres, Jean [2 ,3 ]
Perret, Bertrand [4 ]
Carayol, Marion [1 ]
Drouet, Ludovic [5 ]
Ruidavets, Jean-Bernard [1 ]
机构
[1] CHU Toulouse, Fac Med, Dept Epidemiol, INSERM,U558, F-31073 Toulouse, France
[2] CHU Toulouse, Fac Med, Dept Cardiol, F-31073 Toulouse, France
[3] CHU Toulouse, Fac Med, Dept Epidemiol, F-31073 Toulouse, France
[4] CHU Toulouse, INSERM, U563, Dept Lipoprot & Lipid Mediators, F-31059 Toulouse, France
[5] CHU Lariboisiere Paris, Fac Med Paris 7, Serv Angiohematol Biol Thrombol & Hemostase, F-75475 Paris 10, France
关键词
CORONARY-HEART-DISEASE; LOW-DENSITY-LIPOPROTEIN; POPULATION-BASED SAMPLE; EASTERN FINNISH MEN; BODY IRON; SERUM FERRITIN; CARDIOVASCULAR-DISEASE; MYOCARDIAL-INFARCTION; RISK; STORES;
D O I
10.3945/jn.109.110353
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Although the iron-heart disease hypothesis is prevalent, the epidemiological findings are incongruent. The relationship of serum ferritin with early cardiovascular disease (CVD), particularly atherosclerosis, has not been evaluated extensively, particularly with accounting for inflammation. We examined this association in a case-control study of 124 age- and sex-matched pairs embedded in the population-based random sample (MONICA survey) in Southwest France, taking into account inflammation status. Cases had >= 2 carotid atherosclerotic plaques and controls had none. Inflammation was assessed using several markers, including serum alpha-1 acid glycoprotein (AGP) and high sensitivity C-reactive protein. There was an interaction of inflammation with group (case/control) for serum ferritin. In adults without elevated AGP, serum ferritin was significantly greater in atherosclerotic cases than in adults in the control group. In models adjusted for CVD risk factors, the odds of atherosclerosis increased with the increase in serum ferritin in individuals without elevated AGP; for every 10-mu g/L increase in serum ferritin, the risk for atherosclerosis increased by 3% (odds ratio [95% CI]: 1.03 [1.01-1.06]). In conclusion, carotid atherosclerosis was positively associated with serum ferritin in individuals free from subclinical inflammation based on AGP. Further prospective and/or experimental studies are needed to corroborate the observed association of iron status with atherosclerosis. J. Nutr. 140: 812-816, 2010.
引用
收藏
页码:812 / 816
页数:5
相关论文
共 38 条
[1]   IRON-DEFICIENCY AND ANEMIA OF CHRONIC DISEASE IN ELDERLY WOMEN - A DISCRIMINANT-ANALYSIS APPROACH FOR DIFFERENTIATION [J].
AHLUWALIA, N ;
LAMMIKEEFE, CJ ;
BENDEL, RB ;
MORSE, EE ;
BEARD, JL ;
HALEY, NR .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1995, 61 (03) :590-596
[2]   Metabolic syndrome is associated with markers of subclinical atherosclerosis in a French population-based sample [J].
Ahluwalia, N. ;
Drouet, L. ;
Ruidavets, J. -B. ;
Perret, B. ;
Amar, J. ;
Boccalon, H. ;
Hanaire-Broutin, H. ;
Ferrieres, J. .
ATHEROSCLEROSIS, 2006, 186 (02) :345-353
[3]  
ALI MAM, 1978, CAN MED ASSOC J, V118, P945
[4]  
Auer J, 2002, NUTR METAB CARDIOVAS, V12, P285
[5]   Soluble intercellular adhesion molecule-1 is associated with carotid and femoral atherosclerosis but not with intima-media thickness in a population-based sample [J].
Bongard, V ;
Elias, A ;
Sollier, CBD ;
Ruidavets, JB ;
Boccalon, H ;
Drouet, L ;
Ferrières, J .
ATHEROSCLEROSIS, 2002, 164 (02) :297-304
[6]   The influence of high-altitude living on body iron [J].
Cook, JD ;
Boy, E ;
Flowers, C ;
Daroca, MD .
BLOOD, 2005, 106 (04) :1441-1446
[7]   Coronary heart disease and iron status - Meta-analyses of prospective studies [J].
Danesh, J ;
Appleby, P .
CIRCULATION, 1999, 99 (07) :852-854
[8]   Chronic iron administration increases vascular oxidative stress and accelerates arterial thrombosis [J].
Day, SM ;
Duquaine, D ;
Mundada, LV ;
Menon, RG ;
Khan, BV ;
Rajagopalan, S ;
Fay, WP .
CIRCULATION, 2003, 107 (20) :2601-2606
[9]  
Feelders RA, 1998, EUR J CLIN INVEST, V28, P520
[10]  
FRIEDEWALD WT, 1972, CLIN CHEM, V18, P499