Dietary iron intake, body iron stores, and the risk of type 2 diabetes: a systematic review and meta-analysis

被引:199
作者
Bao, Wei [1 ,2 ]
Rong, Ying [1 ,2 ]
Rong, Shuang [1 ,2 ]
Liu, Liegang [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Sch Publ Hlth, Dept Nutr & Food Hyg,Hubei Key Lab Food Nutr & Sa, Wuhan 430030, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Med Coll, Sch Publ Hlth, Minist Educ,Key Lab Environm & Hlth, Wuhan 430030, Peoples R China
来源
BMC MEDICINE | 2012年 / 10卷
基金
中国国家自然科学基金;
关键词
GENE PROMOTER POLYMORPHISMS; BETA-CELL FUNCTION; SERUM FERRITIN; INSULIN-RESISTANCE; METABOLIC SYNDROME; OXIDATIVE STRESS; TREND ESTIMATION; ASSOCIATION; GLUCOSE; MEN;
D O I
10.1186/1741-7015-10-119
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Excess iron has been shown to induce diabetes in animal models. However, the results from human epidemiologic studies linking body iron stores and iron intake to the risk of type 2 diabetes mellitus (T2DM) are conflicting. In this study, we aimed to systematically evaluate the available evidence for associations between iron intake, body iron stores, and the risk of T2DM. Methods: A systematic search of the PubMed/MEDLINE and EMBASE databases to the end of 22 April 2012 was performed, and reference lists of retrieved articles were screened. Two reviewers independently evaluated the eligibility of inclusion and extracted the data. Pooled relative risks (RRs) and 95% confidence intervals (CIs) were calculated using random-effects models. Results: We reviewed 449 potentially relevant articles, and 11 prospective studies were included in the analysis. A meta-analysis of five studies gave a pooled RR for T2DM of 1.33 (95% CI 1.19 to 1.48; P<0.001) in individuals with the highest level of heme iron intake, compared with those with the lowest level. The pooled RR for T2DM for a daily increment of 1 mg of heme iron intake was 1.16 (1.09 to 1.23, P<0.001). Body iron stores, as measured by ferritin, soluble transferrin receptor (sTfR) and the sTfR: ferritin ratio, were significantly associated with the risk of T2DM. The pooled RRs for T2DM in individuals with the highest versus the lowest intake of ferritin levels was 1.70 (1.27-2.27, P<0.001) before adjustment for inflammatory markers and 1.63 (1.03-2.56, P = 0.036) after adjustment. We did not find any significant association of dietary intakes of total iron, non-heme, or supplemental iron intake with T2DM risk. Conclusion: Higher heme iron intake and increased body iron stores were significantly associated with a greater risk of T2DM. Dietary total iron, non-heme iron, or supplemental iron intakes were not significantly associated with T2DM risk.
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页数:13
相关论文
共 53 条
[1]   Relationships of serum ferritin, transferrin saturation, and HFE mutations and self-reported diabetes in the hemochromatosis and iron overload screening (HEIRS) study [J].
Acton, Ronald T. ;
Reboussin, David M. ;
Barton, James C. ;
McLaren, Gordon D. ;
Passmore, Leah V. ;
Harris, Emily L. ;
Adams, Paul C. ;
Bent, Thomas C. ;
Speechley, Mark R. ;
Vogt, Thomas M. ;
Castro, Oswaldo ;
Sholinsky, Phyliss .
DIABETES CARE, 2006, 29 (09) :2084-2089
[2]   Medical progress: Disorders of iron metabolism [J].
Andrews, NC .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (26) :1986-1995
[3]   DIETARY IRON INTAKE AND RISK OF CORONARY-DISEASE AMONG MEN [J].
ASCHERIO, A ;
WILLETT, WC ;
RIMM, EB ;
GIOVANNUCCI, EL ;
STAMPFER, MJ .
CIRCULATION, 1994, 89 (03) :969-974
[4]   Meat consumption and the risk of type 2 diabetes: a systematic review and meta-analysis of cohort studies [J].
Aune, D. ;
Ursin, G. ;
Veierod, M. B. .
DIABETOLOGIA, 2009, 52 (11) :2277-2287
[5]  
AWAI M, 1979, AM J PATHOL, V95, P663
[6]   Association Between Heme Oxygenase-1 Gene Promoter Polymorphisms and Type 2 Diabetes Mellitus: A HuGE Review and Meta-Analysis [J].
Bao, Wei ;
Song, Fangfang ;
Li, Xiangyang ;
Rong, Shuang ;
Yang, Wei ;
Wang, Di ;
Xu, Jiqu ;
Fu, Juan ;
Zhao, Yanting ;
Liu, Liegang .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2010, 172 (06) :631-636
[7]   Diabetes in Asia Epidemiology, Risk Factors, and Pathophysiology [J].
Chan, Juliana C. N. ;
Malik, Vasanti ;
Jia, Weiping ;
Kadowaki, Takashi ;
Yajnik, Chittaranjan S. ;
Yoon, Kun-Ho ;
Hu, Frank B. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2009, 301 (20) :2129-2140
[8]   The worldwide epidemiology of type 2 diabetes mellitus-present and future perspectives [J].
Chen, Lei ;
Magliano, Dianna J. ;
Zimmet, Paul Z. .
NATURE REVIEWS ENDOCRINOLOGY, 2012, 8 (04) :228-236
[9]   Oxidative stress, β-cell apoptosis, and decreased insulin secretory capacity in mouse models of hemochromatosis [J].
Cooksey, RC ;
Jouihan, HA ;
Ajioka, RS ;
Hazel, MW ;
Jones, DL ;
Kushner, JP ;
McClain, DA .
ENDOCRINOLOGY, 2004, 145 (11) :5305-5312
[10]   Dietary iron restriction or iron chelation protects from diabetes and loss of β-cell function in the obese (ob/ob lep-/-) mouse [J].
Cooksey, Robert C. ;
Jones, Deborah ;
Gabrielsen, Scott ;
Huang, Jingyu ;
Simcox, Judith A. ;
Luo, Bai ;
Soesanto, Yudi ;
Rienhoff, Hugh ;
Abel, E. Dale ;
McClain, Donald A. .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2010, 298 (06) :E1236-E1243