Intakes of heme iron and zinc and colorectal cancer incidence: a meta-analysis of prospective studies

被引:61
作者
Qiao, Lei [1 ]
Feng, Yong [1 ]
机构
[1] China Med Univ, Shengjing Hosp, Dept Colorectal Surg & Oncol, Shenyang 110004, Liaoning, Peoples R China
关键词
Heme iron; Zinc; Cohort studies; Colorectal cancer; Meta-analysis; OXIDE-MEDIATED NITROSATION; COLON-CANCER; RED MEAT; DIETARY HEME; ALCOHOL-CONSUMPTION; BEEF MEAT; RISK; COHORT; WOMEN; CARCINOGENESIS;
D O I
10.1007/s10552-013-0197-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epidemiologic findings concerning the associations between intakes of heme iron and zinc and colorectal cancer (CRC) incidence yielded conflicting results. We aimed to investigate the associations by performing a meta-analysis of prospective studies. We conducted a literature search on PubMed and EMBASE databases up to December 2012 to identify the prospective studies that investigated the relationships between heme iron or zinc intake and risk of CRC. We also reviewed the bibliographies of the retrieved articles to identify additional studies. We used a random-effects model to calculate the summary relative risks (RRs) with 95 % confidence intervals (CIs). Eight studies on heme iron intake and six studies on zinc intake met the inclusion criteria. The summary RR of CRC for the highest versus the lowest intake was 1.14 (95 % CI = 1.04-1.24) for heme iron and 0.83 (95 % CI = 0.72-0.94) for zinc, respectively. The observed associations were not significantly modified by subsites within the colorectum, sex, geographic area, study duration, the number of cases, or the range of intakes. In the dose-response analyses, the summary RR of CRC was 1.11 (95 % CI = 1.03-1.18) for heme iron intake of 1 mg/day, and 0.86 (95 % CI = 0.78-0.96) for zinc intake of 5 mg/day, respectively. There was little evidence of publication bias. This meta-analysis suggests a significant positive dose-response association of heme iron intake and a significant inverse dose-response association of zinc intake with risk of CRC.
引用
收藏
页码:1175 / 1183
页数:9
相关论文
共 34 条
[21]   Effect of zinc supplementation on serum leptin levels and insulin resistance of obese women [J].
Marreiro, Dilina do Nascimento ;
Geloneze, Bruno ;
Tambascia, Marcos A. ;
Lerario, Antonio C. ;
Halpern, Alfredo ;
Franciscato Cozzolino, Silvia Maria .
BIOLOGICAL TRACE ELEMENT RESEARCH, 2006, 112 (02) :109-118
[22]   DIETARY IRON AND COLORECTAL-CANCER RISK [J].
NELSON, RL .
FREE RADICAL BIOLOGY AND MEDICINE, 1992, 12 (02) :161-168
[23]   Beef meat and blood sausage promote the formation of azoxymethane-induced mucin-depleted foci and aberrant crypt foci in rat colons [J].
Pierre, F ;
Freeman, A ;
Taché, S ;
Van der Meer, R ;
Corpet, DE .
JOURNAL OF NUTRITION, 2004, 134 (10) :2711-2716
[24]   Meat and cancer:: haemoglobin and haemin in a low-calcium diet promote colorectal carcinogenesis at the aberrant crypt stage in rats [J].
Pierre, F ;
Taché, S ;
Petit, CR ;
Van der Meer, R ;
Corpet, DE .
CARCINOGENESIS, 2003, 24 (10) :1683-1690
[25]   Beef meat promotion of dimethylhydrazine-induced colorectal carcinogenesis biomarkers is suppressed by dietary calcium [J].
Pierre, Fabrice ;
Santarelli, Raphaelle ;
Tache, Sylviane ;
Gueraud, Francoise ;
Corpet, Denis E. .
BRITISH JOURNAL OF NUTRITION, 2008, 99 (05) :1000-1006
[26]   Red meat and colon cancer: dietary haem-induced colonic cytotoxicity and epithelial hyperproliferation are inhibited by calcium [J].
Sesink, ALA ;
Termont, DSML ;
Kleibeuker, JH ;
Van der Meer, R .
CARCINOGENESIS, 2001, 22 (10) :1653-1659
[27]  
Sesink ALA, 1999, CANCER RES, V59, P5704
[28]   Red meat and colon cancer: dietary haem, but not fat, has cytotoxic and hyperproliferative effects on rat colonic epithelium [J].
Sesink, ALA ;
Termont, DSML ;
Kleibeuker, JH ;
Van der Meer, R .
CARCINOGENESIS, 2000, 21 (10) :1909-1915
[29]   Dietary zinc supplementation attenuates hyperglycemia in db/db mice [J].
Simon, SF ;
Taylor, CG .
EXPERIMENTAL BIOLOGY AND MEDICINE, 2001, 226 (01) :43-51
[30]   Meta-analysis of observational studies in epidemiology - A proposal for reporting [J].
Stroup, DF ;
Berlin, JA ;
Morton, SC ;
Olkin, I ;
Williamson, GD ;
Rennie, D ;
Moher, D ;
Becker, BJ ;
Sipe, TA ;
Thacker, SB .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 283 (15) :2008-2012