Mulholland Helen G, Murray Liam J, Cardwell Chris R, Cantwell Marie M
Cancer Epidemiology & Prevention Research Group, Centre for Clinical & Population Sciences, Queen's University Belfast, Mulhouse Building, Royal Victoria Hospital Site, Belfast, Northern Ireland.
Am J Clin Nutr. 2009 Feb;89(2):568-76. doi: 10.3945/ajcn.2008.26823. Epub 2008 Dec 16.
Habitual consumption of diets with a high glycemic index (GI) and a high glycemic load (GL) may influence cancer risk via hyperinsulinemia and the insulin-like growth factor axis.
The objective was to conduct a systematic review to assess the association between GI, GL, and risk of digestive tract cancers.
Medline and Embase were searched for relevant publications from inception to July 2008. When possible, adjusted results from a comparison of cancer risk of the highest compared with the lowest category of GI and GL intake were combined by using random-effects meta-analyses.
Cohort and case-control studies that examined the risk between GI or GL intake and colorectal cancer (n = 12) and adenomas (n = 2), pancreatic cancer (n = 6), gastric cancer (n = 2), and squamous-cell esophageal carcinoma (n = 1) were retrieved. Most case-control studies observed positive associations between GI and GL intake and these cancers. However, pooled cohort study results showed no associations between colorectal cancer risk and GI intake [relative risk (RR): 1.04; 95% CI: 0.92, 1.12; n = 7 studies] or GL intake (RR: 1.06; 95% CI: 0.95, 1.17; n = 8 studies). Furthermore, no significant associations were observed in meta-analyses of cohort study results of colorectal cancer subsites and GI and GL intake. Similarly, no significant associations emerged between pancreatic cancer risk and GI intake (RR: 0.99; 95% CI: 0.83, 1.19; n = 5 studies) or GL intake (RR: 1.01; 95% CI: 0.86, 1.19; n = 6 studies) in combined cohort studies.
The findings from our meta-analyses indicate that GI and GL intakes are not associated with risk of colorectal or pancreatic cancers. There were insufficient data available regarding other digestive tract cancers to make any conclusions about GI or GL intake and risk.
习惯性食用高血糖指数(GI)和高血糖负荷(GL)的饮食可能通过高胰岛素血症和胰岛素样生长因子轴影响癌症风险。
进行一项系统评价,以评估GI、GL与消化道癌症风险之间的关联。
检索Medline和Embase数据库中从建库至2008年7月的相关出版物。如有可能,通过随机效应荟萃分析合并最高与最低GI和GL摄入量类别癌症风险比较的校正结果。
检索到队列研究和病例对照研究,这些研究探讨了GI或GL摄入量与结直肠癌(n = 12)、腺瘤(n = 2)、胰腺癌(n = 6)、胃癌(n = 2)和食管鳞状细胞癌(n = 1)之间的风险。大多数病例对照研究观察到GI和GL摄入量与这些癌症之间存在正相关。然而,汇总的队列研究结果显示,结直肠癌风险与GI摄入量[相对风险(RR):1.04;95%可信区间(CI):0.92,1.12;n = 7项研究]或GL摄入量(RR:1.06;95%CI:0.95,1.17;n = 8项研究)之间无关联。此外,在结直肠癌亚部位与GI和GL摄入量的队列研究结果的荟萃分析中未观察到显著关联。同样,在合并的队列研究中,胰腺癌风险与GI摄入量(RR:0.99;95%CI:0.83,1.19;n = 5项研究)或GL摄入量(RR:1.01;95%CI:0.86,1.19;n = 6项研究)之间也未出现显著关联。
我们的荟萃分析结果表明,GI和GL摄入量与结直肠癌或胰腺癌风险无关。关于其他消化道癌症,现有数据不足以得出关于GI或GL摄入量与风险的任何结论。