Defining determinants of pancreatic cancer risk: are we making progress?
Defining determinants of pancreatic cancer risk: are we making progress?
复制标题
确定胰腺癌风险的决定因素:我们正在取得进展吗?
DOI:
10.1093/jnci/djp182
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发表时间:
2009
期刊:
影响因子:
--
通讯作者:
Stampfer,MeirJ
中科院分区:
文献类型:
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作者:
Wolpin,BrianM;Stampfer,MeirJ
Brian M. Wolpin, Meir J. Stampfer current study (6), they work to extend this finding and demonstrate a modest increase in risk among those participants who consumed total fat, saturated fat, and monounsaturated fat in the highest vs the lowest quintile, with multivariable-adjusted hazard ratios between 1.2 and 1.4. Interestingly, only fatty acids from animal sources were statistically significantly associated with risk. The study by Thiébaut et al.(6) has several notable and important strengths. The large base population leads to an impressively large number of pancreatic cancer cases available for analysis. The prospective design of the study without the need for proxy respondents increases the interpretability of the results, by limiting the potential for bias and misclassification. The data collected on dietary habits were sufficiently detailed to capture information on the diversity of food products, such as “low-fat” versions of foods, and nicely demonstrate the utility of well-designed food-frequency questionnaires in prospective studies of diet and cancer. Overall, this well-performed prospective cohort study is a welcome addition to our understanding of a disease that is in great need of new insights. However, the available epidemiological and laboratory evidence are insufficient to confirm the importance of animal fats, per se, or even that meat is the important factor, as opposed to other dietary or lifestyle preferences associated with meat consumption. Nonetheless, sufficient evidence already suggests health benefits from limiting meat and saturated fat intake (8), and the current study provides additional support for these recommendations. Also, with further investigation, this work has the potential to provide interesting clues to the mechanisms underlying pancreatic tumorigenesis. Although large prospective cohort studies with questionnairebased analyses will continue to have much to offer in defining predisposing factors for difficult diseases, such as pancreatic cancer, how can we move beyond what has been done before? Two principles are worth mentioning: increased collaboration and greater use of participant-derived biological samples. Because of the relatively low incidence rate of pancreatic cancer, collaboration is vital to provide the critical mass of cases for meaningful analyses. Second, there is great potential for well-designed studies using banked plasma, germline DNA, and tumor tissue samples to advance our understanding of pancreatic cancer pathogenesis.