The role of dietary factors in nonalcoholic fatty liver disease to hepatocellular carcinoma progression: A systematic review

被引:21
|
作者
Zheng, Jiali [1 ]
Zhao, Longgang [2 ]
Dong, Jingwen [1 ]
Chen, Huiyi [1 ]
Li, Donghui [3 ]
Zhang, Xuehong [4 ,5 ]
Hassan, Manal M. [6 ]
Steck, Susan E. [2 ]
Li, Xiaoguang [1 ]
Xiang, Yong-Bing [7 ,8 ]
Wang, Hui [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Publ Hlth, Sch Med, 227 South Chongqing Rd,Rm 415, Shanghai, Peoples R China
[2] Univ South Carolina, Dept Epidemiol & Biostat, Arnold Sch Publ Hlth, Columbia, SC 29208 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Houston, TX 77030 USA
[4] Brigham & Womens Hosp, Dept Med, Channing Div Network Med, 75 Francis St, Boston, MA 02115 USA
[5] Harvard Med Sch, Boston, MA 02115 USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Epidemiol, Houston, TX 77030 USA
[7] Shanghai Jiao Tong Univ, Sch Med, State Key Lab Oncogene & Related Genes, 25 Lane 2200,Xie Tu Rd, Shanghai, Peoples R China
[8] Shanghai Jiao Tong Univ, Sch Med, Dept Epidemiol, Renji Hosp,Shanghai Canc Inst, 25 Lane 2200,Xie Tu Rd, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
Dietary factors; Chronic liver diseases; NAFLD-to-HCC progression; Systematic review; Observational studies; RED MEAT CONSUMPTION; COFFEE CONSUMPTION; RISK-FACTORS; LIFE-STYLE; VEGETABLE CONSUMPTION; INVERSE ASSOCIATION; PROSPECTIVE COHORT; TEA CONSUMPTION; SUBSEQUENT RISK; REDUCES RISK;
D O I
10.1016/j.clnu.2022.08.018
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
Background and aims: Dietary factors play an important role in promoting nonalcoholic fatty liver disease (NAFLD)-related hepatocellular carcinoma (HCC) development through regulation of metabolism and inflammation. However, so far there was no evidence regarding how dietary factors may influence different disease outcomes in the NAFLD to HCC progression. Our study aimed to comprehensively evaluate the role of dietary factors on the risk of progression from NAFLD to HCC. Methods: A comprehensive literature research was conducted in PubMed, Web of Science and Embase databases to identify case-control and cohort studies published up to March 15, 2022 in English. We included studies investigating associations of food and beverage items (excluding alcohol), food groups, dietary patterns, and dietary habits with incidence risk of four main chronic liver diseases involved in the NAFLD-to-HCC progression (i.e., NAFLD, liver fibrosis, liver cirrhosis, and HCC). Three researchers inde-pendently performed the literature search, selected eligible articles, performed data abstraction and evaluated study quality. After evaluating adequacy and credibility of the associations reported for each dietary factor and each liver disease outcome, we summarized and evaluated the consistency of asso-ciations based on a priori determined criteria considering study design and the proportion of significant associations. Results: There were 109 studies included in this review (47 on NAFLD, 1 on liver fibrosis, 6 on liver cirrhosis, and 55 on HCC). Consistent evidence suggested that higher dietary inflammatory potential was associated with increased risk of both NAFLD and HCC whereas Mediterranean diet was associated with lower risk of both diseases. Additionally, greater conformity to the Healthy Eating Index, Dietary Approaches to Stop Hypertension score, and Mediterranean Diet Score, and dietary patterns with high dietary antioxidant capacity reduced NAFLD risk. Some specific foods including soft drinks and red and/or processed meat were associated with increased NAFLD risk while total vegetables and spinach were associated with reduced NAFLD risk. Coffee and white meat consumption were inversely related to HCC risk. Conclusions: Dietary patterns or individual foods representing a more anti-inflammatory potential were associated with reduced risk of both NAFLD and HCC, which implied diet-induced inflammation may impact NAFLD progression towards HCC. (c) 2022 Elsevier Ltd and European Society for Clinical Nutrition and Metabolism. All rights reserved.
引用
收藏
页码:2295 / 2307
页数:13
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