Circulating adipokines and risk of obesity related cancers: A systematic review and meta-analysis

被引:79
|
作者
Yoon, Yeong Sook [1 ]
Kwon, A. Rom [2 ]
Lee, Yoon Kyung [2 ]
Oh, Sang Woo [3 ]
机构
[1] Inje Univ, Ilsan Paik Hosp, Dept Family Med, 170 Juhwa Ro, Goyang Si 10380, Gyeonggi Do, South Korea
[2] Dongguk Univ, Ilsan Hosp, Smart Healthcare Ctr, 27 Dongguk Ro, Goyang Si 10326, Gyeonggi Do, South Korea
[3] Dongguk Univ, Ilsan Hosp, Ctr Obes Metab & Nutr, Dept Family Med, 27 Dongguk Ro, Goyang Si 10326, Gyeonggi Do, South Korea
关键词
Obesity; Cancer; Adipokine; Inflammation; Meta-analysis; MOLECULAR-WEIGHT ADIPONECTIN; C-REACTIVE PROTEIN; RENAL-CELL CARCINOMA; SOLUBLE LEPTIN RECEPTOR; MULTIPLE-MYELOMA RISK; COLORECTAL-CANCER; BREAST-CANCER; ENDOMETRIAL CANCER; PLASMA ADIPONECTIN; SERUM ADIPONECTIN;
D O I
10.1016/j.orcp.2019.03.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Obesity can influence on carcinogenesis through alterations in adipokines and subsequent inflammatory changes. This meta-analysis was aimed to comprehensively assess the association between circulating adipokines and risk of obesity-related cancers. Methods: Pubmed and Embase were searched up to October 2017 for observational studies investigating the relationship between adipokines and cancers. Pooled odds ratio and the corresponding 95% confidence interval was estimated through the meta-analysis using a random-effects model. Findings A total of 93 observational studies (adiponectin = 60, high molecular weight adiponectin = 9, leptin = 39, IL-6 = 16, TNF-alpha = 10, and resistin = 17) were included. Adiponectin was significantly associated with decreased risk of cancer (pooled OR 0.70, 95% CI 0.60-0.80; I-2 = 71.9%; P-heterogeneity < 0.01). Leptin was significantly associated with increased risk of cancer (1.26, 1.05-1.51; I-2 = 65.7%; P-heterogeneity < 0.01). For each 5 mu g/ml increase in adiponectin and 5 ng/ml increase in leptin, the pooled OR was 0.88 (0.83-0.93; I-2 = 80.2%; P-heterogeneity < 0.01) and 1.05 (1.01-1.09; I-2 = 67.9%; P-heterogeneity < 0.01)), respectively. There was nonlinear dose-response association (P-nonlinearity for adiponectin = 0.01; P-nonlinearity for leptin = 0.003). IL-6 (1.09, 0.94-1.25), TNF-alpha (1.65, 0.99-2.74), and resistin (1.28, 0.78-2.11) was not associated with risk of cancer. By cancer site and type, highest category of adiponectin was associated with decreased risk of breast (OR 0.74, 0.60-0.91), colorectal (0.74, 0.60-0.91), and endometrial cancer (0.49, 0.34-0.72). Higher leptin was associated with increased risk of endometrial (1.88, 1.24-2.87) and kidney cancer (2.07, 1.51-2.83). Conclusion: Our study suggests that adiponectin and leptin may play a role in the etiology of cancer. (C) 2019 Published by Elsevier Ltd on behalf of Asia Oceania Association for the Study of Obesity.
引用
收藏
页码:329 / 339
页数:11
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