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

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dc.contributor.authorYoon, Yeong Sook-
dc.contributor.authorKwon, A. Rom-
dc.contributor.authorLee, Yoon Kyung-
dc.contributor.authorOh, Sang Woo-
dc.date.accessioned2023-04-28T03:40:51Z-
dc.date.available2023-04-28T03:40:51Z-
dc.date.issued2019-07-
dc.identifier.issn1871-403X-
dc.identifier.issn1878-0318-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/7935-
dc.description.abstractBackground: 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.-
dc.format.extent11-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER SCI LTD-
dc.titleCirculating adipokines and risk of obesity related cancers: A systematic review and meta-analysis-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.orcp.2019.03.006-
dc.identifier.scopusid2-s2.0-85064260997-
dc.identifier.wosid000480688600001-
dc.identifier.bibliographicCitationOBESITY RESEARCH & CLINICAL PRACTICE, v.13, no.4, pp 329 - 339-
dc.citation.titleOBESITY RESEARCH & CLINICAL PRACTICE-
dc.citation.volume13-
dc.citation.number4-
dc.citation.startPage329-
dc.citation.endPage339-
dc.type.docTypeReview-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEndocrinology & Metabolism-
dc.relation.journalResearchAreaNutrition & Dietetics-
dc.relation.journalWebOfScienceCategoryEndocrinology & Metabolism-
dc.relation.journalWebOfScienceCategoryNutrition & Dietetics-
dc.subject.keywordPlusMOLECULAR-WEIGHT ADIPONECTIN-
dc.subject.keywordPlusC-REACTIVE PROTEIN-
dc.subject.keywordPlusRENAL-CELL CARCINOMA-
dc.subject.keywordPlusSOLUBLE LEPTIN RECEPTOR-
dc.subject.keywordPlusMULTIPLE-MYELOMA RISK-
dc.subject.keywordPlusCOLORECTAL-CANCER-
dc.subject.keywordPlusBREAST-CANCER-
dc.subject.keywordPlusENDOMETRIAL CANCER-
dc.subject.keywordPlusPLASMA ADIPONECTIN-
dc.subject.keywordPlusSERUM ADIPONECTIN-
dc.subject.keywordAuthorObesity-
dc.subject.keywordAuthorCancer-
dc.subject.keywordAuthorAdipokine-
dc.subject.keywordAuthorInflammation-
dc.subject.keywordAuthorMeta-analysis-
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