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Adiponectin and the risk of gastrointestinal cancers in East Asians: Mendelian randomization analysis

BACKGROUND: Adiponectin is an important adipocytokine and has been associated with the risks of gastrointestinal cancers (GICs). Mendelian randomization (MR) analysis is needed to assess the causal relationships between adiponectin and GICs. METHODS: We retrieved the summary data of genome‐wide asso...

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Autores principales: Jiang, Hua, Hu, Daojun, Wang, Jun, Zhang, Bo, He, Chiyi, Ning, Jiyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9189470/
https://www.ncbi.nlm.nih.gov/pubmed/35384390
http://dx.doi.org/10.1002/cam4.4735
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author Jiang, Hua
Hu, Daojun
Wang, Jun
Zhang, Bo
He, Chiyi
Ning, Jiyu
author_facet Jiang, Hua
Hu, Daojun
Wang, Jun
Zhang, Bo
He, Chiyi
Ning, Jiyu
author_sort Jiang, Hua
collection PubMed
description BACKGROUND: Adiponectin is an important adipocytokine and has been associated with the risks of gastrointestinal cancers (GICs). Mendelian randomization (MR) analysis is needed to assess the causal relationships between adiponectin and GICs. METHODS: We retrieved the summary data of genome‐wide association studies for adiponectin and six types of GICs in East Asians. A series of quality control steps were performed to select the eligible genetic instrumental tools. Horizontal pleiotropy and between‐SNP heterogeneity were tested to choose the primary MR method. We also conducted sensitivity analyses to test the robustness of the main findings. RESULTS: We detected neither heterogeneity nor horizontal pleiotropy for the eligible SNPs in all of the MR analyses. Inverse variance weighted (IVW) was therefore used as the primary method, and suggested that per 10% increase in log‐transformed adiponectin level was significantly associated with a decreased risk of gastric cancer (odds ratio [OR] = 0.88, 95% CI 0.81, 0.96), whereas with an increased risk of hepatocellular carcinoma (OR = 1.26, 95% CI 1.09, 1.44) and of biliary tract cancer (OR = 1.54, 95% CI 1.12, 2.12). However, only the association between adiponectin and HCC risk was statistically significant after correction for multiple testing. No statistically significant association was detected between adiponectin and esophageal (OR = 1.05, 95% CI 0.89, 1.23), pancreatic (OR = 1.04, 95% CI 0.78, 1.37), and colorectal cancers (OR = 1.00, 95% CI 0.93, 1.07). Sensitivity analyses did not find contradictory results. CONCLUSION: High level of adiponectin may have a causal effect on and can serve as a biomarker for the carcinogenesis of gastric cancer, hepatocellular carcinoma, and biliary tract cancer.
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spelling pubmed-91894702022-06-16 Adiponectin and the risk of gastrointestinal cancers in East Asians: Mendelian randomization analysis Jiang, Hua Hu, Daojun Wang, Jun Zhang, Bo He, Chiyi Ning, Jiyu Cancer Med RESEARCH ARTICLES BACKGROUND: Adiponectin is an important adipocytokine and has been associated with the risks of gastrointestinal cancers (GICs). Mendelian randomization (MR) analysis is needed to assess the causal relationships between adiponectin and GICs. METHODS: We retrieved the summary data of genome‐wide association studies for adiponectin and six types of GICs in East Asians. A series of quality control steps were performed to select the eligible genetic instrumental tools. Horizontal pleiotropy and between‐SNP heterogeneity were tested to choose the primary MR method. We also conducted sensitivity analyses to test the robustness of the main findings. RESULTS: We detected neither heterogeneity nor horizontal pleiotropy for the eligible SNPs in all of the MR analyses. Inverse variance weighted (IVW) was therefore used as the primary method, and suggested that per 10% increase in log‐transformed adiponectin level was significantly associated with a decreased risk of gastric cancer (odds ratio [OR] = 0.88, 95% CI 0.81, 0.96), whereas with an increased risk of hepatocellular carcinoma (OR = 1.26, 95% CI 1.09, 1.44) and of biliary tract cancer (OR = 1.54, 95% CI 1.12, 2.12). However, only the association between adiponectin and HCC risk was statistically significant after correction for multiple testing. No statistically significant association was detected between adiponectin and esophageal (OR = 1.05, 95% CI 0.89, 1.23), pancreatic (OR = 1.04, 95% CI 0.78, 1.37), and colorectal cancers (OR = 1.00, 95% CI 0.93, 1.07). Sensitivity analyses did not find contradictory results. CONCLUSION: High level of adiponectin may have a causal effect on and can serve as a biomarker for the carcinogenesis of gastric cancer, hepatocellular carcinoma, and biliary tract cancer. John Wiley and Sons Inc. 2022-04-05 /pmc/articles/PMC9189470/ /pubmed/35384390 http://dx.doi.org/10.1002/cam4.4735 Text en © 2022 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle RESEARCH ARTICLES
Jiang, Hua
Hu, Daojun
Wang, Jun
Zhang, Bo
He, Chiyi
Ning, Jiyu
Adiponectin and the risk of gastrointestinal cancers in East Asians: Mendelian randomization analysis
title Adiponectin and the risk of gastrointestinal cancers in East Asians: Mendelian randomization analysis
title_full Adiponectin and the risk of gastrointestinal cancers in East Asians: Mendelian randomization analysis
title_fullStr Adiponectin and the risk of gastrointestinal cancers in East Asians: Mendelian randomization analysis
title_full_unstemmed Adiponectin and the risk of gastrointestinal cancers in East Asians: Mendelian randomization analysis
title_short Adiponectin and the risk of gastrointestinal cancers in East Asians: Mendelian randomization analysis
title_sort adiponectin and the risk of gastrointestinal cancers in east asians: mendelian randomization analysis
topic RESEARCH ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9189470/
https://www.ncbi.nlm.nih.gov/pubmed/35384390
http://dx.doi.org/10.1002/cam4.4735
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