Genetic variants of adiponectin and risk of colorectal cancer |
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Authors: | Mingyang Song Jian Gong Edward L. Giovannucci Sonja I. Berndt Hermann Brenner Jenny Chang‐Claude Keith R. Curtis Tabitha A. Harrison Michael Hoffmeister Li Hsu Shuo Jiao Loic Le Marchand John D. Potter Robert E. Schoen Daniela Seminara Martha L. Slattery Emily White Kana Wu Shuji Ogino Charles S. Fuchs David J. Hunter Shelley S. Tworoger Frank B. Hu Eric Rimm Majken Jensen Ulrike Peters Andrew T. Chan |
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Affiliation: | 1. Department of Nutrition, Harvard School of Public Health, Boston, MA;2. Department of Epidemiology, Harvard School of Public Health, Boston, MA;3. Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA;4. Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA;5. Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD;6. Division of Clinical Epidemiology and Aging Research, German Cancer Research Center (DKFZ), Heidelberg, Germany;7. German Consortium for Translational Cancer Research (DKTK), German Cancer Research Center (DKFZ), Heidelberg, Germany;8. Division of Cancer Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany;9. Department of Biostatistics, School of Public Health, University of Washington, Seattle, WA;10. University of Hawaii Cancer Center, Honolulu, HI;11. Department of Epidemiology, School of Public Health, University of Washington, Seattle, WA;12. Centre for Public Health Research, Massey University, Wellington, New Zealand;13. Department of Medicine and Epidemiology, University of Pittsburgh Medical Center, Pittsburgh, PA;14. Division of Cancer Control and Population Sciences, National Cancer Institute, National Institutes of Health, Bethesda, MD;15. Department of Internal Medicine, University of Utah Health Sciences Center, Salt Lake City, UT;16. Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA;17. Department of Medical Oncology, Dana‐Farber Cancer Institute and Harvard Medical School, Boston, MA;18. Division of Gastroenterology, Massachusetts General Hospital and Harvard Medical School, Boston, MA |
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Abstract: | Circulating adiponectin has been associated with lower risk of colorectal cancer (CRC). Genome‐wide association studies have identified several single‐nucleotide polymorphisms (SNPs) associated with adiponectin levels. However, it is unclear whether these SNPs are associated with CRC risk. In addition, previous data on SNPs in the adiponectin pathway and their associations with CRC are inconsistent. Therefore, we examined 19 SNPs in genes related to adiponectin or its receptors and their associations with CRC using logistic regression among 7,020 cases and 7,631 controls drawn from ten studies included in the Genetics and Epidemiology of Colorectal Cancer Consortium. Using data from a subset of two large cohort studies, we also assessed the contribution of individual SNPs and an adiponectin genetic score to plasma adiponectin after accounting for lifestyle factors among 2,217 women and 619 men. We did not find any statistically significant association between the 19 adiponectin‐associated SNPs and CRC risk (multivariable‐adjusted odds ratios ranged from 0.89 to 1.05, all p > 0.05). Each SNP explained less than 2.50% of the variance of plasma adiponectin, and the genetic score collectively accounted for 2.95 and 1.42% of the variability of adiponectin in women and men, respectively, after adjustment for age, body mass index, physical activity, smoking, alcohol consumption, regular use of aspirin or nonsteroidal anti‐inflammatory drug and postmenopausal hormone use. In conclusion, our findings do not support an association between known adiponectin‐related common SNPs and CRC incidence. However, known common SNPs account for only a limited proportion of the interindividual variance in circulating adiponectin. Further work is warranted to investigate the relationship between adiponectin and CRC while accounting for other components in the pathway. |
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Keywords: | adiponectin single‐nucleotide polymorphism Mendelian randomization colorectal cancer lifestyle factors |
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