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The influence of obesity-related factors in the etiology of renal cell carcinoma-A mendelian randomization study

  • Mattias Johansson
  • , Robert Carreras-Torres
  • , Ghislaine Scelo
  • , Mark P. Purdue
  • , Daniela Mariosa
  • , David C. Muller
  • , Nicolas J. Timpson
  • , Philip C. Haycock
  • , Kevin M. Brown
  • , Zhaoming Wang
  • , Yuanqing Ye
  • , Jonathan N. Hofmann
  • , Matthieu Foll
  • , Valerie Gaborieau
  • , Mitchell J. Machiela
  • , Leandro M. Colli
  • , Peng Li
  • , Jean Guillaume Garnier
  • , Helene Blanche
  • , Anne Boland
  • Laurie Burdette, Egor Prokhortchouk, Konstantin G. Skryabin, Meredith Yeager, Sanja Radojevic-Skodric, Simona Ognjanovic, Lenka Foretova, Ivana Holcatova, Vladimir Janout, Dana Mates, Anush Mukeriya, Stefan Rascu, David Zaridze, Vladimir Bencko, Cezary Cybulski, Eleonora Fabianova, Viorel Jinga, Jolanta Lissowska, Jan Lubinski, Marie Navratilova, Peter Rudnai, Simone Benhamou, Geraldine Cancel-Tassin, Olivier Cussenot, Elisabete Weiderpass, Börje Ljungberg, Raviprakash Tumkur Sitaram, Christel Häggström, Fiona Bruinsma, Susan J. Jordan, Gianluca Severi, Ingrid Winship, Kristian Hveem, Lars J. Vatten, Tony Fletcher, Susanna C. Larsson, Alicja Wolk, Rosamonde E. Banks, Peter J. Selby, Douglas F. Easton, Gabriella Andreotti, Laura E. Beane Freeman, Stella Koutros, Satu Männistö, Stephanie Weinstein, Peter E. Clark, Todd L. Edwards, Loren Lipworth, Susan M. Gapstur, Victoria L. Stevens, Hallie Carol, Matthew L. Freedman, Mark M. Pomerantz, Eunyoung Cho, Kathryn M. Wilson, J. Michael Gaziano, Howard D. Sesso, Neal D. Freedman, Alexander S. Parker, Jeanette E. Eckel-Passow, Wen Yi Huang, Richard J. Kahnoski, Brian R. Lane, Sabrina L. Noyes, David Petillo, Bin Tean Teh, Ulrike Peters, Emily White, Garnet L. Anderson, Lisa Johnson, Juhua Luo, Julie Buring, I. Min Lee, Wong Ho Chow, Lee E. Moore, Timothy Eisen, Marc Henrion, James Larkin, Poulami Barman, Bradley C. Leibovich, Toni K. Choueiri, G. Mark Lathrop, Jean Francois Deleuze, Marc Gunter, James D. McKay, Xifeng Wu, Richard S. Houlston, Stephen J. Chanock, Caroline Relton, J. Brent Richards, Richard M. Martin, George Davey Smith, Paul Brennan
  • International Agency for Research on Cancer
  • National Institutes of Health
  • Imperial College London
  • University of Bristol
  • St. Jude Children Research Hospital
  • University of Texas MD Anderson Cancer Center
  • Max Planck Institute for Demographic Research
  • Evry
  • Centre d'Etude du Polymorphisme Humain (CEPH)
  • Russian Academy of Sciences
  • Kurchatov Scientific Center
  • Medical School of Belgrade
  • Clinical Center of Serbia
  • Mayo Clinic College of Medicine and Science
  • International Organization for Cancer Prevention and Research
  • Masaryk Memorial Cancer Institute
  • Charles University
  • Palacký University Olomouc
  • National Institute of Public Health
  • Russian Academy of Medical Sciences - N.N. Blokhin Russian Cancer Research Center
  • Carol Davila University of Medicine and Pharmacy
  • Pomeranian Medical University in Szczecin
  • Regional Authority of Public Health in Banska Bystrica
  • Maria Sklodowska-Curie Institute of Oncology
  • National Directorate of Environmental Health
  • Institut national de la santé et de la recherche médicale
  • Gustave Roussy Cancer Campus
  • CeRePP
  • Sorbonne Université
  • Paris-Hôpital Tenon
  • Cancer Registry of Norway Institute of Population-Based Cancer Research
  • Karolinska Institutet
  • Folkhalsan
  • University of Tromsø – The Arctic University of Norway
  • Umeå University
  • Uppsala University
  • Cancer Council Victoria
  • Queensland Institute of Medical Research
  • University of Queensland
  • INSERM, Center for Research in Epidemiology and Population Health, Lifelong Epidemiology of Obesity, Diabetes, and Renal Disease Team
  • HuGeF Foundation
  • University of Melbourne
  • Norwegian University of Science and Technology
  • London School of Hygiene and Tropical Medicine
  • University of Leeds
  • Imperial College Healthcare NHS Trust
  • University of Cambridge
  • National Institute for Health and Welfare
  • Vanderbilt University
  • American Cancer Society
  • Dana-Farber Cancer Institute
  • Brown University
  • Harvard University
  • Brigham and Women’s Hospital
  • Mayo Clinic Jacksonville, FL
  • Mayo Clinic Rochester, MN
  • Spectrum Health
  • Michigan State University
  • Van Andel Institute
  • Ferris State University
  • Cancer and Stem Cell Biology Program
  • Agency for Science, Technology and Research, Singapore
  • National Cancer Centre
  • National University of Singapore
  • Fred Hutchinson Cancer Research Center
  • Indiana University Bloomington
  • Institute of Cancer Research
  • Icahn School of Medicine at Mount Sinai
  • Royal Marsden NHS Foundation Trust
  • McGill University
  • Department of Medicine, McGill University
  • University Hospitals Bristol and Weston NHS Foundation Trust

Research output: Contribution to journalArticlepeer-review

74 Citations (Scopus)

Abstract

Background: Several obesity-related factors have been associated with renal cell carcinoma (RCC), but it is unclear which individual factors directly influence risk. We addressed this question using genetic markers as proxies for putative risk factors and evaluated their relation to RCC risk in a mendelian randomization (MR) framework. This methodology limits bias due to confounding and is not affected by reverse causation. Methods and findings: Genetic markers associated with obesity measures, blood pressure, lipids, type 2 diabetes, insulin, and glucose were initially identified as instrumental variables, and their association with RCC risk was subsequently evaluated in a genome-wide association study (GWAS) of 10,784 RCC patients and 20,406 control participants in a 2-sample MR framework. The effect on RCC risk was estimated by calculating odds ratios (OR SD ) for a standard deviation (SD) increment in each risk factor. The MR analysis indicated that higher body mass index increases the risk of RCC (OR SD : 1.56, 95% confidence interval [CI] 1.44-1.70), with comparable results for waist-to-hip ratio (OR SD : 1.63, 95% CI 1.40-1.90) and body fat percentage (OR SD : 1.66, 95% CI 1.44-1.90). This analysis further indicated that higher fasting insulin (OR SD : 1.82, 95% CI 1.30-2.55) and diastolic blood pressure (DBP; OR SD : 1.28, 95% CI 1.11-1.47), but not systolic blood pressure (OR SD : 0.98, 95% CI 0.84-1.14), increase the risk for RCC. No association with RCC risk was seen for lipids, overall type 2 diabetes, or fasting glucose. Conclusions: This study provides novel evidence for an etiological role of insulin in RCC, as well as confirmatory evidence that obesity and DBP influence RCC risk.
Original languageEnglish
Article numbere1002724
JournalPLoS Medicine
Volume16
Issue number1
DOIs
Publication statusPublished - 1 Jan 2019
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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