Shiu Lun Au Yeung1, C Mary Schooling2. 1. School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong. Electronic address: ayslryan@hku.hk. 2. School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong; City University of New York, Graduate School of Public Health and Health Policy, New York, NY, USA.
Abstract
BACKGROUND: Observational studies have found adiponectin inversely associated with cardiovascular disease thereby indicating a potential target of intervention, but genetically higher adiponectin appears unrelated to coronary artery disease (CAD). To clarify, we examined the role of genetically predicted adiponectin in CAD in a larger study and additionally examined the role of genetically predicted CAD in adiponectin using a bi-directional Mendelian randomization study. METHODS: We obtained estimates using inverse variance weighting (IVW) with multiplicative random effects, based on 21 single nucleotide polymorphism (SNPs) to predict adiponectin and 28 SNPs for CAD, using two large genome wide association studies of adiponectin (ADIPOGen Consortium (n = 39,883)) and CAD CARDIoGRAMplusC4D 1000 Genomes based GWAS (n = 60,801 CAD cases; n = 123,504 controls). Sensitivity analyses included using MR-Egger, weighted median method, and exclusion of potentially invalid (pleiotropic) SNPs. RESULTS: Adiponectin was inversely associated with CAD (odds ratio 0.82 per unit increase log transformed adiponectin, 95% confidence interval (CI) 0.71 to 0.94) using IVW. However, the association was null using a weighted median method or MR-Egger, or after exclusion of pleiotropic SNPs acting on obesity related traits. CAD was not associated with adiponectin (-0.011 log transformed adiponectin unit per log odds CAD, 95% CI -0.039 to 0.017), with similar findings from MR-Egger, weighted median method or exclusion of pleiotropic SNPs. CONCLUSION: Adiponectin is unlikely a cause of CAD although we cannot completely rule out the possibility. Previous observational studies are likely driven by factors driving both adiponectin and CAD, whose elucidation might provide new insights concerning interventions for CAD.
BACKGROUND: Observational studies have found adiponectin inversely associated with cardiovascular disease thereby indicating a potential target of intervention, but genetically higher adiponectin appears unrelated to coronary artery disease (CAD). To clarify, we examined the role of genetically predicted adiponectin in CAD in a larger study and additionally examined the role of genetically predicted CAD in adiponectin using a bi-directional Mendelian randomization study. METHODS: We obtained estimates using inverse variance weighting (IVW) with multiplicative random effects, based on 21 single nucleotide polymorphism (SNPs) to predict adiponectin and 28 SNPs for CAD, using two large genome wide association studies of adiponectin (ADIPOGen Consortium (n = 39,883)) and CAD CARDIoGRAMplusC4D 1000 Genomes based GWAS (n = 60,801 CAD cases; n = 123,504 controls). Sensitivity analyses included using MR-Egger, weighted median method, and exclusion of potentially invalid (pleiotropic) SNPs. RESULTS:Adiponectin was inversely associated with CAD (odds ratio 0.82 per unit increase log transformed adiponectin, 95% confidence interval (CI) 0.71 to 0.94) using IVW. However, the association was null using a weighted median method or MR-Egger, or after exclusion of pleiotropic SNPs acting on obesity related traits. CAD was not associated with adiponectin (-0.011 log transformed adiponectin unit per log odds CAD, 95% CI -0.039 to 0.017), with similar findings from MR-Egger, weighted median method or exclusion of pleiotropic SNPs. CONCLUSION:Adiponectin is unlikely a cause of CAD although we cannot completely rule out the possibility. Previous observational studies are likely driven by factors driving both adiponectin and CAD, whose elucidation might provide new insights concerning interventions for CAD.
Authors: Y Zhang; M Peltonen; J C Andersson-Assarsson; P-A Svensson; C Herder; A Rudin; Lms Carlsson; C Maglio Journal: Scand J Rheumatol Date: 2020-07-15 Impact factor: 3.641
Authors: Cassandra N Spracklen; Tugce Karaderi; Hanieh Yaghootkar; Claudia Schurmann; Rebecca S Fine; Zoltan Kutalik; Michael H Preuss; Yingchang Lu; Laura B L Wittemans; Linda S Adair; Matthew Allison; Najaf Amin; Paul L Auer; Traci M Bartz; Matthias Blüher; Michael Boehnke; Judith B Borja; Jette Bork-Jensen; Linda Broer; Daniel I Chasman; Yii-Der Ida Chen; Paraskevi Chirstofidou; Ayse Demirkan; Cornelia M van Duijn; Mary F Feitosa; Melissa E Garcia; Mariaelisa Graff; Harald Grallert; Niels Grarup; Xiuqing Guo; Jeffrey Haesser; Torben Hansen; Tamara B Harris; Heather M Highland; Jaeyoung Hong; M Arfan Ikram; Erik Ingelsson; Rebecca Jackson; Pekka Jousilahti; Mika Kähönen; Jorge R Kizer; Peter Kovacs; Jennifer Kriebel; Markku Laakso; Leslie A Lange; Terho Lehtimäki; Jin Li; Ruifang Li-Gao; Lars Lind; Jian'an Luan; Leo-Pekka Lyytikäinen; Stuart MacGregor; David A Mackey; Anubha Mahajan; Massimo Mangino; Satu Männistö; Mark I McCarthy; Barbara McKnight; Carolina Medina-Gomez; James B Meigs; Sophie Molnos; Dennis Mook-Kanamori; Andrew P Morris; Renee de Mutsert; Mike A Nalls; Ivana Nedeljkovic; Kari E North; Craig E Pennell; Aruna D Pradhan; Michael A Province; Olli T Raitakari; Chelsea K Raulerson; Alex P Reiner; Paul M Ridker; Samuli Ripatti; Neil Roberston; Jerome I Rotter; Veikko Salomaa; America A Sandoval-Zárate; Colleen M Sitlani; Tim D Spector; Konstantin Strauch; Michael Stumvoll; Kent D Taylor; Betina Thuesen; Anke Tönjes; Andre G Uitterlinden; Cristina Venturini; Mark Walker; Carol A Wang; Shuai Wang; Nicholas J Wareham; Sara M Willems; Ko Willems van Dijk; James G Wilson; Ying Wu; Jie Yao; Kristin L Young; Claudia Langenberg; Timothy M Frayling; Tuomas O Kilpeläinen; Cecilia M Lindgren; Ruth J F Loos; Karen L Mohlke Journal: Am J Hum Genet Date: 2019-06-06 Impact factor: 11.025
Authors: Ge Li; Ling Zhong; Lanwen Han; Yonghui Wang; Bo Li; Dongmei Wang; Yanglu Zhao; Yu Li; Qian Zhang; Lu Qi; John R Speakman; Steven M Willi; Ming Li; Shan Gao Journal: Int J Obes (Lond) Date: 2021-10-29 Impact factor: 5.551