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Weak Association Between Genetic Markers of Hyperuricemia and Cardiorenal Outcomes: Insights From the STANISLAS Study Cohort With a 20‐Year Follow‐Up

Authors :
Mehmet Kanbay
Constance Xhaard
Edith Le Floch
Claire Dandine‐Roulland
Nicolas Girerd
João Pedro Ferreira
Jean‐Marc Boivin
Sandra Wagner
Delphine Bacq‐Daian
Jean‐François Deleuze
Faiez Zannad
Patrick Rossignol
Koç University
Défaillance Cardiovasculaire Aiguë et Chronique (DCAC)
Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lorraine (UL)
Centre d'investigation clinique plurithématique Pierre Drouin [Nancy] (CIC-P)
Centre d'investigation clinique [Nancy] (CIC)
Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lorraine (UL)-Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lorraine (UL)
Cardiovascular and Renal Clinical Trialists [Vandoeuvre-les-Nancy] (INI-CRCT)
Institut Lorrain du Coeur et des Vaisseaux Louis Mathieu [Nancy]
French-Clinical Research Infrastructure Network - F-CRIN [Paris] (Cardiovascular & Renal Clinical Trialists - CRCT )
Centre National de Recherche en Génomique Humaine (CNRGH)
Commissariat à l'énergie atomique et aux énergies alternatives (CEA)
Institut de Biologie François JACOB (JACOB)
Direction de Recherche Fondamentale (CEA) (DRF (CEA))
Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)
The STANISLAS (Suivi Temporaire Annuel Non‐Invasif de la Santé des Lorrains Assurés Sociaux) study is sponsored by the Nancy Centre Hospitalier Régional Universitaire. This work is supported by the French Ministry of Health 'Programme Hospitalier de Recherche Clinique Inter regional 2013,' by the Contrat de Plan Etat‐Lorraine and Fonds Européen de Développement Régional Lorraine, and a public grant overseen by the French National Research Agency (ANR) as part of the second 'Investissements d’Avenir' program FIGHT‐heart failure (reference: ANR‐15‐RHU‐0004) and by the French Plan d'Investissement d'Avenir project 'Lorraine Université d’Excellence,' reference ANR‐15‐IDEX‐04‐LUE. It is also supported by the European Fibro‐Targets Project (grant agreement No. SP7#602904), European HOMAGE project (grant agreement No. Heart 'Omics' in Ageing, 7th Framework Program grant No. 305507), the MEDIA project (Européen 'Cooperation'–Theme 'Health'/FP7‐HEALTH‐2010‐single‐stage (reference: 261409), FOCUS‐MR (reference: ANR‐15‐CE14‐0032‐01), ERA‐CVD EXPERT (reference: ANR‐16‐ECVD‐0002‐02), and the Fondation de Recherche en Hypertension Artérielle.
ANR-15-RHUS-0004,FIGHT-HF,Combattre l'insuffisance cardiaque(2015)
ANR-15-IDEX-0004,LUE,Isite LUE(2015)
ANR-15-CE14-0032,MR-focus,Régulation, Diagnostique et Thérapeutique ciblée du récepteur minéralocorticoïde dans le remodelage cardiaque(2015)
ANR-16-ECVD-0002,EXPERT,Exploring new pathways in age-related heart diseases(2016)
European Project: SP7#602904
European Project: 305507
European Project: 261409,EU FP 7 MEDIA project
Université de Lorraine (UL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy)
Université de Lorraine (UL)-Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lorraine (UL)-Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy)-Institut National de la Santé et de la Recherche Médicale (INSERM)
BOZEC, Erwan
Combattre l'insuffisance cardiaque - - FIGHT-HF2015 - ANR-15-RHUS-0004 - RHUS - VALID
ISITE - Isite LUE - - LUE2015 - ANR-15-IDEX-0004 - IDEX - VALID
Régulation, Diagnostique et Thérapeutique ciblée du récepteur minéralocorticoïde dans le remodelage cardiaque - - MR-focus2015 - ANR-15-CE14-0032 - AAPG2015 - VALID
Exploring new pathways in age-related heart diseases - - EXPERT2016 - ANR-16-ECVD-0002 - ERA-CVD - VALID
European Fibro‐Targets Project - SP7#602904 - INCOMING
HOMAGE (Heart Omics in Ageing consortium) - 305507 - INCOMING
The MEtabolic Road to DIAstolic Heart Failure - EU FP 7 MEDIA project - 261409 - INCOMING
Kanbay, Mehmet (ORCID 0000-0002-1297-0675 & YÖK ID 110580)
Xhaard, C.
Le Floch, E.
Dandine-Roulland, C.
Girerd, N.
Ferreira, J.P.
Boivin, J.M.
Wagner, S.
Bacq Daian, D.
Deleuze, J.F.
Zannad, F.
Rossignol, P.
School of Medicine
Source :
Journal of the American Heart Association, Journal of the American Heart Association, 2022, pp.e023301. ⟨10.1161/JAHA.121.023301⟩, Journal of the American Heart Association, Wiley-Blackwell, 2022, pp.e023301. ⟨10.1161/JAHA.121.023301⟩
Publication Year :
2022
Publisher :
HAL CCSD, 2022.

Abstract

Background: Hyperuricemia is associated with poor cardiovascular outcomes, although it is uncertain whether this relationship is causal in nature. This study aimed to: (1) assess the heritability of serum uric acid (SUA) levels, (2) conduct a genome-wide association study on SUA levels, and (3) investigate the association between certain single-nucleotide polymorphisms and target organ damage. Methods and results: the STANISLAS (Suivi Temporaire Annuel Non-Invasif de la Sante des Lorrains Assures Sociaux) study cohort is a single-center longitudinal cohort recruited between 1993 and 1995 (visit 1), with a last visit (visit 4 [V4]) performed approximate to 20 years apart. Serum lipid profile, SUA, urinary albumin/creatinine ratio, estimated glomerular filtration rate, 24-hour ambulatory blood pressure monitoring, transthoracic echocardiography, pulse wave velocity, and genotyping for each participant were assessed at V4. A total of 1573 participants were included at V4, among whom 1417 had available SUA data at visit 1. Genome-wide association study results highlighted multiple single-nucleotide polymorphisms on the SLC2A9 gene linked to SUA levels. Carriers of the most associated mutated SLC2A9 allele (rs16890979) had significantly lower SUA levels. Although SUA level at V4 was highly associated with diabetes, prediabetes, higher body mass index, CRP (C-reactive protein) levels, estimated glomerular filtration rate variation (visit 1-V4), carotid intima-media thickness, and pulse wave velocity, rs16890979 was only associated with higher carotid intima-media thickness. Conclusions: our findings demonstrate that rs16890979, a genetic determinant of SUA levels located on the SLC2A9 gene, is associated with carotid intima-media thickness despite significant associations between SUA levels and several clinical outcomes, thereby lending support to the hypothesis of a link between SUA and cardiovascular disease.<br />Nancy Centre Hospitalier Regional Universitaire; French Ministry of Health; French National Research Agency (ANR); Contrat de Plan Etat?Lorraine and Fonds Européen de Développement Régional Lorraine; Programme Hospitalier de Recherche Clinique Inter regional 2013; Investissements d’Avenir; FIGHT?heart failure; French Plan d'Investissement d'Avenir project “Lorraine Université d’Excellence; European Union (EU); European Fibro?Targets Project; European HOMAGE project; 7th Framework Program; MEDIA project; FOCUS?MR; ERA?CVD EXPERT; Fondation de Recherche en Hypertension Artérielle

Details

Language :
English
ISSN :
20479980
Database :
OpenAIRE
Journal :
Journal of the American Heart Association, Journal of the American Heart Association, 2022, pp.e023301. ⟨10.1161/JAHA.121.023301⟩, Journal of the American Heart Association, Wiley-Blackwell, 2022, pp.e023301. ⟨10.1161/JAHA.121.023301⟩
Accession number :
edsair.doi.dedup.....1beebd65c7706d0e81ebe4123301ba19