Evidence map›Paper›PMID 19503597›Full record

SynthesisPLoS genetics2009

Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations.

Melanie Kolz, Toby Johnson, Serena Sanna, Alexander Teumer, Veronique Vitart, Markus Perola, Massimo Mangino, Eva Albrecht, Chris Wallace, Martin Farrall and 51 more

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in PLoS genetics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 344 papers, 13 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
344citing papers in PubMed, 13 pooled it
25.1field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

344 citing papers in PubMed, 13 syntheses or guidelines pooled it, 655 citations in OpenAlex.

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284 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

61 authors at 20 institutions in 11 countries.

Melanie KolzInstitute of Epidemiology, Helmholtz Zentrum München, National Research Center for Environment and Health, Neuherberg, Germany.
Toby Johnson
Serena Sanna
Alexander Teumer
Veronique Vitart
Markus Perola
Massimo Mangino
Eva Albrecht
Chris Wallace
Martin Farrall
Asa Johansson
Dale R Nyholt
Yurii Aulchenko
Jacques S Beckmann
Sven Bergmann
Murielle Bochud
Morris Brown
Harry Campbell
EUROSPAN Consortium
John Connell
Anna Dominiczak
Georg Homuth
Claudia Lamina
Mark I McCarthy
ENGAGE Consortium
Thomas Meitinger
Vincent Mooser
Patricia Munroe
Matthias Nauck
John Peden
Holger Prokisch
Perttu Salo
Veikko Salomaa
Nilesh J Samani
David Schlessinger
Manuela Uda
Uwe Völker
Gérard Waeber
Dawn Waterworth
Rui Wang-Sattler
Alan F Wright
Jerzy Adamski
John B Whitfield
Ulf Gyllensten
James F Wilson
Igor Rudan
Peter Pramstaller
Hugh Watkins
PROCARDIS Consortium
Angela Doering
H-Erich Wichmann
KORA Study
Tim D Spector
Leena Peltonen
Henry Völzke
Ramaiah Nagaraja
Peter Vollenweider
Mark Caulfield
WTCCC
Thomas Illig
Christian Gieger
Helmholtz Zentrum München · DECentre for Human Genetics · GBUniversität Greifswald · DEFinnish Institute for Health and Welfare · FIKing's College London · GBNational Institutes of Health · USQueen Mary University of London · GBUniversity Hospital of Lausanne · CHGlaxoSmithKline (United States) · USInstitute of Genetic and Biomedical Research · ITQIMR Berghofer Medical Research Institute · AUSIB Swiss Institute of Bioinformatics · CHUniversity of Cambridge · GBUniversity of Edinburgh · GBUniversity of Glasgow · GBUppsala University · SEWestern General Hospital · GBErasmus MC · NLEurac Research · ITInnsbruck Medical University · AT

Funding

Aging-related Traits and Disease Risk Factors in a Sardinian Population CohortZIAAG000675 · NIA · NATIONAL INSTITUTE ON AGING · PI GOROSPE, MYRIAM · 2009 to 2021
$5.7M
PERSISTENCE &CHANGE IN DRINKING HABITS: TWIN STUDYR01AA007535 · NIAAA · WASHINGTON UNIVERSITY · PI HEATH, ANDREW C. · 1989 to 1996
–
Arthritis Research UKBritish Heart Foundation FS/05/061/19501British Heart Foundation PG02/128Chief Scientist Office CZB/4/710Medical Research Council G0400874Medical Research Council G9521010Medical Research Council G9521010DMedical Research Council MC_U127561128NIAAA NIH HHS AA007535NIAAA NIH HHS R01 AA007535NIA NIH HHS N01-AG-1-2109Wellcome TrustWellcome Trust 076113/B/04/Z
6 · The paper itself

Abstract

Elevated serum uric acid levels cause gout and are a risk factor for cardiovascular disease and diabetes. To investigate the polygenetic basis of serum uric acid levels, we conducted a meta-analysis of genome-wide association scans from 14 studies totalling 28,141 participants of European descent, resulting in identification of 954 SNPs distributed across nine loci that exceeded the threshold of genome-wide significance, five of which are novel. Overall, the common variants associated with serum uric acid levels fall in the following nine regions: SLC2A9 (p = 5.2x10(-201)), ABCG2 (p = 3.1x10(-26)), SLC17A1 (p = 3.0x10(-14)), SLC22A11 (p = 6.7x10(-14)), SLC22A12 (p = 2.0x10(-9)), SLC16A9 (p = 1.1x10(-8)), GCKR (p = 1.4x10(-9)), LRRC16A (p = 8.5x10(-9)), and near PDZK1 (p = 2.7x10(-9)). Identified variants were analyzed for gender differences. We found that the minor allele for rs734553 in SLC2A9 has greater influence in lowering uric acid levels in women and the minor allele of rs2231142 in ABCG2 elevates uric acid levels more strongly in men compared to women. To further characterize the identified variants, we analyzed their association with a panel of metabolites. rs12356193 within SLC16A9 was associated with DL-carnitine (p = 4.0x10(-26)) and propionyl-L-carnitine (p = 5.0x10(-8)) concentrations, which in turn were associated with serum UA levels (p = 1.4x10(-57) and p = 8.1x10(-54), respectively), forming a triangle between SNP, metabolites, and UA levels. Taken together, these associations highlight additional pathways that are important in the regulation of serum uric acid levels and point toward novel potential targets for pharmacological intervention to prevent or treat hyperuricemia. In addition, these findings strongly support the hypothesis that transport proteins are key in regulating serum uric acid levels.

Indexed as

Genetic VariationFemaleGenome-Wide Association StudyGoutHumansMaleUric AcidUric Acid

Identifiers

PMID19503597
PMCPMC2683940
OpenAlexW2128934212

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.