Evidence map›Paper›PMID 25477429›Full record

SynthesisCirculation. Cardiovascular genetics2015

Genome-wide meta-analyses of plasma renin activity and concentration reveal association with the kininogen 1 and prekallikrein genes.

Wolfgang Lieb, Ming-Huei Chen, Alexander Teumer, Rudolf A de Boer, Honghuang Lin, Ervin R Fox, Solomon K Musani, James G Wilson, Thomas J Wang, Henry Völzke and 26 more

Open access · bronzeAbstract readMeta-AnalysisReview
In one paragraph

Synthesis in Circulation. Cardiovascular genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
1.6field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 28 citations in OpenAlex.

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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

36 authors at 15 institutions in 14 countries.

Wolfgang Lieb
Ming-Huei Chen
Alexander Teumer
Rudolf A de Boer
Honghuang Lin
Ervin R Fox
Solomon K Musani
James G Wilson
Thomas J Wang
Henry Völzke
Ann-Kristin Petersen
Christine Meisinger
Matthias Nauck
Sabrina Schlesinger
Yong Li
Jöel Menard
Serge Hercberg
H-Erich Wichmann
Uwe Völker
Rajesh Rawal
Martin Bidlingmaier
Anke Hannemann
Marcus Dörr
Rainer Rettig
Wiek H van Gilst
Dirk J van Veldhuisen
Stephan J L Bakker
Gerjan Navis
Henri Wallaschofski
Pierre Meneton
Pim van der Harst
Martin Reincke
Ramachandran S Vasan
CKDGen Consortium
ICBP
EchoGen Consortium
Universitätsmedizin Greifswald · DEHelmholtz Zentrum München · DEUniversity of Groningen · NLUniversity of Mississippi Medical Center · USBoston University · USKiel University · DEBureau van Dijk (Belgium) · BEHilti (Liechtenstein) · LIInserm · FRLaboratoire d'Informatique Médicale et d'Ingénierie des Connaissances en e-SantéMenard (Poland) · PLMölnlycke Health Care (United Kingdom) · GBNational University of General San Martín · ARRatio · SEYong In University · KR

Funding

Ventricular Vascular Coupling: Correlates and PrognosisR01HL080124 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI RAMACHANDRAN, VASAN S · 2005 to 2009
$3.4M
Biomarkers of Ventricular and Vascular RemodelingR01HL077447 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI RAMACHANDRAN, VASAN S · 2005 to 2009
$2.6M
Genome-wide Association Study of Cardiac Structure and FunctionR01HL093328 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI RAMACHANDRAN, VASAN S · 2008 to 2011
$2.4M
Biomarkers of Metabolic and Vascular Risk in ObesityR01DK080739 · NIDDK · BOSTON UNIVERSITY MEDICAL CAMPUS · PI RAMACHANDRAN, VASAN S · 2008 to 2011
$2.1M
Nutriuretic Peptides, the Renin-Angiotensin System, and Metabolic Risk in ObesityR01HL086875 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI WANG, THOMAS J. · 2007 to 2010
$1.7M
SLEEP AND ENTRAINMENT OF SCN FUNCTIONR01HL064278 · NHLBI · CASE WESTERN RESERVE UNIVERSITY · PI STROHL, KINGMAN PERKINS · 1999 to 2002
$871k
ASYMPTOMATIC LEFT VENTRICULAR DYSFUNCTIONK24HL004334 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI RAMACHANDRAN, VASAN S · 2001 to 2008
$707k
THE FRAMINGHAM HEART STUDY-N01HC25195-268025195-268025195N01HC025195 · HC · TRUSTEES OF BOSTON UNIVERSITY · PI WOLF, PHILIP A · 2002 to 2006
–
NHLBI NIH HHS 2K24HL04334NHLBI NIH HHS K24 HL004334NHLBI NIH HHS N01 HC025195NHLBI NIH HHS N01-HC-25195NHLBI NIH HHS N02-HL-6-4278NHLBI NIH HHS R01 HL077447NHLBI NIH HHS R01HL077477NHLBI NIH HHS R01HL080124NHLBI NIH HHS R01-HL-086875NHLBI NIH HHS R01 HL093328NHLBI NIH HHS R01HL093328NIDDK NIH HHS R01 DK080739
6 · The paper itself

Abstract

backgroundThe renin-angiotensin-aldosterone system (RAAS) is critical for regulation of blood pressure and fluid balance and influences cardiovascular remodeling. Dysregulation of the RAAS contributes to cardiovascular and renal morbidity. The genetic architecture of circulating RAAS components is incompletely understood. METHODS AND

resultsWe meta-analyzed genome-wide association data for plasma renin activity (n=5275), plasma renin concentrations (n=8014), and circulating aldosterone (n=13289) from ≤4 population-based cohorts of European and European-American ancestry, and assessed replication of the top results in an independent sample (n=6487). Single-nucleotide polymorphisms (SNPs) in 2 independent loci displayed associations with plasma renin activity at genome-wide significance (P<5×10(-8)). A third locus was close to this threshold (rs4253311 in kallikrein B [KLKB1], P=5.5×10(-8)). Two of these loci replicated in an independent sample for both plasma renin and aldosterone concentrations (SNP rs5030062 in kininogen 1 [KNG1]: P=0.001 for plasma renin, P=0.024 for plasma aldosterone concentration; and rs4253311 with P<0.001 for both plasma renin and aldosterone concentration). SNPs in the NEBL gene reached genome-wide significance for plasma renin concentration in the discovery sample (top SNP rs3915911; P=8.81×10(-9)), but did not replicate (P=0.81). No locus reached genome-wide significance for aldosterone. SNPs rs5030062 and rs4253311 were not related to blood pressure or renal traits; in a companion study, variants in the kallikrein B locus were associated with B-type natriuretic peptide concentrations in blacks.

conclusionsWe identified 2 genetic loci (kininogen 1 and kallikrein B) influencing key components of the RAAS, consistent with the close interrelation between the kallikrein-kinin system and the RAAS.

Indexed as

Cardiovascular DiseasesKidney DiseasesKininogensPolymorphism, Single NucleotidePrekallikreinAldosteroneGenome-Wide Association StudyHumansQuantitative Trait, HeritableReninRenin-Angiotensin SystemAldosteroneKininogensKNG1 protein, humanPrekallikreinReninaldosteronegenome-wide association studyrenin-angiotensin system

Identifiers

PMID25477429
PMCPMC4354880
OpenAlexW2107517347

What Socratic holds

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Read underepoch 390

Registered trials

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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 Socratic graph.