Evidence map›Paper›PMID 19996987›Full record

ArticleJournal of hypertension2010

Blood pressure response to potassium supplementation is associated with genetic variation in endothelin 1 and interactions with E selectin in rural Chinese.

May E Montasser, Lawrence C Shimmin, Donfeng Gu, Jing Chen, Charles Gu, Tanika N Kelly, Cashell E Jaquish, Treva Rice, D C Rao, Jie Cao and 5 more

Open access · greenAbstract read
In one paragraph

Article in Journal of hypertension, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. Potassium and Its Discontents: New Insight, New Treatments.Journal of the American Society of Nephrology : JASN · 2016
    Review
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 7 institutions in 3 countries.

May E MontasserHuman Genetics Center, School of Public Health, University of Texas Health Science Center at Houston, Houston, Texas 77030, USA.
Lawrence C Shimmin
Donfeng Gu
Jing Chen
Charles Gu
Tanika N Kelly
Cashell E Jaquish
Treva Rice
D C Rao
Jie Cao
Jichun Chen
De-Pei Liu
Paul Whelton
Jiang He
James E Hixson
Tulane University · USThe University of Texas Health Science Center at Houston · USWashington University in St. Louis · USAcademy of Medical Sciences · GBChinese Academy of Medical Sciences & Peking Union Medical College · CNLoyola University Chicago · USNational Institutes of Health · US

Funding

Genetic Epidemiology of Blood Pressure InterventionU01HL072507 · NHLBI · TULANE UNIVERSITY OF LOUISIANA · PI HE, JIANG · 2002 to 2008
$7.6M
Family-Based Genome-wide Association Study for Salt-Sensitivity of Blood PressureR01HL090682 · NHLBI · TULANE UNIVERSITY OF LOUISIANA · PI HE, JIANG · 2008 to 2011
$2.8M
NHLBI NIH HHS R01 HL090682NHLBI NIH HHS U01 HL072507NHLBI NIH HHS U01HL072507
6 · The paper itself

Abstract

objectiveAlthough beneficial effects of potassium intake on blood pressure (BP) are well established, little is known about genetic factors that underlie interindividual variability in BP response to dietary potassium. In a previous study, we reported the first evidence for significant heritabilities for BP response in a dietary intervention study in rural Chinese. In this report, we extend our genetic studies to examine associations with polymorphisms in genes in vascular endothelial pathways.

methodsWe genotyped study participants for 23 single nucleotide polymorphisms (SNPs) in endothelin 1 (EDN1), nitric oxide synthase 3, and E selectin (SELE). We tested 17 of these SNPs for associations with BP response to potassium supplementation in 1843 participants. Association tests used population-based [generalized estimation equation (GEE)] and family-based (quantitative transmission disequilibrium test) methods, as well as tests for gene-by-gene (GxG) interaction (generalized multifactor dimensionalilty reduction and GEE).

resultsSingle SNP analysis identified significant associations for several SNPs in EDN1 with multiple measures of BP response to potassium supplementation. The cumulative effects of the minor EDN1 alleles that showed significant associations were to reduce measures of BP response by 0.5-0.9 mmHg. We found significant evidence for effects of GxG interactions between EDN1 and SELE, even in the absence of individual associations with SELE variants.

conclusionOur results implicate variability in EDN1 and SELE as genetic factors that influence BP response to potassium intake. Although such epidemiological studies do not allow direct determination of physiologic mechanisms, our findings of joint effects identify EDN1 and SELE as targets for functional studies to determine their interactions in BP response to potassium intake.

Indexed as

Genetic VariationAdultAllelesAsian PeopleBlood PressureChinaEndothelin-1Epidemiologic StudiesE-SelectinFemaleGenotypeHumansMaleNitric Oxide Synthase Type IIIPolymorphism, Single NucleotidePotassium, DietaryEndothelin-1E-SelectinNitric Oxide Synthase Type IIINOS3 protein, humanPotassium, Dietary

Identifiers

PMID19996987
PMCPMC2919321
OpenAlexW2073856713

What OpenQuestion holds

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Registered trials

None linked

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.