Evidence map›Paper›PMID 25615575›Full record

ArticlePloS one2015

A functional 12T-insertion polymorphism in the ATP1A1 promoter confers decreased susceptibility to hypertension in a male Sardinian population.

Victoria L Herrera, Khristine A Pasion, Ann Marie Moran, Roberta Zaninello, Maria Francesca Ortu, Giovanni Fresu, Daniela Antonella Piras, Giuseppe Argiolas, Chiara Troffa, Valeria Glorioso and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 42% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. A Single Nucleotide Polymorphism inCirculation research · 2022
    Article
  3. Article
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

13 authors at 2 institutions in 2 countries.

Victoria L HerreraWhitaker Cardiovascular Institute, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, United States of America.
Khristine A PasionWhitaker Cardiovascular Institute, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, United States of America.
Ann Marie MoranWhitaker Cardiovascular Institute, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, United States of America.
Roberta ZaninelloHypertension and Related Diseases Center, AOU-Universita' di Sassari, Sassari, Sardinia, Italy.
Maria Francesca OrtuHypertension and Related Diseases Center, AOU-Universita' di Sassari, Sassari, Sardinia, Italy.
Giovanni FresuHypertension and Related Diseases Center, AOU-Universita' di Sassari, Sassari, Sardinia, Italy.
Daniela Antonella PirasHypertension and Related Diseases Center, AOU-Universita' di Sassari, Sassari, Sardinia, Italy.
Giuseppe ArgiolasHypertension and Related Diseases Center, AOU-Universita' di Sassari, Sassari, Sardinia, Italy.
Chiara TroffaHypertension and Related Diseases Center, AOU-Universita' di Sassari, Sassari, Sardinia, Italy.
Valeria GloriosoHypertension and Related Diseases Center, AOU-Universita' di Sassari, Sassari, Sardinia, Italy.
Wanda MasalaHypertension and Related Diseases Center, AOU-Universita' di Sassari, Sassari, Sardinia, Italy.
Nicola GloriosoHypertension and Related Diseases Center, AOU-Universita' di Sassari, Sassari, Sardinia, Italy.
Nelson Ruiz-OpazoWhitaker Cardiovascular Institute, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, United States of America.
University of Sassari · ITBoston University · US

Funding

Functional characterization of ATP1A1 and DEspR variants associated with essentiaR21HL098939 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI RUIZ-OPAZO, NELSON · 2009 to 2010
$772k
NHLBI NIH HHS HL098939NHLBI NIH HHS R21 HL098939
6 · The paper itself

Abstract

Identification of susceptibility genes for essential hypertension in humans has been a challenge due to its multifactorial pathogenesis complicated by gene-gene and gene-environment interactions, developmental programing and sex specific differences. These concurrent features make identification of causal hypertension susceptibility genes with a single approach difficult, thus requiring multiple lines of evidence involving genetic, biochemical and biological experimentation to establish causal functional mutations. Here we report experimental evidence encompassing genetic, biochemical and in vivo modeling that altogether support ATP1A1 as a hypertension susceptibility gene in males in Sardinia, Italy. ATP1A1 encodes the α1Na,K-ATPase isoform, the sole sodium pump in vascular endothelial and renal tubular epithelial cells. DNA-sequencing detected a 12-nucleotide long thymidine (12T) insertion(ins)/deletion(del) polymorphism within a poly-T sequence (38T vs 26T) in the ATP1A1 5'-regulatory region associated with hypertension in a male Sardinian population. The 12T-insertion allele confers decreased susceptibility to hypertension (P = 0.035; OR = 0.50 [0.28-0.93]) accounting for 12.1 mmHg decrease in systolic BP (P = 0.02) and 6.6 mmHg in diastolic BP (P = 0.046). The ATP1A1 promoter containing the 12T-insertion exhibited decreased transcriptional activity in in vitro reporter-assay systems, indicating decreased α1Na,K-ATPase expression with the 12T-insertion, compared with the 12T-deletion ATP1A1 promoter. To test the effects of decreased α1Na,K-ATPase expression on blood pressure, we measured blood pressure by radiotelemetry in three month-old, highly inbred heterozygous knockout ATP1A1+/- male mice with resultant 58% reduction in ATP1A1 protein levels. Male ATP1A1+/- mice showed significantly lower blood pressure (P < 0.03) than age-matched male wild-type littermate controls. Concordantly, lower ATP1A1 expression is expected to lower Na-reabsorption in the kidney thereby decreasing sodium-associated risk for hypertension and sodium-induced endothelial stiffness and dysfunction. Altogether, data support ATP1A1 as a hypertension susceptibility gene in a male Sardinian population, and mandate further investigation of its involvement in hypertension in the general population.

Indexed as

INDEL MutationAdultAgedAnimalsDisease Models, AnimalEssential HypertensionGenetic Predisposition to DiseaseHumansHypertensionItalyMaleMiceMiddle AgedPromoter Regions, GeneticSequence Analysis, DNASex FactorsATP1A1 protein, humanSodium-Potassium-Exchanging ATPaseThymidine

Identifiers

PMID25615575
PMCPMC4304799
OpenAlexW2021010770

What OpenQuestion holds

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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 OpenQuestion graph.