Evidence map›Paper›PMID 31407515›Full record

ArticleMolecular genetics & genomic medicine2019

PPARA genetic variants increase the risk for cardiac pumping function reductions following acute high-altitude exposure: A self-controlled study.

Jie Yang, Chuan Liu, Zhang Jihang, Jie Yu, Limeng Dai, Xiaohan Ding, Youzhu Qiu, Sanjiu Yu, Yuanqi Yang, Yuzhang Wu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics & genomic medicine, 2019. 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 36% 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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 2 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

11 authors at 1 institution in 1 country.

Jie YangDepartment of Cardiology, the Second Affiliated Hospital, Army Medical University (Third Military Medical University), Chongqing, PR China.
Chuan LiuDepartment of Cardiology, the Second Affiliated Hospital, Army Medical University (Third Military Medical University), Chongqing, PR China.
Zhang JihangDepartment of Cardiology, the Second Affiliated Hospital, Army Medical University (Third Military Medical University), Chongqing, PR China.
Jie YuDepartment of Cardiology, the Second Affiliated Hospital, Army Medical University (Third Military Medical University), Chongqing, PR China.
Limeng DaiDepartment of Medical Genetics, College of Basic Medical Science, Army Medical University (Third Military Medical University), Chongqing, PR China.
Xiaohan DingDepartment of Cardiology, the Second Affiliated Hospital, Army Medical University (Third Military Medical University), Chongqing, PR China.
Youzhu QiuDepartment of Cardiology, the Second Affiliated Hospital, Army Medical University (Third Military Medical University), Chongqing, PR China.
Sanjiu YuDepartment of Cardiology, the Second Affiliated Hospital, Army Medical University (Third Military Medical University), Chongqing, PR China.
Yuanqi YangDepartment of Cardiology, the Second Affiliated Hospital, Army Medical University (Third Military Medical University), Chongqing, PR China.
Yuzhang WuInstitute of Immunology, Army Medical University (Third Military Medical University), Chongqing, PR China.
Lan HuangDepartment of Cardiology, the Second Affiliated Hospital, Army Medical University (Third Military Medical University), Chongqing, PR China.ORCID 0000-0002-0616-575X
Army Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLeft cardiac pumping function determines the compensatory capacity of the cardiovascular system following acute high-altitude exposure. Variations in cardiac output (CO) at high altitude are inconsistent between individuals, and genetic susceptibility may play a crucial role. We sought to identify genetic causes of cardiac pumping function variations and describe the genotype-phenotype correlations.

methodsA total of 151 young male volunteers were recruited and transferred to Lhasa (3,700 m) from Chengdu (<500 m) by plane. Genetic information related to hypoxic signaling and cardiovascular-related pathways was collected before departure. Echocardiography was performed both before departure and 24 hr after arrival at high altitude.

resultsHere we reported that PPARA variants were closely related to high-altitude cardiac function. The variants of rs6520015 C-allele and rs7292407 A-allele significantly increased the risk for cardiac pumping function reductions following acute high-altitude exposure. In addition, the individuals carrying haplotypes in PPARA, namely, rs135538 C-allele, rs4253623 A-allele, rs6520015 C-allele and rs7292407 A-allele (C-A-C-A), suffered a 7.27-fold risk for cardiac pumping function reduction (95% CI: 2.39-22.15, p = .0006) compared with those carrying the wild-type haplotype.

conclusionsThis self-controlled study revealed that PPARA variations significantly increased the risk for cardiac pumping function reductions following acute high-altitude exposure, providing a potential predictive marker before high-altitude exposure and targets in mechanistic studies.

Indexed as

AdolescentAdultAllelesAltitude SicknessEchocardiographyGenotypeHaplotypesHumansLinkage DisequilibriumMalePolymorphism, Single NucleotidePPAR alphaProspective StudiesRisk FactorsYoung AdultPPAR alphaPPARA protein, humancardiac functiongenotype-phenotype correlationhaplotypeshigh altitudePPARA

Identifiers

PMID31407515
PMCPMC6785441
OpenAlexW2968060335

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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.