Evidence map›Paper›PMID 24348460›Full record

ArticleFrontiers in endocrinology2013

Endothelin Type A Receptor Genotype is a Determinant of Quantitative Traits of Metabolic Syndrome in Asian Hypertensive Families: A SAPPHIRe Study.

Low-Tone Ho, Yung-Pei Hsu, Chin-Fu Hsiao, Chih-Tai Ting, Kuang-Chung Shih, Lee-Ming Chuang, Kamal Masaki, John Grove, Thomas Quertermous, Chi-Chung Juan and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 84% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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 11 institutions in 2 countries.

Low-Tone HoDepartment of Medical Research and Education, Taipei Veterans General Hospital , Taipei , Taiwan ; School of Medicine, National Yang-Ming University , Taipei , Taiwan ; Faculty of Medicine, National Yang-Ming University , Taipei , Taiwan ; Institute of Physiology, National Yang-Ming University , Taipei , Taiwan ; Institute of Clinical Medicine, National Yang-Ming University , Taipei , Taiwan.
Yung-Pei HsuDepartment of Medical Research and Education, Taipei Veterans General Hospital , Taipei , Taiwan.
Chin-Fu HsiaoDivision of Biostatistics and Bioinformatics, National Health Research Institutes , Taipei , Taiwan.
Chih-Tai TingCardiovascular Center, Taichung Veterans General Hospital , Taichung , Taiwan.
Kuang-Chung ShihDivision of Endocrinology and Metabolism, Tri-Service General Hospital , Taipei , Taiwan.
Lee-Ming ChuangDepartment of Internal Medicine, National Taiwan University Hospital , Taipei , Taiwan ; Graduate Institute of Clinical Medicine, National Taiwan University , Taipei , Taiwan.
Kamal MasakiKuakini Medical Center , Honolulu , Hawaii.
John GroveDepartment of Public Health Sciences and Epidemiology, John A. Burns School of Medicine, University of Hawaii and Pacific Health Research Institute , Honolulu , Hawaii.
Thomas QuertermousDivision of Cardiovascular Medicine, Falk Cardiovascular Research Center, Stanford University , Stanford, CA , USA.
Chi-Chung JuanDepartment of Medical Research and Education, Taipei Veterans General Hospital , Taipei , Taiwan ; Institute of Physiology, National Yang-Ming University , Taipei , Taiwan ; Institute of Clinical Medicine, National Yang-Ming University , Taipei , Taiwan.
Ming-Wei LinDepartment of Medical Research and Education, Taipei Veterans General Hospital , Taipei , Taiwan ; Faculty of Medicine, National Yang-Ming University , Taipei , Taiwan.
Shu-Chiung ChiangInformation Service Center, Taipei Veterans General Hospital , Taipei , Taiwan.
Yii-Der I ChenMedical Genetics Institute, Cedars-Sinai Medical Center, University of California at Los Angeles , Los Angeles, CA , USA.
National Yang Ming Chiao Tung University · TWTaipei Veterans General Hospital · TWKuakini Medical Center · USNational Health Research Institutes · TWNational Taiwan University · TWNational Yang Ming Chiao Tung University · TWStanford University · USTaichung Veterans General Hospital · TWTri-Service General Hospital · TWUniversity of California, Los Angeles · USUniversity of Hawaiʻi at Mānoa · US

Funding

UCLA Clinical and Translational Science InstituteUL1TR000124 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DUBINETT, STEVEN M. · 2012 to 2015
$57.0M
NCATS NIH HHS UL1 TR000124
6 · The paper itself

Abstract

Co-heritability of hypertension and insulin resistance (IR) within families not only implies genetic susceptibility may be responsible for these complex traits but also suggests a rational that biological candidate genes for hypertension may serve as markers for features of the metabolic syndrome (MetS). Thus we determined whether the T323C polymorphism (rs5333) of endothelin type A (ETA) receptor, a predominant receptor evoking potent vasoconstrictive action of endothelin-1, contributes to susceptibility to IR-associated hypertension in 1694 subjects of Chinese and Japanese origins. Blood pressures (BPs) and biochemistries were measured. Fasting insulin level, insulin-resistance homeostasis model assessment (HOMAIR) score, and area under curve of insulin concentration (AUCINS) were selected for assessing insulin sensitivity. Genotypes were obtained by methods of polymerase chain reaction-restriction fragment length polymorphism. Foremost findings were that minor allele frequency of the T323C polymorphism was noticeable lower in our overall Asian subjects compared to multi-national population reported in gene database; moreover both the genotypic and allelic frequencies of the polymorphism were significantly different between the two ethnic groups we studied. The genotype distributions at TT/TC/CC were 65, 31, 4% in Chinese and 51, 41, 8% in Japanese, respectively (p < 0.0001). Additionally, carriers of the C homozygote revealed characteristics of IR, namely significantly higher levels of fasting insulin, HOMAIR score, and AUCINS at 29.3, 35.3, and 39.3%, respectively, when compared to their counterparts with TT/TC genotypes in Chinese. Meanwhile, the CC genotype was associated with a higher level of high density lipoprotein cholesterol in Japanese. No association of the polymorphism with BP was observed. This study demonstrated for the first time that T323C polymorphism of ETA receptor gene was associated with an adverse insulin response in Chinese and a favorite atherogenic index in Japanese.

Indexed as

ETA receptorhypertensionmetabolic syndromeT323C polymorphism

Identifiers

PMID24348460
PMCPMC3842518
OpenAlexW2148908324

What OpenQuestion holds

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LicenceCC BY
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 OpenQuestion graph.