Evidence map›Paper›PMID 32034489›Full record

ArticleHeart and vessels2020

Association of combined genetic variations in SOD3, GPX3, PON1, and GSTT1 with hypertension and severity of coronary artery disease.

Nisa Decharatchakul, Chatri Settasatian, Nongnuch Settasatian, Nantarat Komanasin, Upa Kukongviriyapan, Pongsak Intharapetch, Vichai Senthong, Kittisak Sawanyawisuth

Abstract read
PubMed Publisher
In one paragraph

Article in Heart and vessels, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 3 pooled it
3.0field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 3 syntheses or guidelines pooled it, 31 citations in OpenAlex.

  1. Serum Malondialdehyde Levels in Hypertensive Patients: A Non-invasive Marker of Oxidative Stress. A Systematic Review and Meta-analysis.High blood pressure & cardiovascular prevention : the official journal of the Italian Society of Hypertension · 2022
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  16. Paraoxonase Role in Human Neurodegenerative Diseases.Antioxidants (Basel, Switzerland) · 2020
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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

8 authors at 1 institution in 1 country.

Nisa DecharatchakulBiomedical Sciences Program, Graduate School, Khon Kaen University, Khon Kaen, 40002, Thailand.
Chatri SettasatianDepartment of Pathology, Faculty of Medicine, Khon Kaen University, Khon Kaen, 40002, Thailand. schatr@kku.ac.th.
Nongnuch SettasatianSchool of Medical Technology, Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, 40002, Thailand.
Nantarat KomanasinSchool of Medical Technology, Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, 40002, Thailand.
Upa KukongviriyapanDepartment of Physiology, Faculty of Medicine, Khon Kaen University, Khon Kaen, 40002, Thailand.
Pongsak IntharapetchQueen Sirikit Heart Center of the Northeast, Khon Kaen University, Khon Kaen, 40002, Thailand.
Vichai SenthongDepartment of Medicine, Faculty of Medicine, Khon Kaen University, Khon Kaen, 40002, Thailand.
Kittisak SawanyawisuthDepartment of Medicine, Faculty of Medicine, Khon Kaen University, Khon Kaen, 40002, Thailand.
Khon Kaen University · TH

Funding

Graduate School, Khon Kaen University (TH) 57212108National Research Council of Thailand 555854
6 · The paper itself

Abstract

Oxidative stress plays a critical role in the pathophysiology of hypertension (HT) and the progression of atherosclerotic coronary artery disease (CAD). Genetic variations in superoxide dismutase (SOD), glutathione peroxidase 3 (GPX3), paraoxonase 1 (PON1) and glutathione S-transferase theta 1 (GSTT1) may modulate their gene functions, affecting protein functions. These changes could have an impact on the pathogenesis of HT and progression of CAD. The present study investigated the associations of individual and combined antioxidant-related gene polymorphisms with the incidence of HT and severity of CAD. Two study populations were enrolled. The HT-associated study comprised 735 control and 735 hypertensive subjects (mean age 59.3 ± 9.0 years), matched for age and sex. The CAD study, hospital-based subjects (mean age 62.1 ± 9.5 years), included 279 CAD patients and 165 non-CAD subjects. Gene polymorphisms were identified in genomic DNA using polymerase chain reaction (PCR)-based technique. Genetic variations were assessed for their associations with HT and severity of CAD. Antioxidant gene variants, SOD3 rs2536512-GG, GPX3 rs3828599-GG, PON1 rs705379-TT, and GSTT1

Indexed as

Polymorphism, GeneticAdultAgedAged, 80 and overAryldialkylphosphataseCoronary Artery DiseaseFemaleGenetic Association StudiesGenetic Predisposition to DiseaseGlutathione PeroxidaseGlutathione TransferaseHeart Disease Risk FactorsHumansHypertensionIncidenceLipid PeroxidationAryldialkylphosphataseGlutathione Peroxidaseglutathione S-transferase T1Glutathione TransferaseGPX3 protein, humanPON1 protein, humanSOD3 protein, humanSuperoxide DismutaseGenetic risk scoreGlutathione peroxidaseGlutathione S-transferaseOxidative stressParaoxonaseSuperoxide dismutase

Identifiers

PMID32034489
OpenAlexW3004958741

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.