Evidence map›Paper›PMID 33382484›Full record

ArticleJournal of clinical laboratory analysis2021

A comprehensive association analysis between homocysteine metabolic pathway gene methylation and ischemic stroke in a Chinese hypertensive population.

Bo Li, Yuying Li, Shan Xu, Hongen Chen, Shudong Dai, Xiaoling Peng, Li Wang, Yaping Liang, Cheng Li, Biwei Tang and 5 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

5 citing papers in PubMed, 10 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

15 authors at 3 institutions in 1 country.

Bo LiShenzhen Nanshan Center for Chronic Disease Control, Shenzhen, China.
Yuying LiShenzhen Polytechnic, Shenzhen, China.
Shan XuShenzhen Nanshan Center for Chronic Disease Control, Shenzhen, China.
Hongen ChenShenzhen Nanshan Center for Chronic Disease Control, Shenzhen, China.
Shudong DaiShenzhen Nanshan Center for Chronic Disease Control, Shenzhen, China.
Xiaoling PengShenzhen Nanshan Center for Chronic Disease Control, Shenzhen, China.
Li WangShenzhen Nanshan Center for Chronic Disease Control, Shenzhen, China.
Yaping LiangShenzhen Nanshan Center for Chronic Disease Control, Shenzhen, China.
Cheng LiShenzhen Nanshan Center for Chronic Disease Control, Shenzhen, China.
Biwei TangShenzhen Nanshan Center for Chronic Disease Control, Shenzhen, China.
Liqing ZhuShenzhen Nanshan Center for Chronic Disease Control, Shenzhen, China.
Tao ZhangShenzhen Nanshan Center for Chronic Disease Control, Shenzhen, China.
Chunfang LvShenzhen Nanshan Center for Chronic Disease Control, Shenzhen, China.
Changyi WangShenzhen Nanshan Center for Chronic Disease Control, Shenzhen, China.
Liyuan HanHwa Mei Hospital, University of Chinese Academy of Sciences, Ningbo, China.ORCID https://orcid.org/0000-0002-3329-3212
Shenzhen Nanshan Center for Chronic Disease Control · CNShenzhen Polytechnic University · CNUniversity of Chinese Academy of Sciences · CN

Funding

Guangdong Medical Science and Technology Research Foundation A2019421Nanshan Health Science and Technology Plan 2019011Nanshan Health Science and Technology Plan 2019067Nanshan Health Science and Technology Plan 2020008National Natural Science Foundation of China 81803316Ningbo Health Branding Subject Fund PPXK2018-02Ningbo Science and Technology Project 202002N3152SanMing Project of Medicine in Shenzhen SZSM201803080The Characteristic Innovation Program (Natural Science) of Guangdong Education Department 2018GKTSCX077the Innovative Talent Support Plan of the Medical and Health Technology Project in Zhejiang Province 2021422878
6 · The paper itself

Abstract

backgroundIschemic stroke (IS) is a serious global health burden. In order to improve our understanding of the risk factors associated with IS, we investigated the combined effect of the methylation of five genes related to the metabolism of homocysteine on developing IS.

methodsQuantitative methylation-specific PCR was used to measure the levels of promoter methylation in hypertensive and stroke patients. The cutoff value calculated by the maximum Youden index was used to classify the levels of gene methylation as hypomethylation and hypermethylation. Logistic regression was used to explore the relationship between gene methylation and IS.

resultsThe methylation levels of the genes encoding methylenetetrahydrofolate dehydrogenase 1 [MTHFD1], cystathionine β-synthase [CBS], and dihydrofolate reductase [DHFR] in hypertensive patients were higher than those in stroke patients (all p < 0.01). MTHFD1 hypermethylation, CBS hypermethylation, and DHFR hypermethylation were protective factors for stroke after adjustment for confounding factors. Compared with individuals carrying none of the biomarkers, the ORs [95% CIs] for stroke of those with 1 and 2 elevated biomarkers were 4.068 [1.670-9.913] and 15.345 [6.198-37.994] after adjustment for confounding factors. The participants with a larger number of biomarkers had an increased risk of stroke (p for trend <0.001). For the combination biomarkers, the area under the curve of the receiver operating characteristic was 0.716.

conclusionA significant linear relationship between the number of elevated biomarkers and the risk of stroke has been observed, suggesting that elevations of these biomarkers could be used for potentially predicting the disease.

Indexed as

DNA MethylationAdenosylhomocysteinaseAgedAsian PeopleCase-Control StudiesCross-Sectional StudiesCystathionine beta-SynthaseFemaleGlycine HydroxymethyltransferaseHomocysteineHumansHypertensionIschemic StrokeMaleMethylenetetrahydrofolate Dehydrogenase (NADP)Middle AgedAdenosylhomocysteinaseAHCY protein, humanCystathionine beta-SynthaseGlycine HydroxymethyltransferaseHomocysteineMethylenetetrahydrofolate Dehydrogenase (NADP)Minor Histocompatibility AntigensMTHFD1 protein, humanSHMT protein, humanTetrahydrofolate DehydrogenaseassociationDNA methylationhyperhomocysteinehypertensionischemic stroke

Identifiers

PMID33382484
PMCPMC7957978
OpenAlexW3113475372

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.