Evidence map›Paper›PMID 31873176›Full record

ArticleScientific reports2019

Associations of ACE I/D polymorphism with the levels of ACE, kallikrein, angiotensin II and interleukin-6 in STEMI patients.

Shuhong Dai, Mei Ding, Na Liang, Zhuo Li, Daqing Li, Lianyue Guan, Hongyu Liu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 48 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

7 authors at 5 institutions in 1 country.

Shuhong DaiDepartment of Cardiology, Zibo Central Hospital, Shandong University, No.54, Gong Qing Tuan Xi Road, Zibo, 255036, Shandong, China.
Mei DingDepartment of Cardiology, China-Japan Union Hospital of Jilin University, Changchun, 130033, Jilin, China.
Na LiangOffice of Surgical Nursing Changchun Medical College, Changchun, Jilin, China.
Zhuo LiDepartment of Emergency, Hospital of Weifang Medical College, Weifang, Shandong, China.
Daqing LiDepartment of Cardiology, Qilu Hospital, Shandong University, Jinan, Shandong, China.
Lianyue GuanDepartment of Hepatobiliary-Pancreatic Surgery, China-Japan Union Hospital of Jilin University, Changchun, 130033, Jilin, China. 13504310464@163.com.
Hongyu LiuDepartment of Hepatobiliary-Pancreatic Surgery, China-Japan Union Hospital of Jilin University, Changchun, 130033, Jilin, China. yuhongliu0101@163.com.
Jilin University · CNQilu Hospital of Shandong University · CNShandong University · CNUnion Hospital · CNWeifang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to compare the plasma levels of angiotensin-I converting enzyme (ACE), Angiotensin II (AngII), kallikrein (KLK1) and interleukin-6 (IL-6) in ST segment elevation myocardial infarction (STEMI) patients with different ACE Insertion/deletion (I/D) polymorphisms in a Chinese population. The ACE genotypes were determined in the 199 STEMI patients and 216 control subjects. STEMI patients were divided into three groups based on the ACE genotypes. Single polymerase chain reaction (PCR) was performed to characterize ACE I/D polymorphisms. Plasma levels of ACE, AngII, KLK1 and IL-6 were measured by enzyme-linked immunosorbent assay (ELISA). We found that the DD or ID genotype was significantly independently associated with high ACE (OR = 4.697; 95% CI = 1.927-11.339), KLK1 (3.339; 1.383-8.063) and IL-6 levels (OR = 2.10; 1.025-4.327) in STEMI patients. However, there was no statistical significance between the ACE I/D polymorphism and AngII plasma levels whether in univariate or multivariate logistic regression. Additionally, we detected a significantly positive correlation between plasma KLK1 levels and IL-6 levels in STEMI patients (r = 0.584, P < 0.001). The study showed high levels of ACE, KLK1 and IL-6 were detected when the D allele was present, but AngII plasma levels was not influenced by the ACE I/D polymorphism.

Indexed as

Genetic Association StudiesPolymorphism, GeneticAngiotensin IIFemaleGenetic Predisposition to DiseaseHumansINDEL MutationInterleukin-6KallikreinsLogistic ModelsMaleMiddle AgedMultivariate AnalysisPeptidyl-Dipeptidase ARisk FactorsST Elevation Myocardial InfarctionAngiotensin IIInterleukin-6KallikreinsPeptidyl-Dipeptidase A

Identifiers

PMID31873176
PMCPMC6927979
OpenAlexW2995586820

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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.