Evidence map›Paper›PMID 34104831›Full record

ArticleJournal of clinical and translational research2021

Plasma circulating microRNAs in patients with stable coronary artery disease - Impact of different cardiovascular risk profiles and glomerular filtration rates.

Karlis Trusinskis, Maris Lapsovs, Sandra Paeglite, Evija Knoka, Laima Caunite, Mairita Mazule, Ieva Briede, Sanda Jegere, Indulis Kumsars, Inga Narbute and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Journal of clinical and translational research, 2021. 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
0.4field-weighted citation impact, top 47% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
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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

13 authors at 1 institution in 1 country.

Karlis TrusinskisLatvian Centre of Cardiology, Pauls Stradins Clinical University Hospital, Riga, LV-1002, Latvia.
Maris LapsovsDepartment of Internal Diseases, Riga Stradins University, Riga, LV-1007, Latvia.
Sandra PaegliteDepartment of Internal Diseases, Riga Stradins University, Riga, LV-1007, Latvia.
Evija KnokaLatvian Centre of Cardiology, Pauls Stradins Clinical University Hospital, Riga, LV-1002, Latvia.
Laima CauniteLatvian Centre of Cardiology, Pauls Stradins Clinical University Hospital, Riga, LV-1002, Latvia.
Mairita MazuleDepartment of Internal Diseases, Riga Stradins University, Riga, LV-1007, Latvia.
Ieva BriedeLatvian Centre of Cardiology, Pauls Stradins Clinical University Hospital, Riga, LV-1002, Latvia.
Sanda JegereLatvian Centre of Cardiology, Pauls Stradins Clinical University Hospital, Riga, LV-1002, Latvia.
Indulis KumsarsLatvian Centre of Cardiology, Pauls Stradins Clinical University Hospital, Riga, LV-1002, Latvia.
Inga NarbuteLatvian Centre of Cardiology, Pauls Stradins Clinical University Hospital, Riga, LV-1002, Latvia.
Ilze KonradeDepartment of Endocrinology and Internal Medicine, Riga East Clinical University Hospital, Riga, LV-1038, Latvia.
Andrejs ErglisLatvian Centre of Cardiology, Pauls Stradins Clinical University Hospital, Riga, LV-1002, Latvia.
Aivars LejnieksDepartment of Internal Diseases, Riga Stradins University, Riga, LV-1007, Latvia.
Riga East University Hospital · LV

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimPlasma circulating microRNA (miRNA)-126, -145, and -155 are associated with vascular remodeling, atherosclerotic lesion formation, and plaque vulnerability. In this study, we evaluated the levels of plasma circulating miRNAs in patients with stable coronary artery disease (CAD), different cardiovascular risk profiles, and different glomerular filtration rates (GFR). METHODS AND

resultsForty patients with stable CAD admitted for elective percutaneous coronary intervention (PCI) were enrolled in a prospective study. Before PCI, fasting blood samples were obtained to evaluate clinical parameters and miRNA-126 and miRNA-155 expression. The GFR was calculated by the MDRD and CKD-EPI formulas, and the severity of CAD was calculated according to the SYNTAX score. All these parameters were correlated with miRNAs. The association between miRNA levels and clinical characteristics was evaluated. The expression of miRNA-126 positively correlated with a higher SYNTAX score (r = 0.337; p=0.034); however, no significant correlations between miR-126, GFR, and clinical characteristics were observed. Higher plasma levels of miRNA-155 correlated with increased levels of triglycerides (r = 0.317; P = 0.049), C-peptide (r = 0.452; P = 0.011), and the HOMA index (r = 0.447; P = 0.012) and a higher body mass index (BMI) (r = 0.385; P = 0.015). GFR and miRNA-155 (MDRD - Rho=0.353; P = 0.027. CKD-EPI - Rho=0.357; P = 0.026) were found to have a moderate correlation, although miRNA-155 had no correlation with the SYNTAX score.

conclusionPlasma circulating miRNA-126 levels were increased in patients with severe atherosclerosis as determined by the SYNTAX score. Elevated miRNA-155 expression was observed in patients with Stage 1 GFR but was lower in patients with Stages 2 and 3 GFR. Plasma circulating miRNA-155 had positive correlations with higher levels of BMI, HOMA index, C-peptide, and triglycerides. RELEVANCE FOR PATIENTS: Although further investigations are needed to confirm the role of miRNA-155 and miRNA-126, they may serve as potential biomarkers detecting severity of CAD, lowering of kidney function and metabolic syndrome.

Indexed as

coronary artery diseasemicroRNA-126microRNA-145microRNA-155SYNTAX score

Identifiers

PMID34104831
PMCPMC8177841
OpenAlexW3173135019

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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.