Evidence map›Paper›PMID 31035988›Full record

ArticleBMC endocrine disorders2019

Can MiR-503 be used as a marker in diabetic patients with ischemic stroke?

Saba Sheikhbahaei, Danesh Manizheh, Saadatnia Mohammad, Tajaddini Mohamad Hasan, Nazemian Saman, Rafiee Laleh, Motieian Mahsa, Amoushahi Khouzani Sanaz, Haghjooy Javanmard Shaghayegh

Open access · goldAbstract read
In one paragraph

Article in BMC endocrine disorders, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 3 pooled it
1.4field-weighted citation impact, top 22% 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

16 citing papers in PubMed, 3 syntheses or guidelines pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. MicroRNAs in diabetic macroangiopathy.Cardiovascular diabetology · 2024
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Sex-Specific MicroRNAs in Neurovascular Units in Ischemic Stroke.International journal of molecular sciences · 2021
    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

9 authors at 2 institutions in 1 country.

Saba SheikhbahaeiAcquired Immunodeficiency Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.ORCID http://orcid.org/0000-0002-0995-2097
Danesh ManizhehStudent Research Committee, Isfahan University of Medical Sciences, Isfahan, Iran.
Saadatnia MohammadIsfahan Neurosciences Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Tajaddini Mohamad HasanApplied Physiology Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Nazemian SamanMashhad University of Medical Sciences, Mashhad, Iran.
Rafiee LalehApplied Physiology Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Motieian MahsaIsfahan University of Medical Sciences, Isfahan, Iran.
Amoushahi Khouzani SanazStudent Research Committee, Isfahan University of Medical Sciences, Isfahan, Iran.
Haghjooy Javanmard ShaghayeghApplied Physiology Research Center, Isfahan University of Medical Sciences, Isfahan, Iran. shaghayegh.haghjoo@gmail.com.
Isfahan University of Medical Sciences · IRMashhad University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSome microRNAs are involved in diabetes pathology and some are known to have role in stroke. MiR-503 causes endothelial dysfunction in diabetic patients, predisposing to ischemia. There has been no study evaluating Mir-503 level in diabetic patients with or without ischemic stroke.

methodsWe designed a cross-sectional study to assess and compare serum level of MiR-503 in 4 groups of diabetic patients with ischemic stroke (I), non-diabetic patients with stroke (II), diabetic patients (III), and healthy controls (IV) in acute phase and 3 months later.

resultsOur data analysis showed that mean relative expression of MiR-503 in group (I) was significantly higher than 3 other groups (p < 0.05). The level of miR-503 was related to the patients' fasting blood glucose, Cholesterol level, NIHSS score and acute-phase modified Rankin Scale (mRS) (r = 0.49, p = 0.001, r = 0.5, p = 0.009, r = 0.45, p = 0.009, r = 0.48, p = 0.003, CI = 95%). Relative expression of miR in patients with mRS ≤ 2 (good outcome) was lower than in patients with mRS > 2 (poor outcome) (p = 0.008). After 3 months, level of miR decreased significantly only in group (I) (p = 0.002). Mean relative expression of miR-503 in chronic phase was not significantly different among groups (p-value> 0.05). There was no relation between miRNA level and mRS in chronic phase.

conclusionHyperglycemia and ischemia together raise the level of MiR-503 acutely but it does not remain at high level after 3 months. Although higher miR was related to more disability in acute phase, it does not affect long-term outcome in ischemic patients. As MiR-503 is stable enough in blood it can be used as a potential diagnostic marker of an ischemic stroke in diabetic patient. Its level also is an indicator of stroke severity and patients' short-term outcome. It is recommended to study whether antagomiR-503 is a new therapeutic agent reducing the severity of and disability due to stroke.

Indexed as

AgedBiomarkersBrain IschemiaCase-Control StudiesCross-Sectional StudiesDiabetes ComplicationsDiabetes MellitusFemaleFollow-Up StudiesHumansMaleMicroRNAsMiddle AgedPrognosisStrokeBiomarkersMicroRNAsMIRN503 microRNA, humanDiabetesHyperglycemiaIschemiaIschemic strokeMicroRNAmiR-503MiRNA

Identifiers

PMID31035988
PMCPMC6489259
OpenAlexW2947050313

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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.