Evidence map›Paper›PMID 35892612›Full record

ArticleChildren (Basel, Switzerland)2022

MicroRNA-126-3p/5p and Aortic Stiffness in Patients with Turner Syndrome.

Masood Abu-Halima, Felix Sebastian Oberhoffer, Viktoria Wagner, Mohamed Abd El Rahman, Anna-Maria Jung, Michael Zemlin, Tilman R Rohrer, Eckart Meese, Hashim Abdul-Khaliq

Open access · goldAbstract read
In one paragraph

Article in Children (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 30% 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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 9 citations in OpenAlex.

  1. Guideline
  2. Non-coding rnas in Turner syndrome: a systematic review.Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo · 2024
    Pooled it
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
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.

Masood Abu-HalimaInstitute of Human Genetics, Saarland University, 66421 Homburg, Germany.ORCID 0000-0001-9048-4958
Felix Sebastian OberhofferDepartment of Pediatric Cardiology, Saarland University Hospital, 66421 Homburg, Germany.
Viktoria WagnerInstitute of Human Genetics, Saarland University, 66421 Homburg, Germany.ORCID 0000-0002-1957-0658
Mohamed Abd El RahmanDepartment of Pediatric Cardiology, Saarland University Hospital, 66421 Homburg, Germany.
Anna-Maria JungDepartment of General Pediatrics and Neonatology, Saarland University Hospital, 66421 Homburg, Germany.
Michael ZemlinDepartment of General Pediatrics and Neonatology, Saarland University Hospital, 66421 Homburg, Germany.ORCID 0000-0001-9528-7419
Tilman R RohrerDepartment of General Pediatrics and Neonatology, Saarland University Hospital, 66421 Homburg, Germany.
Eckart MeeseInstitute of Human Genetics, Saarland University, 66421 Homburg, Germany.
Hashim Abdul-KhaliqDepartment of Pediatric Cardiology, Saarland University Hospital, 66421 Homburg, Germany.
Saarland University · DELMU Klinikum · DE

Funding

Hedwig-Stalter-Foundation
6 · The paper itself

Abstract

Background: Turner Syndrome (TS) is a relatively rare X-chromosomal disease with increased cardiovascular morbidity and mortality. This study aimed to identify whether the circulating miR-126-3p/5p are involved in the pathophysiology of vascular dysfunction in TS. Methods: Using the RT-qPCR, the abundance levels of miR-126-3p and miR-126-5p were determined in 33 TS patients and 33 age-matched healthy volunteers (HVs). Vascular screening, including the assessment of blood pressure, pulse wave velocity, augmentation index, aortic deformation, arterial distensibility, and arterial elastance, was conducted in TS patients and HVs. Results: The abundance levels of miR-126-3p and miR-126-5p were significantly higher in TS patients compared to HVs (p < 0.0001). Within the TS cohort, miR-126-3p/5p correlated significantly with aortic deformation (r = 0.47, p = 0.01; r = 0.48, p < 0.01) and arterial distensibility (r = 0.55, p < 0.01; r = 0.48, p < 0.01). In addition, a significant negative correlation was demonstrated between miR-126-3p and arterial elastance (r = −0.48, p = 0.01). The receiver operating characteristic analysis showed that miR-126-3p and miR-126-5p separated the tested groups with high sensitivity and specificity. Conclusions: The abundance levels of miR-126-3p and miR-126-5p were significantly higher in TS patients compared to HVs. Within the TS cohort, a lower abundance level of miR-126-3p and miR-126-5p was linked with a significantly higher aortic stiffness.

Indexed as

MicroRNAsTurner Syndromevascular dysfunction

Identifiers

PMID35892612
PMCPMC9394385
OpenAlexW4287009922

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.