Evidence map›Paper›PMID 35937842›Full record

ArticleFrontiers in endocrinology2022

Characteristic MicroRNAs Linked to Dysregulated Metabolic Pathways in Qatari Adult Subjects With Obesity and Metabolic Syndrome.

Fayaz Ahmad Mir, Raghvendra Mall, Ahmad Iskandarani, Ehsan Ullah, Tareq A Samra, Farhan Cyprian, Aijaz Parray, Meis Alkasem, Ibrahem Abdalhakam, Faisal Farooq and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

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  9. Characterizing Circulating microRNA Signatures of Type 2 Diabetes Subtypes.International journal of molecular sciences · 2025
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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

11 authors at 4 institutions in 2 countries.

Fayaz Ahmad MirQatar Metabolic Institute, Academic Health System, Hamad Medical Corporation, Doha, Qatar.
Raghvendra MallQatar Computing Research Institute (QCRI), Hamad Bin Khalifa University, Doha, Qatar.
Ahmad IskandaraniQatar Metabolic Institute, Academic Health System, Hamad Medical Corporation, Doha, Qatar.
Ehsan UllahQatar Computing Research Institute (QCRI), Hamad Bin Khalifa University, Doha, Qatar.
Tareq A SamraQatar Metabolic Institute, Academic Health System, Hamad Medical Corporation, Doha, Qatar.
Farhan CyprianCollege of Medicine, Qatar University (QU) Health, Qatar University, Doha, Qatar.
Aijaz ParrayQatar Neuroscience Institute, Academic Health System, Hamad Medical Corporation, Doha, Qatar.
Meis AlkasemQatar Metabolic Institute, Academic Health System, Hamad Medical Corporation, Doha, Qatar.
Ibrahem AbdalhakamQatar Metabolic Institute, Academic Health System, Hamad Medical Corporation, Doha, Qatar.
Faisal FarooqQatar Computing Research Institute (QCRI), Hamad Bin Khalifa University, Doha, Qatar.
Abdul-Badi Abou-SamraQatar Metabolic Institute, Academic Health System, Hamad Medical Corporation, Doha, Qatar.
Hamad Medical Corporation · QAHamad bin Khalifa University · QAQatar University · QASt. Jude Children's Research Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Obesity-associated dysglycemia is associated with metabolic disorders. MicroRNAs (miRNAs) are known regulators of metabolic homeostasis. We aimed to assess the relationship of circulating miRNAs with clinical features in obese Qatari individuals. Methods: We analyzed a dataset of 39 age-matched patients that includes 18 subjects with obesity only (OBO) and 21 subjects with obesity and metabolic syndrome (OBM). We measured 754 well-characterized human microRNAs (miRNAs) and identified differentially expressed miRNAs along with their significant associations with clinical markers in these patients. Results: A total of 64 miRNAs were differentially expressed between metabolically healthy obese (OBO) versus metabolically unhealthy obese (OBM) patients. Thirteen out of 64 miRNAs significantly correlated with at least one clinical trait of the metabolic syndrome. Six out of the thirteen demonstrated significant association with HbA1c levels; miR-331-3p, miR-452-3p, and miR-485-5p were over-expressed, whereas miR-153-3p, miR-182-5p, and miR-433-3p were under-expressed in the OBM patients with elevated HbA1c levels. We also identified, miR-106b-3p, miR-652-3p, and miR-93-5p that showed a significant association with creatinine; miR-130b-5p, miR-363-3p, and miR-636 were significantly associated with cholesterol, whereas miR-130a-3p was significantly associated with LDL. Additionally, miR-652-3p's differential expression correlated significantly with HDL and creatinine. Conclusions: MicroRNAs associated with metabolic syndrome in obese subjects may have a pathophysiologic role and can serve as markers for obese individuals predisposed to various metabolic diseases like diabetes.

Indexed as

Metabolic SyndromeMicroRNAsAdultBiomarkersCreatinineGlycated HemoglobinHumansMetabolic Networks and PathwaysObesityBiomarkersCreatinineGlycated HemoglobinMicroRNAsMIRN153 microRNA, humanMIRN363 microRNA, humanMIRN433 microRNA, humanMIRN485 microRNA, humanHbA1cmetabolic disordermirDIPmiRNAnetwork analysisobesity

Identifiers

PMID35937842
PMCPMC9352892
OpenAlexW4286447697

What OpenQuestion holds

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LicenceCC BY
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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.