Evidence map›Paper›PMID 41975450›Full record

ArticleNutrition & metabolism2026

Negative correlation between microRNA and insulin sensitivity gene expression in adipose tissue: potential implications for diabetes and neurodegenerative diseases.

Jakub Podraza, Michał Wąsowski, Marta Izabela Jonas, Wojciech Lisik, Maurycy Jonas, Artur Binda, Paweł Jaworski, Wiesław Tarnowski, Bartłomiej Noszczyk, Monika Puzianowska-Kuźnicka and 1 more

Abstract read
In one paragraph

Article in Nutrition & metabolism, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

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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

1 citing paper in PubMed.

  1. 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

11 authors.

Jakub PodrazaThe Faculty of Biology and Biotechnology, Warsaw University of Life Sciences, Warsaw, 02-787, Poland.
Michał WąsowskiMedical Centre of Postgraduate Education, Department of General Medicine and Geriatric Cardiology, Warsaw, 00-401, Poland.
Marta Izabela JonasMossakowski Medical Research Centre, Department of Human Epigenetics, Polish Academy of Sciences, Warsaw, 02-106, Poland.
Wojciech LisikDepartment of General and Transplantation Surgery, The Medical University of Warsaw, Warsaw, 00-694, Poland.
Maurycy JonasDepartment of General and Transplantation Surgery, The Medical University of Warsaw, Warsaw, 00-694, Poland.
Artur BindaMedical Centre of Postgraduate Education, Department of General, Oncological and Bariatric Surgery, Warsaw, 00-401, Poland.
Paweł JaworskiMedical Centre of Postgraduate Education, Department of General, Oncological and Bariatric Surgery, Warsaw, 00-401, Poland.
Wiesław TarnowskiMedical Centre of Postgraduate Education, Department of General, Oncological and Bariatric Surgery, Warsaw, 00-401, Poland.
Bartłomiej NoszczykMedical Centre of Postgraduate Education, Department of Plastic Surgery, Warsaw, 00-401, Poland.
Monika Puzianowska-KuźnickaMossakowski Medical Research Centre, Department of Human Epigenetics, Polish Academy of Sciences, Warsaw, 02-106, Poland.
Alina KuryłowiczMedical Centre of Postgraduate Education, Department of General Medicine and Geriatric Cardiology, Warsaw, 00-401, Poland. akurylowicz@imdik.pan.pl.ORCID http://orcid.org/0000-0001-8632-4927

Funding

National Science Centre, Poland 2018/31/B/NZ5/01556
6 · The paper itself

Abstract

backgroundObesity-related adipose tissue dysfunction leads to a chronic inflammatory state affecting distant organs and tissues. This metabolic inflammation has a detrimental impact on the expression of genes related to glucose metabolism, leading to systemic insulin resistance, which also affects the central nervous system and contributes to cognitive decline. Adipose tissue-derived microRNAs (miRNAs) have been implicated in this phenomenon. This study aimed to investigate whether the expression of genes critical for both insulin action and neuronal metabolism (APP, SOCS3, PTPN1, PTPN2) is altered in the adipose tissue of patients with obesity due to miRNA interference, predisposing them directly to the development of insulin resistance and metabolic inflammation, while indirectly leading to a decline in cognitive function.

methodsThe expression of mRNAs of the above-mentioned genes, selected adipokines (interleukins 1β, 6, 8, 15, tumor necrosis factor-alpha, resistin, adiponectin) and miRNAs was measured by real-time PCR in adipose tissue of 75 patients with obesity, 19 patients who successfully reduced body mass after metabolic surgery and 25 normal weight subjects, stratified by insulin sensitivity and diabetic status. The results were correlated with patients' clinical and biochemical parameters.

resultsmRNA levels of genes promoting insulin sensitivity, APP and PTPN2, were significantly (p < 0.05) decreased in adipose tissue from patients with obesity, in both visceral (VAT) and subcutaneous (SAT) depots. After stratification by the triglyceride/high-density lipoprotein ratio (an indirect marker of insulin sensitivity), we found that individuals diagnosed with insulin resistance had lower VAT and SAT APP and PTPN2 mRNA levels, whereas APP expression was significantly decreased in VAT from patients with both obesity and type 2 diabetes compared to normoglycemic individuals with obesity, too. We also observed significant positive correlations between the mRNA levels of these genes and the expression of the above-mentioned adipokines. Finally, we analysed the levels of miRNAs targeting the mRNAs of the genes studied and observed significant negative correlations between APP mRNA levels and hsa-miR-579-5p and hsa-miR-142-3p, and between PTPN2 mRNA levels and hsa-miR-142-3p.

conclusionAdipose tissues of patients with obesity are characterised by altered expression of genes that are key for both insulin action and neuronal metabolism, and miRNAs may be involved in this phenomenon. However, due to the descriptive nature of our experiments, these results require verification in functional studies.

Indexed as

AdipokinesAdipose tissueInsulin resistanceInsulin sensitivityMetabolic inflammationMicroRNAObesity

Identifiers

PMID41975450
PMCPMC13185245

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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.