Evidence map›Paper›PMID 38902687›Full record

ArticleCardiovascular diabetology2024

Cholesin receptor signalling is active in cardiovascular system-associated adipose tissue and correlates with SGLT2i treatment in patients with diabetes.

Aleksandra Ryk, Anna Marcinkiewicz, Jędrzej Chrzanowski, Arkadiusz Mariusz Michalak, Izabela Dróżdz, Jacek Burzyński, Michał Krejca, Wojciech Fendler

Abstract read
In one paragraph

Article in Cardiovascular diabetology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

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.

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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

8 authors.

Aleksandra RykDepartment of Biostatistics and Translational Medicine, Medical University of Lodz, Mazowiecka 15, 92-215, Lodz, Poland.ORCID 0000-0002-6146-2888
Anna MarcinkiewiczDepartment of Cardiac Surgery, Medical University of Lodz, Lodz, Poland.ORCID 0000-0003-4494-3724
Jędrzej ChrzanowskiDepartment of Biostatistics and Translational Medicine, Medical University of Lodz, Mazowiecka 15, 92-215, Lodz, Poland.ORCID 0000-0001-6204-8622
Arkadiusz Mariusz MichalakDepartment of Biostatistics and Translational Medicine, Medical University of Lodz, Mazowiecka 15, 92-215, Lodz, Poland.ORCID 0000-0002-6088-9636
Izabela DróżdzDepartment of Clinical Genetics, Medical University of Lodz, Lodz, Poland.ORCID 0000-0003-1956-5063
Jacek BurzyńskiDepartment of Biostatistics and Translational Medicine, Medical University of Lodz, Mazowiecka 15, 92-215, Lodz, Poland.
Michał KrejcaDepartment of Cardiac Surgery, Medical University of Lodz, Lodz, Poland.ORCID 0000-0002-6812-6027
Wojciech FendlerDepartment of Biostatistics and Translational Medicine, Medical University of Lodz, Mazowiecka 15, 92-215, Lodz, Poland. wojciech.fendler@umed.lodz.pl.ORCID 0000-0002-5083-9168

Funding

Minister of Education and Science program "Perły Nauki" PN/01/0025/2022National Science Center, Poland 2022/45/N/NZ4/01206
6 · The paper itself

Abstract

backgroundRecently deorphanized G protein-coupled receptor 146 (GPR146) was shown to respond to signal from a newly identified hormone-cholesin-and to play a role in hepatic lipid metabolism. However, the importance of its biological activity in human organism remains elusive, mainly due to the lack of studies on human tissues up to this point. This study aimed to identify the cholesin receptor-associated genes and clinical factors linked with their expression in cardiovascular system and associated adipose tissues.

methodsRight cardiac auricle, aortic wall, saphenous vein, and adipose tissue (periaortic-PAT, epicardial-EAT, thymic-TAT) samples were collected during coronary artery bypass grafting. Clinical records of the study participants were assessed for the presence of diabetes, medications taken and serum cholesterol levels. GPR146 mRNA expression in all gathered tissues was assessed with qPCR, and RNA seqencing was performed in selected tissues of 20 individuals to identify pathways associated with GPR146 expression.

resultsWe included 46 participants [37 male, 23 with type 2 diabetes, median age 68.50 (Q1-Q3: 63.00-72.00) years, BMI 28.39 (26.06-31.49) kg/m

conclusionsGPR146 expression is associated with serum lipids and metabolically-relevant transcriptomic changes in EAT similar to SGLT2i-associated ones.

Indexed as

Adipose TissueDiabetes Mellitus, Type 2Receptors, G-Protein-CoupledSignal TransductionSodium-Glucose Transporter 2 InhibitorsAgedBiomarkersFemaleHumansMaleMiddle AgedTreatment OutcomeBiomarkersReceptors, G-Protein-CoupledSodium-Glucose Transporter 2 InhibitorsAdipose tissueCholesinDiabetesGPR146SGLT2i

Identifiers

PMID38902687
PMCPMC11191148

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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.