Evidence map›Paper›PMID 37791312›Full record

ArticleJACC. Basic to translational science2023

Empagliflozin Suppresses the Differentiation/Maturation of Human Epicardial Preadipocytes and Improves Paracrine Secretome Profile.

Masayuki Takano, Hidekazu Kondo, Taisuke Harada, Masaki Takahashi, Yumi Ishii, Hirochika Yamasaki, Tong Shan, Kumiko Akiyoshi, Takashi Shuto, Yasushi Teshima and 6 more

Open access · goldAbstract read
In one paragraph

Article in JACC. Basic to translational science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
8.3field-weighted citation impact, top 2% 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

29 citing papers in PubMed, 38 citations in OpenAlex.

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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

16 authors at 1 institution in 1 country.

Masayuki TakanoDepartment of Cardiology and Clinical Examination, Faculty of Medicine, Oita University, Yufu-city, Oita, Japan.
Hidekazu KondoDepartment of Cardiology and Clinical Examination, Faculty of Medicine, Oita University, Yufu-city, Oita, Japan.
Taisuke HaradaDepartment of Cardiology and Clinical Examination, Faculty of Medicine, Oita University, Yufu-city, Oita, Japan.
Masaki TakahashiDepartment of Cardiology and Clinical Examination, Faculty of Medicine, Oita University, Yufu-city, Oita, Japan.
Yumi IshiiDepartment of Cardiology and Clinical Examination, Faculty of Medicine, Oita University, Yufu-city, Oita, Japan.
Hirochika YamasakiDepartment of Cardiology and Clinical Examination, Faculty of Medicine, Oita University, Yufu-city, Oita, Japan.
Tong ShanDepartment of Cardiology and Clinical Examination, Faculty of Medicine, Oita University, Yufu-city, Oita, Japan.
Kumiko AkiyoshiDepartment of Cardiology and Clinical Examination, Faculty of Medicine, Oita University, Yufu-city, Oita, Japan.
Takashi ShutoDepartment of Cardiovascular Surgery, Faculty of Medicine Oita University, Yufu-city, Oita, Japan.
Yasushi TeshimaDepartment of Cardiology and Clinical Examination, Faculty of Medicine, Oita University, Yufu-city, Oita, Japan.
Tomoyuki WadaDepartment of Cardiovascular Surgery, Faculty of Medicine Oita University, Yufu-city, Oita, Japan.
Kunio YufuDepartment of Cardiology and Clinical Examination, Faculty of Medicine, Oita University, Yufu-city, Oita, Japan.
Hidenori SakoDepartment of Cardiovascular Surgery, Oka Hospital, Oita-city, Oita, Japan.
Hirofumi AnaiDepartment of Cardiovascular Surgery, Faculty of Medicine Oita University, Yufu-city, Oita, Japan.
Shinji MiyamotoDepartment of Cardiovascular Surgery, Faculty of Medicine Oita University, Yufu-city, Oita, Japan.
Naohiko TakahashiDepartment of Cardiology and Clinical Examination, Faculty of Medicine, Oita University, Yufu-city, Oita, Japan.
Oita University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sodium-glucose cotransporter 2 (SGLT2) inhibitors reduce epicardial adipose tissue (EAT) in humans, enhancing cardioprotective effects on heart failure and atrial fibrillation. We investigated the direct effect of the SGLT2 inhibitor empagliflozin on human primary epicardial adipocytes and preadipocytes. SGLT2 is primarily expressed in human preadipocytes in the EAT. The expression levels of SGLT2 significantly diminished when the preadipocytes were terminally differentiated. Adipogenesis of preadipocytes was attenuated by empagliflozin treatment without affecting cell proliferation. The messenger RNA levels and secreted protein levels of interleukin 6 and monocyte chemoattractant protein 1 were significantly decreased in empagliflozin-treated adipocytes. Coculture of human induced pluripotent stem cell-derived atrial cardiomyocytes and adipocytes pretreated with or without empagliflozin revealed that empagliflozin significantly suppressed reactive oxygen species.

Indexed as

epicardial adipose tissueinterleukin 6paracrine effectpreadipocytesodium-glucose cotransporter 2 inhibitor

Identifiers

PMID37791312
PMCPMC10544075
OpenAlexW4385694190

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.