Evidence map›Paper›PMID 41133257›Full record

ArticleJournal of the Endocrine Society2025

SGLT2 Inhibitors Modify Fibrosis-4 Index and Mitigate the Development of DKD: Role of Background Antidiabetic Drugs.

Keisuke Takano, Koichi Hayashi, Koichi Kitamura, Mutsuo Kanda, Kei Ito, Taro Hirai, Yuki Hara, Akihiro Miyake, Keita Endo, Kaede Yoshino and 3 more

Abstract read
In one paragraph

Article in Journal of the Endocrine Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

13 authors.

Keisuke TakanoDepartment of Nephrology, Endocrinology and Diabetes, Tokyo Bay Urayasu Ichikawa Medical Center, Urayasu, 3-4-32 Todaijima Urayasu-city, Chiba 2790001, Japan.ORCID https://orcid.org/0009-0009-9671-924X
Koichi HayashiDepartment of Emergency and Critical Care Medicine, St Marianna University School of Medicine, 2-16-1 Sugao Miyamae-ku Kawasaki-city, Kanagawa 2168511, Japan.
Koichi KitamuraDepartment of Nephrology, Endocrinology and Diabetes, Tokyo Bay Urayasu Ichikawa Medical Center, Urayasu, 3-4-32 Todaijima Urayasu-city, Chiba 2790001, Japan.
Mutsuo KandaDepartment of Nephrology, Endocrinology and Diabetes, Tokyo Bay Urayasu Ichikawa Medical Center, Urayasu, 3-4-32 Todaijima Urayasu-city, Chiba 2790001, Japan.
Kei ItoDepartment of Nephrology, Endocrinology and Diabetes, Tokyo Bay Urayasu Ichikawa Medical Center, Urayasu, 3-4-32 Todaijima Urayasu-city, Chiba 2790001, Japan.
Taro HiraiDepartment of Nephrology, Endocrinology and Diabetes, Tokyo Bay Urayasu Ichikawa Medical Center, Urayasu, 3-4-32 Todaijima Urayasu-city, Chiba 2790001, Japan.ORCID https://orcid.org/0000-0002-7278-3417
Yuki HaraDepartment of Nephrology, Endocrinology and Diabetes, Tokyo Bay Urayasu Ichikawa Medical Center, Urayasu, 3-4-32 Todaijima Urayasu-city, Chiba 2790001, Japan.
Akihiro MiyakeDepartment of Nephrology, Endocrinology and Diabetes, Tokyo Bay Urayasu Ichikawa Medical Center, Urayasu, 3-4-32 Todaijima Urayasu-city, Chiba 2790001, Japan.
Keita EndoDepartment of Nephrology, Endocrinology and Diabetes, Tokyo Bay Urayasu Ichikawa Medical Center, Urayasu, 3-4-32 Todaijima Urayasu-city, Chiba 2790001, Japan.ORCID https://orcid.org/0000-0001-8521-0573
Kaede YoshinoDepartment of Nephrology, Endocrinology and Diabetes, Tokyo Bay Urayasu Ichikawa Medical Center, Urayasu, 3-4-32 Todaijima Urayasu-city, Chiba 2790001, Japan.
Shinsuke ItoDepartment of Nephrology, Endocrinology and Diabetes, Tokyo Bay Urayasu Ichikawa Medical Center, Urayasu, 3-4-32 Todaijima Urayasu-city, Chiba 2790001, Japan.
Shigeki FujitaniDepartment of Emergency and Critical Care Medicine, St Marianna University School of Medicine, 2-16-1 Sugao Miyamae-ku Kawasaki-city, Kanagawa 2168511, Japan.
Toshihiko SuzukiDepartment of Nephrology, Endocrinology and Diabetes, Tokyo Bay Urayasu Ichikawa Medical Center, Urayasu, 3-4-32 Todaijima Urayasu-city, Chiba 2790001, Japan.ORCID https://orcid.org/0000-0002-4545-9769

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Context: The fibrosis-4 (FIB-4) index is a noninvasive marker for liver fibrosis and is associated with the occurrence of diabetic kidney disease (DKD). Although sodium-glucose cotransporter-2 inhibitors (SGLT2is) are recognized to provide cardiovascular and renal benefits, the role of SGLT2is in regulating FIB-4 index and the subsequent effect on renal events remain unclear. Objective: This work aimed to clarify whether the FIB-4 index was associated with the development of DKD (estimated glomerular filtration rate < 60 mL/min/1.73 m Methods: A retrospective cohort study was conducted that included 136 patients with type 2 diabetes mellitus who were newly given SGLT2is for 3 years. Results: Patients with a high FIB-4 index (≥1.3) at baseline exhibited a higher incidence of de novo DKD, compared to those with a lower FIB-4 index (<1.3). This association was ameliorated in patients whose FIB-4 index was decreased during the SGLT2i treatment. Finally, among the background therapies, metformin use was associated with a decrease in FIB-4 index and a lower cumulative incidence of de novo DKD. Conclusion: Elevated FIB-4 index at baseline is a potent predictor for developing DKD, and combination therapy with SGLT2is and metformin may enhance renal protection by modulating FIB-4 index.

Indexed as

diabetic kidney diseasefibrosis-4 indexmetforminSGLT2 inhibitorstype 2 diabetes mellitus

Identifiers

PMID41133257
PMCPMC12543019

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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.