Evidence map›Paper›PMID 41476904›Full record

ArticleFrontiers in clinical diabetes and healthcare2025

Real-world effectiveness and safety of imeglimin: a single-center retrospective cohort study in Japan.

Taro Fujisawa, Takehiro Kato, Kazuhisa Takami, Shinya Fukuda, Risako Imai, Tomoya Kawashima, Ryosuke Horita, Katsuhisa Sakai, Akiko Yamada, Shin Tsunekawa and 1 more

Abstract read
In one paragraph

Article in Frontiers in clinical diabetes and healthcare, 2025. 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

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

1 citing paper in PubMed.

  1. Trial
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.

Taro FujisawaDepartment of Diabetes, Endocrinology and Metabolism, Gifu University Graduate School of Medicine, Gifu, Japan.
Takehiro KatoDepartment of Diabetes, Endocrinology and Metabolism, Gifu University Graduate School of Medicine, Gifu, Japan.
Kazuhisa TakamiDepartment of Endocrinology and Metabolism/Diabetes Center, Central Japan International Medical Center, Minokamo, Japan.
Shinya FukudaDepartment of Endocrinology and Metabolism/Diabetes Center, Central Japan International Medical Center, Minokamo, Japan.
Risako ImaiDepartment of Endocrinology and Metabolism/Diabetes Center, Central Japan International Medical Center, Minokamo, Japan.
Tomoya KawashimaDepartment of Endocrinology and Metabolism/Diabetes Center, Central Japan International Medical Center, Minokamo, Japan.
Ryosuke HoritaDepartment of Endocrinology and Metabolism/Diabetes Center, Central Japan International Medical Center, Minokamo, Japan.
Katsuhisa SakaiDepartment of Endocrinology and Metabolism/Diabetes Center, Central Japan International Medical Center, Minokamo, Japan.
Akiko YamadaDepartment of Endocrinology and Metabolism/Diabetes Center, Central Japan International Medical Center, Minokamo, Japan.
Shin TsunekawaDepartment of Diabetes, Endocrinology and Metabolism, Gifu University Graduate School of Medicine, Gifu, Japan.
Daisuke YabeDepartment of Diabetes, Endocrinology and Metabolism, Gifu University Graduate School of Medicine, Gifu, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aims/Introduction: This study aimed to evaluate the real-world effectiveness and safety of imeglimin in individuals with type 2 diabetes. Materials and methods: We retrospectively reviewed 79 individuals (52 men, 27 women) with type 2 diabetes who newly initiated imeglimin (1,000 mg twice daily) and were followed for 12 months at the Central Japan International Medical Center between September 2022 and December 2023. Individuals were stratified by age (<65, 65-74, ≥75 years) and by the presence or absence of biguanide dose reduction at imeglimin initiation. The primary endpoint was the change in HbA1c from baseline to 12 months. Secondary endpoints included the achievement rate of glycemic targets, incidence of adverse events, and changes in body weight, blood pressure, liver and renal function, lipid profile, and uric acid. Results: HbA1c significantly decreased one month after initiation and the improvement was sustained through 12 months (mean change from baseline -0.8 ± 1.2%). Effectiveness and safety did not differ significantly among age groups. Gastrointestinal symptoms were the most common adverse events (21.5%), with no age-related differences. HbA1c reduction was greater in individuals without biguanide dose reduction compared with those with dose reduction (-1.5 ± 1.7% Conclusions: Imeglimin demonstrated sustained glycemic effectiveness and favorable tolerability in real-world practice, including among elderly individuals with type 2 diabetes. These findings suggest imeglimin as a valuable therapeutic option for older adults with type 2 diabetes. Caution is warranted when co-administered with high-dose metformin, whereas combination with <1,000 mg/day appears relatively safe.

Indexed as

effectiveness and safetyimegliminolder adultsreal-world evidencetype 2 diabetes

Identifiers

PMID41476904
PMCPMC12747980

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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.