Evidence map›Paper›PMID 41275238›Full record

ArticleBMC pharmacology & toxicology2025

Association between daily dose of dipeptidyl peptidase-4 inhibitors and change in glycated hemoglobin in patients with type 2 diabetes: interpretation of mixed-effects machine-learning models using electronic medical records.

Takashi Hayakawa, Hayato Akimoto, Takuya Nagashima, Kimino Minagawa, Yasuo Takahashi, Satoshi Asai

Abstract read
In one paragraph

Article in BMC pharmacology & toxicology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
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

6 authors.

Takashi HayakawaDivision of Pharmacology, Department of Biomedical Sciences, Nihon University School of Medicine, Oyaguchi-kamicho 30-1, Itabashi-ku, Tokyo, 173-8610, Japan.
Hayato AkimotoDivision of Genomic Epidemiology and Clinical Trials, Clinical Trials Research Center, Nihon University School of Medicine, Oyaguchi-kamicho 30-1, Itabashi-ku, Tokyo, 173-8610, Japan. akimoto.hayato@nihon-u.ac.jp.
Takuya NagashimaDivision of Pharmacology, Department of Biomedical Sciences, Nihon University School of Medicine, Oyaguchi-kamicho 30-1, Itabashi-ku, Tokyo, 173-8610, Japan.
Kimino MinagawaDivision of Genomic Epidemiology and Clinical Trials, Clinical Trials Research Center, Nihon University School of Medicine, Oyaguchi-kamicho 30-1, Itabashi-ku, Tokyo, 173-8610, Japan.
Yasuo TakahashiDivision of Genomic Epidemiology and Clinical Trials, Clinical Trials Research Center, Nihon University School of Medicine, Oyaguchi-kamicho 30-1, Itabashi-ku, Tokyo, 173-8610, Japan.
Satoshi AsaiDivision of Pharmacology, Department of Biomedical Sciences, Nihon University School of Medicine, Oyaguchi-kamicho 30-1, Itabashi-ku, Tokyo, 173-8610, Japan.

Funding

Japan Agency for Medical Research and Development JP223fa627011Japan Society for the Promotion of Science JP24K18341
6 · The paper itself

Abstract

backgroundMany randomized, placebo-controlled trials suggest that the dose–response relationship between dipeptidyl peptidase-4 (DPP-4) inhibitors and change in HbA1c (ΔHbA1c) is non-linear. However, in the real world, patients with type 2 diabetes (T2D) receive varying doses over time depending on their glycemic control. Therefore, to accurately capture real-world HbA1c variability, longitudinal medical records reflecting these dose changes must be analyzed. Crucially, the analysis must also account for the influence of potential confounding factors on HbA1c. Linear mixed-effects models cannot adequately assess this non-linear relationship. The aim of this study was to evaluate the association between daily dose of DPP-4 inhibitors and ΔHbA1c in the real world by developing and interpreting tree-based machine-learning models with random effects.

methodsLongitudinal information on T2D patients was extracted from electronic medical records. Four machine-learning models with random effects were constructed to predict change in HbA1c: linear mixed-effects models (LMMs) with/without a backward elimination method, a mixed-effects random forest model (MERF), and a combining tree-boosting with Gaussian process and mixed-effects model (GPBoost). The MERF and GPBoost were interpreted by SHapley Additive exPlanations and partial dependence.

resultsNon-linear machine-learning models such as MERF and GPBoost had better predictive performance than LMMs. When interpreting MERF and GPBoost, HbA1c level decreased in a dose-dependent manner within the range of sitagliptin 0–50 mg/day, but no difference was observed between 50 and 100 mg/day. For teneligliptin, while 10 mg/day was suggested to have a slightly weaker HbA1c-lowering effect than 20 or 40 mg/day, there was no difference between 20 and 40 mg/day. Regarding vildagliptin, 100 mg/day showed a tendency to lower HbA1c level more than 50 mg/day.

conclusionsNon-linear machine-learning models can clearly demonstrate the dose–response relationship of the HbA1c-lowering effects of DPP-4 inhibitors in real-world T2D patients. For sitagliptin and teneligliptin, the HbA1c-lowering effect plateaued within the approved dose range. With regard to vildagliptin, it is unclear whether dose–response saturation was observed due to the limited number of dosing regimens. Our findings support the results of previous trials, and machine-learning models demonstrated that it is possible to evaluate the dose–response relationship in the real world.

Indexed as

Diabetes Mellitus, Type 2Dipeptidyl-Peptidase IV InhibitorsGlycated HemoglobinHypoglycemic AgentsMachine LearningAgedDose-Response Relationship, DrugElectronic Health RecordsFemaleHumansMaleMiddle AgedPredictive Learning ModelsRandom ForestDipeptidyl-Peptidase IV InhibitorsGlycated Hemoglobinhemoglobin A1c protein, humanHypoglycemic AgentsDose–responseDPP-4 inhibitorMachine-learningReal-worldType 2 diabetes

Identifiers

PMID41275238
PMCPMC12751167

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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.