Evidence map›Paper›PMID 25802725›Full record

ArticleJournal of diabetes investigation2015

Response to the dipeptidyl peptidase-4 inhibitors in Japanese patients with type 2 diabetes might be associated with a diplotype of two single nucleotide polymorphisms on the interleukin-6 promoter region under a certain level of physical activity.

Mizue Matsui, Yoshihiko Takahashi, Noriko Takebe, Kazuma Takahashi, Kan Nagasawa, Hiroyuki Honma, Tomoyasu Oda, Mitsutaka Ono, Riyuki Nakagawa, Takayoshi Sasai and 6 more

Open access · goldAbstract read
In one paragraph

Article in Journal of diabetes investigation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Pharmacogenetics of new classes of antidiabetic drugs.Bosnian journal of basic medical sciences · 2021
    Review
  2. Review
  3. Pharmacogenetics of Type 2 Diabetes-Progress and Prospects.International journal of molecular sciences · 2020
    Review
  4. 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

16 authors at 1 institution in 1 country.

Mizue MatsuiDivision of Diabetes and Metabolism, Department of Internal Medicine, Iwate Medical University Morioka, Japan.
Yoshihiko TakahashiDivision of Diabetes and Metabolism, Department of Internal Medicine, Iwate Medical University Morioka, Japan.
Noriko TakebeDivision of Diabetes and Metabolism, Department of Internal Medicine, Iwate Medical University Morioka, Japan.
Kazuma TakahashiDivision of Diabetes and Metabolism, Department of Internal Medicine, Iwate Medical University Morioka, Japan.
Kan NagasawaDivision of Diabetes and Metabolism, Department of Internal Medicine, Iwate Medical University Morioka, Japan.
Hiroyuki HonmaDivision of Diabetes and Metabolism, Department of Internal Medicine, Iwate Medical University Morioka, Japan.
Tomoyasu OdaDivision of Diabetes and Metabolism, Department of Internal Medicine, Iwate Medical University Morioka, Japan.
Mitsutaka OnoDivision of Diabetes and Metabolism, Department of Internal Medicine, Iwate Medical University Morioka, Japan.
Riyuki NakagawaDivision of Diabetes and Metabolism, Department of Internal Medicine, Iwate Medical University Morioka, Japan.
Takayoshi SasaiDivision of Diabetes and Metabolism, Department of Internal Medicine, Iwate Medical University Morioka, Japan.
Hirobumi TogashiDivision of Diabetes and Metabolism, Department of Internal Medicine, Iwate Medical University Morioka, Japan.
Mari HangaiDivision of Diabetes and Metabolism, Department of Internal Medicine, Iwate Medical University Morioka, Japan.
Takashi KajiwaraDivision of Diabetes and Metabolism, Department of Internal Medicine, Iwate Medical University Morioka, Japan.
Haruhito TaneichiDivision of Diabetes and Metabolism, Department of Internal Medicine, Iwate Medical University Morioka, Japan.
Yasushi IshigakiDivision of Diabetes and Metabolism, Department of Internal Medicine, Iwate Medical University Morioka, Japan.
Jo SatohDivision of Diabetes and Metabolism, Department of Internal Medicine, Iwate Medical University Morioka, Japan.
Iwate Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

AIMS/

introductionMuscle-derived interleukin-6 (IL-6) has been reported to promote glucagon-like peptide-1 (GLP-1) secretion, and we explored the association of single nucleotide polymorphisms (SNPs) in the human IL-6 promoter region with the responsiveness to dipeptidyl peptidase-4 inhibitors (DPP-4Is), drugs that increase circulating GLP-1. MATERIALS AND

methodsThe present observational study enrolled Japanese patients with type 2 diabetes who took a DPP-4I over 3 months, and most of the clinical information was collected retrospectively. We defined non-responders as those having less than a 0.2% decrease of the glycated hemoglobin level at 3 or 4 months after starting DPP-4I treatment. Physical activity was retrospectively estimated by the Japanese short version of International Physical Activity Questionnaire.

resultsWe studied 316 patients whose physical activity corresponding to the season of the DPP-4I administration was estimated. The non-responder rate was 29.7%. We analyzed rs1800796 and rs2097677, both are suggested to be functional in Japanese. Multivariate analysis for all patients showed that the adjusted odds ratio for the non-responder risk of the diplotype rs1800796 G/*-rs2097677 A/* against C/C-G/G (OR_G*A*) was 0.445 (P = 0.068). When patients were stratified by the International Physical Activity Questionnaire into low (n = 149) and moderate/high (n = 167) activity groups, however, OR_G*A* in each group was 1.58 (P = 0.615) and 0.153 (P = 0.003), respectively.

conclusionsThe diplotype rs1800796 G/*-rs2097677 A/* might contribute to responsiveness to DPP-4Is in Japanese patients with type 2 diabetes under a certain level of physical activity. However, further investigation is warranted to confirm this.

Indexed as

Glucagon-like peptide-1Interleukin-6Single nucleotide polymorphism

Identifiers

PMID25802725
PMCPMC4364852
OpenAlexW2021766042

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.