Evidence map›Paper›PMID 31822955›Full record

ArticleEuropean journal of clinical pharmacology2020

Association between dipeptidyl peptidase-4 inhibitor and aspiration pneumonia: disproportionality analysis using the spontaneous reporting system in Japan.

Yoshihiro Noguchi, Hiroki Esaki, Azusa Murayama, Mayuko Sugioka, Aisa Koyama, Tomoya Tachi, Hitomi Teramachi

Abstract read
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Article in European journal of clinical pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Sodium-Glucose Cotransporter 2 Inhibitors and the Risk of Pneumonia and Septic Shock.The Journal of clinical endocrinology and metabolism · 2022
    Article
  3. Article
  4. Article
  5. 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

7 authors at 1 institution in 1 country.

Yoshihiro NoguchiLaboratory of Clinical Pharmacy, Gifu Pharmaceutical University, Gifu, Japan. noguchiy@gifu-pu.ac.jp.ORCID http://orcid.org/0000-0002-9110-9604
Hiroki EsakiLaboratory of Clinical Pharmacy, Gifu Pharmaceutical University, Gifu, Japan.
Azusa MurayamaLaboratory of Clinical Pharmacy, Gifu Pharmaceutical University, Gifu, Japan.
Mayuko SugiokaLaboratory of Clinical Pharmacy, Gifu Pharmaceutical University, Gifu, Japan.
Aisa KoyamaLaboratory of Clinical Pharmacy, Gifu Pharmaceutical University, Gifu, Japan.
Tomoya TachiLaboratory of Clinical Pharmacy, Gifu Pharmaceutical University, Gifu, Japan.
Hitomi TeramachiLaboratory of Clinical Pharmacy, Gifu Pharmaceutical University, Gifu, Japan. teramachih@gifu-pu.ac.jp.
Gifu Pharmaceutical University · JP

Funding

Japan Society for the Promotion of Science (JP) 19K20731
6 · The paper itself

Abstract

purposeDipeptidyl peptidase-4 inhibitor (DPP-4-Is), a kind of drug used for the treatment of diabetes, is considered to prevent the degradation of substance P that suppresses the occurrence of dysphagia. On the other hand, DPP-4 inhibitors are also known to act on the immune system. In this study, we used a spontaneous reporting system to evaluate the signals for dysphagia and aspiration pneumonia with DPP-4-Is.

methodsWe calculated reporting odds ratio (ROR) and information coefficients (IC) as disproportionality analysis to evaluate DPP-4-Is induced dysphagia and aspiration pneumonia using the Japanese Adverse Drug Event Report (JADER) database.

resultsFor DPP-4-Is as a class, no signals were detected for dysphagia, but the signal for aspiration pneumonia was detected at ROR 1.67 (95% confidence interval [95% CI]: 1.20 to 2.34) and IC 0.70 (95% CI: 0.21 to 1.19). For aspiration pneumonia, trelagliptin was the only drug among the DPP-4-Is for which both ROR and IC signals were detected (ROR 9.99, 95% CI: 4.10 to 24.36; IC: 1.98, 95% CI: 0.78 to 3.18). ROR signals, but not IC signals, were detected for linagliptin (ROR 2.66, 95% CI: 1.19 to 5.94; IC: 1.09, 95% CI: - 0.004 to 2.19) and sitagliptin (ROR 1.84, 95% CI: 1.04 to 3.25; IC: 0.78, 95% CI: - 0.03 to 1.58).

conclusionSince DPP-4 inhibitors prevent the degradation of substance P involved in swallowing reflex, DPP-4 inhibitors were expected to prevent dysphagia and aspiration pneumonia. However, this study revealed that DPP-4 inhibitors strongly were associated with onset rather than preventing aspiration pneumonia. This result suggests that DPP-4 inhibitors may affect the immune function associated with the development of aspiration pneumonia. Furthermore, there is a possibility that the amount of DPP-4-Is used clinically cannot increase the amount of substance P in sufficient quantity to prevent aspiration pneumonia.

Indexed as

Adverse Drug Reaction Reporting SystemsDatabases, FactualDeglutition DisordersDipeptidyl-Peptidase IV InhibitorsHumansHypoglycemic AgentsJapanOdds RatioPneumonia, AspirationDipeptidyl-Peptidase IV InhibitorsHypoglycemic AgentsAspiration pneumoniaDipeptidyl peptidase-4 inhibitorsDisproportionality analysisDysphagiaJapanese Adverse Drug Event Report (JADER) databaseSpontaneous reporting system

Identifiers

PMID31822955
OpenAlexW2992219210

What OpenQuestion holds

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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.