Evidence map›Paper›PMID 35309321›Full record

ArticleFrontiers in immunology2022

Case Report: Appearance of Various Disease-Specific Antibodies After the Onset of Dipeptidyl Peptidase-4 Inhibitor-Associated Bullous Pemphigoid.

Yuichiro Iwamoto, Takatoshi Anno, Katsumasa Koyama, Fumiko Kawasaki, Kohei Kaku, Koichi Tomoda, Seiko Sugiyama, Yumi Aoyama, Hideaki Kaneto

Abstract readCase Reports
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Yuichiro IwamotoDepartment of General Internal Medicine 1, Kawasaki Medical School, Okayama, Japan.
Takatoshi AnnoDepartment of General Internal Medicine 1, Kawasaki Medical School, Okayama, Japan.
Katsumasa KoyamaDepartment of General Internal Medicine 1, Kawasaki Medical School, Okayama, Japan.
Fumiko KawasakiDepartment of General Internal Medicine 1, Kawasaki Medical School, Okayama, Japan.
Kohei KakuDepartment of General Internal Medicine 1, Kawasaki Medical School, Okayama, Japan.
Koichi TomodaDepartment of General Internal Medicine 1, Kawasaki Medical School, Okayama, Japan.
Seiko SugiyamaDepartment of Dermatology, Kawasaki Medical School, Okayama, Japan.
Yumi AoyamaDepartment of Dermatology, Kawasaki Medical School, Okayama, Japan.
Hideaki KanetoDepartment of Diabetes, Endocrinology and Metabolism, Kawasaki Medical School, Kurashiki, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bullous pemphigoid (BP) is a rare autoimmune blistering disease, and the prevalence of type 2 diabetes mellitus (T2DM) is relatively high in subjects with BP. It is known that dipeptidyl peptidase-4 inhibitor (DPP-4i), one kind of antidiabetic drugs, can cause BP, although precise mechanism of DPP-4i-related BP remains unclear. In this report, we showed a case with appearance of various disease-specific antibodies after the onset of DPP-4i-related BP. Furthermore, various disease-specific antibodies became positive and showed high titers two years after the onset of DPP-4i-related BP and discontinuation of DPP-4i. These data showed that it is possible for immune tolerance to be broken after the onset of DPP-4i-related BP, and it may be important to check autoimmune antibodies in DPP-4i-related BP subjects even when BP symptoms are improved.

Indexed as

Diabetes Mellitus, Type 2Dipeptidyl-Peptidase IV InhibitorsPemphigoid, BullousDipeptidyl-Peptidases and Tripeptidyl-PeptidasesHumansHypoglycemic AgentsDipeptidyl-Peptidase IV InhibitorsDipeptidyl-Peptidases and Tripeptidyl-PeptidasesHypoglycemic Agentsautoantibodiesbullous pemphigoiddipeptidyl peptidase-4 inhibitordipeptidyl peptidase-4 inhibitor-associated bullous pemphigoidtype 2 diabetes mellitus

Identifiers

PMID35309321
PMCPMC8927025

What Socratic holds

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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 Socratic graph.