Evidence map›Paper›PMID 30800564›Full record

ArticleDiabetology international2019

Characteristics and clinical course of type 1 diabetes mellitus related to anti-programmed cell death-1 therapy.

Megu Yamaguchi Baden, Akihisa Imagawa, Norio Abiru, Takuya Awata, Hiroshi Ikegami, Yasuko Uchigata, Yoichi Oikawa, Haruhiko Osawa, Hiroshi Kajio, Eiji Kawasaki and 13 more

Open access · bronzeAbstract read
In one paragraph

Article in Diabetology international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 3 pooled it
7.2field-weighted citation impact, top 3% 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

69 citing papers in PubMed, 3 syntheses or guidelines pooled it, 105 citations in OpenAlex.

  1. Pooled it
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  9. Fulminant and Slowly Progressive Type 1 Diabetes Associated with Pregnancy.International journal of molecular sciences · 2025
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9 more citing papers are in PubMed but not listed here.

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

23 authors at 17 institutions in 1 country.

Megu Yamaguchi Baden1Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, Suita, Osaka Japan.
Akihisa Imagawa2Department of Internal Medicine (I), Osaka Medical College, 2-7 Daigakucho, Takatsuki, Osaka 569-8686 Japan.ORCID 0000-0002-4213-3229
Norio Abiru3Department of Endocrinology and Metabolism, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Takuya Awata4Department of Diabetes, Endocrinology and Metabolism, International University of Health and Welfare Hospital, Otawara, Tochigi Japan.
Hiroshi Ikegami5Department of Endocrinology, Metabolism and Diabetes, Kindai University Faculty of Medicine, Higashi-osaka, Osaka Japan.
Yasuko Uchigata6Tokyo Women's Medical University Medical Center East, Tokyo, Japan.
Yoichi Oikawa7Department of Endocrinology and Diabetes, School of Medicine, Saitama Medical University, Saitama, Japan.
Haruhiko Osawa8Department of Laboratory Medicine, Ehime University School of Medicine, Toon, Ehime Japan.
Hiroshi Kajio9Department of Diabetes, Endocrinology, and Metabolism, Center Hospital of the National Center for Global Health and Medicine, Tokyo, Japan.
Eiji Kawasaki10Diabetes Center, Shin-Koga Hospital, Kurume, Fukuoka Japan.
Yumiko Kawabata5Department of Endocrinology, Metabolism and Diabetes, Kindai University Faculty of Medicine, Higashi-osaka, Osaka Japan.
Junji Kozawa1Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, Suita, Osaka Japan.
Akira Shimada7Department of Endocrinology and Diabetes, School of Medicine, Saitama Medical University, Saitama, Japan.
Kazuma Takahashi11Faculty of Nursing and Graduate School of Nursing, Iwate Prefectural University, Takizawa, Iwate Japan.
Shoichiro TanakaAi Home Clinic Toshima, Tokyo, Japan.
Daisuke Chujo9Department of Diabetes, Endocrinology, and Metabolism, Center Hospital of the National Center for Global Health and Medicine, Tokyo, Japan.
Tomoyasu Fukui13Department of Internal Medicine, Division of Diabetes and Endocrinology, Showa University School of Medicine, Tokyo, Japan.
Junnosuke Miura14Diabetes Center, Tokyo Women's Medical University School of Medicine, Tokyo, Japan.
Kazuki Yasuda15Department of Metabolic Disorder, Diabetes Research Center, Research Institute, National Center for Global Health and Medicine, Tokyo, Japan.
Hisafumi Yasuda16Division of Health Sciences, Department of Community Health Sciences, Kobe University Graduate School of Health Sciences, Kobe, Hyogo Japan.
Tetsuro Kobayashi17Okinaka Memorial Institute for Medical Research, Tokyo, Japan.
Toshiaki HanafusaSakai City Medical Center, Sakai, Osaka Japan.
consultation of the Japan Diabetes Society Committee on Type 1 Diabetes Mellitus Research
National Center for Global Health and Medicine · JPKindai University · JPSaitama Medical University · JPThe University of Osaka · JPEhime University · JPHyogo University of Health Sciences · JPInternational University of Health and Welfare · JPIwate Prefectural University · JPKoga Hospital · JPOkinaka Memorial Adult Disease Research Institute · JPOsaka Medical and Pharmaceutical University · JPSakai Municipal Hospital · JPShowa University · JPTokyo Women's Medical University · JPTokyo Women's Medical University Adachi Medical Center · JPToshima Hospital · JPUniversity of Nagasaki · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsWe conducted a national survey to clarify the characteristics and clinical course of type 1 diabetes related to anti-programmed cell death-1 therapy.

methodsWe analyzed the detailed data of 22 patients that were collected using a Japan Diabetes Society survey and a literature database search.

resultsAmong the 22 patients, 11 (50.0%) met the criteria for fulminant type 1 diabetes and 11 (50.0%) met the criteria for acute-onset type 1 diabetes. The average patient age was 63 years. The mean duration between the date of the first anti-PD-1 antibody injection and development of type 1 diabetes was 155 days and ranged from 13 to 504 days. Flu-like symptoms, abdominal symptoms, and drowsiness were observed in 27.8, 31.6, and 16.7% patients, respectively. Mean ± standard deviation or median (first quartile-third quartile) glucose levels, HbA1c levels, urinary C-peptide immunoreactivity levels, and fasting serum C-peptide immunoreactivity levels were 617 ± 248 mg/dl, 8.1 ± 1.3%, 4.1 (1.4-9.4) μg/day, and 0.46 (0.20-0.70) ng/ml, respectively. Seventeen of 20 patients (85.0%) developed ketosis, and 7 of 18 patients (38.9%) developed diabetic ketoacidosis. Ten of 19 patients (52.6%) showed at least one elevated pancreatic enzyme level at the onset and two of seven patients showed this elevation before diabetes onset. Only one of 21 patients was anti-glutamic acid decarboxylase antibody positive.

conclusionsAnti-programmed cell death-1 antibody-related type 1 diabetes varies from typical fulminant type 1 diabetes to acute-onset type 1 diabetes. However, diabetic ketoacidosis was frequently observed at the onset of diabetes. An appropriate diagnosis and treatment should be provided to avoid life-threatening metabolic alterations.

Indexed as

Anti-PD-1 antibodyFulminant type 1 diabetesImmune-checkpoint inhibitorsNivolumabPembrolizumabType 1 diabetes

Identifiers

PMID30800564
PMCPMC6357237
OpenAlexW2810537535

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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.