Evidence map›Paper›PMID 35255603›Full record

ArticleEndocrinology and metabolism (Seoul, Korea)2022

Human Leukocyte Antigens and Biomarkers in Type 1 Diabetes Mellitus Induced by Immune-Checkpoint Inhibitors.

Hidefumi Inaba, Yosuke Kaido, Saya Ito, Tomonao Hirobata, Gen Inoue, Takakazu Sugita, Yuki Yamamoto, Masatoshi Jinnin, Hiroaki Kimura, Tomoko Kobayashi and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Endocrinology and metabolism (Seoul, Korea), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

22 citing papers in PubMed, 30 citations in OpenAlex.

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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

13 authors at 4 institutions in 1 country.

Hidefumi InabaDepartment of Diabetes and Endocrinology, Japanese Red Cross Wakayama Medical Center, Wakayama, Japan.
Yosuke KaidoDepartment of Diabetes and Endocrinology, Japanese Red Cross Wakayama Medical Center, Wakayama, Japan.
Saya ItoDepartment of Diabetes and Endocrinology, Japanese Red Cross Wakayama Medical Center, Wakayama, Japan.
Tomonao HirobataDepartment of Diabetes and Endocrinology, Japanese Red Cross Wakayama Medical Center, Wakayama, Japan.
Gen InoueDepartment of Diabetes and Endocrinology, Japanese Red Cross Wakayama Medical Center, Wakayama, Japan.
Takakazu SugitaDepartment of Respiratory Medicine, Japanese Red Cross Wakayama Medical Center, Wakayama, Japan.
Yuki YamamotoDepartment of Dermatology, Wakayama Medical University, Wakayama, Japan.
Masatoshi JinninDepartment of Dermatology, Wakayama Medical University, Wakayama, Japan.
Hiroaki KimuraDepartment of Pharmaceutical Health Sciences, Kyushu University of Health and Welfare, Nobeoka, Japan.
Tomoko KobayashiDepartment of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Shintaro IwamaDepartment of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Hiroshi ArimaDepartment of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Takaaki MatsuokaThe First Department of Medicine, Wakayama Medical University, Wakayama, Japan.
Japanese Red Cross Society Wakayama Medical Center · JPWakayama Medical University · JPNagoya University · JPKyushu University of Health and Welfare · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundType 1 diabetes mellitus induced by immune-checkpoint inhibitors (ICI-T1DM) is a rare critical entity. However, the etiology of ICI-T1DM remains unclear.

methodsIn order to elucidate risk factors for ICI-T1DM, we evaluated the clinical course and immunological status of patients with ICI-T1DM who had been diagnosed during 2016 to 2021.

resultsSeven of 871 (0.8%, six men and one woman) patients developed ICI-T1DM. We revealed that the allele frequencies of human leukocyte antigen (HLA)-DPA1*02:02 and DPB1*05:01 were significantly higher in the patients with ICI-T1DM In comparison to the controls who received ICI (11/14 vs. 10/26, P=0.022; 11/14 vs. 7/26, P=0.0027, respectively). HLA-DRB1*04:05, which has been found to be a T1DM susceptibility allele in Asians, was also observed as a high-risk allele for ICI-T1DM. The significance of the HLA-DPB1*05:01 and DRB1*04:05 alleles was confirmed by an analysis of four additional patients. The absolute/relative neutrophil count, neutrophils-lymphocyte ratio, and neutrophil-eosinophil ratio increased, and the absolute lymphocyte count and absolute/relative eosinophil count decreased at the onset as compared with 6 weeks before. In two patients, alterations in cytokines and chemokines were found at the onset.

conclusionNovel high-risk HLA alleles and haplotypes were identified in ICI-T1DM, and peripheral blood factors may be utilized as biomarkers.

Indexed as

Diabetes Mellitus, Type 1AllelesBiomarkersFemaleGene FrequencyHumansImmune Checkpoint InhibitorsMaleBiomarkersImmune Checkpoint InhibitorsBiomarkersChemokinesCytokinesDiabetes mellitus, type 1Immune checkpoint inhibitorsImmune-related adverse events

Identifiers

PMID35255603
PMCPMC8901959
OpenAlexW4214601866

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.