Evidence map›Paper›PMID 34799942›Full record

ArticleJournal of clinical laboratory analysis2022

Low serum interleukin-38 levels in patients with Graves' disease and Hashimoto's thyroiditis.

Jialu Xu, Guoqing Huang, Linjie Weng, Luping Gong, Yushan Mao, Yan Li, Mingcai Li

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

8 citing papers in PubMed, 17 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

7 authors at 1 institution in 1 country.

Jialu XuDepartment of Clinical Laboratory, The Affiliated Lihuili Hospital, Ningbo University, Ningbo, China.
Guoqing HuangDepartment of Immunology, Zhejiang Key Laboratory of Pathophysiology, Ningbo University School of Medicine, Ningbo, China.
Linjie WengDepartment of Immunology, Zhejiang Key Laboratory of Pathophysiology, Ningbo University School of Medicine, Ningbo, China.
Luping GongDepartment of Immunology, Zhejiang Key Laboratory of Pathophysiology, Ningbo University School of Medicine, Ningbo, China.
Yushan MaoDepartment of Endocrinology, The Affiliated Hospital of Medical School, Ningbo University, Ningbo, China.
Yan LiDepartment of Immunology, Zhejiang Key Laboratory of Pathophysiology, Ningbo University School of Medicine, Ningbo, China.
Mingcai LiDepartment of Immunology, Zhejiang Key Laboratory of Pathophysiology, Ningbo University School of Medicine, Ningbo, China.ORCID https://orcid.org/0000-0003-3910-6964
Ningbo University · CN

Funding

National Natural Science Foundation of China 81970735Natural Science Foundation of Ningbo 202003N4115Natural Science Foundation of Ningbo 202003N4118
6 · The paper itself

Abstract

backgroundAutoimmune thyroid disease (AITD) mainly includes Graves' disease (GD) and Hashimoto's thyroiditis (HT), which is caused by individual genetics, autoimmune dysfunction, and a variety of external environmental factors. Interleukin (IL)-38 is involved in a wide range of autoimmune diseases, but little is known about IL-38 expression in AITD.

methodsFifty patients with GD, 50 with HT, and 50 healthy controls (HC) were enrolled in this study. Basic information of the participants was obtained through a physical examination. Immunological data were obtained by an automatic chemiluminescence immunoanalyzer. C-reactive protein (CRP) concentrations and the white blood cell count were measured. Serum IL-38 levels were determined by an enzyme-linked immunosorbent assay.

resultsSerum IL-38 levels were significantly lower in the GD and HT groups than in the HC group (both p < 0.01). Serum CRP concentrations were significantly lower in the HT group than in the HC group (p < 0.05). Receiver operating characteristic curve analysis showed that the area under the curve was 0.7736 (p < 0.01) for IL-38 and 0.7972 (p < 0.01) for IL-38 combined with CRP in the GD group. In the HT group, the area under the curve was 0.7276 (p < 0.01) for IL-38 and 0.7300 for IL-38 combined with CRP (p < 0.01).

conclusionsThe results suggest that serum IL-38 level is a potential new diagnostic biomarker in patients with GD and HT.

Indexed as

AdultCase-Control StudiesC-Reactive ProteinFemaleGraves DiseaseHashimoto DiseaseHumansInterleukinsMaleMiddle AgedC-Reactive ProteinIL-38 protein, humanInterleukinsautoimmune thyroid diseaseC-reactive proteinGraves’ diseaseHashimoto's thyroiditisinterleukin-38

Identifiers

PMID34799942
PMCPMC8761401
OpenAlexW3213345334

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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.