Evidence map›Paper›PMID 41293179›Full record

ArticleFrontiers in immunology2025

Serum lactate dehydrogenase and rapidly progressive interstitial lung disease are associated with increased mortality in anti-melanoma differentiation-associated gene 5 antibody-positive dermatomyositis.

Gang Wang, Dong Yan, Yujie Zhang, Chang Liu, Zhichun Liu

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Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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0cells of the map it votes in
3citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Gang Wang *Department of Rheumatology and Immunology, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Dong Yan *Department of Rheumatology and Immunology, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Yujie ZhangDepartment of Rheumatology and Immunology, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Chang LiuDepartment of Rheumatology and Immunology, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Zhichun LiuDepartment of Rheumatology and Immunology, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: This study aims to evaluate the clinical characteristics and prognostic significance of serum lactate dehydrogenase (LDH) in patients with anti-MDA5+ dermatomyositis (anti-MDA5+ DM). Methods: We assessed 246 consecutive patients with anti-MDA5+ DM. The patients were divided into two groups based on LDH levels: the LDH ≤ 338 U/L group and the LDH > 338 U/L group. We compared the clinical characteristics, laboratory findings, and long-term prognosis between the two groups. Results: Overall, the one-year mortality rate in patients with anti-MDA5+ DM was high, at 24.39% (60/246). LDH levels exhibited a nonlinear, inverted S-shaped relationship with the overall mortality risk in anti-MDA5+ DM patients (nonlinear P = 0.001). Patients in the LDH > 338 U/L group had significantly higher levels of ALT [64.0 (32.0, 121.0) vs 40.0 (23.0, 66.5), P<0.001], AST [75.0 (47.5, 134.0) vs 40.0 (26.0, 60.6), P<0.001], CK [107.0 (42.0, 208.8) vs 50.0 (35.5, 100.5), P<0.001], CRP [8.5 (3.5, 17.6) vs 4.7 (2.7, 10.2), P<0.001], and serum ferritin levels [1307.6 (679.8, 1565.5) vs 1001.0 (391.2, 1307.6), P<0.001] compared to the LDH ≤ 338 U/L group. Additionally, the positivity rate of Anti-Ro52 antibodies (70.7% vs 57.7%, P = 0.033), the incidence of rapidly progressive interstitial lung disease (RPILD) (42.3% vs 29.3%, P = 0.033), and the mortality rate (35.0% vs 13.8%, P<0.001) were significantly higher in the LDH > 338 U/L group than in the LDH ≤ 338 U/L group. Multivariable regression analysis revealed that LDH > 338 U/L and the presence of RPILD were associated with poor prognosis [hazard ratios of 2.253 (95% CI 1.258, 4.035, P = 0.006) and 10.293 (95% CI 4.683, 22.623, P < 0.001), respectively]. Conclusion: Patients with different LDH levels exhibit distinct clinical characteristics, laboratory findings, and long-term prognosis. Elevated LDH levels (> 338 U/L) and the presence of RPILD are associated with poor prognosis.

Indexed as

AutoantibodiesDermatomyositisInterferon-Induced Helicase, IFIH1L-Lactate DehydrogenaseLung Diseases, InterstitialAdultAgedBiomarkersDisease ProgressionFemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesAutoantibodiesBiomarkersIFIH1 protein, humanInterferon-Induced Helicase, IFIH1L-Lactate Dehydrogenaseanti-MDA5 antibodyanti-MDA5 positive dermatomyositisclinical characteristicsdermatomyositislactate dehydrogenaseprognosisrapidly progressive interstitial lung disease

Identifiers

PMID41293179
PMCPMC12640893

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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.