Evidence map›Paper›PMID 42058432›Full record

ArticleFrontiers in medicine2026

Integrated inflammatory-immune-nutritional signatures differentiate lung phenotypes in systemic sclerosis.

Huichen Luo, Danhui Hu, Xu Wang, Daming Ou, Ling Lei

Abstract read
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Article in Frontiers in medicine, 2026. 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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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Huichen LuoDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Danhui HuDepartment of Neonatology, The First Affiliated Hospital of University of South China, Hengyang, Hunan, China.
Xu WangDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Daming OuDepartment of Rheumatology and Immunology, The First Affiliated Hospital of University of South China, Hengyang, Hunan, China.
Ling LeiDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Systemic sclerosis (SSc) exhibits heterogeneous pulmonary involvement, most commonly interstitial lung disease (ILD) and pulmonary arterial hypertension (PAH). How systemic inflammatory, immune, and nutritional states differ across these lung phenotypes remains incompletely understood. Objective: To characterize integrated inflammatory-immune-nutritional signatures across SSc lung phenotypes and validate their robustness using multivariable modeling and unsupervised clustering. Methods: We conducted a retrospective cross-sectional study of 314 consecutive SSc inpatients fulfilling the 2013 ACR/EULAR criteria (2018-2023). Patients were stratified into four lung phenotypes: ILD-/PAH- ( Results: ILD + /PAH + patients showed a higher systemic inflammatory burden, including higher ESR (38 [21-61.5] vs. 23 [10-45] mm/h, Conclusion: SSc lung phenotypes defined by ILD/PAH co-occurrence display distinct integrated inflammatory-immune-nutritional signatures. The ILD + /PAH + phenotype reflects a high-burden systemic inflammatory state, and a small set of coherent markers (ESR, triglycerides, IgA, and autoantibodies) provides a reproducible framework for phenotype-oriented stratification.

Indexed as

biomarkersinterstitial lung diseasephenotypingpulmonary arterial hypertensionsystemic sclerosis

Identifiers

PMID42058432
PMCPMC13120917

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