Evidence map›Paper›PMID 42393475›Full record

ArticleLung2026

Circulating Adipokines as Diagnostic and Prognostic Markers in Idiopathic Pulmonary Fibrosis.

Ju Hyun Oh, Ganghee Chae, Yeyoung Kim, Jin Woo Song

Abstract read
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Article in Lung, 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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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ju Hyun OhDepartment of Pulmonary and Critical Care Medicine, Ajou University Medical Center, Ajou University School of Medicine, Suwon, Republic of Korea.
Ganghee ChaeDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Republic of Korea.
Yeyoung KimDepartment of Pulmonary and Critical Care Medicine, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Republic of Korea.
Jin Woo SongDepartment of Pulmonary and Critical Care Medicine, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Republic of Korea. jwsongasan@gmail.com.

Funding

Asan Institute for Life Sciences, Asan Medical Center 2024IP0078-1Korea Environmental Industry and Technology Institute RS-2022-KE002197Korea Health Industry Development Institute RS-2026-25517592National Research Foundation of Korea (NRF) NRF-2022M3A9E4082647
6 · The paper itself

Abstract

purposeDysregulation of lipid metabolism has been implicated in the pathogenesis of idiopathic pulmonary fibrosis (IPF). We aimed to evaluated the predictive value of adipokines in IPF diagnosis and prognosis.

methodsClinical data of patients with IPF (n = 100) and healthy controls (n = 64) were retrospectively analysed. Plasma adipokine levels including leptin and adiponectin were measured using enzyme-linked immunosorbent assay.

resultsThe mean age of patients with IPF was 68.4 years and 83.0% were male; they were older than controls. The plasma leptin levels were higher in patients with IPF than those in controls and were independently associated with IPF presence (odds ratio: 1.007, 95% confidence interval [CI]: 1.003-1.011; P < 0.001) after adjusting age. Patients with high adiponectin levels (≥ 2700 ng/mL) had poorer survival than those without (median survival time: 25.0 vs. 62.0 months; P = 0.019). High adiponectin levels (≥ 2700 ng/mL) demonstrated an increased risk of mortality (hazard ratio [HR]: 2.304, 95% CI 1.041-5.102; P = 0.040) after adjusting the body mass index, forced vital capacity (FVC), diffusing capacity of the lung for carbon monoxide (DLCO), and treatment. Additionally, high adiponectin group demonstrated higher risk of acute exacerbation (AE) than low adiponectin group in the Kaplan-Meier analysis (log rank, P = 0.021). High adiponectin levels were also significantly associated with AE in the unadjusted Cox analysis (HR: 4.748; 95% CI 1.100-20.507; P = 0.037), but this association was not significant after adjusted for FVC and DLCO (HR: 3.821; 95% CI 0.872-16.742; P = 0.075).

conclusionPlasma adipokines are useful biomarkers for IPF diagnosis and prognosis.

Indexed as

AdiponectinIdiopathic Pulmonary FibrosisLeptinAgedBiomarkersCase-Control StudiesEnzyme-Linked Immunosorbent AssayFemaleHumansMaleMiddle AgedPredictive Value of TestsPrognosisRetrospective StudiesRisk FactorsVital CapacityAdiponectinADIPOQ protein, humanBiomarkersLeptinBiomarkerDiagnosisIdiopathic pulmonary fibrosisMortalityPrognosis

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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.