Evidence map›Paper›PMID 41703565›Full record

ArticleRespiratory research2026

High density lipoproteins, disease severity and clinical outcomes in patients with idiopathic pulmonary fibrosis.

Anna J Podolanczuk, Hillary Mulder, John S Kim, Megan L Neely, Robert J Kaner, Jamie L Todd

Abstract read
In one paragraph

Article in Respiratory research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

1 citing paper in PubMed.

  1. Article
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

6 authors.

Anna J PodolanczukWeill Cornell Medicine, New York, USA. ajp9012@med.cornell.edu.
Hillary MulderDuke Clinical Research Institute, Durham, USA.
John S KimUniversity of Virginia, Charlottesville, USA.
Megan L NeelyDuke Clinical Research Institute, Durham, USA.
Robert J KanerWeill Cornell Medicine, New York, USA.
Jamie L ToddDuke Clinical Research Institute, Durham, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDysregulation of lipid metabolism is implicated in the pathogenesis of idiopathic pulmonary fibrosis (IPF). We assessed associations between circulating levels of high-density lipoprotein-cholesterol (HDL-C) and its components apolipoprotein A-1 (ApoA1) and paraoxonase-1 (PON-1) and disease severity and outcomes in patients with IPF.

methodsThe cohort comprised 284 patients enrolled in the IPF-PRO Registry. We analyzed associations between HDL-C, ApoA1 and PON-1 levels at enrollment and measures of disease severity at enrollment (using linear regression) and outcomes during follow-up (using Cox models). Models were adjusted for demographic and clinical variables, including cardiovascular disease and statin use, assessed at enrollment.

resultsIn unadjusted models, higher ApoA1 and lower PON-1 were associated with higher FVC % predicted at enrollment. Median follow-up was 40 months. In unadjusted models, higher ApoA1 at enrollment was associated with lower risks of all-cause mortality (hazard ratio [HR] 0.32 [95% CI: 0.16, 0.64] per unit higher log2 ApoA1) and respiratory hospitalization (HR 0.25 [0.11, 0.57] per unit higher log2 ApoA1). In analyses adjusted for demographic and clinical variables, the association with respiratory hospitalization remained significant (HR 0.30 [95% CI: 0.10, 0.88; p = 0.029]), but the association with all-cause mortality was no longer significant (HR 0.44 [95% CI: 0.18, 1.08; p = 0.074]). Levels of PON-1 or HDL-C were not associated with all-cause mortality or respiratory hospitalization.

conclusionIn a real-world cohort of patients with IPF, a higher circulating level of ApoA1 was associated with a lower risk of respiratory hospitalization. ApoA1 is a potential prognostic biomarker in patients with IPF.

Indexed as

Apolipoprotein A-ICholesterol, HDLIdiopathic Pulmonary FibrosisLipoproteins, HDLSeverity of Illness IndexAgedAryldialkylphosphataseBiomarkersCohort StudiesFemaleFollow-Up StudiesHumansMaleMiddle AgedRegistriesAPOA1 protein, humanApolipoprotein A-IAryldialkylphosphataseBiomarkersCholesterol, HDLLipoproteins, HDLPON1 protein, humanBiomarkersDisease progressionLipidsLung diseases, interstitial

Identifiers

PMID41703565
PMCPMC12911027

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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.