» Articles » PMID: 18314323

Profusion of Fibroblast Foci in Patients with Idiopathic Pulmonary Fibrosis Does Not Predict Outcome

Overview
Journal Respir Med
Publisher Elsevier
Specialty Pulmonary Medicine
Date 2008 Mar 4
PMID 18314323
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Rationale: The prognostic significance of fibroblast foci in surgical lung biopsies from patients with idiopathic pulmonary fibrosis (IPF) is unclear.

Objectives: We assessed the relationship between profusion of fibroblast foci and survival in 43 patients with IPF seen at a tertiary referral medical center from 1996 to 2002.

Methods: Fibroblast foci in surgical lung biopsies were counted using a systematic morphometric point-counting technique. Patients with either clinical or pathologic evidence of accelerated disease were excluded from analysis. The association of fibroblast counts with survival was assessed using proportional hazards regression.

Results: The mean age (+/-SD) of the study population was 64+/-9 years; 26 (60%) patients were male. The mean (%+/-SD) profusion of fibroblastic foci was 0.6+/-0.7, expressed as a percentage of total points counted. Fibroblast foci counts did not differ markedly between upper, middle, and lower lobes. Median survival from the time of biopsy was 2.4 years; there were 25 (58%) deaths in the follow up period. There was no significant relationship between profusion of fibroblast foci and survival in the overall group (p=0.250).

Conclusions: Higher prevalence of fibroblast foci assessed using a simple point-counting technique applied to surgical lung biopsies is not associated with survival in patients with clinically stable IPF.

Citing Articles

Digital quantification of p16-positive foci in fibrotic interstitial lung disease is associated with a phenotype of idiopathic pulmonary fibrosis with reduced survival.

Keow J, Cecchini M, Jayawardena N, Zompatori M, Joseph M, Mura M Respir Res. 2022; 23(1):147.

PMID: 35672770 PMC: 9175499. DOI: 10.1186/s12931-022-02067-w.


The Extent of Inflammatory Cell Infiltrate and Fibrosis in Lungs of Telomere- and Surfactant-Related Familial Pulmonary Fibrosis.

van Batenburg A, van Oosterhout M, Knoppert S, Kazemier K, van der Vis J, Grutters J Front Med (Lausanne). 2021; 8:736485.

PMID: 34631753 PMC: 8497799. DOI: 10.3389/fmed.2021.736485.


The diagnosis of idiopathic pulmonary fibrosis: current and future approaches.

Martinez F, Chisholm A, Collard H, Flaherty K, Myers J, Raghu G Lancet Respir Med. 2016; 5(1):61-71.

PMID: 27932290 PMC: 5524148. DOI: 10.1016/S2213-2600(16)30325-3.


Three-dimensional characterization of fibroblast foci in idiopathic pulmonary fibrosis.

Jones M, Fabre A, Schneider P, Cinetto F, Sgalla G, Mavrogordato M JCI Insight. 2016; 1(5).

PMID: 27275013 PMC: 4889020. DOI: 10.1172/jci.insight.86375.


Lymphangiogenesis and Lesion Heterogeneity in Interstitial Lung Diseases.

Yamashita M Clin Med Insights Circ Respir Pulm Med. 2016; 9(Suppl 1):111-21.

PMID: 26823655 PMC: 4725607. DOI: 10.4137/CCRPM.S33856.