» Articles » PMID: 23728869

The Impact of Emphysema in Pulmonary Fibrosis

Overview
Journal Eur Respir Rev
Specialty Pulmonary Medicine
Date 2013 Jun 4
PMID 23728869
Citations 53
Authors
Affiliations
Soon will be listed here.
Abstract

Several groups have described a syndrome in which idiopathic pulmonary fibrosis (IPF) coexists with pulmonary emphysema. This comes as no surprise since both diseases are associated with a history of exposure to cigarette smoke. The syndrome of combined pulmonary fibrosis and emphysema (CPFE) is characterised by upper lobe emphysema and lower lobe fibrosis. Physiological testing of these patients reveals preserved lung volume indices contrasted by markedly impaired diffusion capacity. The incidence of CPFE remains unknown but several case series suggest that this subgroup may comprise up to 35% of patients with IPF. CPFE is a strong determinant of associated pulmonary hypertension (PH). In addition, CPFE has major effects on measures of physiological function, exercise capacity and prognosis, and may affect the results of pulmonary fibrosis trials. Further studies are needed to ascertain the aetiology, morbidity, mortality and management of the CPFE syndrome, with or without PH, and to evaluate novel therapeutic options in CPFE.

Citing Articles

Identifying health risk determinants and molecular targets in patients with idiopathic pulmonary fibrosis via combined differential and weighted gene co-expression analysis.

Moin A, Ullah M, Nipa J, Rahman M, Emran A, Islam M Front Genet. 2025; 15:1496462.

PMID: 39944354 PMC: 11813903. DOI: 10.3389/fgene.2024.1496462.


Research progress of SIRTs activator resveratrol and its derivatives in autoimmune diseases.

Yu X, Chen M, Wu J, Song R Front Immunol. 2024; 15:1390907.

PMID: 38962006 PMC: 11219927. DOI: 10.3389/fimmu.2024.1390907.


Impact of combined pulmonary fibrosis and emphysema on lung cancer risk and mortality in rheumatoid arthritis: A multicenter retrospective cohort study.

Mori S, Ueki Y, Hasegawa M, Nakamura K, Nakashima K, Hidaka T PLoS One. 2024; 19(2):e0298573.

PMID: 38412181 PMC: 10898759. DOI: 10.1371/journal.pone.0298573.


Transitional cell states sculpt tissue topology during lung regeneration.

Konkimalla A, Konishi S, Macadlo L, Kobayashi Y, Farino Z, Miyashita N Cell Stem Cell. 2023; 30(11):1486-1502.e9.

PMID: 37922879 PMC: 10762634. DOI: 10.1016/j.stem.2023.10.001.


The effect of CALIPER-derived parameters for idiopathic pulmonary fibrosis in predicting prognosis, progression, and mortality: a systematic review.

Jiao X, Song H, Liu W, Yang J, Wang Z, Yang D Eur Radiol. 2023; 33(10):7262-7273.

PMID: 37528299 DOI: 10.1007/s00330-023-10010-w.


References
1.
Rogliani P, Mura M, Mattia P, Ferlosio A, Farinelli G, Mariotta S . HRCT and histopathological evaluation of fibrosis and tissue destruction in IPF associated with pulmonary emphysema. Respir Med. 2008; 102(12):1753-61. DOI: 10.1016/j.rmed.2008.07.010. View

2.
Savale L, Chaouat A, Bastuji-Garin S, Marcos E, Boyer L, Maitre B . Shortened telomeres in circulating leukocytes of patients with chronic obstructive pulmonary disease. Am J Respir Crit Care Med. 2009; 179(7):566-71. PMC: 4850213. DOI: 10.1164/rccm.200809-1398OC. View

3.
Hiwatari N, Shimura S, Takishima T . Pulmonary emphysema followed by pulmonary fibrosis of undetermined cause. Respiration. 1993; 60(6):354-8. DOI: 10.1159/000196235. View

4.
Valdes A, Andrew T, Gardner J, Kimura M, Oelsner E, Cherkas L . Obesity, cigarette smoking, and telomere length in women. Lancet. 2005; 366(9486):662-4. DOI: 10.1016/S0140-6736(05)66630-5. View

5.
Galie N, Hoeper M, Humbert M, Torbicki A, Vachiery J, Barbera J . Guidelines for the diagnosis and treatment of pulmonary hypertension. Eur Respir J. 2009; 34(6):1219-63. DOI: 10.1183/09031936.00139009. View