Diagnostic and prognostic implications of family history of fibrotic interstitial lung diseases

Patients with familial fibrotic interstitial lung disease (ILD) experience worse survival than patients with sporadic disease. Current guidelines do not consider family aggregation or genetic information in the diagnostic algorithm for idiopathic pulmonary fibrosis or other fibrotic ILDs. Better cha...

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Veröffentlicht in:	Respiratory research 2024-12, Vol.25 (1), p.433-10
Hauptverfasser:	Duminy-Luppi, D, Alcaide-Aldeano, A, Planas-Cerezales, L, Bermudo, G, Vicens-Zygmunt, V, Luburich, P, Del Río-Carrero, B, Llatjós, R, Pijuan, L, Escobar, I, Rivas, F, Montes-Worboys, A, Gutiérrez-Rodríguez, Y, Rodríguez-Plaza, D, Padró-Miquel, A, Esteve-Garcia, A, Fernández-Varas, B, Flores, C, Fuentes, M, Dorca, J, Santos, S, Perona, R, Günther, A, Shull, J, Molina-Molina, M
Format:	Artikel
Sprache:	eng
Schlagworte:	Aged Bacterial pneumonia Biopsy Cohort Studies Development and progression Disease Progression Diseases Epidemiology Female Follow-Up Studies Genetic aspects Health aspects Humans Idiopathic Pulmonary Fibrosis - diagnosis Idiopathic Pulmonary Fibrosis - epidemiology Idiopathic Pulmonary Fibrosis - genetics Idiopathic Pulmonary Fibrosis - pathology Lung Lung diseases, interstitial Lung Diseases, Interstitial - diagnosis Lung Diseases, Interstitial - epidemiology Lung Diseases, Interstitial - genetics Male Medical colleges Medical research Medicine, Experimental Middle Aged Pneumonia Prognosis Retrospective Studies Telomerase Telomere Shortening Telomeres
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