%0 Journal Article %T Prevalence and incidence of interstitial lung diseases in a multi-ethnic county of Greater Paris %+ Service de pneumologie [Avicenne] %+ Hypoxie et Poumon : pneumopathologies fibrosantes, modulations ventilatoires et circulatoires (H&P - U1272 Inserm) %+ Institut Pierre Louis d'Epidémiologie et de Santé Publique (iPLESP) %+ DRSM %+ Hôpital Avicenne [AP-HP] %+ Hôpital Robert Ballanger [Aulnay-sous-Bois] %+ CHU Tenon [AP-HP] %+ AP-HP - Hôpital Bichat - Claude Bernard [Paris] %+ Hôpital Jean Verdier [AP-HP] %+ Centre Hospitalier de Saint-Denis [Ile-de-France] %+ Sciences Po (Sciences Po) %A Duchemann, Boris %A Annesi-Maesano, Isabella %A Jacobé de Naurois, Charlotte %A Sanyal, Shreosi %A Brillet, Pierre-Yves %A Kambouchner, Marianne %A Phin Huynh, Sophie %A Naccache, Jean-Marc %A Borie, Raphael %A Piquet, Jacques %A Mekinian, Arsène %A Virally, Jérôme %A Uzunhan, Yurdagul %A Cadranel, Jacques %A Crestani, Bruno %A Fain, Olivier %A Lhote, Francois %A Dhote, Robin %A Saidenberg-Kermanac'H, Nathalie %A Rosental, Paul-Andre %A Valeyre, Dominique %A Nunes, Hilario %< avec comité de lecture %Z 2441/2pgnlfr3bc8mqrapog6oi5ptvo %@ 0903-1936 %J European Respiratory Journal %I European Respiratory Society %V 50 %N 2 %P . %8 2017-08 %D 2017 %R 10.1183/13993003.02419-2016 %K Interstitial lung diseases %K Great Paris %K Multi-ethnic county %Z Environmental Sciences/Environmental and Society %Z Humanities and Social Sciences/History, Philosophy and Sociology of SciencesJournal articles %X The objective of the study was to estimate the prevalence and incidence of interstitial lung diseases (ILDs) in Seine-Saint-Denis, a multi-ethnic county of Greater Paris, France. Patients with ILDs were identified between January and December 2012 by using several sources; all potentially involved medical specialists from public and private hospitals, community-based pulmonologists and general practitioners, and the Social Security system. Diagnoses were validated centrally by an expert multidisciplinary discussion. 1170 ILD cases were reported (crude overall prevalence: 97.9/10⁵ and incidence: 19.4/10⁵/year). In the 848 reviewed cases, the most prevalent diagnoses were sarcoidosis (42.6%), connective tissue diseases associated ILDs (CTDs-ILDs) (16%), idiopathic pulmonary fibrosis (IPF) (11.6%), and occupational ILDs (5.0%), which corresponded to a crude prevalence of 30.2/10⁵ for sarcoidosis, 12.1/10⁵ for CTDs-ILDs and 8.2/10⁵ for IPF. The prevalence of fibrotic idiopathic interstitial pneumonias, merging IPF, nonspecific interstitial pneumonia and cases registered with code J84.1 was 16.34/10⁵. An adjusted multinomial model demonstrated an increased risk of sarcoidosis in North Africans and Afro-Caribbeans and of CTDs-ILDs in Afro-Caribbeans, compared to that in Europeans. This study, with a comprehensive recruitment and stringent diagnostic criteria, emphasises the importance of secondary ILDs, particularly CTDs-ILDs and the relatively low prevalence of IPF, and confirms that sarcoidosis is a rare disease in France. [résumé éditeur] %G English %L hal-03435018 %U https://sciencespo.hal.science/hal-03435018 %~ SHS %~ SDE %~ UNIV-PARIS13 %~ SCIENCESPO %~ APHP %~ OPENAIRE %~ GIP-BE %~ HIPHISCITECH %~ IPLESP %~ USPC %~ SORBONNE-UNIVERSITE %~ SU-INF-2018 %~ SU-MEDECINE %~ SU-MED %~ SORBONNE-PARIS-NORD %~ SU-TI %~ ALLIANCE-SU