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Pulmonary Hypertension in Patients with Common Variable Immunodeficiency

Authors :
Matthieu Devilder
Laurent Savale
Pascal de Groote
Frédéric Gagnadoux
Pierre Thoré
Julie Mankikian
Clément Boissin
Nicolas Noel
E. Boiffard
Xavier Jaïs
Athénaïs Boucly
Céline Chabanne
Jérémie Pichon
Peter Dorfmüller
Olivier Meyrignac
Olivier Sitbon
Marc Humbert
Anne Bergeron
Marianne Riou
David Montani
Source :
Journal of Clinical Immunology. 41:1549-1562
Publication Year :
2021
Publisher :
Springer Science and Business Media LLC, 2021.

Abstract

Common variable immunodeficiency (CVID) is known to cause infectious, inflammatory, and autoimmune manifestations. Pulmonary hypertension (PH) is an unusual complication of CVID with largely unknown characteristics and mechanisms. We report the clinical, functional, hemodynamics, radiologic and histologic characteristics, and outcomes of CVID-associated PH patients from the French PH Network. Ten patients were identified. The median (range) age at CVID diagnosis was 36.5 (4–49) years and the median delay between CVID and PH diagnosis was 12 (0–30) years. CVID-associated PH affected predominantly women (female-to-male ratio 9:1). Most patients were New York Heart Association functional class III with a severe hemodynamic profile and frequent portal hypertension (n = 6). Pulmonary function tests were almost normal in 70% of patients and showed a mild restrictive syndrome in 30% of patients while the diffusing capacity for carbon monoxide was decreased in all but one patient. High-resolution computed tomography found enlarged mediastinal nodes, mild interstitial infiltration with reticulations and nodules. Two patients had a CIVD-interstitial lung disease, and one presented with bronchiectasis. Pathologic assessment of lymph nodes performed in 5 patients revealed the presence of granulomas (n = 5) and follicular lymphoid hyperplasia (n = 3). At last follow-up (median 24.5 months), 9 patients were alive, and one patient died of Hodgkin disease. PH is a possible complication of CVID whose pathophysiological mechanisms, while still unclear, would be due to the inflammatory nature of CVID. CVID-associated PH presents as precapillary PH with multiple possible causes, acting in concert in some patients: a portal hypertension, a pulmonary vascular remodeling, sometimes a pulmonary parenchymal involvement and occasionally an extrinsic compression by mediastinal lymphadenopathies, which would be consistent with its classification in group 5 of the current PH classification.

Details

ISSN :
15732592 and 02719142
Volume :
41
Database :
OpenAIRE
Journal :
Journal of Clinical Immunology
Accession number :
edsair.doi...........1a511a3c44e8bfeb24ce6bd7624cb20c