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Pulmonary Hypertension in Patients with Common Variable Immunodeficiency.
Thoré, Pierre; Jaïs, Xavier; Savale, Laurent; Dorfmuller, Peter; Boucly, Athénaïs; Devilder, Matthieu; Meyrignac, Olivier; Pichon, Jérémie; Mankikian, Julie; Riou, Marianne; Boiffard, Emmanuel; Boissin, Clément; De Groote, Pascal; Chabanne, Céline; Gagnadoux, Frédéric; Bergeron, Anne; Noel, Nicolas; Sitbon, Olivier; Humbert, Marc; Montani, David.
Affiliation
  • Thoré P; Assistance Publique - Hôpitaux de Paris (AP-HP), Department of Respiratory and Intensive Care Medicine, Pulmonary Hypertension National Referral Center, Hôpital Bicêtre, Le Kremlin-Bicêtre, France.
  • Jaïs X; Centre Hospitalier Régional Universitaire (CHRU) de Nancy, Department of Pneumology, Hôpital Brabois, Vandoeuvre-lès-Nancy, France.
  • Savale L; INSERM UMR_S 1116 "Défaillance Cardiovasculaire Aigüe Et Chronique", School of Medicine of Nancy, University of Lorraine, Nancy, France.
  • Dorfmuller P; Assistance Publique - Hôpitaux de Paris (AP-HP), Department of Respiratory and Intensive Care Medicine, Pulmonary Hypertension National Referral Center, Hôpital Bicêtre, Le Kremlin-Bicêtre, France.
  • Boucly A; School of Medicine, University Paris-Saclay, Le Kremlin-Bicêtre, France.
  • Devilder M; INSERM UMR_S 999 "Pulmonary Hypertension: Pathophysiology and Novel Therapies", Hôpital Marie Lannelongue, Le Plessis-Robinson, France.
  • Meyrignac O; Assistance Publique - Hôpitaux de Paris (AP-HP), Department of Respiratory and Intensive Care Medicine, Pulmonary Hypertension National Referral Center, Hôpital Bicêtre, Le Kremlin-Bicêtre, France.
  • Pichon J; School of Medicine, University Paris-Saclay, Le Kremlin-Bicêtre, France.
  • Mankikian J; INSERM UMR_S 999 "Pulmonary Hypertension: Pathophysiology and Novel Therapies", Hôpital Marie Lannelongue, Le Plessis-Robinson, France.
  • Riou M; Department of Pathology, University Hospital of Giessen and Marburg (UKGM), Giessen, Germany.
  • Boiffard E; Assistance Publique - Hôpitaux de Paris (AP-HP), Department of Respiratory and Intensive Care Medicine, Pulmonary Hypertension National Referral Center, Hôpital Bicêtre, Le Kremlin-Bicêtre, France.
  • Boissin C; School of Medicine, University Paris-Saclay, Le Kremlin-Bicêtre, France.
  • De Groote P; INSERM UMR_S 999 "Pulmonary Hypertension: Pathophysiology and Novel Therapies", Hôpital Marie Lannelongue, Le Plessis-Robinson, France.
  • Chabanne C; School of Medicine, University Paris-Saclay, Le Kremlin-Bicêtre, France.
  • Gagnadoux F; Assistance Publique - Hôpitaux de Paris (AP-HP), Department of Radiology, Hôpital Bicêtre, Le Kremlin-Bicêtre, France.
  • Bergeron A; School of Medicine, University Paris-Saclay, Le Kremlin-Bicêtre, France.
  • Noel N; Assistance Publique - Hôpitaux de Paris (AP-HP), Department of Radiology, Hôpital Bicêtre, Le Kremlin-Bicêtre, France.
  • Sitbon O; Assistance Publique - Hôpitaux de Paris (AP-HP), Department of Respiratory and Intensive Care Medicine, Pulmonary Hypertension National Referral Center, Hôpital Bicêtre, Le Kremlin-Bicêtre, France.
  • Humbert M; School of Medicine, University Paris-Saclay, Le Kremlin-Bicêtre, France.
  • Montani D; INSERM UMR_S 999 "Pulmonary Hypertension: Pathophysiology and Novel Therapies", Hôpital Marie Lannelongue, Le Plessis-Robinson, France.
J Clin Immunol ; 41(7): 1549-1562, 2021 10.
Article in En | MEDLINE | ID: mdl-34110542
PURPOSE: 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. METHODS: We report the clinical, functional, hemodynamics, radiologic and histologic characteristics, and outcomes of CVID-associated PH patients from the French PH Network. RESULTS: 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. CONCLUSION: 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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Common Variable Immunodeficiency / Hypertension, Pulmonary Type of study: Prognostic_studies Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: J Clin Immunol Year: 2021 Document type: Article Affiliation country: Francia Country of publication: Países Bajos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Common Variable Immunodeficiency / Hypertension, Pulmonary Type of study: Prognostic_studies Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: J Clin Immunol Year: 2021 Document type: Article Affiliation country: Francia Country of publication: Países Bajos