Chronic Granulomatous Disease: The European Experience |
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| Authors: | J. Merlijn van den Berg, Elsbeth van Koppen, Anders hlin, Bernd H. Belohradsky, Ewa Bernatowska, Lucien Corbeel, Teresa Espa ol, Alain Fischer, Magdalena Kurenko-Deptuch, Richard Mouy, Theoni Petropoulou, Joachim Roesler, Reinhard Seger, Marie-Jos Stasia, Niels H. Valerius, Ron S. Weening, Baruch Wolach, Dirk Roos, Taco W. Kuijpers |
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| Affiliation: | J. Merlijn van den Berg, Elsbeth van Koppen, Anders Åhlin, Bernd H. Belohradsky, Ewa Bernatowska, Lucien Corbeel, Teresa Español, Alain Fischer, Magdalena Kurenko-Deptuch, Richard Mouy, Theoni Petropoulou, Joachim Roesler, Reinhard Seger, Marie-José Stasia, Niels H. Valerius, Ron S. Weening, Baruch Wolach, Dirk Roos, and Taco W. Kuijpers |
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| Abstract: | CGD is an immunodeficiency caused by deletions or mutations in genes that encode subunits of the leukocyte NADPH oxidase complex. Normally, assembly of the NADPH oxidase complex in phagosomes of certain phagocytic cells leads to a “respiratory burst”, essential for the clearance of phagocytosed micro-organisms. CGD patients lack this mechanism, which leads to life-threatening infections and granuloma formation. However, a clear picture of the clinical course of CGD is hampered by its low prevalence (~1![[ratio]](corehtml/pmc/pmcents/x2236.gif "/>250,000). Therefore, extensive clinical data from 429 European patients were collected and analyzed. Of these patients 351 were males and 78 were females. X-linked (XL) CGD (gp91<em><sup>phox</sup></em> deficient) accounted for 67% of the cases, autosomal recessive (AR) inheritance for 33%. AR-CGD was diagnosed later in life, and the mean survival time was significantly better in AR patients (49.6 years) than in XL CGD (37.8 years), suggesting a milder disease course in AR patients. The disease manifested itself most frequently in the lungs (66% of patients), skin (53%), lymph nodes (50%), gastrointestinal tract (48%) and liver (32%). The most frequently cultured micro-organisms per episode were <em>Staphylococcus aureus</em> (30%), <em>Aspergillus spp.</em> (26%), and <em>Salmonella spp.</em> (16%). Surprisingly, <em>Pseudomonas spp.</em> (2%) and <em>Burkholderia cepacia</em> (<1%) were found only sporadically. Lesions induced by inoculation with BCG occurred in 8% of the patients. Only 71% of the patients received antibiotic maintenance therapy, and 53% antifungal prophylaxis. 33% were treated with γ-interferon. 24 patients (6%) had received a stem cell transplantation. The most prominent reason of death was pneumonia and pulmonary abscess (18/84 cases), septicemia (16/84) and brain abscess (4/84). These data provide further insight in the clinical course of CGD in Europe and hopefully can help to increase awareness and optimize the treatment of these patients.</td>
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