Short- and long-term response to corticosteroid therapy in chronic beryllium disease
Chronic beryllium disease (CBD) is a granulomatous disorder that affects the lung after exposure to beryllium. The present study reports short- and long-term evolution of granulomatous and fibrotic components in eight patients with severe CBD receiving corticosteroid therapy. Eight patients with con...
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Veröffentlicht in: | The European respiratory journal 2008-09, Vol.32 (3), p.687-693 |
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description | Chronic beryllium disease (CBD) is a granulomatous disorder that affects the lung after exposure to beryllium. The present study reports short- and long-term evolution of granulomatous and fibrotic components in eight patients with severe CBD receiving corticosteroid therapy. Eight patients with confirmed CBD were studied at baseline, after initial corticosteroid treatment (4-12 months), at relapse and at the final visit. Beryllium exposure, Glu(69) (HLA-DPB1 genes coding for glutamate at position beta69) polymorphism, symptoms, pulmonary function tests (PFT), serum angiotensin-converting enzyme (SACE) and high-resolution computed tomography (HRCT) quantification of pulmonary lesions were analysed. The CBD patients were observed for a median (range) of 69 (20-180) months. After stopping beryllium exposure, corticosteroids improved symptoms and PFT (vital capacity +26%, diffusing capacity of the lung for carbon monoxide +15%), and decreased SACE level and active lesion HRCT score. In total, 18 clinical relapses occurred after the treatment was tapered and these were associated with SACE and active lesion HRCT score impairment. At the final visit, corticosteroids had completely stabilised all parameters including both HRCT scores of active lesions and fibrotic lesions in six out of eight patients. Corticosteroids were beneficial in chronic beryllium disease. They were effective in suppressing granulomatosis lesions in all cases and in stopping the evolution to pulmonary fibrosis in six out of eight patients. |
doi_str_mv | 10.1183/09031936.00149607 |
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W ; Lamberto, C ; Lepage, V ; Naccache, J-M ; Valeyre, D</creator><creatorcontrib>Marchand-Adam, S ; El Khatib, A ; Guillon, F ; Brauner, M. W ; Lamberto, C ; Lepage, V ; Naccache, J-M ; Valeyre, D</creatorcontrib><description>Chronic beryllium disease (CBD) is a granulomatous disorder that affects the lung after exposure to beryllium. The present study reports short- and long-term evolution of granulomatous and fibrotic components in eight patients with severe CBD receiving corticosteroid therapy. Eight patients with confirmed CBD were studied at baseline, after initial corticosteroid treatment (4-12 months), at relapse and at the final visit. Beryllium exposure, Glu(69) (HLA-DPB1 genes coding for glutamate at position beta69) polymorphism, symptoms, pulmonary function tests (PFT), serum angiotensin-converting enzyme (SACE) and high-resolution computed tomography (HRCT) quantification of pulmonary lesions were analysed. The CBD patients were observed for a median (range) of 69 (20-180) months. After stopping beryllium exposure, corticosteroids improved symptoms and PFT (vital capacity +26%, diffusing capacity of the lung for carbon monoxide +15%), and decreased SACE level and active lesion HRCT score. In total, 18 clinical relapses occurred after the treatment was tapered and these were associated with SACE and active lesion HRCT score impairment. At the final visit, corticosteroids had completely stabilised all parameters including both HRCT scores of active lesions and fibrotic lesions in six out of eight patients. Corticosteroids were beneficial in chronic beryllium disease. They were effective in suppressing granulomatosis lesions in all cases and in stopping the evolution to pulmonary fibrosis in six out of eight patients.</description><identifier>ISSN: 0903-1936</identifier><identifier>EISSN: 1399-3003</identifier><identifier>DOI: 10.1183/09031936.00149607</identifier><identifier>PMID: 18757698</identifier><language>eng</language><publisher>Leeds: Eur Respiratory Soc</publisher><subject>Adrenal Cortex Hormones - therapeutic use ; Adult ; Berylliosis - complications ; Berylliosis - drug therapy ; Berylliosis - immunology ; Biological and medical sciences ; Bones, joints and connective tissue. Antiinflammatory agents ; Bronchoalveolar Lavage Fluid - cytology ; Bronchoalveolar Lavage Fluid - immunology ; Chemical and industrial products toxicology. Toxic occupational diseases ; Humans ; Inorganic dusts (pneumoconiosises) and organic dusts (byssinosis etc.) ; Longitudinal Studies ; Mass Screening ; Medical sciences ; Middle Aged ; Pharmacology. Drug treatments ; Pneumology ; Pulmonary Fibrosis - etiology ; Pulmonary Fibrosis - prevention & control ; Recovery of Function ; Respiratory Function Tests ; Retrospective Studies ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. 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W</creatorcontrib><creatorcontrib>Lamberto, C</creatorcontrib><creatorcontrib>Lepage, V</creatorcontrib><creatorcontrib>Naccache, J-M</creatorcontrib><creatorcontrib>Valeyre, D</creatorcontrib><title>Short- and long-term response to corticosteroid therapy in chronic beryllium disease</title><title>The European respiratory journal</title><addtitle>Eur Respir J</addtitle><description>Chronic beryllium disease (CBD) is a granulomatous disorder that affects the lung after exposure to beryllium. The present study reports short- and long-term evolution of granulomatous and fibrotic components in eight patients with severe CBD receiving corticosteroid therapy. Eight patients with confirmed CBD were studied at baseline, after initial corticosteroid treatment (4-12 months), at relapse and at the final visit. Beryllium exposure, Glu(69) (HLA-DPB1 genes coding for glutamate at position beta69) polymorphism, symptoms, pulmonary function tests (PFT), serum angiotensin-converting enzyme (SACE) and high-resolution computed tomography (HRCT) quantification of pulmonary lesions were analysed. The CBD patients were observed for a median (range) of 69 (20-180) months. After stopping beryllium exposure, corticosteroids improved symptoms and PFT (vital capacity +26%, diffusing capacity of the lung for carbon monoxide +15%), and decreased SACE level and active lesion HRCT score. In total, 18 clinical relapses occurred after the treatment was tapered and these were associated with SACE and active lesion HRCT score impairment. At the final visit, corticosteroids had completely stabilised all parameters including both HRCT scores of active lesions and fibrotic lesions in six out of eight patients. Corticosteroids were beneficial in chronic beryllium disease. They were effective in suppressing granulomatosis lesions in all cases and in stopping the evolution to pulmonary fibrosis in six out of eight patients.</description><subject>Adrenal Cortex Hormones - therapeutic use</subject><subject>Adult</subject><subject>Berylliosis - complications</subject><subject>Berylliosis - drug therapy</subject><subject>Berylliosis - immunology</subject><subject>Biological and medical sciences</subject><subject>Bones, joints and connective tissue. Antiinflammatory agents</subject><subject>Bronchoalveolar Lavage Fluid - cytology</subject><subject>Bronchoalveolar Lavage Fluid - immunology</subject><subject>Chemical and industrial products toxicology. Toxic occupational diseases</subject><subject>Humans</subject><subject>Inorganic dusts (pneumoconiosises) and organic dusts (byssinosis etc.)</subject><subject>Longitudinal Studies</subject><subject>Mass Screening</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacology. Drug treatments</subject><subject>Pneumology</subject><subject>Pulmonary Fibrosis - etiology</subject><subject>Pulmonary Fibrosis - prevention & control</subject><subject>Recovery of Function</subject><subject>Respiratory Function Tests</subject><subject>Retrospective Studies</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</subject><subject>Toxicology</subject><issn>0903-1936</issn><issn>1399-3003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkEtLAzEYRYMotlZ_gBvJxuXUZDKTx1KKLyi4sK5DMkk6KTOTkkyR_ntTWu0qfNxzL-EAcI_RHGNOnpBABAtC5wjhSlDELsAUEyEKghC5BNNDXhyACbhJaZMpWhF8DSaYs5pRwadg9dWGOBZQDQZ2YVgXo409jDZtw5AsHANscu6bkHIQvIFja6Pa7qEfYNPGMPgGahv3Xed3PTQ-WZXsLbhyqkv27vTOwPfry2rxXiw_3z4Wz8uiqSgfC126WhvhHKkrQ2k-lKGs5rhkmjgueP4mR0wpQbUzBpe2tpaWuiq1U5gpMgP4uNvEkFK0Tm6j71XcS4zkwZD8MyT_DOXOw7Gz3enemnPjpCQDjydApUZ1Lqqh8emfK1Et8jQ6c61ftz8-Wpl61XV5FksbN6SURFLOyC9vEXwK</recordid><startdate>20080901</startdate><enddate>20080901</enddate><creator>Marchand-Adam, S</creator><creator>El Khatib, A</creator><creator>Guillon, F</creator><creator>Brauner, M. 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W ; Lamberto, C ; Lepage, V ; Naccache, J-M ; Valeyre, D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c468t-b2f5bd9ff354d66f5bad6758127b3f898187807aa96bfdd12e5ee62b42bfa17a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adrenal Cortex Hormones - therapeutic use</topic><topic>Adult</topic><topic>Berylliosis - complications</topic><topic>Berylliosis - drug therapy</topic><topic>Berylliosis - immunology</topic><topic>Biological and medical sciences</topic><topic>Bones, joints and connective tissue. Antiinflammatory agents</topic><topic>Bronchoalveolar Lavage Fluid - cytology</topic><topic>Bronchoalveolar Lavage Fluid - immunology</topic><topic>Chemical and industrial products toxicology. Toxic occupational diseases</topic><topic>Humans</topic><topic>Inorganic dusts (pneumoconiosises) and organic dusts (byssinosis etc.)</topic><topic>Longitudinal Studies</topic><topic>Mass Screening</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pharmacology. Drug treatments</topic><topic>Pneumology</topic><topic>Pulmonary Fibrosis - etiology</topic><topic>Pulmonary Fibrosis - prevention & control</topic><topic>Recovery of Function</topic><topic>Respiratory Function Tests</topic><topic>Retrospective Studies</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marchand-Adam, S</creatorcontrib><creatorcontrib>El Khatib, A</creatorcontrib><creatorcontrib>Guillon, F</creatorcontrib><creatorcontrib>Brauner, M. W</creatorcontrib><creatorcontrib>Lamberto, C</creatorcontrib><creatorcontrib>Lepage, V</creatorcontrib><creatorcontrib>Naccache, J-M</creatorcontrib><creatorcontrib>Valeyre, D</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>The European respiratory journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marchand-Adam, S</au><au>El Khatib, A</au><au>Guillon, F</au><au>Brauner, M. 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Beryllium exposure, Glu(69) (HLA-DPB1 genes coding for glutamate at position beta69) polymorphism, symptoms, pulmonary function tests (PFT), serum angiotensin-converting enzyme (SACE) and high-resolution computed tomography (HRCT) quantification of pulmonary lesions were analysed. The CBD patients were observed for a median (range) of 69 (20-180) months. After stopping beryllium exposure, corticosteroids improved symptoms and PFT (vital capacity +26%, diffusing capacity of the lung for carbon monoxide +15%), and decreased SACE level and active lesion HRCT score. In total, 18 clinical relapses occurred after the treatment was tapered and these were associated with SACE and active lesion HRCT score impairment. At the final visit, corticosteroids had completely stabilised all parameters including both HRCT scores of active lesions and fibrotic lesions in six out of eight patients. Corticosteroids were beneficial in chronic beryllium disease. They were effective in suppressing granulomatosis lesions in all cases and in stopping the evolution to pulmonary fibrosis in six out of eight patients.</abstract><cop>Leeds</cop><pub>Eur Respiratory Soc</pub><pmid>18757698</pmid><doi>10.1183/09031936.00149607</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adrenal Cortex Hormones - therapeutic use Adult Berylliosis - complications Berylliosis - drug therapy Berylliosis - immunology Biological and medical sciences Bones, joints and connective tissue. Antiinflammatory agents Bronchoalveolar Lavage Fluid - cytology Bronchoalveolar Lavage Fluid - immunology Chemical and industrial products toxicology. Toxic occupational diseases Humans Inorganic dusts (pneumoconiosises) and organic dusts (byssinosis etc.) Longitudinal Studies Mass Screening Medical sciences Middle Aged Pharmacology. Drug treatments Pneumology Pulmonary Fibrosis - etiology Pulmonary Fibrosis - prevention & control Recovery of Function Respiratory Function Tests Retrospective Studies Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis Toxicology |
title | Short- and long-term response to corticosteroid therapy in chronic beryllium disease |
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