Increasing nontuberculous mycobacteria infection in cystic fibrosis

被引:113
作者
Bar-On, Ophir [1 ]
Mussaffi, Huda [1 ,2 ]
Mei-Zahav, Meir [1 ,2 ]
Prais, Dario [1 ,2 ]
Steuer, Guy [1 ]
Stafler, Patrick [1 ,2 ]
Hananya, Shai [1 ]
Blau, Hannah [1 ,2 ]
机构
[1] Schneider Childrens Med Ctr Israel, Graub CF Ctr, Pulm Inst, IL-49202 Petah, Tikva, Israel
[2] Tel Aviv Univ, Sackler Fac Med, IL-69978 Tel Aviv, Israel
关键词
Cystic fibrosis; Nontuberculous mycobacteria; Mycobacterium abscessus; Allergic bronchopulmonary aspergillosis; RAPIDLY GROWING MYCOBACTERIA; LUNG-DISEASE; ABSCESSUS; AVIUM; DIAGNOSIS; ADULTS;
D O I
10.1016/j.jcf.2014.05.008
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
100201 [内科学];
摘要
Background: Nontuberculous mycobacteria (NTM) are emerging infections in the CF population. Aims: To assess NTM infection prevalence and associated features in our CF clinic population. Methods: Patient records, 2002-2011, were reviewed for NTM infection. FEV1, pancreatic function, sputum microbiology, and serum cytokines were compared in patients with and without NTM infection. Results: Incidence rate of NTM infection increased from 0 in 2002 to 8.7% in 2011 (p < 0.001). NTM infection prevalence increased 3-fold from 5% (4/79) in 2003 to 14.5% (16/110) in 2011 (p = 0.05). Prevalence of chronic NTM lung disease has decreased somewhat since a peak in 2009, with institution of aggressive triple therapy. Of NTM-infected compared to uninfected patients, 88.2% vs. 60.3% had a known 'severe' CFTR genotype (p = 0.04), 88.2% vs. 58.9% were pancreatic insufficient (p = 0.02); 70.6% vs. 43.8% had chronic Pseudomonas aeruginosa (p = 0.06); 75% vs. 32% had Aspergillus infection (p = 0.007) and 23.5% vs 2.7% had allergic bronchopulmonary aspergillosis (p = 0.01). Patients infected with Mycobacterium abscessus had increased TGF-beta, TNF-alpha, IL-1 beta, IL-2, IL-4 and IL-5 levels (p < 0.05). There was no difference in cytokine levels for all NTM infected compared to uninfected patients. M abscessus comprised 46% of all NTM infections. Comparing M abscessus versus other NTM, duration was 10.5 (1-118) months versus 1 (1-70) month, median (range) (p = 0.004); lung disease occurred in 69% versus 17% (p = 0.0004), with sputum conversion in 4/11 versus 5/6, respectively (NS). Conclusions: NTM incidence and prevalence have increased dramatically in our CF clinic, associated with a severe CF genotype and phenotype. M abscessus, the most prevalent NTM, caused prolonged infection despite therapy. There has been some decrease in the prevalence of NTM lung disease since 2009. (C) 2014 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:53 / 62
页数:10
相关论文
共 30 条
[1]
[Anonymous], 2011, UK CF REG ANN DAT RE
[2]
[Anonymous], 2012, ECFS PAT REG ANN DAT
[3]
ISOLATION OF RAPIDLY GROWING MYCOBACTERIA IN PATIENTS WITH CYSTIC-FIBROSIS [J].
BOXERBAUM, B .
JOURNAL OF PEDIATRICS, 1980, 96 (04) :689-691
[4]
Whole-genome sequencing to identify transmission of Mycobacterium abscessus between patients with cystic fibrosis: a retrospective cohort study [J].
Bryant, Josephine M. ;
Grogono, Dorothy M. ;
Greaves, Daniel ;
Foweraker, Juliet ;
Roddick, Iain ;
Inns, Thomas ;
Reacher, Mark ;
Haworth, Charles S. ;
Curran, Martin D. ;
Harris, Simon R. ;
Peacock, Sharon J. ;
Parkhill, Julian ;
Floto, R. Andres .
LANCET, 2013, 381 (9877) :1551-1560
[5]
Mycobacterium avium and Mycobacterium abscessus complex target distinct cystic fibrosis patient subpopulations [J].
Catherinot, Emilie ;
Roux, Anne-Laure ;
Vibet, Marie-Anne ;
Bellis, Gil ;
Ravilly, Sophie ;
Lemonnier, Lydie ;
Le Roux, Evelyne ;
Bernede-Bauduin, Claire ;
Le Bourgeois, Muriel ;
Herrmann, Jean-Louis ;
Guillemot, Didier ;
Gaillard, Jean-Louis .
JOURNAL OF CYSTIC FIBROSIS, 2013, 12 (01) :74-80
[6]
Host Immune Response to Rapidly Growing Mycobacteria, an Emerging Cause of Chronic Lung Disease [J].
Chan, Edward D. ;
Bai, Xiyuan ;
Kartalija, Marinka ;
Ormes, Ian M. ;
Ordways, Diane J. .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2010, 43 (04) :387-393
[7]
Surrounded by mycobacteria: nontuberculous mycobacteria in the human environment [J].
Falkinham, J. O., III .
JOURNAL OF APPLIED MICROBIOLOGY, 2009, 107 (02) :356-367
[8]
Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report [J].
Farrell, Philip M. ;
Rosenstein, Beryl J. ;
White, Terry B. ;
Accurso, Frank J. ;
Castellani, Carlo ;
Cutting, Garry R. ;
Durie, Peter R. ;
LeGrys, Vicky A. ;
Massie, John ;
Parad, Richard B. ;
Rock, Michael J. ;
Campbell, Preston W., III .
JOURNAL OF PEDIATRICS, 2008, 153 (02) :S4-S14
[9]
Pathological and radiological changes in resected lung specimens in Mycobacterium avium intracellulare complex disease [J].
Fujita, J ;
Ohtsuki, Y ;
Suemitsu, I ;
Shigeto, E ;
Yamadori, I ;
Obayashi, Y ;
Miyawaki, H ;
Dobashi, N ;
Matsushima, T ;
Takahara, J .
EUROPEAN RESPIRATORY JOURNAL, 1999, 13 (03) :535-540
[10]
Mutations that permit residual CFTR function delay acquisition of multiple respiratory pathogens in CF patients [J].
Green, Deanna M. ;
McDougal, Kathryn E. ;
Blackman, Scott M. ;
Sosnay, Patrick R. ;
Henderson, Lindsay B. ;
Naughton, Kathleen M. ;
Collaco, J. Michael ;
Cutting, Garry R. .
RESPIRATORY RESEARCH, 2010, 11