Longitudinal study of Stenotrophomonas maltophilia antibody levels and outcomes in cystic fibrosis patients

被引:13
作者
Wettlaufer, Jillian [1 ]
Klingel, Michelle [2 ]
Yau, Yvonne [3 ]
Stanojevic, Sanja [2 ]
Tullis, Elizabeth [4 ,5 ]
Ratjen, Felix [2 ]
Waters, Valerie [1 ]
机构
[1] Univ Toronto, Hosp Sick Children, Dept Pediat, Div Infect Dis, 555 Univ Ave, Toronto, ON M5G IX8, Canada
[2] Univ Toronto, Hosp Sick Children, Div Resp Med, Dept Pediat, Toronto, ON, Canada
[3] Univ Toronto, Hosp Sick Children, Dept Pediat Lab Med, Div Microbiol, 555 Univ Ave, Toronto, ON M5G 1X8, Canada
[4] Univ Toronto, St Michaels Hosp, Dept Med, Div Respirol, 30 Bond St, Toronto, ON M5B 1W8, Canada
[5] Univ Toronto, St Michaels Hosp, Li Ka Shing Knowledge Inst, Keenan Res Ctr,Dept Med, 30 Bond St, Toronto, ON M5B IW8, Canada
关键词
Cystic fibrosis; Stenotrophomonas maltophilia; Antibodies; Pulmonary exacerbation; PSEUDOMONAS-AERUGINOSA; ACQUISITION; INFECTION; MORTALITY;
D O I
10.1016/j.jcf.2016.06.007
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Previous studies have shown an association between higher Stenotrophomonas maltophilia antibody levels and decreased lung function in patients with cystic fibrosis (CF). The purpose of this study was to assess the serologic response to S. maltophilia over time and to determine whether changes in antibody levels could predict clinical outcomes. Methods: Changes in S. maltophilia antibody levels in adult and pediatric patients with CF from 2008 to 2014 were assessed between groups of infection patterns. Regression models accounting for repeated measures were used to assess whether antibody levels could predict subsequent S. maltophilia microbiological status, and whether they are associated with lung function and subsequent pulmonary exacerbation. Results: A total of 409 S. maltophilia antibody samples from 135 CF patients showed that antibody levels did not change significantly between study visits, regardless of infection group. Higher antibody levels were independently associated with future culture positivity (OR 1.62; 95% CI 1.09, 2.41; p = 0.02). While higher antibody levels were not independently associated with decreases in FEV1% predicted, they were associated with an increased hazard ratio for subsequent pulmonary exacerbation (HR 1.3; 95% CI 1.1, 1.6; p < 0.001). Conclusions: S. maltophilia antibody levels may be helpful to identify individuals at risk of exacerbation who may benefit from earlier antimicrobial treatment. (C) 2016 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:58 / 63
页数:6
相关论文
共 19 条
[1]  
Amin R, 2014, COCHRANE DB SYST REV, V4
[2]   Clinical and Epidemiologic Phenotypes of Childhood Asthma [J].
Depner, Martin ;
Fuchs, Oliver ;
Genuneit, Jon ;
Karvonen, Anne M. ;
Hyvarinen, Anne ;
Kaulek, Vincent ;
Roduit, Caroline ;
Weber, Juliane ;
Schaub, Bianca ;
Lauener, Roger ;
Kabesch, Michael ;
Pfefferle, Petra Ina ;
Frey, Urs ;
Pekkanen, Juha ;
Dalphin, Jean-Charles ;
Riedler, Josef ;
Braun-Fahrlaender, Charlotte ;
von Mutius, Erika ;
Ege, Markus J. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2014, 189 (02) :129-138
[3]  
DORING G, 1983, INFECT IMMUN, V42, P197
[4]   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
[5]   Pathophysiology and management of pulmonary infections in cystic fibrosis [J].
Gibson, RL ;
Burns, JL ;
Ramsey, BW .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2003, 168 (08) :918-951
[6]   PHARYNGEAL CARRIAGE AND ACQUISITION OF ANTICAPSULAR ANTIBODY TO HAEMOPHILUS-INFLUENZAE TYPE-B IN A HIGH-RISK POPULATION IN SOUTHWESTERN ALASKA [J].
HALL, DB ;
LUM, MKW ;
KNUTSON, LR ;
HEYWARD, WL ;
WARD, JI .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1987, 126 (06) :1190-1197
[7]   Distinguishing Asthma Phenotypes Using Machine Learning Approaches [J].
Howard, Rebecca ;
Rattray, Magnus ;
Prosperi, Mattia ;
Custovic, Adnan .
CURRENT ALLERGY AND ASTHMA REPORTS, 2015, 15 (07)
[8]   PREDICTION OF MORTALITY IN PATIENTS WITH CYSTIC-FIBROSIS [J].
KEREM, E ;
REISMAN, J ;
COREY, M ;
CANNY, GJ ;
LEVISON, H .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (18) :1187-1191
[9]  
Lee Tim W R, 2003, J Cyst Fibros, V2, P29, DOI 10.1016/S1569-1993(02)00141-8
[10]   Multi-ethnic reference values for spirometry for the 3-95-yr age range: the global lung function 2012 equations [J].
Quanjer, Philip H. ;
Stanojevic, Sanja ;
Cole, Tim J. ;
Baur, Xaver ;
Hall, Graham L. ;
Culver, Bruce H. ;
Enright, Paul L. ;
Hankinson, John L. ;
Ip, Mary S. M. ;
Zheng, Jinping ;
Stocks, Janet .
EUROPEAN RESPIRATORY JOURNAL, 2012, 40 (06) :1324-1343