Antibiotic Exposure and IBD Development Among Children: A Population-Based Cohort Study

被引:308
作者
Kronman, Matthew P. [1 ]
Zaoutis, Theoklis E. [2 ,3 ]
Haynes, Kevin [3 ]
Feng, Rui [3 ]
Coffin, Susan E. [2 ,3 ]
机构
[1] Univ Washington, Div Infect Dis, Seattle Childrens Hosp, Seattle, WA 98105 USA
[2] Childrens Hosp Philadelphia, Div Infect Dis, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Biostat & Epidemiol, Ctr Clin Epidemiol & Biostat, Perelman Sch Med, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院; 美国医疗保健研究与质量局;
关键词
antimicrobials; epidemiology; inflammatory bowel disease; pediatric; population-based studies; INFLAMMATORY-BOWEL-DISEASE; PRACTICE RESEARCH DATABASE; CROHNS-DISEASE; ULCERATIVE-COLITIS; RISK-FACTORS; 1ST YEAR; ASSOCIATION; INFECTIONS; CHILDHOOD; RATES;
D O I
10.1542/peds.2011-3886
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
OBJECTIVE: To determine whether childhood antianaerobic antibiotic exposure is associated with the development of inflammatory bowel disease (IBD). METHODS: This retrospective cohort study employed data from 464 UK ambulatory practices participating in The Health Improvement Network. All children with >= 2 years of follow-up from 1994 to 2009 were followed between practice enrollment and IBD development, practice deregistration, 19 years of age, or death; those with previous IBD were excluded. All antibiotic prescriptions were captured. Antianaerobic antibiotic agents were defined as penicillin, amoxicillin, ampicillin, penicillin/beta-lactamase inhibitor combinations, tetracyclines, clindamycin, metronidazole, cefoxitin, carbapenems, and oral vancomycin. RESULTS: A total of 1 072 426 subjects contributed 6.6 million person-years of follow-up; 748 developed IBD. IBD incidence rates among antianaerobic antibiotic unexposed and exposed subjects were 0.83 and 1.52/10 000 person-years, respectively, for an 84% relative risk increase. Exposure throughout childhood was associated with developing IBD, but this relationship decreased with increasing age at exposure. Exposure before 1 year of age had an adjusted hazard ratio of 5.51 (95% confidence interval [CI]: 1.66-18.28) but decreased to 2.62 (95% CI: 1.61-4.25) and 1.57 (95% CI: 1.35-1.84) by 5 and 15 years, respectively. Each antibiotic course increased the IBD hazard by 6% (4%-8%). A dose-response effect existed, with receipt of >2 antibiotic courses more highly associated with IBD development than receipt of 1 to 2 courses, with adjusted hazard ratios of 4.77 (95% CI: 2.13-10.68) versus 3.33 (95% CI: 1.69-6.58). CONCLUSIONS: Childhood antianaerobic antibiotic exposure is associated with IBD development. Pediatrics 2012; 130: e794-e803
引用
收藏
页码:E794 / E803
页数:10
相关论文
共 34 条
[1]   Mechanisms of disease: The effect of infections on susceptibility to autoimmune and allergic diseases [J].
Bach, JF .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (12) :911-920
[2]   Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease [J].
Barrett, Jeffrey C. ;
Hansoul, Sarah ;
Nicolae, Dan L. ;
Cho, Judy H. ;
Duerr, Richard H. ;
Rioux, John D. ;
Brant, Steven R. ;
Silverberg, Mark S. ;
Taylor, Kent D. ;
Barmada, M. Michael ;
Bitton, Alain ;
Dassopoulos, Themistocles ;
Datta, Lisa Wu ;
Green, Todd ;
Griffiths, Anne M. ;
Kistner, Emily O. ;
Murtha, Michael T. ;
Regueiro, Miguel D. ;
Rotter, Jerome I. ;
Schumm, L. Philip ;
Steinhart, A. Hillary ;
Targan, Stephan R. ;
Xavier, Ramnik J. ;
Libioulle, Cecile ;
Sandor, Cynthia ;
Lathrop, Mark ;
Belaiche, Jacques ;
Dewit, Olivier ;
Gut, Ivo ;
Heath, Simon ;
Laukens, Debby ;
Mni, Myriam ;
Rutgeerts, Paul ;
Van Gossum, Andre ;
Zelenika, Diana ;
Franchimont, Denis ;
Hugot, Jean-Pierre ;
de Vos, Martine ;
Vermeire, Severine ;
Louis, Edouard ;
Cardon, Lon R. ;
Anderson, Carl A. ;
Drummond, Hazel ;
Nimmo, Elaine ;
Ahmad, Tariq ;
Prescott, Natalie J. ;
Onnie, Clive M. ;
Fisher, Sheila A. ;
Marchini, Jonathan ;
Ghori, Jilur .
NATURE GENETICS, 2008, 40 (08) :955-962
[3]   Antibiotic use and the development of Crohn's disease [J].
Card, T ;
Logan, RFA ;
Rodrigues, LC ;
Wheeler, JG .
GUT, 2004, 53 (02) :246-250
[4]  
CSD Medical Research UK, THIN DAT STAT
[5]   The Pervasive Effects of an Antibiotic on the Human Gut Microbiota, as Revealed by Deep 16S rRNA Sequencing [J].
Dethlefsen, Les ;
Huse, Sue ;
Sogin, Mitchell L. ;
Relman, David A. .
PLOS BIOLOGY, 2008, 6 (11) :2383-2400
[6]   Mycobacterium avium subspecies paratuberculosis and Crohn's disease: a systematic review and meta-analysis [J].
Feller, Martin ;
Huwiler, Karin ;
Stephan, Roger ;
Altpeter, Ekkehardt ;
Shang, Aijing ;
Furrer, Hansjakob ;
Pfyffer, Gaby E. ;
Jemmi, Thomas ;
Baumgartner, Andreas ;
Egger, Matthias .
LANCET INFECTIOUS DISEASES, 2007, 7 (09) :607-613
[7]   Communicable ulcerative colitis induced by T-bet deficiency in the innate immune system [J].
Garrett, Wendy S. ;
Lord, Graham M. ;
Punit, Shivesh ;
Lugo-Villarino, Geanncarlo ;
Mazmanian, Sarkis K. ;
Ito, Susumu ;
Glickman, Jonathan N. ;
Glimcher, Laurie H. .
CELL, 2007, 131 (01) :33-45
[8]   Population-based cases control study of inflammatory bowel disease risk factors [J].
Gearry, Richard B. ;
Richardson, Ann K. ;
Frampton, Christopher M. ;
Dodgshun, Andrew J. ;
Barclay, Murray L. .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2010, 25 (02) :325-333
[9]   CHILDHOOD FACTORS IN ULCERATIVE-COLITIS AND CROHNS-DISEASE - AN INTERNATIONAL COOPERATIVE STUDY [J].
GILAT, T ;
HACOHEN, D ;
LILOS, P ;
LANGMAN, MJS .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1987, 22 (08) :1009-1024
[10]   Increased Short- and Long-Term Risk of Inflammatory Bowel Disease After Salmonella or Campylobacter Gastroenteritis [J].
Gradel, Kim O. ;
Nielsen, Hans L. ;
Schonheyder, Henrik C. ;
Ejlertsen, Tove ;
Kristensen, Brian ;
Nielsen, Henrik .
GASTROENTEROLOGY, 2009, 137 (02) :495-501