Probiotic Supplementation Affects Pulmonary Exacerbations in Patients With Cystic Fibrosis: A Pilot Study

被引:89
作者
Weiss, Batia [1 ,2 ]
Bujanover, Yoram [1 ]
Yahav, Yaakov [2 ,3 ]
Vilozni, Daphna [2 ,3 ]
Fireman, Elizabeth [4 ]
Efrati, On [2 ,3 ]
机构
[1] Safra Childrens Hosp, Div Pediat Gastroenterol & Nutr, IL-526265 Tel Hashomer, Israel
[2] Tel Aviv Univ, Sackler Fac Med, IL-69978 Tel Aviv, Israel
[3] Safra Childrens Hosp, Div Pediat Pulmonol, Natl Ctr Cyst Fibrosis, IL-526265 Tel Hashomer, Israel
[4] Tel Aviv Univ, Tel Aviv Sourasky Med Ctr, Pulm & Allergy Dept, Lab Pulm & Allerg Dis,Natl Serv Interstitial Lung, IL-69978 Tel Aviv, Israel
关键词
probiotics; cystic fibrosis; pulmonary; interleukin-8; sputum; INTESTINAL PERMEABILITY; CYTOKINE PRODUCTION; LACTOBACILLUS-GG; EXPRESSION; MANAGEMENT; INFLAMMATION; DISEASE;
D O I
10.1002/ppul.21138
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective: Probiotics reduce intestinal inflammation in, and Lactobacillus GG (LGG) reduces pulmonary exacerbation rate cystic fibrosis (CF) patients. We intended to determine the effect of a mixed probiotic preparation on pulmonary exacerbations and inflammatory characteristics of the sputum in CF patients. Study Design: A prospective pilot study of 10 CF patients with mild moderate lung disease and Pseudomonas aeruginosa colonization, treated with probiotics for 6 months. Pulmonary function tests (PFT's), sputum cultures with semi-quantitative bacterial analysis, and sputum neutrophil count and interleukin-8 (IL-8) levels were compared to pretreatment and post-treatment values. The rate of pulmonary exacerbations was compared to 2 years prior to the study. Results: The exacerbation rate was significantly reduced in comparison to the previous 2 years and to 6 months post-treatment (P=0.002). PFT's have not changed at the end of treatment and during 6 months post-treatment. No change in sputum bacteria, neutrophil count, and IL-8 levels was observed. Conclusion: Probiotics reduce pulmonary exacerbations rate in patients with CF Probiotics may have a preventive potential for pulmonary deterioration in CF patients. Pediatr Pulmonol. 2010; 45:536-540. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:536 / 540
页数:5
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