Inam Zaina, Felton Erin, Burrell Aszia, Chaney Hollis, Sami Iman, Koumbourlis Anastassios C, Freishtat Robert J, Zemanick Edith T, Crandall Keith A, Hahn Andrea
Pediatric Residency Program, Children's National Hospital, Washington, District of Columbia, USA.
George Washington University School of Medicine and Health Sciences, Washington, District of Columbia, USA.
Open Forum Infect Dis. 2022 Sep 12;9(9):ofac466. doi: 10.1093/ofid/ofac466. eCollection 2022 Sep.
Cystic fibrosis (CF) is characterized by recurrent pulmonary exacerbations (PEx) and lung function decline. PEx are frequently treated with antibiotics. However, little is known about the effects of antibiotics on the airway microbiome of persons with CF over time. The purpose of this study was to evaluate changes in the microbiome and lung function in persons with CF over 1 year following an initial study pulmonary exacerbation (iPEx).
Twenty children aged ≤18 years with CF were enrolled in the study, which occurred prior to the routine administration of highly effective modulator therapy. Respiratory samples and spirometry were obtained at a minimum of quarterly visits and up to 1 year after an iPEx. Metagenomic sequencing was performed, and bacterial taxa were assigned using MetaPhlAn 2.0. Paired test, analysis of variance, and generalized least squares regression were used to compare outcome variables.
The mean age of study participants at the time of the iPEx was 10.6 years. There were 3 ± 1.6 PEx treated with antibiotics per person during the study period. Bacterial richness was similar at 1 year compared to iPEx (40.3 vs 39.3, = .852), whereas the mean Shannon diversity index was significantly higher at 1 year (2.84 vs 1.62, < .001). The number of PEx treated with antibiotics was not associated with changes in microbial diversity but was associated with changes in lung function.
In our 1-year prospective study, we found that microbial diversity increased despite decreases in lung function associated with repeated PEx events requiring antibiotic therapy.
囊性纤维化(CF)的特征为反复的肺部加重(PEx)和肺功能下降。PEx通常用抗生素治疗。然而,随着时间的推移,抗生素对CF患者气道微生物群的影响知之甚少。本研究的目的是评估CF患者在首次研究性肺部加重(iPEx)后1年内微生物群和肺功能的变化。
20名年龄≤18岁的CF儿童参与了本研究,该研究在常规给予高效调节剂治疗之前进行。在iPEx后至少每季度进行一次访视,并持续1年,期间采集呼吸样本并进行肺活量测定。进行宏基因组测序,并使用MetaPhlAn 2.0分配细菌分类群。采用配对检验、方差分析和广义最小二乘回归比较结果变量。
iPEx时研究参与者的平均年龄为10.6岁。在研究期间,每人接受3±1.6次用抗生素治疗的PEx。与iPEx时相比,1年时细菌丰富度相似(40.3对39.3,P = 0.852),而平均香农多样性指数在1年时显著更高(2.84对1.62,P < 0.001)。用抗生素治疗的PEx次数与微生物多样性的变化无关,但与肺功能的变化有关。
在我们为期1年的前瞻性研究中,我们发现尽管与需要抗生素治疗的反复PEx事件相关的肺功能下降,但微生物多样性仍有所增加。