抗生素
医学
罗红霉素
强力霉素
鼻窦炎
失调
内科学
微生物群
功能性内窥镜鼻窦手术
胃肠病学
微生物学
肠道菌群
免疫学
红霉素
生物
生物信息学
作者
Joey Siu,Brett Wagner Mackenzie,Lilian Klingler,Kristi Biswas,Yi Wang,Cheung‐Tak Hung,Soo Hee Jeong,Daniel Bunout Barnett,Malcolm D. Tingle,Richard Douglas
摘要
Abstract Background Despite the widespread prescription of antibiotics for the treatment of chronic rhinosinusitis (CRS), their efficacy remains uncertain. Limited penetration of systemic antibiotics into the sinonasal mucosa has been reported previously by this group. This study aimed to investigate the short‐term effects of antibiotics on the sinus and gut microbiota as well as any relationships these had with drug distribution. Methods Thirty subjects undergoing functional endoscopic sinus surgery for CRS were randomized to one of three groups: (1) doxycycline (100 mg daily for 7 days); (2) roxithromycin (300 mg daily for 7 days); and (3) control (no antibiotics given). Sinonasal and stool samples collected before and after treatment were analyzed using 16S ribosomal RNA (rRNA) gene‐targeted amplicon sequencing and Droplet Digital polymerase chain reaction (PCR) for bacterial community composition and the quantification of bacterial DNA, respectively. Results There were no significant major bacterial community shifts or changes to bacterial diversity and load following the treatment period in all patient groups. Non‐significant trend reductions were observed in gut microbial diversity with antibiotics. For the roxithromycin group, sinonasal bacterial diversity was negatively correlated with serum drug levels and reduced overall compared to controls ( p < 0.05). The relative abundance of Staphylococcus ASV129 in sinonasal samples reduced with increasing mucus doxycycline levels ( p = 0.01). Conclusion Antibiotic prescription for CRS should be further investigated because of preliminary evidence of poor sinonasal drug penetration, unproven efficacy, and the potential impact of dysbiosis in the sinuses and off‐target sites. Further studies should consider distinguishing the presence of DNA from viable and nonviable bacteria.
科研通智能强力驱动
Strongly Powered by AbleSci AI