Zhang Wei, Wang Yang, Cai Li-Jun
Hubei Maternal and Child Health Care Hospital , Wuhan 430016, China.
Zhongguo Dang Dai Er Ke Za Zhi. 2024 Nov 15;26(11):1176-1181. doi: 10.7499/j.issn.1008-8830.2407129.
To detect multidrug resistance gene locus mutations in children with pneumonia through targeted high-throughput sequencing and to explore its clinical significance.
A retrospective analysis was conducted on the clinical data of 2 899 children with pneumonia, who underwent respiratory pathogen-targeted high-throughput sequencing, treated at Hubei Maternal and Child Health Care Hospital between January and December 2023. The patients were divided into a mutation group (=885) and a non-mutation group (=2 014) based on whether there was a mutation in the 23SrRNA macrolide-resistant gene of . Multivariate logistic regression analysis was used to investigate the risk factors for multidrug resistance gene locus mutations in children with pneumonia.
Among the 2 899 children, 885 cases (30.53%) had mutations in the 23SrRNA resistance gene, including 884 cases with the A2063G mutation and 1 case with the A2064G mutation. In children with 23SrRNA resistance gene mutations, treatment with doxycycline or ofloxacin was more effective than with azithromycin or clarithromycin, and doxycycline was more effective than ofloxacin (<0.05). The mutation rate of resistance genes in children with pneumonia increased with age (<0.001). Multivariate logistic regression analysis showed that increased age, extrapulmonary infection, lung consolidation, prolonged fever, prolonged hospitalization, and elevated CRP levels were risk factors for 23SrRNA gene locus mutations (<0.05).
Age, extrapulmonary infections, lung consolidation, duration of fever, length of hospitalization, and CRP levels are closely related to 23SrRNA resistance gene locus mutations. Detecting multidrug resistance gene locus mutations in children with pneumonia can aid in early diagnosis and prediction of treatment efficacy, promoting rational clinical treatment.
通过靶向高通量测序检测肺炎患儿多药耐药基因位点突变,并探讨其临床意义。
回顾性分析2023年1月至12月在湖北省妇幼保健院接受呼吸道病原体靶向高通量测序治疗的2899例肺炎患儿的临床资料。根据肺炎链球菌23SrRNA大环内酯类耐药基因是否存在突变,将患者分为突变组(n = 885)和非突变组(n = 2014)。采用多因素logistic回归分析探讨肺炎患儿多药耐药基因位点突变的危险因素。
2899例患儿中,885例(30.53%)23SrRNA耐药基因发生突变,其中A2063G突变884例,A2064G突变1例。在23SrRNA耐药基因突变的患儿中,使用多西环素或氧氟沙星治疗比使用阿奇霉素或克拉霉素更有效,且多西环素比氧氟沙星更有效(P < 0.05)。肺炎患儿耐药基因的突变率随年龄增长而增加(P < 0.001)。多因素logistic回归分析显示,年龄增加、肺外感染、肺部实变、发热时间延长、住院时间延长和CRP水平升高是23SrRNA基因位点突变的危险因素(P < 0.05)。
年龄、肺外感染、肺部实变、发热持续时间、住院时间和CRP水平与23SrRNA耐药基因位点突变密切相关。检测肺炎患儿多药耐药基因位点突变有助于早期诊断和预测治疗效果,促进临床合理治疗。