Enterococcus Intestinal Domination Is Associated With Increased Mortality in the Acute Leukemia Chemotherapy Population

CLINICAL INFECTIOUS DISEASES(2024)

引用 8|浏览4
暂无评分
摘要
Background. Enterococcus intestinal domination (EID), a state of dysbiosis wherein enterococci comprise >= 30% abundance within the microbiota, has been associated with Enterococcus bacteremia, graft-versus-host disease, and mortality in the allogeneic hematopoietic stem cell transplant (allo HCT) population. The acute leukemia (AL) chemotherapy population includes patients receiving intensive chemotherapy, but not all patients go on to have an allo HCT. The impact of EID on outcomes including mortality in the AL chemotherapy population is unknown. Methods. Microbiota composition from weekly stool samples was analyzed using 16S ribosomal RNA gene sequencing. Patients were analyzed in 2 cohorts: AL chemotherapy cohort and allo HCT cohort. a -diversity and richness were calculated. Kaplan-Meier analysis was used to analyze mortality. Results. A total of 929 stool samples were collected from 139 patients. Both allo HCT and AL cohorts had a decline in alpha-diversity and richness over the course of treatment that tended not to return to baseline months later. EID was observed in at least 1 sample in 36% of allo HCT patients and 49% of AL patients. Patients with observed EID had lower a-diversity over time. Similar to the HCT cohort, AL patients with EID had reduced overall survival. We identified 4 other genera that were commonly found in >= 30% relative abundance within the microbiota, but none were associated with mortality. In fact, in allo HCT, Bacteroides abundance =30% was associated with improved survival. Conclusions. EID is associated with increased all-cause mortality in HCT and AL cohorts. Unlike EID, relative abundance >= 30% by other genera is not associated with increased all-cause mortality.
更多
查看译文
关键词
microbiome,Enterococcus,intestinal domination,acute leukemia,hematopoietic stem cell transplant
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要