Department of Traumatology and Acute Critical Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, 565-0871, Japan.
Department of Infection Metagenomics, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.
Dig Dis Sci. 2022 Jun;67(6):2420-2432. doi: 10.1007/s10620-021-07000-7. Epub 2021 May 3.
The gut microbiota are reported to be altered in critical illness. The pattern and impact of dysbiosis on prognosis has not been thoroughly investigated in the ICU setting.
We aimed to evaluate changes in the gut microbiota of ICU patients via 16S rRNA gene deep sequencing, assess the association of the changes with antibiotics use or disease severity, and explore the association of gut microbiota changes with ICU patient prognosis.
Seventy-one mechanically ventilated patients were included. Fecal samples were collected serially on days 1-2, 3-4, 5-7, 8-14, and thereafter when suitable. Microorganisms of the fecal samples were profiled by 16S rRNA gene deep sequencing.
Proportions of the five major phyla in the feces were diverse in each patient at admission. Those of Bacteroidetes and Firmicutes especially converged and stabilized within the first week from admission with a reduction in α-diversity (p < 0.001). Significant differences occurred in the proportional change of Actinobacteria between the carbapenem and non-carbapenem groups (p = 0.030) and that of Actinobacteria according to initial SOFA score and changes in the SOFA score (p < 0.001). An imbalance in the ratio of Bacteroidetes to Firmicutes within seven days from admission was associated with higher mortality when the ratio was > 8 or < 1/8 (odds ratio: 5.54, 95% CI: 1.39-22.18, p = 0.015).
Broad-spectrum antibiotics and disease severity may be associated with gut dysbiosis in the ICU. A progression of dysbiosis occurring in the gut of ICU patients might be associated with mortality.
据报道,危重病患者的肠道微生物群会发生改变。在重症监护病房(ICU)环境中,尚未彻底研究菌群失调的模式及其对预后的影响。
我们旨在通过 16S rRNA 基因测序评估 ICU 患者肠道微生物群的变化,评估这些变化与抗生素使用或疾病严重程度的关系,并探讨肠道微生物群变化与 ICU 患者预后的关系。
纳入 71 例机械通气患者。在入院第 1-2 天、第 3-4 天、第 5-7 天、第 8-14 天以及适合时采集粪便标本进行连续检测。通过 16S rRNA 基因测序对粪便样本中的微生物进行分析。
入院时每位患者粪便中的五个主要菌群比例各不相同。入院后第一周内,厚壁菌门和拟杆菌门的比例趋于集中且稳定,α多样性降低(p<0.001)。碳青霉烯类和非碳青霉烯类抗生素组之间放线菌的比例变化(p=0.030)和根据初始 SOFA 评分和 SOFA 评分变化的放线菌比例变化存在显著差异(p<0.001)。入院后 7 天内,拟杆菌门与厚壁菌门的比例失衡与死亡率升高有关,当该比值>8 或<1/8 时(比值比:5.54,95%置信区间:1.39-22.18,p=0.015)。
广谱抗生素和疾病严重程度可能与 ICU 中的肠道菌群失调有关。在 ICU 患者肠道中发生的菌群失调进展可能与死亡率相关。