Research Institute of Internal Medicine, Oslo University Hospital, 0424, Oslo, Norway.
Section of Clinical Immunology and Infectious Diseases, Oslo University Hospital, 0424, Oslo, Norway.
Crit Care. 2023 Feb 23;27(1):69. doi: 10.1186/s13054-023-04356-2.
Gut microbiota alterations have been reported in hospitalized COVID-19 patients, with reduced alpha diversity and altered microbiota composition related to respiratory failure. However, data regarding gut microbiota and mortality are scarce.
Rectal swabs for gut microbiota analyses were collected within 48 h after hospital admission (baseline; n = 123) and three-month post-admission (n = 50) in a subset of patients included in the Norwegian SARS-CoV2 cohort study. Samples were analysed by sequencing the 16S rRNA gene. Gut microbiota diversity and composition at baseline were assessed in relation to need for intensive care unit (ICU) admission during hospitalization. The primary objective was to investigate whether the ICU-related gut microbiota was associated with 60-day mortality.
Gut microbiota diversity (Shannon index) at baseline was lower in COVID-19 patients requiring ICU admission during hospitalization than in those managed in general wards. A dysbiosis index representing a balance of enriched and reduced taxa in ICU compared with ward patients, including decreased abundance of butyrate-producing microbes and enrichment of a partly oral bacterial flora, was associated with need of ICU admission independent of antibiotic use, dexamethasone use, chronic pulmonary disease, PO/FiO ratio, C-reactive protein, neutrophil counts or creatinine levels (adjusted p < 0.001). The ICU-related dysbiosis index at baseline correlated with systemic inflammation and was associated with 60-day mortality in univariate analyses (Hazard ratio 3.70 [2.00-8.6], p < 0.001), as well as after separate adjustment for covariates. At the three-month follow-up, the dysbiosis index remained elevated in ICU patients compared with ward patients (adjusted p = 0.007).
Although our data should be regarded as exploratory due to low number of clinical end points, they suggest that gut microbiota alterations during hospitalization could be related to poor prognosis after severe COVID-19. Larger studies of gut involvement during COVID-19 in relation to long-term clinical outcome are warranted. Trial registration NCT04381819 . Retrospectively registered May 11, 2020.
有报道称,住院的 COVID-19 患者肠道微生物群发生改变,α多样性降低,与呼吸衰竭相关的微生物群落组成发生改变。然而,关于肠道微生物群与死亡率的数据还很缺乏。
在挪威 SARS-CoV2 队列研究中,纳入的部分患者在入院后 48 小时内(基线;n=123)和入院后三个月(n=50)采集直肠拭子进行肠道微生物组分析。通过 16S rRNA 基因测序分析样本。在基线时评估肠道微生物群的多样性和组成与住院期间需要入住重症监护病房(ICU)之间的关系。主要目的是研究与 ICU 相关的肠道微生物群是否与 60 天死亡率有关。
与在普通病房接受治疗的 COVID-19 患者相比,住院期间需要入住 ICU 的患者的肠道微生物群多样性(Shannon 指数)较低。与普通病房患者相比,ICU 患者的肠道微生物群中富集和减少的细菌种类的平衡(即丁酸产生菌丰度降低和部分口腔细菌菌群的富集),与 ICU 入住无关,独立于抗生素使用、地塞米松使用、慢性肺部疾病、PO/FiO 比值、C 反应蛋白、中性粒细胞计数或肌酐水平(调整后 p<0.001)。基线时与 ICU 相关的肠道微生态失调指数与全身炎症相关,在单因素分析中与 60 天死亡率相关(危险比 3.70 [2.00-8.6],p<0.001),并且在单独调整协变量后仍然相关。在三个月的随访中,与普通病房患者相比,ICU 患者的微生态失调指数仍然升高(调整后 p=0.007)。
尽管由于临床终点数量较少,我们的数据应被视为探索性的,但它们表明住院期间肠道微生物群的改变可能与严重 COVID-19 后的不良预后有关。有必要开展更大规模的研究,以了解 COVID-19 期间肠道变化与长期临床结局的关系。试验注册 NCT04381819 。2020 年 5 月 11 日回顾性注册。