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益生菌改善新冠病毒门诊患者的症状和病毒清除:一项随机、四盲、安慰剂对照试验。

Probiotic improves symptomatic and viral clearance in Covid19 outpatients: a randomized, quadruple-blinded, placebo-controlled trial.

机构信息

Centro de Investigación Translacional en Ciencias de la Salud, Hospital General Dr. Manuel Gea Gonzalez, Ciudad de México, (CDMX), México.

International Scientific Council for Probiotics, Ciudad de México, (CDMX), México.

出版信息

Gut Microbes. 2022 Jan-Dec;14(1):2018899. doi: 10.1080/19490976.2021.2018899.

Abstract

Intestinal bacteria may influence lung homeostasis via the gut-lung axis. We conducted a single-center, quadruple-blinded, randomized trial in adult symptomatic Coronavirus Disease 2019 (Covid19) outpatients. Subjects were allocated 1:1 to probiotic formula (strains KABP022, KABP023, and KAPB033, plus strain KABP021, totaling 2 × 10 colony-forming units (CFU)) or placebo, for 30 days. Co-primary endpoints included: i) proportion of patients in complete symptomatic and viral remission; ii) proportion progressing to moderate or severe disease with hospitalization, or death; and iii) days on Intensive Care Unit (ICU). Three hundred subjects were randomized (median age 37.0 years [range 18 to 60], 161 [53.7%] women, 126 [42.0%] having known metabolic risk factors), and 293 completed the study (97.7%). Complete remission was achieved by 78 of 147 (53.1%) in probiotic group compared to 41 of 146 (28.1%) in placebo (RR: 1.89 [95 CI 1.40-2.55]; < .001), significant after multiplicity correction. No hospitalizations or deaths occurred during the study, precluding the assessment of remaining co-primary outcomes. Probiotic supplementation was well-tolerated and reduced nasopharyngeal viral load, lung infiltrates and duration of both digestive and non-digestive symptoms, compared to placebo. No significant compositional changes were detected in fecal microbiota between probiotic and placebo, but probiotic supplementation significantly increased specific IgM and IgG against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV2) compared to placebo. It is thus hypothesized this probiotic primarily acts by interacting with the host's immune system rather than changing colonic microbiota composition. Future studies should replicate these findings and elucidate its mechanism of action (Registration: NCT04517422). AE: Adverse Event; BMI: Body Mass Index; CONSORT: CONsolidated Standards of Reporting Trials; CFU: Colony-Forming Units; eDRF: Electronic Daily Report Form; GLA: Gut-Lung Axis; GSRS: Gastrointestinal Symptoms Rating Scale; hsCRP: High-sensitivity C-Reactive Protein; HR: Hazard Ratio; ICU: Intensive Care Unit; OR: Odds Ratio; PCoA: Principal Coordinate Analysis; RR: Relative Risk; RT-qPCR: Real-Time Quantitative Polymerase Chain Reaction; SARS-CoV2: Severe acute respiratory syndrome coronavirus 2; SpO: Peripheral Oxygen Saturation; WHO: World Health Organization.

摘要

肠道细菌可能通过肠-肺轴影响肺内稳态。我们在成年有症状的 2019 冠状病毒病(COVID-19)门诊患者中进行了一项单中心、四重盲、随机试验。将受试者按照 1:1 分配至益生菌配方(菌株 KABP022、KABP023 和 KAPB033,加菌株 KABP021,总计 2×10 菌落形成单位(CFU))或安慰剂组,疗程 30 天。主要复合终点包括:i)完全缓解症状和病毒清除的患者比例;ii)进展为需要住院或死亡的中重度疾病的患者比例;以及 iii)入住重症监护病房(ICU)的天数。300 名受试者被随机分组(中位年龄 37.0 岁[范围 18 至 60],161 名[53.7%]女性,126 名[42.0%]有已知代谢危险因素),293 名完成了研究(97.7%)。益生菌组中 147 名患者中有 78 名(53.1%)达到完全缓解,而安慰剂组中 146 名患者中有 41 名(28.1%)(RR:1.89[95%CI 1.40-2.55];<0.001),在多重校正后有统计学意义。研究期间无住院或死亡事件发生,因此无法评估其余主要复合终点。与安慰剂相比,益生菌补充剂可更好地缓解症状,降低鼻咽病毒载量,减少肺部浸润,并缩短消化和非消化症状的持续时间。与安慰剂相比,粪便微生物群的组成在益生菌和安慰剂之间没有明显变化,但益生菌补充剂可显著增加针对严重急性呼吸综合征冠状病毒 2(SARS-CoV2)的特异性 IgM 和 IgG,与安慰剂相比(RR:1.89[95%CI 1.40-2.55];<0.001)。因此,研究假设这种益生菌主要通过与宿主免疫系统相互作用而不是改变结肠微生物群的组成来发挥作用。未来的研究应复制这些发现并阐明其作用机制(注册:NCT04517422)。AE:不良事件;BMI:体重指数;CONSORT:临床试验的统一报告标准;CFU:集落形成单位;eDRF:电子每日报告表;GLA:肠-肺轴;GSRS:胃肠道症状评分量表;hsCRP:高敏 C 反应蛋白;HR:危险比;ICU:重症监护病房;OR:比值比;PCoA:主坐标分析;RR:相对风险;RT-qPCR:实时定量聚合酶链反应;SARS-CoV2:严重急性呼吸综合征冠状病毒 2;SpO:外周血氧饱和度;WHO:世界卫生组织。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eb6/8757475/2c88aedc06f8/KGMI_A_2018899_F0001_B.jpg

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