Efficacy of a Multistrain Synbiotic Treatment in Acute and Post-Acute COVID-19 Patients: A Double-Blind, Placebo-Controlled Randomized Trial.

Publication date: Jul 16, 2024

Several studies reported the effect of COVID-19 on inducing gut dysbiosis, which is also correlated with disease severity. This study aims to investigate the effect of a nutraceutical formula on the shift of microbiota profiles and, secondly, on the clinical-pathological parameters of acute and post-acute COVID-19 patients. In this randomised, double-blind, placebo-controlled trial conducted at National Institute for Infectious diseases (INMI) Lazzaro Spallanzani (Italy), 52 patients were randomly assigned (1:1) to receive a multistrain synbiotic formula (Kebirah) or placebo orally for 35 days at COVID-19 diagnosis. Health professionals, investigators, and patients were masked to group assignments. The V3-V4 hypervariable region of 16S rRNA gene sequencing was employed to study the gut microbiota composition in the two groups. Supplementation with Kebirah prevented the decrease in the Shannon diversity index of gut microbiota, which was instead observed in patients receiving the placebo. In addition, decreases in lymphocyte count and haemoglobin levels were observed only in the placebo group and not in the treated group, which was also characterised by an amelioration of the gut microbial profile, with an enrichment in beneficial bacteria and a preservation of species diversity. Our data suggest that modulating the gut microbiota in acute disease through administration of a specific symbiotic formula could be a useful strategy in the frame of SARS-CoV-2 infections.

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Concepts Keywords
16s microbiota
Dysbiosis probiotics
Italy SARS-CoV-2
Nutraceutical
Synbiotic

Semantics

Type Source Name
disease MESH COVID-19
disease MESH dysbiosis
disease MESH Infectious diseases
disease VO gene
disease VO Bacteria
disease MESH acute disease
drug DRUGBANK Coenzyme M
disease MESH infections
disease IDO infection
disease MESH sequelae
disease MESH long COVID
disease MESH morbidities
disease IDO host
pathway REACTOME Immune System
disease MESH inflammation
disease IDO intervention
disease VO protocol
disease MESH allergy
disease VO pregnant women
drug DRUGBANK Oxygen
disease VO stomach
disease IDO blood
drug DRUGBANK Dextrose unspecified form
disease MESH hair loss
disease MESH chest pain
disease MESH sore throat
disease MESH insomnia
disease MESH paresthesias
disease VO time
drug DRUGBANK Quercetin
drug DRUGBANK Calcium
drug DRUGBANK Butyric Acid
drug DRUGBANK Maltodextrin
drug DRUGBANK Silicon dioxide
disease VO manufacturer
disease VO USA
disease VO device
disease IDO quality
disease MESH clinical relevance
disease VO ANOVA

Original Article

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