Probiotics Administration in Cystic Fibrosis: What Is the Evidence?

In the last 20 years, gut microbiota in patients with cystic fibrosis (CF) has become an object of interest. It was shown that these patients had gut dysbiosis and this could explain not only the intestinal manifestations of the disease but also part of those involving the respiratory tract. The acq...

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Main Authors: Susanna Esposito, Ilaria Testa, Elena Mariotti Zani, Daniela Cunico, Lisa Torelli, Roberto Grandinetti, Valentina Fainardi, Giovanna Pisi, Nicola Principi
Format: Article
Language:English
Published: MDPI AG 2022-07-01
Series:Nutrients
Subjects:
Online Access:https://www.mdpi.com/2072-6643/14/15/3160
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author Susanna Esposito
Ilaria Testa
Elena Mariotti Zani
Daniela Cunico
Lisa Torelli
Roberto Grandinetti
Valentina Fainardi
Giovanna Pisi
Nicola Principi
author_facet Susanna Esposito
Ilaria Testa
Elena Mariotti Zani
Daniela Cunico
Lisa Torelli
Roberto Grandinetti
Valentina Fainardi
Giovanna Pisi
Nicola Principi
author_sort Susanna Esposito
collection DOAJ
description In the last 20 years, gut microbiota in patients with cystic fibrosis (CF) has become an object of interest. It was shown that these patients had gut dysbiosis and this could explain not only the intestinal manifestations of the disease but also part of those involving the respiratory tract. The acquisition of previously unknown information about the importance of some bacteria, i.e., those partially or totally disappeared in the gut of CF patients, in the regulation of the activity and function of the gut and the lung was the base to suggest the use of probiotics in CF patients. The main aim of this paper is to discuss the biological basis for probiotic administration to CF patients and which results could be expected. Literature analysis showed that CF intestinal dysbiosis depends on the same genetic mutations that condition the clinical picture of the diseases and is aggravated by a series of therapeutic interventions, such as dietary modifications, the use of antibiotics, and the administration of antacids. All this translates into a significant worsening of the structure and function of organs, including the lung and intestine, already deeply penalized by the genetic alterations of CF. Probiotics can intervene on dysbiosis, reducing the negative effects derived from it. However, the available data cannot be considered sufficient to indicate that these bacteria are essential elements of CF therapy. Further studies that take into account the still unsolved aspects on how to use probiotics are absolutely necessary.
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spelling doaj.art-36e349e565b84159a78bc620bd9779aa2023-11-30T22:44:20ZengMDPI AGNutrients2072-66432022-07-011415316010.3390/nu14153160Probiotics Administration in Cystic Fibrosis: What Is the Evidence?Susanna Esposito0Ilaria Testa1Elena Mariotti Zani2Daniela Cunico3Lisa Torelli4Roberto Grandinetti5Valentina Fainardi6Giovanna Pisi7Nicola Principi8Pediatric Clinic, Department of Medicine and Surgery, University of Parma, 43126 Parma, ItalyRespiratory Unit, Great Ormond Street Hospital for Children, Foundation Trust, London WC1N 1LE, UKPediatric Clinic, Department of Medicine and Surgery, University of Parma, 43126 Parma, ItalyPediatric Clinic, Department of Medicine and Surgery, University of Parma, 43126 Parma, ItalyPediatric Clinic, Department of Medicine and Surgery, University of Parma, 43126 Parma, ItalyPediatric Clinic, Department of Medicine and Surgery, University of Parma, 43126 Parma, ItalyRespiratory Unit, Great Ormond Street Hospital for Children, Foundation Trust, London WC1N 1LE, UKRespiratory Unit, Great Ormond Street Hospital for Children, Foundation Trust, London WC1N 1LE, UKUniversità degli Studi di Milano, 20122 Milan, ItalyIn the last 20 years, gut microbiota in patients with cystic fibrosis (CF) has become an object of interest. It was shown that these patients had gut dysbiosis and this could explain not only the intestinal manifestations of the disease but also part of those involving the respiratory tract. The acquisition of previously unknown information about the importance of some bacteria, i.e., those partially or totally disappeared in the gut of CF patients, in the regulation of the activity and function of the gut and the lung was the base to suggest the use of probiotics in CF patients. The main aim of this paper is to discuss the biological basis for probiotic administration to CF patients and which results could be expected. Literature analysis showed that CF intestinal dysbiosis depends on the same genetic mutations that condition the clinical picture of the diseases and is aggravated by a series of therapeutic interventions, such as dietary modifications, the use of antibiotics, and the administration of antacids. All this translates into a significant worsening of the structure and function of organs, including the lung and intestine, already deeply penalized by the genetic alterations of CF. Probiotics can intervene on dysbiosis, reducing the negative effects derived from it. However, the available data cannot be considered sufficient to indicate that these bacteria are essential elements of CF therapy. Further studies that take into account the still unsolved aspects on how to use probiotics are absolutely necessary.https://www.mdpi.com/2072-6643/14/15/3160cystic fibrosisdysbiosisgut-lung axismicrobiotaprobiotic
spellingShingle Susanna Esposito
Ilaria Testa
Elena Mariotti Zani
Daniela Cunico
Lisa Torelli
Roberto Grandinetti
Valentina Fainardi
Giovanna Pisi
Nicola Principi
Probiotics Administration in Cystic Fibrosis: What Is the Evidence?
Nutrients
cystic fibrosis
dysbiosis
gut-lung axis
microbiota
probiotic
title Probiotics Administration in Cystic Fibrosis: What Is the Evidence?
title_full Probiotics Administration in Cystic Fibrosis: What Is the Evidence?
title_fullStr Probiotics Administration in Cystic Fibrosis: What Is the Evidence?
title_full_unstemmed Probiotics Administration in Cystic Fibrosis: What Is the Evidence?
title_short Probiotics Administration in Cystic Fibrosis: What Is the Evidence?
title_sort probiotics administration in cystic fibrosis what is the evidence
topic cystic fibrosis
dysbiosis
gut-lung axis
microbiota
probiotic
url https://www.mdpi.com/2072-6643/14/15/3160
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