Effect of an enteral amino acid blend on muscle and gut functionality in critically ill patients: a proof-of-concept randomized controlled trial.


Journal

Critical care (London, England)
ISSN: 1466-609X
Titre abrégé: Crit Care
Pays: England
ID NLM: 9801902

Informations de publication

Date de publication:
17 11 2022
Historique:
received: 10 08 2022
accepted: 21 10 2022
entrez: 18 11 2022
pubmed: 19 11 2022
medline: 22 11 2022
Statut: epublish

Résumé

A defining feature of prolonged critical illness is muscle wasting, leading to impaired recovery. Supplementation with a tailored blend of amino acids may bolster the innate gut defence, promote intestinal mucosa repair and limit muscle loss. This was a monocentric, randomized, double-blind, placebo-controlled study that included patients with sepsis or acute respiratory distress syndrome. Patients received a specific combination of five amino acids or placebo mixed with enteral feeding for 21 days. Markers of renal function, gut barrier structure and functionality were collected at baseline and 1, 2, 3 and 8 weeks after randomization. Muscle structure and function were assessed through MRI measurements of the anterior quadriceps volume and by twitch airway pressure. Data were compared between groups relative to the baseline. Thirty-five critically ill patients were randomized. The amino acid blend did not impair urine output, blood creatinine levels or creatinine clearance. Plasma citrulline levels increased significantly along the treatment period in the amino acid group (difference in means [95% CI] 5.86 [1.72; 10.00] nmol/mL P = 0.007). Alanine aminotransferase and alkaline phosphatase concentrations were lower in the amino acid group than in the placebo group at one week (ratio of means 0.5 [0.29; 0.86] (P = 0.015) and 0.73 [0.57; 0.94] (P = 0.015), respectively). Twitch airway pressure and volume of the anterior quadriceps were greater in the amino acid group than in the placebo group 3 weeks after randomization (difference in means 10.6 [0.99; 20.20] cmH Amino acid supplementation increased plasma citrulline levels, reduced alanine aminotransferase and alkaline phosphatase levels, and improved twitch airway pressure and anterior quadriceps volume. Trial registration ClinicalTrials.gov, NCT02968836. Registered November 21, 2016.

Sections du résumé

BACKGROUND
A defining feature of prolonged critical illness is muscle wasting, leading to impaired recovery. Supplementation with a tailored blend of amino acids may bolster the innate gut defence, promote intestinal mucosa repair and limit muscle loss.
METHODS
This was a monocentric, randomized, double-blind, placebo-controlled study that included patients with sepsis or acute respiratory distress syndrome. Patients received a specific combination of five amino acids or placebo mixed with enteral feeding for 21 days. Markers of renal function, gut barrier structure and functionality were collected at baseline and 1, 2, 3 and 8 weeks after randomization. Muscle structure and function were assessed through MRI measurements of the anterior quadriceps volume and by twitch airway pressure. Data were compared between groups relative to the baseline.
RESULTS
Thirty-five critically ill patients were randomized. The amino acid blend did not impair urine output, blood creatinine levels or creatinine clearance. Plasma citrulline levels increased significantly along the treatment period in the amino acid group (difference in means [95% CI] 5.86 [1.72; 10.00] nmol/mL P = 0.007). Alanine aminotransferase and alkaline phosphatase concentrations were lower in the amino acid group than in the placebo group at one week (ratio of means 0.5 [0.29; 0.86] (P = 0.015) and 0.73 [0.57; 0.94] (P = 0.015), respectively). Twitch airway pressure and volume of the anterior quadriceps were greater in the amino acid group than in the placebo group 3 weeks after randomization (difference in means 10.6 [0.99; 20.20] cmH
CONCLUSIONS
Amino acid supplementation increased plasma citrulline levels, reduced alanine aminotransferase and alkaline phosphatase levels, and improved twitch airway pressure and anterior quadriceps volume. Trial registration ClinicalTrials.gov, NCT02968836. Registered November 21, 2016.

Identifiants

pubmed: 36397118
doi: 10.1186/s13054-022-04232-5
pii: 10.1186/s13054-022-04232-5
pmc: PMC9670468
doi:

Substances chimiques

Citrulline 29VT07BGDA
Creatinine AYI8EX34EU
Alkaline Phosphatase EC 3.1.3.1
Alanine Transaminase EC 2.6.1.2

Banques de données

ClinicalTrials.gov
['NCT02968836']

Types de publication

Randomized Controlled Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

358

Informations de copyright

© 2022. The Author(s).

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Auteurs

Nicholas Heming (N)

General Intensive Care Unit, Raymond Poincaré Hospital (AP-HP), University of Versailles Saint-Quentin en Yvelines, University Paris Saclay, 104, Boulevard Raymond Poincaré, 92380, Garches, France.
Laboratory of Infection and Inflammation - U1173, School of Medicine Simone Veil, INSERM, University Versailles Saint Quentin - University Paris Saclay, Garches, France.
FHU SEPSIS (Saclay and Paris Seine Nord Endeavour to PerSonalize Interventions for Sepsis), 92380, Garches, France.
RHU RECORDS (Rapid rEcognition of CORticosteroiD Resistant or Sensitive Sepsis), 92380, Garches, France.

Robert Carlier (R)

Department of Radiology, APHP, DMU Smart Imaging, GH Université Paris-Saclay, Hôpital Raymond Poincaré, Garches, France.
UFR des Sciences de la Santé Simone-Veil, Université de Versailles Saint-Quentin-en-Yvelines, Montigny-le-Bretonneux, France.

Helene Prigent (H)

Department of Physiology-AP-HP, Hôpital Raymond-Poincaré, Garches, France.
UFR des Sciences de la Santé Simone-Veil, Université de Versailles Saint-Quentin-en-Yvelines, Montigny-le-Bretonneux, France.

Ahmed Mekki (A)

Department of Radiology, APHP, DMU Smart Imaging, GH Université Paris-Saclay, Hôpital Raymond Poincaré, Garches, France.
UFR des Sciences de la Santé Simone-Veil, Université de Versailles Saint-Quentin-en-Yvelines, Montigny-le-Bretonneux, France.

Camille Jousset (C)

Department of Radiology, APHP, DMU Smart Imaging, GH Université Paris-Saclay, Hôpital Raymond Poincaré, Garches, France.
UFR des Sciences de la Santé Simone-Veil, Université de Versailles Saint-Quentin-en-Yvelines, Montigny-le-Bretonneux, France.

Frederic Lofaso (F)

Department of Physiology-AP-HP, Hôpital Raymond-Poincaré, Garches, France.
UFR des Sciences de la Santé Simone-Veil, Université de Versailles Saint-Quentin-en-Yvelines, Montigny-le-Bretonneux, France.

Xavier Ambrosi (X)

General Intensive Care Unit, Raymond Poincaré Hospital (AP-HP), University of Versailles Saint-Quentin en Yvelines, University Paris Saclay, 104, Boulevard Raymond Poincaré, 92380, Garches, France.
Department of Anesthesiology and Intensive Care Medicine, University Hospital of Nantes, Nantes, France.

Rania Bounab (R)

General Intensive Care Unit, Raymond Poincaré Hospital (AP-HP), University of Versailles Saint-Quentin en Yvelines, University Paris Saclay, 104, Boulevard Raymond Poincaré, 92380, Garches, France.

Virginie Maxime (V)

General Intensive Care Unit, Raymond Poincaré Hospital (AP-HP), University of Versailles Saint-Quentin en Yvelines, University Paris Saclay, 104, Boulevard Raymond Poincaré, 92380, Garches, France.

Arnaud Mansart (A)

Laboratory of Infection and Inflammation - U1173, School of Medicine Simone Veil, INSERM, University Versailles Saint Quentin - University Paris Saclay, Garches, France.
FHU SEPSIS (Saclay and Paris Seine Nord Endeavour to PerSonalize Interventions for Sepsis), 92380, Garches, France.
RHU RECORDS (Rapid rEcognition of CORticosteroiD Resistant or Sensitive Sepsis), 92380, Garches, France.

Pascal Crenn (P)

UFR des Sciences de la Santé Simone-Veil, Université de Versailles Saint-Quentin-en-Yvelines, Montigny-le-Bretonneux, France.
Clinical Nutrition Unit and FHU Hepatinov, Hôpital Raymond Poincaré, APHP Université Paris Saclay, Garches, France.

Pierre Moine (P)

General Intensive Care Unit, Raymond Poincaré Hospital (AP-HP), University of Versailles Saint-Quentin en Yvelines, University Paris Saclay, 104, Boulevard Raymond Poincaré, 92380, Garches, France.
Laboratory of Infection and Inflammation - U1173, School of Medicine Simone Veil, INSERM, University Versailles Saint Quentin - University Paris Saclay, Garches, France.
FHU SEPSIS (Saclay and Paris Seine Nord Endeavour to PerSonalize Interventions for Sepsis), 92380, Garches, France.
RHU RECORDS (Rapid rEcognition of CORticosteroiD Resistant or Sensitive Sepsis), 92380, Garches, France.

Fabien Foltzer (F)

Nestlé Research, Société de Produits de Nestlé, Lausanne, Switzerland.

Bernard Cuenoud (B)

Translation Research, Nestlé Health Science, Lausanne, Switzerland.

Tobias Konz (T)

Nestlé Research, Société de Produits de Nestlé, Lausanne, Switzerland.

John Corthesy (J)

Nestlé Research, Société de Produits de Nestlé, Lausanne, Switzerland.

Maurice Beaumont (M)

Nestlé Research, Société de Produits de Nestlé, Lausanne, Switzerland.

Mickaël Hartweg (M)

Nestlé Research, Société de Produits de Nestlé, Lausanne, Switzerland.

Claudia Roessle (C)

Translation Research, Nestlé Health Science, Lausanne, Switzerland.

Jean-Charles Preiser (JC)

Nutrition Team, Erasme University Hospital, Université Libre de Bruxelles, 1070, Brussels, Belgium.

Denis Breuillé (D)

Nestlé Research, Société de Produits de Nestlé, Lausanne, Switzerland.

Djillali Annane (D)

General Intensive Care Unit, Raymond Poincaré Hospital (AP-HP), University of Versailles Saint-Quentin en Yvelines, University Paris Saclay, 104, Boulevard Raymond Poincaré, 92380, Garches, France. djillali.annane@aphp.fr.
Laboratory of Infection and Inflammation - U1173, School of Medicine Simone Veil, INSERM, University Versailles Saint Quentin - University Paris Saclay, Garches, France. djillali.annane@aphp.fr.
FHU SEPSIS (Saclay and Paris Seine Nord Endeavour to PerSonalize Interventions for Sepsis), 92380, Garches, France. djillali.annane@aphp.fr.
RHU RECORDS (Rapid rEcognition of CORticosteroiD Resistant or Sensitive Sepsis), 92380, Garches, France. djillali.annane@aphp.fr.

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