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Real-World data on efficacy of L-glutamine in preventing sickle cell disease-related complications in pediatric and adult patients

BACKGROUND: L-glutamine has been shown to play an important role in the regulation of oxidative stress which is one of the key contributors to the pathophysiology of sickle cell disease (SCD). In a Phase 3 clinical trial, L-glutamine demonstrated a significant reduction in SCD-related complications...

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Autores principales: Elenga, Narcisse, Loko, Gylna, Etienne-Julan, Maryse, Al-Okka, Randa, Adel, Ahmad M., Yassin, Mohamed A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9376442/
https://www.ncbi.nlm.nih.gov/pubmed/35979207
http://dx.doi.org/10.3389/fmed.2022.931925
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author Elenga, Narcisse
Loko, Gylna
Etienne-Julan, Maryse
Al-Okka, Randa
Adel, Ahmad M.
Yassin, Mohamed A.
author_facet Elenga, Narcisse
Loko, Gylna
Etienne-Julan, Maryse
Al-Okka, Randa
Adel, Ahmad M.
Yassin, Mohamed A.
author_sort Elenga, Narcisse
collection PubMed
description BACKGROUND: L-glutamine has been shown to play an important role in the regulation of oxidative stress which is one of the key contributors to the pathophysiology of sickle cell disease (SCD). In a Phase 3 clinical trial, L-glutamine demonstrated a significant reduction in SCD-related complications including vaso-occlusive crises (VOCs), hospitalizations, and acute chest syndrome (ACS) compared to placebo in patients with SCD. OBJECTIVE: The primary objective was to confirm the efficacy of L-glutamine (Endari(®)) therapy in pediatric and adult patients with SCD at follow-up time points of 24, 48 and 72 weeks. METHODS: In the observational study, nineteen patients with SCD were treated orally with L-glutamine twice daily for 72 weeks. Clinical and laboratory parameters were measured at baseline and follow-up time points. Patients with severe VOC and ACS were hospitalized. Blood transfusion was given in case of ACS and uncontrolled pain associated with VOC despite administration of the highest dose of intravenous (IV) narcotic. RESULTS: Compared to baseline, patients had significantly fewer pain crises (median change from 3.0 to 0.0; P < 0.00001), hospitalizations (median change from 3.0 to 0.0; P < 0.00001), days of hospitalization (median change from 15.0 to 0.0; P < 0.00001), and blood transfusions (median change from 3.0 to 0.0; P < 0.00001) at 24, 48, and 72 weeks following L-glutamine therapy. Moreover, there was a drastic decrease in the number of ACS events during this time. A significant increase was observed in mean hemoglobin levels and hematocrit proportions from baseline to 72 weeks (P < 0.001). Conversely, compared to baseline, mean reticulocyte counts and lactate dehydrogenase (LDH) levels were considerably lower at follow-up time points (P = 0.003 and P < 0.001, respectively). No patient reported treatment-related adverse events. CONCLUSION: Although the sample size was small, our data clearly demonstrated that L-glutamine therapy was safe and significantly improved clinical outcomes and hemolysis parameters in patients with SCD.
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spelling pubmed-93764422022-08-16 Real-World data on efficacy of L-glutamine in preventing sickle cell disease-related complications in pediatric and adult patients Elenga, Narcisse Loko, Gylna Etienne-Julan, Maryse Al-Okka, Randa Adel, Ahmad M. Yassin, Mohamed A. Front Med (Lausanne) Medicine BACKGROUND: L-glutamine has been shown to play an important role in the regulation of oxidative stress which is one of the key contributors to the pathophysiology of sickle cell disease (SCD). In a Phase 3 clinical trial, L-glutamine demonstrated a significant reduction in SCD-related complications including vaso-occlusive crises (VOCs), hospitalizations, and acute chest syndrome (ACS) compared to placebo in patients with SCD. OBJECTIVE: The primary objective was to confirm the efficacy of L-glutamine (Endari(®)) therapy in pediatric and adult patients with SCD at follow-up time points of 24, 48 and 72 weeks. METHODS: In the observational study, nineteen patients with SCD were treated orally with L-glutamine twice daily for 72 weeks. Clinical and laboratory parameters were measured at baseline and follow-up time points. Patients with severe VOC and ACS were hospitalized. Blood transfusion was given in case of ACS and uncontrolled pain associated with VOC despite administration of the highest dose of intravenous (IV) narcotic. RESULTS: Compared to baseline, patients had significantly fewer pain crises (median change from 3.0 to 0.0; P < 0.00001), hospitalizations (median change from 3.0 to 0.0; P < 0.00001), days of hospitalization (median change from 15.0 to 0.0; P < 0.00001), and blood transfusions (median change from 3.0 to 0.0; P < 0.00001) at 24, 48, and 72 weeks following L-glutamine therapy. Moreover, there was a drastic decrease in the number of ACS events during this time. A significant increase was observed in mean hemoglobin levels and hematocrit proportions from baseline to 72 weeks (P < 0.001). Conversely, compared to baseline, mean reticulocyte counts and lactate dehydrogenase (LDH) levels were considerably lower at follow-up time points (P = 0.003 and P < 0.001, respectively). No patient reported treatment-related adverse events. CONCLUSION: Although the sample size was small, our data clearly demonstrated that L-glutamine therapy was safe and significantly improved clinical outcomes and hemolysis parameters in patients with SCD. Frontiers Media S.A. 2022-08-01 /pmc/articles/PMC9376442/ /pubmed/35979207 http://dx.doi.org/10.3389/fmed.2022.931925 Text en Copyright © 2022 Elenga, Loko, Etienne-Julan, Al-Okka, Adel and Yassin. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Elenga, Narcisse
Loko, Gylna
Etienne-Julan, Maryse
Al-Okka, Randa
Adel, Ahmad M.
Yassin, Mohamed A.
Real-World data on efficacy of L-glutamine in preventing sickle cell disease-related complications in pediatric and adult patients
title Real-World data on efficacy of L-glutamine in preventing sickle cell disease-related complications in pediatric and adult patients
title_full Real-World data on efficacy of L-glutamine in preventing sickle cell disease-related complications in pediatric and adult patients
title_fullStr Real-World data on efficacy of L-glutamine in preventing sickle cell disease-related complications in pediatric and adult patients
title_full_unstemmed Real-World data on efficacy of L-glutamine in preventing sickle cell disease-related complications in pediatric and adult patients
title_short Real-World data on efficacy of L-glutamine in preventing sickle cell disease-related complications in pediatric and adult patients
title_sort real-world data on efficacy of l-glutamine in preventing sickle cell disease-related complications in pediatric and adult patients
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9376442/
https://www.ncbi.nlm.nih.gov/pubmed/35979207
http://dx.doi.org/10.3389/fmed.2022.931925
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