Double-blind clinical trial of arginine supplementation in the treatment of adult patients with sickle cell anaemia

Detalhes bibliográficos
Autor(a) principal: Eleutério, Renata Mirian Nunes
Data de Publicação: 2019
Outros Autores: Nascimento, Francisco O., Araújo, Tamara G., Castro, Marilena F., Almeida Filho, Tarcísio Paulo de, Maia Filho, Pedro A., Eleutério Júnior, José, Elias, Darcielle Bruna Dias, Lemes, Romélia Pinheiro Gonçalves
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da Universidade Federal do Ceará (UFC)
Texto Completo: http://www.repositorio.ufc.br/handle/riufc/40665
Resumo: Background. Sickle cell anaemia (SCA) is the most prevalentmonogenic disease in Brazil. In SCA, haemoglobin S (HbS) is formed, whichmodifies red blood cell morphology. Intravascular haemolysis occurs, in which free Hb and free radicals degrade nitric oxide (NO) and release arginase, which reduces arginine levels. Because arginine is a substrate for NO formation, this decrease leads to reduced NO (vasodilator) synthesis. SCA treatment uses hydroxyurea (HU) to maintain high foetal haemoglobin (HbF) levels and reduces HbS to avoid haemolytic episodes. Objective. To analyse the efficacy of L-arginine as an adjuvant in the treatment of SCA patients. Setting. The State Blood Centre of Cear´a, Brazil. Methods. This was a randomized double-blind clinical study of adults with SCA with continuous use of HU at the State Blood Centre of Cear´a. The clinical study enrolled 25 patients receiving HU + L-arginine (500mg) and 25 patients receivingHU+ placebo.The treatment was carried out over fourmonths. Laboratory tests were performed to determine the levels of the following: (1) complete blood count; (2) nitrite + nitrate; (3) HbF; and (4) reticulocytes. The clinical experiments were performed by a haematologist. The main outcome measures were nitrite and pain. Results. Statistical analysis showed that the levels of NO were increased in the study group, and there was also a reduction in pain frequency using a pain frequency scale by day, week, and month.The levels of nitrite plus nitrate in the group receiving placebo plus HU did not change among the times evaluated (38.27 ± 17.27 mg/L, 39.49 ± 12.84 mg/L, 34.45 ± 11.25 mg/L, p >0.05), but in the patients who received supplementation with L-arginine plus HU, a significant increase in nitrite plus nitrate levels was observed between M0 and M4 (36.55 ± 20.23 mg/L versus 48.64 ± 20.63 mg/L, p =0.001) and M2 and M4 (35.71 ± 15.11 mg/L versus 48.64 ± 20.63 mg/L, p <0.001). It is important to note that the increase in nitrite plus nitrate levels occurred only in the fourth month of follow-up of patients in the treatment group, showing that at least 4months of supplementation with L-arginine is necessary to show an increase in these metabolites in the serum. Conclusion. The use of L-arginine as a coadjuvant in the treatment of sickle cell anaemia may function as a potential tool for pain relief, consequently improving the life of patients.
id UFC-7_eedce98454c6dad2a31f9be787de5260
oai_identifier_str oai:repositorio.ufc.br:riufc/40665
network_acronym_str UFC-7
network_name_str Repositório Institucional da Universidade Federal do Ceará (UFC)
repository_id_str
spelling Double-blind clinical trial of arginine supplementation in the treatment of adult patients with sickle cell anaemiaEnsaio ClínicoClinical TrialArginineArgininaAnemia FalciformeAnemia, Sickle CellBackground. Sickle cell anaemia (SCA) is the most prevalentmonogenic disease in Brazil. In SCA, haemoglobin S (HbS) is formed, whichmodifies red blood cell morphology. Intravascular haemolysis occurs, in which free Hb and free radicals degrade nitric oxide (NO) and release arginase, which reduces arginine levels. Because arginine is a substrate for NO formation, this decrease leads to reduced NO (vasodilator) synthesis. SCA treatment uses hydroxyurea (HU) to maintain high foetal haemoglobin (HbF) levels and reduces HbS to avoid haemolytic episodes. Objective. To analyse the efficacy of L-arginine as an adjuvant in the treatment of SCA patients. Setting. The State Blood Centre of Cear´a, Brazil. Methods. This was a randomized double-blind clinical study of adults with SCA with continuous use of HU at the State Blood Centre of Cear´a. The clinical study enrolled 25 patients receiving HU + L-arginine (500mg) and 25 patients receivingHU+ placebo.The treatment was carried out over fourmonths. Laboratory tests were performed to determine the levels of the following: (1) complete blood count; (2) nitrite + nitrate; (3) HbF; and (4) reticulocytes. The clinical experiments were performed by a haematologist. The main outcome measures were nitrite and pain. Results. Statistical analysis showed that the levels of NO were increased in the study group, and there was also a reduction in pain frequency using a pain frequency scale by day, week, and month.The levels of nitrite plus nitrate in the group receiving placebo plus HU did not change among the times evaluated (38.27 ± 17.27 mg/L, 39.49 ± 12.84 mg/L, 34.45 ± 11.25 mg/L, p >0.05), but in the patients who received supplementation with L-arginine plus HU, a significant increase in nitrite plus nitrate levels was observed between M0 and M4 (36.55 ± 20.23 mg/L versus 48.64 ± 20.63 mg/L, p =0.001) and M2 and M4 (35.71 ± 15.11 mg/L versus 48.64 ± 20.63 mg/L, p <0.001). It is important to note that the increase in nitrite plus nitrate levels occurred only in the fourth month of follow-up of patients in the treatment group, showing that at least 4months of supplementation with L-arginine is necessary to show an increase in these metabolites in the serum. Conclusion. The use of L-arginine as a coadjuvant in the treatment of sickle cell anaemia may function as a potential tool for pain relief, consequently improving the life of patients.Advances in Hematology2019-04-08T19:09:14Z2019-04-08T19:09:14Z2019-02info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfELEUTÉRIO, Renata M. N. et al. Double-blind clinical trial of arginine supplementation in the treatment of adult patients with sickle cell anaemia. Advances in Hematology, v. 2019, p. 1-6, feb. 2019.0021-89791089-7550 (On line)http://www.repositorio.ufc.br/handle/riufc/40665Eleutério, Renata Mirian NunesNascimento, Francisco O.Araújo, Tamara G.Castro, Marilena F.Almeida Filho, Tarcísio Paulo deMaia Filho, Pedro A.Eleutério Júnior, JoséElias, Darcielle Bruna DiasLemes, Romélia Pinheiro Gonçalvesengreponame:Repositório Institucional da Universidade Federal do Ceará (UFC)instname:Universidade Federal do Ceará (UFC)instacron:UFCinfo:eu-repo/semantics/openAccess2022-03-24T19:16:44Zoai:repositorio.ufc.br:riufc/40665Repositório InstitucionalPUBhttp://www.repositorio.ufc.br/ri-oai/requestbu@ufc.br || repositorio@ufc.bropendoar:2024-09-11T18:52:54.578085Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)false
dc.title.none.fl_str_mv Double-blind clinical trial of arginine supplementation in the treatment of adult patients with sickle cell anaemia
title Double-blind clinical trial of arginine supplementation in the treatment of adult patients with sickle cell anaemia
spellingShingle Double-blind clinical trial of arginine supplementation in the treatment of adult patients with sickle cell anaemia
Eleutério, Renata Mirian Nunes
Ensaio Clínico
Clinical Trial
Arginine
Arginina
Anemia Falciforme
Anemia, Sickle Cell
title_short Double-blind clinical trial of arginine supplementation in the treatment of adult patients with sickle cell anaemia
title_full Double-blind clinical trial of arginine supplementation in the treatment of adult patients with sickle cell anaemia
title_fullStr Double-blind clinical trial of arginine supplementation in the treatment of adult patients with sickle cell anaemia
title_full_unstemmed Double-blind clinical trial of arginine supplementation in the treatment of adult patients with sickle cell anaemia
title_sort Double-blind clinical trial of arginine supplementation in the treatment of adult patients with sickle cell anaemia
author Eleutério, Renata Mirian Nunes
author_facet Eleutério, Renata Mirian Nunes
Nascimento, Francisco O.
Araújo, Tamara G.
Castro, Marilena F.
Almeida Filho, Tarcísio Paulo de
Maia Filho, Pedro A.
Eleutério Júnior, José
Elias, Darcielle Bruna Dias
Lemes, Romélia Pinheiro Gonçalves
author_role author
author2 Nascimento, Francisco O.
Araújo, Tamara G.
Castro, Marilena F.
Almeida Filho, Tarcísio Paulo de
Maia Filho, Pedro A.
Eleutério Júnior, José
Elias, Darcielle Bruna Dias
Lemes, Romélia Pinheiro Gonçalves
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Eleutério, Renata Mirian Nunes
Nascimento, Francisco O.
Araújo, Tamara G.
Castro, Marilena F.
Almeida Filho, Tarcísio Paulo de
Maia Filho, Pedro A.
Eleutério Júnior, José
Elias, Darcielle Bruna Dias
Lemes, Romélia Pinheiro Gonçalves
dc.subject.por.fl_str_mv Ensaio Clínico
Clinical Trial
Arginine
Arginina
Anemia Falciforme
Anemia, Sickle Cell
topic Ensaio Clínico
Clinical Trial
Arginine
Arginina
Anemia Falciforme
Anemia, Sickle Cell
description Background. Sickle cell anaemia (SCA) is the most prevalentmonogenic disease in Brazil. In SCA, haemoglobin S (HbS) is formed, whichmodifies red blood cell morphology. Intravascular haemolysis occurs, in which free Hb and free radicals degrade nitric oxide (NO) and release arginase, which reduces arginine levels. Because arginine is a substrate for NO formation, this decrease leads to reduced NO (vasodilator) synthesis. SCA treatment uses hydroxyurea (HU) to maintain high foetal haemoglobin (HbF) levels and reduces HbS to avoid haemolytic episodes. Objective. To analyse the efficacy of L-arginine as an adjuvant in the treatment of SCA patients. Setting. The State Blood Centre of Cear´a, Brazil. Methods. This was a randomized double-blind clinical study of adults with SCA with continuous use of HU at the State Blood Centre of Cear´a. The clinical study enrolled 25 patients receiving HU + L-arginine (500mg) and 25 patients receivingHU+ placebo.The treatment was carried out over fourmonths. Laboratory tests were performed to determine the levels of the following: (1) complete blood count; (2) nitrite + nitrate; (3) HbF; and (4) reticulocytes. The clinical experiments were performed by a haematologist. The main outcome measures were nitrite and pain. Results. Statistical analysis showed that the levels of NO were increased in the study group, and there was also a reduction in pain frequency using a pain frequency scale by day, week, and month.The levels of nitrite plus nitrate in the group receiving placebo plus HU did not change among the times evaluated (38.27 ± 17.27 mg/L, 39.49 ± 12.84 mg/L, 34.45 ± 11.25 mg/L, p >0.05), but in the patients who received supplementation with L-arginine plus HU, a significant increase in nitrite plus nitrate levels was observed between M0 and M4 (36.55 ± 20.23 mg/L versus 48.64 ± 20.63 mg/L, p =0.001) and M2 and M4 (35.71 ± 15.11 mg/L versus 48.64 ± 20.63 mg/L, p <0.001). It is important to note that the increase in nitrite plus nitrate levels occurred only in the fourth month of follow-up of patients in the treatment group, showing that at least 4months of supplementation with L-arginine is necessary to show an increase in these metabolites in the serum. Conclusion. The use of L-arginine as a coadjuvant in the treatment of sickle cell anaemia may function as a potential tool for pain relief, consequently improving the life of patients.
publishDate 2019
dc.date.none.fl_str_mv 2019-04-08T19:09:14Z
2019-04-08T19:09:14Z
2019-02
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv ELEUTÉRIO, Renata M. N. et al. Double-blind clinical trial of arginine supplementation in the treatment of adult patients with sickle cell anaemia. Advances in Hematology, v. 2019, p. 1-6, feb. 2019.
0021-8979
1089-7550 (On line)
http://www.repositorio.ufc.br/handle/riufc/40665
identifier_str_mv ELEUTÉRIO, Renata M. N. et al. Double-blind clinical trial of arginine supplementation in the treatment of adult patients with sickle cell anaemia. Advances in Hematology, v. 2019, p. 1-6, feb. 2019.
0021-8979
1089-7550 (On line)
url http://www.repositorio.ufc.br/handle/riufc/40665
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Advances in Hematology
publisher.none.fl_str_mv Advances in Hematology
dc.source.none.fl_str_mv reponame:Repositório Institucional da Universidade Federal do Ceará (UFC)
instname:Universidade Federal do Ceará (UFC)
instacron:UFC
instname_str Universidade Federal do Ceará (UFC)
instacron_str UFC
institution UFC
reponame_str Repositório Institucional da Universidade Federal do Ceará (UFC)
collection Repositório Institucional da Universidade Federal do Ceará (UFC)
repository.name.fl_str_mv Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)
repository.mail.fl_str_mv bu@ufc.br || repositorio@ufc.br
_version_ 1813028982205972480