The SLCO1A2 -189_-188InsA polymorphism reduces clearance of rocuronium in patients submitted to elective surgeries

Detalhes bibliográficos
Autor(a) principal: Costa, A. C.C.
Data de Publicação: 2017
Outros Autores: Coelho, E. B., Lanchote, V. L., Correia, B. V. [UNESP], Abumansur, J. T., Lauretti, G. R., de Moraes, N. V. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1007/s00228-017-2243-1
http://hdl.handle.net/11449/169631
Resumo: Purpose: Rocuronium (ROC) is a neuromuscular blocker mainly eliminated by biliary excretion dependent on organic anion transporting polypeptide 1A2 (OATP1A2) hepatocellular uptake. However, the influence of SLCO1A2 (gene encoding OATP1A2) genetic polymorphism on ROC pharmacokinetics was never described before. The objective of this work was to evaluate the influence of genetic polymorphisms of SLCO1A2 on the pharmacokinetics of rocuronium (ROC). Methods: Patients undergoing elective surgeries under general anesthesia using rocuronium as a neuromuscular blocker were genotyped for SLCO1A2 polymorphisms in the coding region (41A>G, 382A>T, 404A>T, 502C>T, 516A>C, 559G>A, 830C>A, and 833delA) and in the promoter region (-1105G>A, -1032G>A, -715T>C, -361G>A, and -189_-188insA). Rocuronium pharmacokinetic parameters were estimated by non-compartmental analysis. Results: None of the patients had heterozygous or homozygous variant of 404A>T, 382A>T, 502C>T, 833delA, 830C>A, 41A>G, and -715T>C. A linkage disequilibrium was found between -1105G>A and -1032G>A genotypes. Patients genotyped as -A or AA (n = 17) for SLCO1A2 -189_-188InsA showed reduced total clearance of ROC compared to patients genotyped as −/− (n = 13) (151.6 vs 207.1 mL/min, p ≤ 0.05). The pharmacokinetics parameters of ROC were not significantly different between other SLCO1A2 genotypes. Conclusion: SLCO1A2 -189_-188InsA polymorphism is related to the reduced clearance of rocuronium in patients submitted to elective surgeries under general anesthesia. Trial registration: NCT 02399397 (ClinicalTrials.gov).
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spelling The SLCO1A2 -189_-188InsA polymorphism reduces clearance of rocuronium in patients submitted to elective surgeriesNeuromuscular blockadePharmacogeneticsPharmacokineticsRocuroniumSNPsPurpose: Rocuronium (ROC) is a neuromuscular blocker mainly eliminated by biliary excretion dependent on organic anion transporting polypeptide 1A2 (OATP1A2) hepatocellular uptake. However, the influence of SLCO1A2 (gene encoding OATP1A2) genetic polymorphism on ROC pharmacokinetics was never described before. The objective of this work was to evaluate the influence of genetic polymorphisms of SLCO1A2 on the pharmacokinetics of rocuronium (ROC). Methods: Patients undergoing elective surgeries under general anesthesia using rocuronium as a neuromuscular blocker were genotyped for SLCO1A2 polymorphisms in the coding region (41A>G, 382A>T, 404A>T, 502C>T, 516A>C, 559G>A, 830C>A, and 833delA) and in the promoter region (-1105G>A, -1032G>A, -715T>C, -361G>A, and -189_-188insA). Rocuronium pharmacokinetic parameters were estimated by non-compartmental analysis. Results: None of the patients had heterozygous or homozygous variant of 404A>T, 382A>T, 502C>T, 833delA, 830C>A, 41A>G, and -715T>C. A linkage disequilibrium was found between -1105G>A and -1032G>A genotypes. Patients genotyped as -A or AA (n = 17) for SLCO1A2 -189_-188InsA showed reduced total clearance of ROC compared to patients genotyped as −/− (n = 13) (151.6 vs 207.1 mL/min, p ≤ 0.05). The pharmacokinetics parameters of ROC were not significantly different between other SLCO1A2 genotypes. Conclusion: SLCO1A2 -189_-188InsA polymorphism is related to the reduced clearance of rocuronium in patients submitted to elective surgeries under general anesthesia. Trial registration: NCT 02399397 (ClinicalTrials.gov).Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Universidade de São Paulo (USP) Faculdade de Ciências Farmacêuticas de Ribeirão PretoUniversidade de São Paulo (USP) Faculdade de Medicina de Ribeirão PretoUniversidade Estadual Paulista (UNESP) Faculdade de Ciências FarmacêuticasUniversidade Estadual Paulista (UNESP) Faculdade de Ciências FarmacêuticasFAPESP: 2013/14730-0Universidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)Costa, A. C.C.Coelho, E. B.Lanchote, V. L.Correia, B. V. [UNESP]Abumansur, J. T.Lauretti, G. R.de Moraes, N. V. [UNESP]2018-12-11T16:46:56Z2018-12-11T16:46:56Z2017-08-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article957-963application/pdfhttp://dx.doi.org/10.1007/s00228-017-2243-1European Journal of Clinical Pharmacology, v. 73, n. 8, p. 957-963, 2017.1432-10410031-6970http://hdl.handle.net/11449/16963110.1007/s00228-017-2243-12-s2.0-850174451152-s2.0-85017445115.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengEuropean Journal of Clinical Pharmacology1,1591,159info:eu-repo/semantics/openAccess2023-12-15T06:21:38Zoai:repositorio.unesp.br:11449/169631Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-12-15T06:21:38Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv The SLCO1A2 -189_-188InsA polymorphism reduces clearance of rocuronium in patients submitted to elective surgeries
title The SLCO1A2 -189_-188InsA polymorphism reduces clearance of rocuronium in patients submitted to elective surgeries
spellingShingle The SLCO1A2 -189_-188InsA polymorphism reduces clearance of rocuronium in patients submitted to elective surgeries
Costa, A. C.C.
Neuromuscular blockade
Pharmacogenetics
Pharmacokinetics
Rocuronium
SNPs
title_short The SLCO1A2 -189_-188InsA polymorphism reduces clearance of rocuronium in patients submitted to elective surgeries
title_full The SLCO1A2 -189_-188InsA polymorphism reduces clearance of rocuronium in patients submitted to elective surgeries
title_fullStr The SLCO1A2 -189_-188InsA polymorphism reduces clearance of rocuronium in patients submitted to elective surgeries
title_full_unstemmed The SLCO1A2 -189_-188InsA polymorphism reduces clearance of rocuronium in patients submitted to elective surgeries
title_sort The SLCO1A2 -189_-188InsA polymorphism reduces clearance of rocuronium in patients submitted to elective surgeries
author Costa, A. C.C.
author_facet Costa, A. C.C.
Coelho, E. B.
Lanchote, V. L.
Correia, B. V. [UNESP]
Abumansur, J. T.
Lauretti, G. R.
de Moraes, N. V. [UNESP]
author_role author
author2 Coelho, E. B.
Lanchote, V. L.
Correia, B. V. [UNESP]
Abumansur, J. T.
Lauretti, G. R.
de Moraes, N. V. [UNESP]
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Costa, A. C.C.
Coelho, E. B.
Lanchote, V. L.
Correia, B. V. [UNESP]
Abumansur, J. T.
Lauretti, G. R.
de Moraes, N. V. [UNESP]
dc.subject.por.fl_str_mv Neuromuscular blockade
Pharmacogenetics
Pharmacokinetics
Rocuronium
SNPs
topic Neuromuscular blockade
Pharmacogenetics
Pharmacokinetics
Rocuronium
SNPs
description Purpose: Rocuronium (ROC) is a neuromuscular blocker mainly eliminated by biliary excretion dependent on organic anion transporting polypeptide 1A2 (OATP1A2) hepatocellular uptake. However, the influence of SLCO1A2 (gene encoding OATP1A2) genetic polymorphism on ROC pharmacokinetics was never described before. The objective of this work was to evaluate the influence of genetic polymorphisms of SLCO1A2 on the pharmacokinetics of rocuronium (ROC). Methods: Patients undergoing elective surgeries under general anesthesia using rocuronium as a neuromuscular blocker were genotyped for SLCO1A2 polymorphisms in the coding region (41A>G, 382A>T, 404A>T, 502C>T, 516A>C, 559G>A, 830C>A, and 833delA) and in the promoter region (-1105G>A, -1032G>A, -715T>C, -361G>A, and -189_-188insA). Rocuronium pharmacokinetic parameters were estimated by non-compartmental analysis. Results: None of the patients had heterozygous or homozygous variant of 404A>T, 382A>T, 502C>T, 833delA, 830C>A, 41A>G, and -715T>C. A linkage disequilibrium was found between -1105G>A and -1032G>A genotypes. Patients genotyped as -A or AA (n = 17) for SLCO1A2 -189_-188InsA showed reduced total clearance of ROC compared to patients genotyped as −/− (n = 13) (151.6 vs 207.1 mL/min, p ≤ 0.05). The pharmacokinetics parameters of ROC were not significantly different between other SLCO1A2 genotypes. Conclusion: SLCO1A2 -189_-188InsA polymorphism is related to the reduced clearance of rocuronium in patients submitted to elective surgeries under general anesthesia. Trial registration: NCT 02399397 (ClinicalTrials.gov).
publishDate 2017
dc.date.none.fl_str_mv 2017-08-01
2018-12-11T16:46:56Z
2018-12-11T16:46:56Z
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 http://dx.doi.org/10.1007/s00228-017-2243-1
European Journal of Clinical Pharmacology, v. 73, n. 8, p. 957-963, 2017.
1432-1041
0031-6970
http://hdl.handle.net/11449/169631
10.1007/s00228-017-2243-1
2-s2.0-85017445115
2-s2.0-85017445115.pdf
url http://dx.doi.org/10.1007/s00228-017-2243-1
http://hdl.handle.net/11449/169631
identifier_str_mv European Journal of Clinical Pharmacology, v. 73, n. 8, p. 957-963, 2017.
1432-1041
0031-6970
10.1007/s00228-017-2243-1
2-s2.0-85017445115
2-s2.0-85017445115.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv European Journal of Clinical Pharmacology
1,159
1,159
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 957-963
application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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