Sources of hepatic glucose production by 2H2O ingestion and Bayesian analysis of 2H glucuronide enrichment

Detalhes bibliográficos
Autor(a) principal: Delgado, T. C.
Data de Publicação: 2008
Outros Autores: Barosa, C., Castro, M. M. C. A., Geraldes, C. F. G. C., Bastos, M., Baptista, C., Fagulha, A., Barros, L., Mota, A., Carvalheiro, M., Jones, J. G., Merritt, Matthew
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/8087
https://doi.org/10.1002/mrm.21681
Resumo: The contribution of gluconeogenesis to hepatic glucose production (GP) was quantified after 2H2O ingestion by Bayesian analysis of the position 2 and 5 2H-NMR signals (H2 and H5) of monoacetone glucose (MAG) derived from urinary acetaminophen glucuronide. Six controls and 10 kidney transplant (KTx) patients with cyclosporine A (CsA) immunosuppressant therapy were studied. Seven KTx patients were lean and euglycemic (BMI = 24.3 ± 1.0 kg/m2; fasting glucose = 4.7 ± 0.1 mM) while three were obese and hyperglycemic (BMI = 30.5 ± 0.7 kg/m2; fasting glucose = 7.1 ± 0.5 mM). For the 16 spectra analyzed, the mean coefficient of variation for the gluconeogenesis contribution was 10% ± 5%. This uncertainty was associated with a mean signal-to-noise ratio (SNR) of 79:1 and 45:1 for the MAG H2 and H5 signals, respectively. For control subjects, gluconeogenesis contributed 54% ± 7% of GP as determined by the mean and standard deviation (SD) of individual Bayesian analyses. For the lean/normoglycemic KTx subjects, the gluconeogenic contribution to GP was 62% ± 7% (P = 0.06 vs. controls), while hyperglycemic/obese KTx patients had a gluconeogenic contribution of 68% ± 3% (P < 0.005 vs. controls). These data suggest that in KTx patients, an increased gluconeogenic contribution to GP is strongly associated with obesity and hyperglycemia. Magn Reson Med 60:517-523, 2008. © 2008 Wiley-Liss, Inc.
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spelling Sources of hepatic glucose production by 2H2O ingestion and Bayesian analysis of 2H glucuronide enrichmentThe contribution of gluconeogenesis to hepatic glucose production (GP) was quantified after 2H2O ingestion by Bayesian analysis of the position 2 and 5 2H-NMR signals (H2 and H5) of monoacetone glucose (MAG) derived from urinary acetaminophen glucuronide. Six controls and 10 kidney transplant (KTx) patients with cyclosporine A (CsA) immunosuppressant therapy were studied. Seven KTx patients were lean and euglycemic (BMI = 24.3 ± 1.0 kg/m2; fasting glucose = 4.7 ± 0.1 mM) while three were obese and hyperglycemic (BMI = 30.5 ± 0.7 kg/m2; fasting glucose = 7.1 ± 0.5 mM). For the 16 spectra analyzed, the mean coefficient of variation for the gluconeogenesis contribution was 10% ± 5%. This uncertainty was associated with a mean signal-to-noise ratio (SNR) of 79:1 and 45:1 for the MAG H2 and H5 signals, respectively. For control subjects, gluconeogenesis contributed 54% ± 7% of GP as determined by the mean and standard deviation (SD) of individual Bayesian analyses. For the lean/normoglycemic KTx subjects, the gluconeogenic contribution to GP was 62% ± 7% (P = 0.06 vs. controls), while hyperglycemic/obese KTx patients had a gluconeogenic contribution of 68% ± 3% (P < 0.005 vs. controls). These data suggest that in KTx patients, an increased gluconeogenic contribution to GP is strongly associated with obesity and hyperglycemia. Magn Reson Med 60:517-523, 2008. © 2008 Wiley-Liss, Inc.2008info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/8087http://hdl.handle.net/10316/8087https://doi.org/10.1002/mrm.21681engMagnetic Resonance in Medicine. 60:3 (2008) 517-523Delgado, T. C.Barosa, C.Castro, M. M. C. A.Geraldes, C. F. G. C.Bastos, M.Baptista, C.Fagulha, A.Barros, L.Mota, A.Carvalheiro, M.Jones, J. G.Merritt, Matthewinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2021-09-29T07:57:45Zoai:estudogeral.uc.pt:10316/8087Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:55:46.347888Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Sources of hepatic glucose production by 2H2O ingestion and Bayesian analysis of 2H glucuronide enrichment
title Sources of hepatic glucose production by 2H2O ingestion and Bayesian analysis of 2H glucuronide enrichment
spellingShingle Sources of hepatic glucose production by 2H2O ingestion and Bayesian analysis of 2H glucuronide enrichment
Delgado, T. C.
title_short Sources of hepatic glucose production by 2H2O ingestion and Bayesian analysis of 2H glucuronide enrichment
title_full Sources of hepatic glucose production by 2H2O ingestion and Bayesian analysis of 2H glucuronide enrichment
title_fullStr Sources of hepatic glucose production by 2H2O ingestion and Bayesian analysis of 2H glucuronide enrichment
title_full_unstemmed Sources of hepatic glucose production by 2H2O ingestion and Bayesian analysis of 2H glucuronide enrichment
title_sort Sources of hepatic glucose production by 2H2O ingestion and Bayesian analysis of 2H glucuronide enrichment
author Delgado, T. C.
author_facet Delgado, T. C.
Barosa, C.
Castro, M. M. C. A.
Geraldes, C. F. G. C.
Bastos, M.
Baptista, C.
Fagulha, A.
Barros, L.
Mota, A.
Carvalheiro, M.
Jones, J. G.
Merritt, Matthew
author_role author
author2 Barosa, C.
Castro, M. M. C. A.
Geraldes, C. F. G. C.
Bastos, M.
Baptista, C.
Fagulha, A.
Barros, L.
Mota, A.
Carvalheiro, M.
Jones, J. G.
Merritt, Matthew
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Delgado, T. C.
Barosa, C.
Castro, M. M. C. A.
Geraldes, C. F. G. C.
Bastos, M.
Baptista, C.
Fagulha, A.
Barros, L.
Mota, A.
Carvalheiro, M.
Jones, J. G.
Merritt, Matthew
description The contribution of gluconeogenesis to hepatic glucose production (GP) was quantified after 2H2O ingestion by Bayesian analysis of the position 2 and 5 2H-NMR signals (H2 and H5) of monoacetone glucose (MAG) derived from urinary acetaminophen glucuronide. Six controls and 10 kidney transplant (KTx) patients with cyclosporine A (CsA) immunosuppressant therapy were studied. Seven KTx patients were lean and euglycemic (BMI = 24.3 ± 1.0 kg/m2; fasting glucose = 4.7 ± 0.1 mM) while three were obese and hyperglycemic (BMI = 30.5 ± 0.7 kg/m2; fasting glucose = 7.1 ± 0.5 mM). For the 16 spectra analyzed, the mean coefficient of variation for the gluconeogenesis contribution was 10% ± 5%. This uncertainty was associated with a mean signal-to-noise ratio (SNR) of 79:1 and 45:1 for the MAG H2 and H5 signals, respectively. For control subjects, gluconeogenesis contributed 54% ± 7% of GP as determined by the mean and standard deviation (SD) of individual Bayesian analyses. For the lean/normoglycemic KTx subjects, the gluconeogenic contribution to GP was 62% ± 7% (P = 0.06 vs. controls), while hyperglycemic/obese KTx patients had a gluconeogenic contribution of 68% ± 3% (P < 0.005 vs. controls). These data suggest that in KTx patients, an increased gluconeogenic contribution to GP is strongly associated with obesity and hyperglycemia. Magn Reson Med 60:517-523, 2008. © 2008 Wiley-Liss, Inc.
publishDate 2008
dc.date.none.fl_str_mv 2008
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/8087
http://hdl.handle.net/10316/8087
https://doi.org/10.1002/mrm.21681
url http://hdl.handle.net/10316/8087
https://doi.org/10.1002/mrm.21681
dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv Magnetic Resonance in Medicine. 60:3 (2008) 517-523
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