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dc.contributor.author | Porcellati, Francesca | es_ES |
dc.contributor.author | Lucidi, Paola | es_ES |
dc.contributor.author | Rossetti, Paolo | es_ES |
dc.contributor.author | Candeloro, Paola | es_ES |
dc.contributor.author | Andreoli, Anna Marinelli | es_ES |
dc.contributor.author | Marzotti, Stefania | es_ES |
dc.contributor.author | Cioli, Patrizia | es_ES |
dc.contributor.author | Bolli, Geremia B. | es_ES |
dc.contributor.author | Fanelli, Carmine G. | es_ES |
dc.date.accessioned | 2013-11-25T13:50:15Z | |
dc.date.issued | 2011 | |
dc.identifier.issn | 0149-5992 | |
dc.identifier.uri | http://hdl.handle.net/10251/33976 | |
dc.description.abstract | [EN] OBJECTIVE-To assess the role of adiposity on the pharmacodynamics of basal insulins NPH, detemir, and glargine in type 2 diabetes mellitus (T2DM), as estimated by glucose infusion rate (GIR) and endogenous glucose production (EGP) rate in the euglycemic clamp. RESEARCH DESIGN AND METHODS-We examined the variables that best predicted GIR and EGP in 32-h clamp studies after treatment with subcutaneous injection of 0.4 units/kg NPH, detemir, and glargine in 18 T2DM subjects (crossover). RESULTS-A multiple regression analysis revealed that BMI best predicted GIR variation during the clamp. BMI was inversely correlated with GIR in all three insulin treatments, but was statistically significant in detemir treatment only. BMI correlated positively with residual suppression of EGP in detemir, but not with glargine and NPH treatments. CONCLUSIONS-Adiposity blunts the pharmacodynamics of all basal insulins in T2DM. However, as adiposity increases, the effect of detemir is lower versus NPH and glargine. | es_ES |
dc.description.sponsorship | F.P., P.L., P.R., and C.G.F. received grants from various companies (sanofi-aventis, Eli Lilly, Bristol-Myers Squibb, Novartis, and Merck Sharp & Dohme) for participating at meetings and congresses. G.B.B. received honoraria for scientific advising and consulting from the following companies: sanofi-aventis, MannKind, and Eli Lilly. No other potential conflicts of interest relevant to this article were reported. | |
dc.language | Inglés | es_ES |
dc.publisher | American Diabetes Association | es_ES |
dc.relation.ispartof | Diabetes Care | es_ES |
dc.rights | Reserva de todos los derechos | es_ES |
dc.title | Differential Effects of Adiposity on Pharmacodynamics of Basal Insulins NPH, Glargine, and Detemir in Type 2 Diabetes | es_ES |
dc.type | Artículo | es_ES |
dc.embargo.lift | 10000-01-01 | |
dc.embargo.terms | forever | es_ES |
dc.identifier.doi | 10.2337/dc11-1064 | |
dc.rights.accessRights | Cerrado | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Instituto Universitario de Automática e Informática Industrial - Institut Universitari d'Automàtica i Informàtica Industrial | es_ES |
dc.description.bibliographicCitation | Porcellati, F.; Lucidi, P.; Rossetti, P.; Candeloro, P.; Andreoli, AM.; Marzotti, S.; Cioli, P.... (2011). Differential Effects of Adiposity on Pharmacodynamics of Basal Insulins NPH, Glargine, and Detemir in Type 2 Diabetes. Diabetes Care. 34(12):2521-2523. doi:10.2337/dc11-1064 | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | http://dx.doi.org/10.2337/dc11-1064 | es_ES |
dc.description.upvformatpinicio | 2521 | es_ES |
dc.description.upvformatpfin | 2523 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 34 | es_ES |
dc.description.issue | 12 | es_ES |
dc.relation.senia | 220375 | |
dc.identifier.pmid | 21972412 | |
dc.identifier.pmcid | PMC3220859 | |
dc.contributor.funder | Bristol-Myers Squibb | es_ES |
dc.contributor.funder | Novartis Foundation | es_ES |
dc.contributor.funder | Eli Lilly and Company | es_ES |