dc.creatorEyzaguirre C., Francisca
dc.creatorCodner Dujovne, Ethel
dc.date.accessioned2019-03-11T12:51:01Z
dc.date.available2019-03-11T12:51:01Z
dc.date.created2019-03-11T12:51:01Z
dc.date.issued2006
dc.identifierRevista Medica de Chile, Volumen 134, Issue 2, 2018, Pages 239-250
dc.identifier00349887
dc.identifier07176163
dc.identifierhttp://repositorio.uchile.cl/handle/2250/164132
dc.description.abstractInsulin analogues, developed by molecular engineering, have structural changes in the A and B insulin chains. These modifications change their action profile, rendering insulin replacement closer to physiology. Rapid acting analogues like lispro, a spart and glulisine, are absorbed rapidly from the subcutaneous tissue to the circulation. In addition, two long acting insulin analogues have been developed: glargine and detemir. The combination of a long acting insulin, to maintain baseline levels, and multiple daily doses of a rapid acting analogue are the mainstay of basal-bolus therapy. Multiples studies have compared human insulin (NPH and regular) with insulin analogues in patients with type 1 or 2 diabetes mellitus, showing an improvement in the metabolic control, fewer hypoglycemic events and better quality of life. In summary, insulin analogues offer new therapeutic options and allow an individualized intensive treatment.
dc.languageen
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceRevista Medica de Chile
dc.subjectDiabetes mellitus, insulin dependent
dc.subjectInsulin
dc.subjectInsulin, long acting
dc.subjectPro insulin
dc.titleInsulin analogues: Searching for a physiological replacement Análoges de insulina: En búsqueda del reemplazo fisiológico
dc.typeArtículos de revistas


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