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Lispro insulin in people with non-alcoholic liver cirrhosis and type 2 diabetes mellitus.
Gentile, S; Guarino, G; Strollo, F; Romano, M; Genovese, S; Masarone, M; Ceriello, A.
Affiliation
  • Gentile S; Unit of Internal Medicine, Department of Clinical and Experimental Medicine, 2nd University of Naples, Italy.
  • Guarino G; Unit of Internal Medicine, Department of Clinical and Experimental Medicine, 2nd University of Naples, Italy.
  • Strollo F; Diabetes and Endocrinology Unit, St. Peter's Hospital FBF, Rome, Italy. Electronic address: felix.strollo@gmail.com.
  • Romano M; Unit of Gastroenterology, Department of Clinical and Experimental Medicine, 2nd University of Naples, Italy.
  • Genovese S; Diabetes and Metabolic Disease Unit, Cardiovascular Department, IRCCS Multimedica, Sesto San Giovanni (MI), Italy.
  • Masarone M; Unit of Internal Medicine, Department of Clinical and Experimental Medicine, 2nd University of Naples, Italy.
  • Ceriello A; Instititut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) and Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), Barcelona, (AC), Spain.
Diabetes Res Clin Pract ; 113: 179-86, 2016 Mar.
Article in En | MEDLINE | ID: mdl-26803356
AIMS: To compare metabolic control under lispro and recombinant regular human insulin (RHI) in people with diet-unresponsive type 2 diabetes mellitus (T2DM) and compensated non-alcoholic liver disease (CLD). METHODS: 108 people with T2DM and CLD were randomly allocated to RHI or lispro according to a 12+12 week cross-over protocol. A 1-week continuous glucose monitoring (CGM) session was performed at the end of each treatment period followed by a standard meal test with a 12IU lispro or RHI shot ahead. RESULTS: CGM showed higher glycemic excursions under RHI than under lispro (p<0.01) with lower glucose levels in the late post-absorption phase (p<0.05) and even more during the night (p<0.01). Post-challenge incremental areas under the curve (ΔAUC) were undistinguishable for insulin but lower for glucose, while insulin peaked higher and earlier and glycemic excursions were lower with lispro than with RHI (0.05
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Blood Glucose / Diabetes Mellitus, Type 2 / Insulin Lispro / Insulin, Regular, Human / Hypoglycemic Agents / Liver Cirrhosis Type of study: Clinical_trials / Guideline Limits: Female / Humans / Male / Middle aged Language: En Journal: Diabetes Res Clin Pract Journal subject: ENDOCRINOLOGIA Year: 2016 Type: Article Affiliation country: Italy

Full text: 1 Database: MEDLINE Main subject: Blood Glucose / Diabetes Mellitus, Type 2 / Insulin Lispro / Insulin, Regular, Human / Hypoglycemic Agents / Liver Cirrhosis Type of study: Clinical_trials / Guideline Limits: Female / Humans / Male / Middle aged Language: En Journal: Diabetes Res Clin Pract Journal subject: ENDOCRINOLOGIA Year: 2016 Type: Article Affiliation country: Italy