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Commencing insulin glargine 100 U/mL therapy in individuals with type 2 diabetes: Determinants of achievement of HbA1c goal less than 7.0.
Owens, David R; Landgraf, Wolfgang; Frier, Brian M; Zhang, Mei; Home, Philip D; Meneghini, Luigi; Bolli, Geremia B.
Afiliação
  • Owens DR; Swansea University, Diabetes Research Group Cymru, College of Medicine, Swansea, UK.
  • Landgraf W; Sanofi, Frankfurt, Germany.
  • Frier BM; The Queen's Medical Research Institute, University of Edinburgh, Edinburgh, UK.
  • Zhang M; Sanofi US, Bridgewater, New Jersey.
  • Home PD; Department of Medical School, Institute of Cellular Medicine, Diabetes, Newcastle University, Newcastle upon Tyne, UK.
  • Meneghini L; Department of Internal Medicine, Endocrinology, University of Texas Southwestern Medical Center and Parkland Health and Hospital System, Dallas, Texas.
  • Bolli GB; Department of Internal Medicine, University of Perugia School of Medicine, Perugia, Italy.
Diabetes Obes Metab ; 21(2): 321-329, 2019 02.
Article em En | MEDLINE | ID: mdl-30520217
AIMS: To identify factors associated with achievement of glycated haemoglobin A1c (HbA1c) target at 24 weeks after commencing basal insulin therapy in individuals with type 2 diabetes mellitus (T2DM). MATERIALS AND METHODS: Post-hoc pooled analysis of 16 randomized, treat-to-target trials involving individuals with T2DM inadequately controlled with oral anti-hyperglycaemic drugs (n = 3415) initiated on once-daily insulin glargine 100 U/mL (Gla-100). Clinical outcomes were assessed by HbA1c response at 24 weeks and individuals were classified as "good responders" with HbA1c <7.0% (<53 mmol/mol) or as "poor responders" with HbA1c ≥7.0% (≥53 mmol/mol). Univariable and multivariable stepwise logistic regression analyses were performed to identify predictive factors for attaining HbA1c <7.0%. RESULTS: Lower levels of baseline HbA1c, fasting plasma glucose (FPG) and post-prandial plasma glucose (PPG), higher body mass index (BMI), shorter diabetes duration and male sex were associated with a good glycaemic response, but not age or baseline C-peptide levels. Gla-100 dose (U/kg) was highest in the poor-responder group, which had the fewest hypoglycaemia episodes. Univariable analysis for achievement of HbA1c <7.0% confirmed these observations. Multivariable analysis retained baseline HbA1c, body weight, BMI, sex, 2-hours PPG and diabetes duration as predictors of a good response. Continued use of sulfonylureas, hypoglycaemia and change in body weight were indicative of poor response. CONCLUSIONS: Baseline HbA1c was the strongest determinant for achieving target HbA1c <7.0% by supplementary Gla-100 therapy, while sex and BMI were also useful indicators. However, age and C-peptide levels at baseline did not predict glycaemic response to the introduction of basal insulin.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Planejamento de Assistência ao Paciente / Hemoglobinas Glicadas / Diabetes Mellitus Tipo 2 / Insulina Glargina Tipo de estudo: Clinical_trials / Prognostic_studies / Systematic_reviews Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Diabetes Obes Metab Assunto da revista: ENDOCRINOLOGIA / METABOLISMO Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Planejamento de Assistência ao Paciente / Hemoglobinas Glicadas / Diabetes Mellitus Tipo 2 / Insulina Glargina Tipo de estudo: Clinical_trials / Prognostic_studies / Systematic_reviews Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Diabetes Obes Metab Assunto da revista: ENDOCRINOLOGIA / METABOLISMO Ano de publicação: 2019 Tipo de documento: Article