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dc.contributor.authorProot, P.
dc.contributor.authorDel Prato, S.
dc.contributor.authorPaldanius, P. M.
dc.contributor.authorFoley, J. E.
dc.contributor.authorStumvoll, M.
dc.contributor.authorMatthews, D. R.
dc.date.accessioned2021-03-03T17:49:33Z
dc.date.available2021-03-03T17:49:33Z
dc.date.issued2019
dc.identifier.citationMatthews D. R. , Paldanius P. M. , Proot P., Foley J. E. , Stumvoll M., Del Prato S., "Baseline characteristics in the VERIFY study: a randomized trial assessing the durability of glycaemic control with early vildagliptin-metformin combination in newly diagnosed Type 2 diabetes", DIABETIC MEDICINE, cilt.36, sa.4, ss.505-513, 2019
dc.identifier.issn0742-3071
dc.identifier.othervv_1032021
dc.identifier.otherav_4bacb428-eed1-438c-9f9d-876226603244
dc.identifier.urihttp://hdl.handle.net/20.500.12627/54293
dc.identifier.urihttps://doi.org/10.1111/dme.13886
dc.description.abstractAim To assess the long-term clinical benefits of early combination treatment with vildagliptin-metformin vs. standard-of-care, metformin monotherapy in the ongoing VERIFY study. Methods We randomized 2001 participants with multi-ethnic background, aged 18-70 years, having HbA(1c) levels 48-58 mmol/mol (6.5-7.5%) and BMI 22-40 kg/m(2). Baseline data included HbA(1c), fasting plasma glucose and homeostasis model beta-cell and insulin sensitivity. Standardized meal-tests, insulin secretion rate relative to glucose, and oral glucose insulin sensitivity were assessed in a subpopulation. Results Out of 4524 screened, data were collected from the 2001 eligible participants (53% women) across Europe (52.4%), Latin America (26.8%), Asia (17.2%), South Africa (3.1%) and Australia (0.5%). The median (interquartile range) disease duration was 3.4 (0.9, 10.2) months; mean (+/- SD) age 54.3 +/- 9.4 years; weight 85.5 +/- 17.5 kg and BMI 31.1 +/- 4.7 kg/m(2). Baseline HbA(1c) was 52 +/- 3 mmol/mol (6.9 +/- 0.3%), fasting plasma glucose 7.5 +/- 1.5 mmol/l and the median (interquartile range) of fasting insulin was 109 (75-160) mU/l. Homeostasis model beta-cell and insulin sensitivity values were 84% (60, 116) and 46% (31, 68), respectively. In those undertaking meal-tests, insulin secretion rate relative to glucose was 28 +/- 12 pmol/min/m(2)/mmol/l and oral glucose insulin sensitivity was 353 +/- 57 ml/min/m(2). Conclusions Our current, multi-ethnic, newly diagnosed VERIFY population reflects a characteristic presence of early insulin resistance in participants with increased demand for insulin associated with obesity. The VERIFY study will provide unique evidence in characterizing therapeutic intervention in a diverse population with hyperglycaemia, focusing on durability of early glycaemic control.
dc.language.isoeng
dc.subjectEndocrinology
dc.subjectEndocrine and Autonomic Systems
dc.subjectEndocrinology, Diabetes and Metabolism
dc.subjectLife Sciences
dc.subjectHealth Sciences
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectEndokrinoloji ve Metabolizma Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectENDOKRİNOLOJİ VE METABOLİZMA
dc.titleBaseline characteristics in the VERIFY study: a randomized trial assessing the durability of glycaemic control with early vildagliptin-metformin combination in newly diagnosed Type 2 diabetes
dc.typeMakale
dc.relation.journalDIABETIC MEDICINE
dc.contributor.departmentUniversity Of Oxford , ,
dc.identifier.volume36
dc.identifier.issue4
dc.identifier.startpage505
dc.identifier.endpage513
dc.contributor.firstauthorID2505361


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