Predicting post one-year durability of glucose-lowering monotherapies in patients with newly-diagnosed type 2 diabetes mellitus – A MASTERMIND precision medicine approach (UKPDS 87)
Autor: | Andrew T. Hattersley, Rury R. Holman, Ewan R. Pearson, Angus G. Jones, Beverley M. Shields, Ruth L. Coleman, Olorunsola F. Agbaje |
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Rok vydání: | 2020 |
Předmět: |
Blood Glucose
Male Chlorpropamide medicine.medical_specialty Time Factors endocrine system diseases Endocrinology Diabetes and Metabolism medicine.medical_treatment 030209 endocrinology & metabolism Type 2 diabetes 03 medical and health sciences 0302 clinical medicine Endocrinology Risk Factors Diabetes mellitus Internal medicine Glyburide Internal Medicine medicine Humans Hypoglycemic Agents Insulin In patient 030212 general & internal medicine Precision Medicine Glycated Hemoglobin Glucose lowering Drug Substitution business.industry nutritional and metabolic diseases Type 2 Diabetes Mellitus General Medicine Middle Aged Prognosis medicine.disease Precision medicine Metformin United Kingdom Treatment Outcome Diabetes Mellitus Type 2 Drug Therapy Combination Female business Follow-Up Studies medicine.drug |
Zdroj: | Diabetes Research and Clinical Practice. 166:108333 |
ISSN: | 0168-8227 |
Popis: | Aims Predicting likely durability of glucose-lowering therapies for people with type 2 diabetes (T2D) could help inform individualised therapeutic choices. Methods We used data from UKPDS patients with newly-diagnosed T2D randomised to first-line glucose-lowering monotherapy with chlorpropamide–glibenclamide–basal insulin or metformin. In 2,339 participants who achieved one-year HbA1c values Results Follow-up was median (IQR) 11.0 (8.0–14.0) years. Monotherapy-failure occurred in 72%–82%–75% and 79% for those randomised to chlorpropamide–glibenclamide–basal insulin or metformin respectively–after median 4.5 (3.0–6.6)–3.7 (2.6–5.6)–4.2 (2.7–6.5) and 3.8 (2.6– 5.2) years. Time-to-monotherapy-failure was predicted primarily by HbA1c and BMI values–with other risk factors varying by type of monotherapy–with predictions to within ±2.5 years for 55%–60%–56% and 57% of the chlorpropamide–glibenclamide–basal insulin and metformin monotherapy cohorts respectively. Conclusions Post one-year glycaemic durability can be predicted robustly in individuals with newly-diagnosed T2D who achieve HbA1c values |
Databáze: | OpenAIRE |
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