Short Course of Insulin Treatment versus Metformin in Newly Diagnosed Patients with Type 2 Diabetes.
Marta SeghieriEleni RebelosAndrea MariLuigi SciangulaCarlo GiordaEleuterio FerranniniPublished in: Journal of clinical medicine (2018)
The ß-cell dysfunction of type 2 diabetes is partly reversible. The optimal time window to induce glycemic remission is uncertain; short courses of insulin treatment have been tested as a strategy to induce remission. In a pilot study in 38 newly-diagnosed patients, we assessed the time-course of insulin sensitivity and ß-cell function (by repeat oral glucose tolerance tests) following a 6-week basal insulin treatment compared to metformin monotherapy in equipoised glycemic control. At 6 weeks, insulin secretion and sensitivity were increased in both groups whilst ß-cell glucose sensitivity was unchanged. From this time onwards, in the insulin group glycemia started to rise at 3 months, and was no longer different from baseline at 1 year. The initial improvement in insulin secretion and sensitivity dissipated. In the metformin group, fasting plasma glucose and HbA1c levels reached a nadir at 8 months, at which time insulin secretion, glucose and insulin sensitivity were significantly better than at baseline and higher than in the insulin group. A short course of basal insulin in newly-diagnosed patients does not appear to offer clinical advantage over recommended initiation with metformin.
Keyphrases
- type diabetes
- newly diagnosed
- glycemic control
- blood glucose
- end stage renal disease
- insulin resistance
- chronic kidney disease
- weight loss
- cardiovascular disease
- peritoneal dialysis
- oxidative stress
- combination therapy
- prognostic factors
- cell therapy
- disease activity
- bone marrow
- replacement therapy
- adipose tissue
- open label
- gestational age
- mesenchymal stem cells
- double blind