TY - JOUR
T1 - Poorly controlled elderly Type 2 diabetic patients
T2 - The effects of increasing sulphonylurea dosages or adding metformin
AU - Gregorio, Franco
AU - Ambrosi, F.
AU - Manfrini, S.
AU - Velussi, M.
AU - Carle, F.
AU - Testa, R.
AU - Merante, D.
AU - Filipponi, P.
PY - 1999
Y1 - 1999
N2 - Aims: To assess the effects and safety of increasing sulphonylurea dosages or adding metformin in poorly controlled elderly Type 2 diabetic patients. Methods: A 18-month multicentre clinical study was performed on sulphonylurea-treated diabetic patients over 70 years of age with well- preserved renal function, steady fasting blood glucose ≥ 200 mg/dl and HbA(1c) ≥ 9%. Patients were randomly assigned to sulphonylurea increased up to its maximum dosage (1st group) or to addition of metformin (2nd group). Glycaemic control, lipid pattern, haemostatic status and safety were monitored during run-in, at baseline and at scheduled intervals for 18 months. Results refer to 85 patients in the 1st group and 89 patients in the 2nd with complete data. Results: Similar improvements in glycaemic levels were observed with both treatments within the first month and a similar decrease in HbA(1c) within the third month. No further changes occurred in glycaemic control. In the 1st group, fasting glucose (mmol/l, mean ± SE) decreased from 14.21 ± 0.49 to 9.88 ± 0.21, average day-long glucose from 14.87 ± 0.27 to 10.69 ± 0.19 and HbA(1c) (%) from 10.32 ± 0.13 to 8.66 ± 0.13. In the 2nd treatment group fasting glucose decreased from 14.59 ± 0.61 to 9.05 ± 37.28, average day-long glucose from 15.09 ± 0.29 to 10.32 ± 0.21 and HbA(1c) from 10.33 ± 0.13 to 8.77 ± 0.12 (for all P <0.0005). In this 2nd group, a decrease in LDL-cholesterol (P <0.05) and an increase in HDL-cholesterol levels (P <0.02) were also observed. In the 1st group, anthrombin III activity increased significantly (P <0.01). In the 2nd group, significant reductions in markers of platelet function (FP4 and βTG, P <0.01), thrombin generation (FPA, F1 + 2 and D-D, P <0.01), and fibrinolysis inhibition (PAI-1 activity, PAI-1 antigen, P <0.001) were observed. Increases in some fibrinolytic activation markers (t-PA activity, and AT-III activity, P <0.01) occurred. Fasting lactate concentrations were unchanged in the metformin-treated group. No serious adverse effects were observed in either group. Conclusions: These results suggest that either high sulphonylurea dosages or a therapy combining lower sulphonylurea dosages with metformin are effective and safe in an aged but healthy population. Metformin provides additional benefits counteracting several cardiovascular risk factors but must be administered with caution, bearing in mind the general contra-indications for the drug but not age alone.
AB - Aims: To assess the effects and safety of increasing sulphonylurea dosages or adding metformin in poorly controlled elderly Type 2 diabetic patients. Methods: A 18-month multicentre clinical study was performed on sulphonylurea-treated diabetic patients over 70 years of age with well- preserved renal function, steady fasting blood glucose ≥ 200 mg/dl and HbA(1c) ≥ 9%. Patients were randomly assigned to sulphonylurea increased up to its maximum dosage (1st group) or to addition of metformin (2nd group). Glycaemic control, lipid pattern, haemostatic status and safety were monitored during run-in, at baseline and at scheduled intervals for 18 months. Results refer to 85 patients in the 1st group and 89 patients in the 2nd with complete data. Results: Similar improvements in glycaemic levels were observed with both treatments within the first month and a similar decrease in HbA(1c) within the third month. No further changes occurred in glycaemic control. In the 1st group, fasting glucose (mmol/l, mean ± SE) decreased from 14.21 ± 0.49 to 9.88 ± 0.21, average day-long glucose from 14.87 ± 0.27 to 10.69 ± 0.19 and HbA(1c) (%) from 10.32 ± 0.13 to 8.66 ± 0.13. In the 2nd treatment group fasting glucose decreased from 14.59 ± 0.61 to 9.05 ± 37.28, average day-long glucose from 15.09 ± 0.29 to 10.32 ± 0.21 and HbA(1c) from 10.33 ± 0.13 to 8.77 ± 0.12 (for all P <0.0005). In this 2nd group, a decrease in LDL-cholesterol (P <0.05) and an increase in HDL-cholesterol levels (P <0.02) were also observed. In the 1st group, anthrombin III activity increased significantly (P <0.01). In the 2nd group, significant reductions in markers of platelet function (FP4 and βTG, P <0.01), thrombin generation (FPA, F1 + 2 and D-D, P <0.01), and fibrinolysis inhibition (PAI-1 activity, PAI-1 antigen, P <0.001) were observed. Increases in some fibrinolytic activation markers (t-PA activity, and AT-III activity, P <0.01) occurred. Fasting lactate concentrations were unchanged in the metformin-treated group. No serious adverse effects were observed in either group. Conclusions: These results suggest that either high sulphonylurea dosages or a therapy combining lower sulphonylurea dosages with metformin are effective and safe in an aged but healthy population. Metformin provides additional benefits counteracting several cardiovascular risk factors but must be administered with caution, bearing in mind the general contra-indications for the drug but not age alone.
KW - Elderly
KW - Metformin
KW - Sulphonylureas
KW - Type 2 diabetes mellitus
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U2 - 10.1046/j.1464-5491.1999.00201.x
DO - 10.1046/j.1464-5491.1999.00201.x
M3 - Article
C2 - 10656230
AN - SCOPUS:0033368928
SN - 0742-3071
VL - 16
SP - 1016
EP - 1024
JO - Diabetic Medicine
JF - Diabetic Medicine
IS - 12
ER -