Beneficial effects of insulin versus sulphonylurea on insulin secretion and metabolic control in recently diagnosed type 2 diabetic patients

被引:123
作者
Alvarsson, M [1 ]
Sundkvist, G
Lager, I
Henricsson, M
Berntorp, K
Fernqvist-Forbes, E
Steen, L
Westermark, G
Westermark, P
Örn, T
Grill, V
机构
[1] Karolinska Hosp, Dept Endocrinol & Diabetol, SE-17176 Stockholm, Sweden
[2] Malmo Univ Hosp, Dept Endocrinol, Malmo, Sweden
[3] Kristianstad Hosp, Dept Med, Kristianstad, Sweden
[4] Helsingborg Hosp, Dept Ophthalmol, Helsingborg, Sweden
[5] Visby Hosp, Dept Med, Visby, Sweden
[6] Malarsjukhuset, Dept Med, Eskilstuna, Sweden
[7] Fac Hlth Sci, Div Cell Biol, Linkoping, Sweden
[8] Blekingesjukhuset, Dept Med, Karlskrona, Sweden
关键词
D O I
10.2337/diacare.26.8.2231
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE - To evaluate whether treatment with insulin in recently diagnosed type 2 diabetes is advantageous compared with glibenclamide treatment. RESEARCH DESIGN AND METHODS - beta-Cell function, glycemic control, and quality of life were monitored over 2 years in 39 patients with islet cell antibody-negative type 2 diabetes diagnosed 0-2 years before inclusion in a Swedish multicenter randomized clinical trial. Patients were randomized to either two daily injections of premixed 30% soluble and 70% NPH insulin or glibenclamide (3.5-10.5 mg daily). C-peptide-glucagon tests were performed yearly in duplicate after 2-3 days of temporary withdrawal of treatment. RESULTS - After 1 year the glucagon-stimulated C-peptide response was increased in the insulin-treated group by 0.14 +/- 0.08 nmol/l, whereas it was decreased by 0.12 +/- 0.08 nmol/l in the glibenclamide group, P < 0.02 for difference between groups. After 2 years, fasting insulin levels were higher after treatment withdrawal in the insulin-treated versus the glibenclamide-treated group (P = 0.02). HbA(1c) levels decreased significantly during the first year in both groups, however, at the end of the second year, HbA(1c) had deteriorated in the glibenclamide group (P < 0.01), but not in the insulin-treated group. The difference in evolution of HbA(1c) during the second year was significant between groups, P < 0.02. A questionnaire indicated no difference in well-being related to treatment. CONCLUSIONS - Early insulin versus glibenclamide treatment in type 2 diabetes temporarily prolongs endogenous insulin secretion and promotes better metabolic control.
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页码:2231 / 2237
页数:7
相关论文
共 22 条
[1]  
[Anonymous], 1995, Diabetes, V44, P1249
[2]   REPRODUCIBILITY OF THE GLUCAGON TEST [J].
ARNOLDLARSEN, S ;
MADSBAD, S ;
KUHL, C .
DIABETIC MEDICINE, 1987, 4 (04) :299-303
[3]   Random C-peptide in the classification of diabetes [J].
Berger, B ;
Stenström, G ;
Sundkvist, G .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 2000, 60 (08) :687-693
[4]   NIDDM: A rapid progressive disease - Results from a long-term, randomised, comparative study of insulin or sulphonylurea treatment [J].
Birkeland, KI ;
Rishaug, U ;
Hanssen, KF ;
Vaaler, S .
DIABETOLOGIA, 1996, 39 (12) :1629-1633
[5]  
Borg H, 1997, CLIN CHEM, V43, P779
[6]   ISLET AMYLOID POLYPEPTIDE IN THE RABBIT AND EUROPEAN HARE - STUDIES ON ITS RELATIONSHIP TO AMYLOIDOGENESIS [J].
CHRISTMANSON, L ;
BETSHOLTZ, C ;
LECKSTROM, A ;
ENGSTROM, U ;
CORTIE, C ;
JOHNSON, KH ;
ADRIAN, TE ;
WESTERMARK, P .
DIABETOLOGIA, 1993, 36 (03) :183-188
[7]   RELATIONSHIPS BETWEEN DIABETES DURATION, METABOLIC CONTROL AND BETA-CELL FUNCTION IN A REPRESENTATIVE POPULATION OF TYPE-2 DIABETIC-PATIENTS IN SWEDEN [J].
CLAUSON, P ;
LINNARSSON, R ;
GOTTSATER, A ;
SUNDKVIST, G ;
GRILL, V .
DIABETIC MEDICINE, 1994, 11 (08) :794-801
[8]  
FRIER BM, 1977, DIABETES, V26, P369
[9]   THE EFFECT OF CHRONIC HYPERGLYCEMIA ON THE ISLET B-CELL RESPONSIVENESS IN NEWLY DIAGNOSED TYPE-2 DIABETES [J].
GJESSING, HJ ;
REINHOLD, B ;
PEDERSEN, O .
DIABETIC MEDICINE, 1992, 9 (07) :601-604
[10]   PANCREATIC BETA-CELL FUNCTION EVALUATED BY INTRAVENOUS GLUCOSE AND GLUCAGON STIMULATION - A COMPARISON BETWEEN INSULIN AND C-PEPTIDE TO MEASURE INSULIN-SECRETION [J].
GOTTSATER, A ;
LANDINOLSSON, M ;
FERNLUND, P ;
GULLBERG, B ;
LERNMARK, A ;
SUNDKVIST, G .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1992, 52 (07) :631-639