Worry vs. knowledge about treatment-associated hypoglycaemia and weight gain in type 2 diabetic patients on metformin and/or sulphonylurea

2012 ◽  
Vol 28 (5) ◽  
pp. 731-736 ◽  
Author(s):  
Asger Lund ◽  
Filip K. Knop
Endocrine ◽  
2010 ◽  
Vol 39 (2) ◽  
pp. 190-197 ◽  
Author(s):  
H. J. Jansen ◽  
J. C. Hendriks ◽  
B. E. de Galan ◽  
G. Penders ◽  
C. J. Tack ◽  
...  

2005 ◽  
Vol 94 (6) ◽  
pp. 931-937 ◽  
Author(s):  
A. Sallé ◽  
M. Ryan ◽  
G. Guilloteau ◽  
B. Bouhanick ◽  
G. Berrut ◽  
...  

Insulin use is common in type 2 diabetes and is frequently accompanied by weight gain, the composition of which is poorly understood. The present study evaluates insulin-induced body composition changes. Body weight and composition of thirty-two type 2 diabetic patients undergoing their first 12 months of insulin therapy were compared with those observed in thirty-two type 2 diabetic patients previously treated on insulin (minimum 1 year). Body composition was determined by simultaneous body water spaces (bioelectrical impedance analysis) and body density measurements. After 6 months, glycosylated Hb (HbA1c) significantly improved in the newly treated group (P<0·0001), but remained stable in those treated previously. HbA1c did not differ between 6 and 12 months in the two groups. Body weight significantly (P=0·04) changed over 12 months in those newly treated only (+2·8 kg), essentially comprising fat-free mass (P=0·044). Fat mass remained unchanged (P=0·85) as did total body water, while extracellular: total body water ratio tended to increase in those newly treated (P=0·059). Weight changes correlated with HbA1c changes (R2 0·134, P=0·002) in the initial 6 months only. Insulin therapy leads to weight gain (2·8 kg), predominantly fat-free mass, over 12 months. After 6 months, newly treated patients continued gaining weight despite an unchanged HbA1c, suggesting the potential anabolic role of insulin in subsequent gains. Therefore, in the initial 6 months, weight gain can be attributed to a ‘glucose control-related effect’ and further gain appears to be due to a ‘non-glucose control-related’ effect of insulin treatment.


Author(s):  
Giuseppe Lisco ◽  
Anna De Tullio ◽  
Edoardo Guastamacchia ◽  
Vincenzo Triggiani

Introduction: New evidences suggest that combining basal insulin with glucagone-like peptide 1 receptor agonists (GLP-1RA) in patients with type 2 diabetes could promptly ameliorate the glucose control and prevent both hypoglycaemia and weight gain compared with more intensive insulin regimens. Aim of the study: To review the efficacy/effectiveness and safety of fixed-ratio combinations of basal insulin and GLP-1RA (FRCs). Methods: We asked the web for freely available medical data concerning the aim of the study, and selected original articles, randomized clinical trials (RCTs), clinical reviews, and meta-analysis written in English. Results: FRCs provide a significative improvement in glucose control in both insulin-naïve (-1.4% to -2% HbA1c from aseline) and insulin-experienced (-1.5% to -2% HbA1c from baseline) type 2 diabetic patients with moderate glucose impairment. More patients achieved the recommended glycaemic targets on FRCs compared to those on mono-therapy with basal insulin or GLP-1RAs. The intensification with FRCs results in a better glycaemic control compared to basal insulin at fasting as well as during the postprandial state. The frequency of hypoglycaemia is similar or lower in patients treated with FRCs than in those on basal insulin alone at similar dose. Weight trend can be variable, ranging from -2.7 to +2 Kg for iDegLira and -0.7 to -1.3 Kg for iGlarLixi. However, a lower weight gain is obtained with iDegLira compared to iDeg (-2.2 to - 2.5 Kg), iGlar (-1.7 to 3.2 Kg), and basal-bolus (-3.6 Kg) as well as with iGlarLixi compared to iGlar (-1.4 Kg). Discussion and Conclusion: FRCs should be considered for safely improve the metabolic control in type 2 diabetic patients.


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