Effect of metformin adjunct therapy on cardiometabolic parameters in Indian adolescents with type 1 diabetes: a randomized controlled trial

被引:0
作者
Mondkar, Shruti [1 ]
Khandagale, Sukeshini [2 ]
Shah, Nikhil [1 ]
Khadilkar, Anuradha [1 ,3 ]
Oza, Chirantap [1 ]
Bhor, Shital [1 ]
Gondhalekar, Ketan [1 ]
Wagle, Aneeta [4 ,5 ]
Kajale, Neha [1 ,3 ]
Khadilkar, Vaman [1 ,3 ]
机构
[1] Hirabai Cowasji Jehangir Med Res Inst HCJMRI, Dept Pediat Endocrinol & Growth, Pune, India
[2] Symbiosis Int Univ, Symbiosis Sch Biol Sci, Pune, India
[3] Savitribai Phule Pune Univ, Interdisciplinary Sch Hlth Sci, Pune, India
[4] Jehangir Hosp, Dept Radiol, Pune, India
[5] Kem Hosp Res Ctr, Dept Rheumatol, Pune, India
来源
FRONTIERS IN CLINICAL DIABETES AND HEALTHCARE | 2024年 / 5卷
关键词
metformin; carotid intima media thickness; dyslipidemia; insulin resistance; T1DM; INSULIN-RESISTANCE; BIOELECTRICAL-IMPEDANCE; SENSITIVITY; CHILDREN; OBESITY;
D O I
10.3389/fcdhc.2024.1353279
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Insulin resistance is being increasingly reported in type-1 Diabetes (T1D) and is known to accelerate microvascular complications. The Asian Indian population has a higher risk of double diabetes development compared to Caucasians. Hence, we studied the effect of adding Metformin to standard insulin therapy on glycemic control, insulin sensitivity (IS), cardiometabolic parameters and body composition in Indian adolescents with T1D. Methods A Randomized controlled trial was conducted spanning 9 months (Registration number:CTRI/2019/11/022126). Inclusion: Age 10-19 years, T1D duration>1year, HbA1c>8% Exclusion: Uncontrolled vascular complications/comorbidities, Metformin intolerance, concomitant drugs affecting insulin sensitivity. Participants were randomized to Metformin/Placebo (n=41 each) groups and age, sex, duration-matched. Assessments were performed at baseline, 3 and 9 months. Results 82 participants aged 14.7 +/- 3years (40 females) were enrolled, with a mean diabetes duration of 5.2 +/- 2.3 years. Over 9 months, HbA1c decreased significantly by 0.8 (95% confidence interval: -1.2 to -0.3) from 9.8 +/- 1.8% to 9.1 +/- 1.7% on Metformin but remained largely unchanged (difference of 0.2, 95% confidence interval: -0.7 to 0.2) i.e. 9.9 +/- 1.6% and 9.7 +/- 2.2% on placebo. HbA1c improvement correlated negatively with baseline IS (EGDR:r= -0.3;SEARCH:r = -0.24, p<0.05) implying better HbA1c-lowering in those with decreased initial IS. CGM-based glycemic variability (standard deviation) reduced by 6.3 mg/dL (95% confidence interval: -12.9 to 0.2) from 100.2 +/- 19.1 mg/dL to 93.7 +/- 19.9 mg/dL in those on Metformin (p=0.05) but not placebo (94.0 +/- 20.5; 90.0 +/- 22.6 mg/dL). Insulin sensitivity: CACTIexa & SEARCH scores demonstrated no change with Metformin but significant worsening on placebo. Significant increase in LDL-C(42%), total cholesterol(133.6 to 151.1 mg/dL), triglyceride (60.0 to 88.0 mg/dL) and carotid intima-media thickness was noted on placebo but not Metformin. Weight, BMI, fat Z-scores increased significantly on placebo but not Metformin. Adverse events (AE) were minor; AE, compliance and safety parameters were similar between the two groups. Conclusion Metformin as an adjunct to insulin in Asian Indian adolescents with T1D demonstrated beneficial effect on glycemic control, glycemic variability, IS, lipid profile, vascular function, weight and body fat, with a good safety profile when administered for 9 months.
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