Efficacy of Liraglutide: GLP 1 Receptor Agonist on Glycemic Control and Weight Loss among Patients with Type 2 Diabetes

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  • Admin PJMD

Abstract

Background: American Diabetes Association (ADA) made conspicuous changes in its 2019 Standards of
Care Diabetes guidelines by choosing Glucagon like Peptide 1 (GLP1) receptor agonists and Sodium
Glucose co-transporter 2 (SGLT2) inhibitors as the second line treatment options after metformin because
both classes of drugs are cardiovascular friendly as proved in the Cardiovascular Outcome Trials (CVOT).
GLP analogs show massive weight loss benefits apart from offering good glycemic control. We aimed to
determine the impact of liraglutide on correction of hyperglycemia and body weight in Asian population.
Methods: A cross sectional pre-post observational study enrolling 49 Type 2 diabetic patients with uncontrolled blood glucose, 15 years and above who agreed to use liraglutide apart from standard care, for
glycemic control were recruited in the study. Study site was general practice clinic in Clifton and family medicine health care center Ziauddin University. Pre and post treatment HbA1C and BMI were observed after
adding on Liraglutide 1.8 mg to metformin 1 gm bid, over a period of 12 weeks. Differences in the changes
in BMI and HbA1C were examined using McNemar’s test.
Results: Mean age of the participants was 44.4 years. Duration of Diabetes was 65.1 months i.e. 5.4 years. At
week 12, liraglutide 1.8 mg significantly reduced HbA1C levels by 0.94% (8.53+1.07 vs. 7.56+1.04 p-value
<0.05) and BMI by 6.2kg (37.23+ 5.3 vs. 31.27.6+5.5 p-value <0.05) statistically significant.
Conclusion: Liraglutide 1.8 mg over a period of 12 weeks, significantly reduced body weight (6.2kg p-value
0.05) and improved glycemic control (0.94% p-value<0.05) without causing hypoglycemia.

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Published

2020-01-24

How to Cite

PJMD, A. (2020). Efficacy of Liraglutide: GLP 1 Receptor Agonist on Glycemic Control and Weight Loss among Patients with Type 2 Diabetes. Pakistan Journal of Medicine and Dentistry, 9(1), 35–40. Retrieved from http://ojs.zu.edu.pk/ojs/index.php/pjmd/article/view/387

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