Dapagliflozin Add-On Therapy Improves Body Composition and Metabolic Parameters in Overweight Type 2 Diabetic Patients: A Pilot Study

Ugo Di Folco, Alessandra Gatti, Maria Rosaria Nardone, Claudio Tubili

Abstract


Background: Sodium-glucose cotransporter-2 inhibitors (SGLT2-i) inhibit renal glucose reabsorption in the proximal tubules, and reduce plasma glucose, body weight and cardiovascular risk in patients with type 2 diabetes mellitus (T2DM). The data on the effect of SGLT-2i on body composition are conflicting: in some reports, they reduce fat mass, while in other reports, they determine reduction of extra- and intra-cellular fluids. The aim of our pilot study was to investigate the body compartments changes and the effects on glycemia and plasma lipids of add-on SGLT2-i dapagliflozin therapy in poorly controlled overweight/obese T2DM patients.

Methods: Fifty-six overweight (body mass index (BMI) > 25) uncontrolled (HbA1c > 53 mmol/mol; 7%) T2DM outpatients were recruited. They were treated with metformin and basal insulin (group A) or metformin (group B). Weight, BMI, waist circumference (WC), fasting blood glucose (FPG), HbA1c, plasma lipids, bioelectric parameters and derived body compartments (phase angle (pA), total body water (TBW), fat free mass (FFM) and fat mass (FM)) were assessed at baseline (T0) and after 16 weeks (T1) of dapagliflozin 10 mg add-on treatment. Students t-test and one-way analysis of variance (ANOVA) were used to compare the T0 and T1 data.

Results: After 16 weeks, all the patients had weight loss (-3.0 0.6 kg, P < 0.0001) and reduced WC (-2.5 0.6 cm, P < 0.0001). Weight reduction was significant in both groups separately (group A: -2.5 0.3 kg, P <= 0.001; group B: -3.4 0.4 kg, P <= 0.001) and was higher in group B. FFM was not impaired in group A (from 60.2 5.2 to 59.5 8.1 kg; ns) and in group B (from 60.4 6.2 to 59.3 6.6 kg; ns). FM decreased in all the patients (29.9 6.84 kg vs. 26.30 7.4 kg, P < 0.000); a higher reduction was found in group B (-3.6 1.2 kg, P < 0.001) vs. group A (-2.3 1.3 kg, P < 0.001). Metabolic control improved in all the patients: FPG 172 49.4 mg/dL vs. 137 36.8 mg/dL at T1, P < 0.0001; HbA1c 69 9.3 mmol/mol (8.51.5%) vs. 60 8.7 mmol/mol (7.61.4%), P = 0.000. In group A, insulin dose was reduced by 9.3%. Cholesterol and triglycerides (TG) levels decreased in overall population (181.8 48.8 mg/dL vs. 170.7 40.7, P = 0.003; 172 93 mg/dL vs. 143.2 87.8, P = 0.000).

Conclusions: Dapagliflozin add-on therapy induced weight loss and metabolic improvement in overweight and obese T2DM patients. Also insulin-treated patients had weight loss (2.5 kg). Bioelectric impedance analysis (BIA) demonstrated FM loss without FFM impairment and was confirmed to be a simple and effective method to assess body composition in clinical practice.




J Endocrinol Metab. 2019;9(4):90-94
doi: https://doi.org/10.14740/jem564


Keywords


Dapagliflozin; Type 2 diabetes mellitus; Obesity; Body composition; Bioelectric impedance analysis

Full Text: HTML PDF
 

Browse  Journals  

 

Journal of Clinical Medicine Research

Journal of Endocrinology and Metabolism

Journal of Clinical Gynecology and Obstetrics

 

World Journal of Oncology

Gastroenterology Research

Journal of Hematology

 

Journal of Medical Cases

Journal of Current Surgery

Clinical Infection and Immunity

 

Cardiology Research

World Journal of Nephrology and Urology

Cellular and Molecular Medicine Research

 

Journal of Neurology Research

International Journal of Clinical Pediatrics

 

 
       
 

Journal of Endocrinology and Metabolism, bimonthly, ISSN 1923-2861 (print), 1923-287X (online), published by Elmer Press Inc.                     
The content of this site is intended for health care professionals.
This is an open-access journal distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, which permits unrestricted
non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Creative Commons Attribution license (Attribution-NonCommercial 4.0 International CC-BY-NC 4.0)


This journal follows the International Committee of Medical Journal Editors (ICMJE) recommendations for manuscripts submitted to biomedical journals,
the Committee on Publication Ethics (COPE) guidelines, and the Principles of Transparency and Best Practice in Scholarly Publishing.

website: www.jofem.org   editorial contact: editor@jofem.org
Address: 9225 Leslie Street, Suite 201, Richmond Hill, Ontario, L4B 3H6, Canada

© Elmer Press Inc. All Rights Reserved.


Disclaimer: The views and opinions expressed in the published articles are those of the authors and do not necessarily reflect the views or opinions of the editors and Elmer Press Inc. This website is provided for medical research and informational purposes only and does not constitute any medical advice or professional services. The information provided in this journal should not be used for diagnosis and treatment, those seeking medical advice should always consult with a licensed physician.