Exenatide, Dapagliflozin, or Phentermine/Topiramate Differentially Affect Metabolic Profiles in Polycystic Ovary Syndrome

Author:

Elkind-Hirsch Karen E12ORCID,Chappell N3,Seidemann Ericka1,Storment John3,Bellanger Drake2

Affiliation:

1. Woman’s Hospital Research Center, Woman’s Hospital, Baton Rouge, Louisiana, USA

2. Woman’s Weight Loss and Metabolic Clinic, Woman’s Hospital, Baton Rouge, Louisiana, USA

3. Fertility Answers, Woman’s Hospital, Baton Rouge, Louisiana, USA

Abstract

Abstract Context Glucagon-like peptide-1 receptor agonists and sodium-glucose cotransporter-2 inhibitors reduce weight and improve insulin sensitivity via different mechanisms. Objective The efficacy of once-weekly exenatide (EQW) and dapagliflozin (DAPA) alone and coadministered (EQW/DAPA), DAPA/extended-release (ER) metformin (DAPA/MET), and phentermine topiramate extended release (PHEN/TPM) on metabolic parameters, body composition, and sex hormones were examined in obese women with PCOS. Methods Nondiabetic women (n = 119; aged 18-45 years) with a body mass index (BMI) greater than 30 and less than 45 and polycystic ovary syndrome (National Institutes of Health criteria) were randomly assigned in a single-blinded fashion to EQW (2 mg weekly); DAPA (10 mg daily), EQW/DAPA (2 mg weekly/10 mg daily), DAPA (10 mg)/MET (2000 mg XR daily), or PHEN (7.5 mg)/TPM (46 mg ER daily) treatment for 24 weeks. Study visits at baseline and 24 weeks included weight, blood pressure (BP), waist (WC) measures, and body composition evaluated by dual-energy x-ray absorptiometry (DXA). Oral glucose tolerance tests were conducted to assess glycemia and mean blood glucose (MBG), and compute insulin sensitivity (SI) and secretion (IS) measures. Sex steroids, free androgen index (FAI), and lipid profiles were measured in the fasting sample. Results EQW/DAPA and PHEN/TPM resulted in the most loss of weight and total body fat by DXA, and WC. Despite equivalent reductions in BMI and WC with PHEN/TPM, only EQW/DAPA and EQW resulted in significant improvements in MBG, SI, and IS. Reductions in fasting glucose, testosterone, FAI, and BP were seen with all drugs. Conclusion Dual therapy with EQW/DAPA was superior to either alone, DAPA/MET and PHEN/TPM in terms of clinical and metabolic benefits in this patient population.

Funder

AstraZeneca

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference39 articles.

1. Polycystic ovary syndrome;Azziz;Nat Rev Dis Primers.,2016

2. Mechanisms of intergenerational transmission of polycystic ovary syndrome;Dumesic;Reproduction.,2020

3. Deciphering the DNA methylome of polycystic ovary syndrome;Tan;Mol Diagn Ther.,2020

4. Insulin resistance and the polycystic ovary syndrome revisited: an update on mechanisms and implications;Diamanti-Kandarakis;Endocr Rev.,2012

5. Insulin resistance and the polycystic ovary syndrome: mechanism and implications for pathogenesis;Dunaif;Endocr Rev.,1997

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