RecruitingNot ApplicableNCT06155708

Exogenous Ketone Supplementation in Females with Polycystic Ovary Syndrome

Exogenous Ketone Supplementation to Improve Cardiovascular Disease Risk Factors in Females with Polycystic Ovary Syndrome


Sponsor

McGill University

Enrollment

60 participants

Start Date

Jan 20, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Polycystic ovary syndrome (PCOS) affects 1 in 5 females of reproductive age. Commonly characterized as a disorder of infertility, PCOS is often accompanied by 3 potent cardiovascular disease (CVD) risk factors: insulin resistance, endothelial dysfunction, and elevated blood pressure. Accordingly, PCOS is associated with the development of CVD, the second leading cause of death in females in Canada. However, effective treatments to improve cardiovascular health in PCOS are lacking. Exogenous ketone monoester (KME) ingestion has been shown to improves outcomes associated with insulin resistance, endothelial function, and blood pressure regulation in healthy individuals and individuals predisposed to CVD. Therefore, oral ketone supplements offer a practical and effective strategy for improving cardiovascular health; however, this treatment has yet to be evaluated in PCOS. Therefore, the overall goal of this project is to employ KME ingestion to improve markers of cardiovascular health in females with PCOS. On two different days, participants will consume either a beverage containing a ketone supplement or a beverage containing a placebo supplement. The objectives are to compare responses between KME and placebo ingestion, and examine all outcomes related to cardiovascular health in females with PCOS in comparison with female controls of similar age and body mass index. The effects of KME ingestion will be quantified on: 1) glycemic control during an oral glucose tolerance test; 2) endothelial function using the flow-mediated dilation test; 3) blood pressure and acute blood pressure regulation; and 4) hemodynamic responses to acute exercise.


Eligibility

Min Age: 18 YearsMax Age: 40 Years

Inclusion Criteria3

  • All female participants will report female sex assigned at birth
  • All participants will be aged 18 to 40
  • PCOS diagnosis

Exclusion Criteria4

  • Current smokers or a prolonged history of smoking
  • Presence or history of overt cardiometabolic disease (e.g., stage 2 hypertension, diabetes, heart disease), neurologic disease, or endocrinopathy (with the exception of PCOS)
  • Current pregnancy or currently breastfeeding
  • Current use of medications which may affect our outcomes of interest (e.g., anti-hypertensives, anti-androgens, metformin)

Interventions

DIETARY_SUPPLEMENTKetone

\- Ketone monoester supplement in the form of (R)-3-hydroxybutyl (R)-3-hydroxybutyrate based on participants' body weight (0.45ml/kg body weight) ingested with water and vanilla-flavored stevia in a total volume of 100 ml.

DIETARY_SUPPLEMENTWater

100 ml water combined with 10ml bitter flavor and vanilla-flavored stevia


Locations(1)

Cardiovascular Health and Autonomic Research Laboratory

Montreal, Quebec, Canada

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NCT06155708


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