GLUCAGON-LIKE PEPTIDE-1 RECEPTOR AGONISTS AND BONE HEALTH: RESULTS FROM A PILOT RANDOMIZED CONTROLLED TRIAL
Electronic Theses and Dissertations
Item Files
Item Details
- title
- GLUCAGON-LIKE PEPTIDE-1 RECEPTOR AGONISTS AND BONE HEALTH: RESULTS FROM A PILOT RANDOMIZED CONTROLLED TRIAL
- author
- Dinkla, Lauren
- abstract
- BACKGROUND: This project’s purpose is to explore the impact of GLP1Ra-based therapy on measures of bone health in older adults. METHODS: Data comes from a 20-week randomized controlled trial (NCT05786521) which enrolled 20 older adults with a BMI ≥27 kg/m2. Participants were allocated to a combination of 1.0 mg/weekly semaglutide + lifestyle counseling (“intervention”; n=10) or lifestyle counseling alone (“control”; n=10). Total body weight, DXA-acquired bone mineral density (BMD), and bone turnover markers (BTM) [C-terminal telopeptide of type 1 collagen (CTX), and procollagen type I N-propeptide (P1NP)] were measured at baseline and 20-weeks. RESULTS: At baseline, participants were 72.7±4.8 years of age, 50% women, 45% Hispanic, and living with obesity (BMI: 32.9±4.0 kg/m2). After 20 weeks, the intervention group experienced greater weight loss than control (-5.3% compared to -0.89%; p=0.006). No significant differences in whole body BMD were reported between the groups, p=0.77. Likewise, no differences in BTM were observed; CTX: p=0.56, P1NP p=0.78. CONCLUSIONS: In this pilot study, 5% weight loss achieved with GLP1Ra use was not associated with significant change in BMD or BTM compared to lifestyle alone, however, CTX and P1NP increased.
- subject
- bone formation
- bone mineral density
- bone resorption
- glucagon‐like peptide‐1 receptor agonist
- older adults
- randomized controlled trial
- contributor
- Beavers, Kristen M (advisor)
- Miller, Gary (committee member)
- Beavers, Daniel P (committee member)
- Cortes, Tiffany (committee member)
- date
- 2025-06-24T08:36:31Z (accessioned)
- 2025 (issued)
- degree
- Health and Exercise Science (discipline)
- embargo
- 2027-06-23 (terms)
- 2027-06-23 (liftdate)
- identifier
- http://hdl.handle.net/10339/111018 (uri)
- language
- en (iso)
- publisher
- Wake Forest University
- type
- Thesis