A pilot study of depot medroxyprogesterone acetate pharmacokinetics and weight gain in adolescent females
- PMID: 24582292
- PMCID: PMC4019679
- DOI: 10.1016/j.contraception.2014.01.017
A pilot study of depot medroxyprogesterone acetate pharmacokinetics and weight gain in adolescent females
Abstract
Objective: To explore the relationship between medroxyprogesterone acetate (MPA) pharmacokinetic (PK) parameter estimates and weight gain.
Study design: Prospective study of adolescents (N=40; age 12-21 years) initiating DMPA. PK parameters were calculated: maximum MPA concentration (Cmax, ng/mL), time to Cmax (Tmax, days) and elimination rate constant (ng/mL/day). Optimal PK cut points were determined for predicting body mass index (BMI) increase ≥10%.
Results: Cmax <2.88 ng/mL and elimination rate constant <0.021 ng/mL/day were associated (p<.05) with BMI increase ≥10%. Elimination rate constant was most predictive of weight gain.
Conclusions: PK evaluation may help identify adolescents at risk of excessive DMPA-associated weight gain.
Keywords: Adolescence; Contraception; Depo Provera; Pharmacokinetics; Weight.
Copyright © 2014 Elsevier Inc. All rights reserved.
Conflict of interest statement
Conflict of Interest/Financial Disclosure: None.
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