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Long-term use of contraceptive depot medroxyprogesterone acetate in young women impairs arterial endothelial function assessed by cardiovascular magnetic resonance

Depot medroxyprogesterone acetate (DMPA) inhibits proliferation of ovarian follicles, resulting in anovulation and a decrease in circulating estrogen; the latter action is potentially disadvantageous to cardiovascular health. We therefore investigated the vascular effects of long-term contraceptive...

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Published in:Circulation (New York, N.Y.) N.Y.), 2002-09, Vol.106 (13), p.1646-1651
Main Authors: SORENSEN, Morten B, COLLINS, Peter, PENNELL, Dudley J, ONG, Paul J. L, WEBB, Carolyn M, HAYWARD, Christopher S, ASBURY, Elizabeth A, GATEHOUSE, Peter D, ELKINGTON, Andrew G, YANG, Guang Z, KUBBA, Ali
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Language:English
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Summary:Depot medroxyprogesterone acetate (DMPA) inhibits proliferation of ovarian follicles, resulting in anovulation and a decrease in circulating estrogen; the latter action is potentially disadvantageous to cardiovascular health. We therefore investigated the vascular effects of long-term contraceptive DMPA in young women. Endothelium-dependent (hyperemia-induced flow-mediated dilatation [FMD]) and -independent (glyceryl trinitrate [GTN]) changes in brachial artery area were measured using cardiovascular magnetic resonance in 13 amenorrheic DMPA users (>1 year use; mean age 29+/-4 years) and in 10 controls (mean age 30+/-4 years, P=0.25) with regular menstrual cycles after validation of the technique. FMD and GTN responses were measured just before repeat MPA injection and 48 hours later (n=12) in DMPA users and during menstruation and midcycle (n=9) in controls. Serum-estradiol levels (S-estradiol) were measured at both visits. FMD was reduced in DMPA users compared with controls during menstruation (1.1% versus 8.0%, respectively P
ISSN:0009-7322
1524-4539
DOI:10.1161/01.cir.0000030940.73167.4e