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Volume 76, Issue 6, Pages 425-431 (December 2007)


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Bone status after cessation of use of injectable progestin contraceptives

Lynn RosenbergaCorresponding Author Informationemail addressweb address, Yuqing Zhanga, Deborah Constantb, Diane Cooperb, Asgar A. Kallac, Lisa Micklesfieldd, Margaret Hoffmanb

Received 10 August 2007; accepted 23 August 2007. published online 12 November 2007.

Abstract 

Background

Women using injectable progestin contraceptives (IPCs) have lower bone mineral density than nonusers. We assessed whether bone loss is completely reversible after cessation of IPC use, whether different IPCs have different effects and whether effects vary by age at first use.

Study Design

In a cross-sectional study in Cape Town, South Africa, 3487 premenopausal black and mixed race women aged 18–44 years were interviewed for information on contraceptive history and risk factors for decreased bone mineral density, and ultrasound measurements of the left calcaneus were taken. Adjusted means of the ultrasound measures for categories of IPC use were obtained using multivariable linear regression.

Results

Current users of IPCs had the lowest ultrasound measures, while the measures of women who had ceased IPC use at least 2–3 years previously were similar to or greater than those of never users of IPCs. The effects of depot medroxyprogesterone acetate and norethisterone enanthate were similar. The calcaneus measures were unrelated to age at which use began after control for confounding factors.

Conclusion

The data suggest that bone loss during IPC use is reversible and that this loss of bone is completely recovered several years after cessation of use.

a Slone Epidemiology Center at Boston University, Boston, MA 02215-1201, USA

b Women’s Health Research Unit, University of Cape Town, Cape Town 7925, South Africa

c Department of Medicine, University of Cape Town, Cape Town 7925, South Africa

d Exercise and Sports Medicine Research Unit, University of Cape Town, Cape Town 925, South Africa

Corresponding Author InformationCorresponding author. Tel.: +1 617 734 6006; fax: +1 617 738 5119.

 The present study was supported by grant HD042360 from the National Institute of Child Health and Human Development.

PII: S0010-7824(07)00414-3

doi:10.1016/j.contraception.2007.08.010


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