Weight change among women using intramuscular depot medroxyprogesterone acetate, a copper intrauterine device, or a levonorgestrel implant for contraception: Findings from a randomised, multicentre, open-label trial

Mags Beksinska, Rodal Issema, Ivana Beesham, Tharnija Lalbahadur, Katherine Thomas, Charles Morrison, G Justus Hofmeyr, Petrus S Steyn, Nelly Mugo, Thesla Palanee-Phillips, Khatija Ahmed, Gonasagrie Nair, Jared M Baeten, Jenni Smit, Mags Beksinska, Rodal Issema, Ivana Beesham, Tharnija Lalbahadur, Katherine Thomas, Charles Morrison, G Justus Hofmeyr, Petrus S Steyn, Nelly Mugo, Thesla Palanee-Phillips, Khatija Ahmed, Gonasagrie Nair, Jared M Baeten, Jenni Smit

Abstract

Background: There is limited evidence on the impact of the use of progestin-only hormonal contraception (POC) on weight change. We conducted a secondary analysis of prospective weight change among women enrolled in the Evidence for Contraceptive options and HIV Outcomes (ECHO) trial.

Methods: The ECHO trial was conducted at 12 sites in eSwatini, Kenya, South Africa and Zambia between December 2015 and October 2018. HIV negative, women aged 16-35 years, desiring contraception, were randomised (1:1:1) to either 3-monthly intramuscular depot medroxyprogesterone acetate (DMPA-IM), levonorgestrel (LNG) implant or copper intrauterine device (IUD). Follow-up was up to 18 months. Weight (kg) was measured at baseline and study exit. Analysis was performed as intention to treat (ITT) and time on continuous contraceptive use. The primary outcome of this secondary analysis is weight change from study enrolment to the final visit at study month 12-18. The ECHO trial is registered with ClinicalTrials.gov, NCT02550067.

Findings: 7829 women were randomly assigned to DMPA-IM (n = 2609), copper IUD (n = 2607) or LNG implant (n = 2613). The ITT population included 7014 women 2293 DMPA-IM group, 2372 copper IUD group and 2349 LNG group) who were not lost to follow-up, pregnant on study, or missing weight data. The mean weight increased in all groups but was significantly different in magnitude: 3.5 kg (SD = 6.3), 2.4 kg (SD = 5.9) and 1.5 kg (SD = 5.7) in the DMPA-IM, LNG implant and copper IUD groups, respectively. Comparative differences between groups were (2.02 kg (95% CI, 1.68, 2.36, p < 0.001) for DMPA-IM versus copper IUD, 0.87 kg (0.53,1.20 p < 0.001) for LNG implant compared to copper IUD and 1.16 kg (0.82, 1.50, p < 0.001) for DMPA-IM compared with LNG implant. Results for continuous contraceptive use were similar.

Interpretation: We found differences in weight gain between POC users compared to the non-hormonal copper IUD group over 12-18 months of use. Women using POCs should be counselled about this potential side effect when choosing a contraceptive method.

Keywords: Body mass index; Contraception; Copper intrauterine device; Depot medroxyprogesterone acetate; Levonorgestrel implant; Weight.

Conflict of interest statement

Dr. Baeten reports grants from USAID, grants from BMGF, during the conduct of the study; personal fees from Gilead Sciences, outside the submitted work; Dr. Smit reports grants from FHI360, during the conduct of the study; No other authors report any conflicts of interest.

© 2021 The Author(s).

Figures

Fig. 1
Fig. 1
Trial profile. 1. Woman who were pregnant at any time during the study. 2. Missed a baseline or exit visit weight/height or data entry error that could not be resolved.
Fig. 2
Fig. 2
Shifts in BMI categories from baseline to final measurement. Fig. 2 displays the number of women within each randomized arm falling into each BMI category at baseline and at final measurement; the proportion of women transitioning from one category to another over time are shown as lighter-intensity paths between baseline and final visit, with the thickness of each path indicating the size of the group falling into a given transition between categories from baseline to final visit.

References

    1. United Nations D of E, and Social Affairs PD (2019). C, (ST/ESA/SER.A/435). Contraceptive Use by Method 2019: data Booklet. 2019.
    1. Le Y.C.L., Rahman M., Berenson A.B. Early weight gain predicting later weight gain among depot medroxyprogesterone acetate users. Obstet Gynecol. 2009;114:279–284.
    1. Modesto W., Dos Santos P.de.N.S., Correia V.M., Borges L., Bahamondes L. Weight variation in users of depot-medroxyprogesterone acetate, the levonorgestrel-releasing intrauterine system and a copper intrauterine device for up to ten years of use. Eur J Contracept Reprod Health Care. 2015;20:57–63.
    1. Paul C., Skegg D.C.G., Williams S. Depot medroxyprogesterone acetate: patterns of use and reasons for discontinuation. Contraception. 1997;56:209–214.
    1. research Who special programme of, HK Toopozada, Koetsawang S. Multinational comparative clinical trial of long-acting injectable contraceptives: norethisterone enanthate given in two dosage regimens and depot-medroxyprogesterone acetate. A preliminary report. Contraception. 1983;28:1–20.
    1. Jain J., Jakimiuk A.J., Bode F.R., Ross D., Kaunitz A.M. Contraceptive efficacy and safety of DMPA-SC. Contraception. 2004;70:269–275.
    1. Lopez L.M., Ramesh S., Chen M. Progestin-only contraceptives: effects on weight. Cochrane Database Syst Rev. 2016 doi: 10.1002/14651858.CD008815.pub2.
    1. Bonny A.E., Ziegler J., Harvey R., Debanne S.M., Secic M., Cromer B.A. Weight gain in obese and nonobese adolescent girls initiating depot medroxyprogesterone, oral contraceptive pills, or no hormonal contraceptive method. Arch Pediatr Adolesc Med. 2006;160:40–45.
    1. Dal'ava N., Bahamondes L., Bahamondes M.V., Bottura B.F., Monteiro I. Body weight and body composition of depot medroxyprogesterone acetate users. Contraception. 2014;90:182–187.
    1. Dos Santos P.D.N.S., Modesto W.O., Dal'Ava N., Bahamondes M.V., Pavin E.J., Fernandes A.M.D.S. Body composition and weight gain in new users of the three-monthly injectable contraceptive, depot-medroxyprogesterone acetate, after 12 months of follow-up. Eur J Contracept Reprod Health Care. 2014;19:432–438.
    1. Dal'Ava N., Bahamondes L., Bahamondes M.V., De Oliveira Santos A., Monteiro I. Body weight and composition in users of levonorgestrel-releasing intrauterine system. Contraception. 2012;86:350–353.
    1. Pantoja M., Medeiros T., Baccarin M.C., Morais S.S., Bahamondes L., dos Santos Fernandes A.M. Variations in body mass index of users of depot-medroxyprogesterone acetate as a contraceptive. Contraception. 2010;81:107–111.
    1. Okunola T.O., Bola-Oyebamiji S.B., Sowemimo O. Comparison of weight gain between levonorgestrel and etonogestrel implants after 12 months of insertion. Int J Gynecol Obstet. 2019;147:54–58.
    1. Amatayakul K., Sivasomboon B., Thanangkul O. A study of the mechanism of weight gain in medroxyprogesterone acetate users. Contraception. 1980;22:605–622.
    1. Clark M.K., Dillon J.S., Sowers M., Nichols S. Weight, fat mass, and central distribution of fat increase when women use depot-medroxyprogesterone acetate for contraception. Int J Obes. 2005;29:1252–1258.
    1. Vickery Z., Madden T., Zhao Q., Secura G., Allsworth J.E., Peipert J.F. Weight change at 12 months in users of three progestin-only contraceptive methods. Contraception. 2013 Oct;88(4):503–508. doi101016/j.contraception201303004; 2013:88.
    1. Beksinska M.E., Smit J.A., Kleinschmidt I., Milford C., Farley T.M.M. Prospective study of weight change in new adolescent users of DMPA, NET-EN, COCs, nonusers and discontinuers of hormonal contraception. Contraception. 2010;81:30–34.
    1. Bahamondes L., Del Castillo S., Tabares G., Arce X.E., Perrotti M., Petta C. Comparison of weight increase in users of depot medroxyprogesterone acetate and copper IUD up to 5 years. Contraception. 2001;64:223–225.
    1. Berenson A.B., Rahman M. Changes in weight, total fat, percent body fat, and central-to-peripheral fat ratio associated with injectable and oral contraceptive use. Am J Obstet Gynecol. 2009;200 329.e1-329.e8.
    1. Mangan S.A., Larsen P.G., Hudson S. Overweight teens at increased risk for weight gain while using depot medroxyprogesterone acetate. J Pediatr Adolesc Gynecol. 2002;15:79–82.
    1. Bonny A.E., Britto M.T., Huang B., Succop P., Slap G.B. Weight gain, adiposity, and eating behaviors among adolescent females on depot medroxyprogesterone acetate (DMPA) J Pediatr Adolesc Gynecol. 2004;17:109–115.
    1. Bahamondes L., Brache V., Ali M., Habib N. A multicenter randomized clinical trial of etonogestrel and levonorgestrel contraceptive implants with nonrandomized copper intrauterine device controls: effect on weight variations up to 3 years after placement. Contraception. 2018;98:181–187.
    1. Romano M.E., Braun-Courville D.K. Assessing weight status in adolescent and young adult users of the etonogestrel contraceptive implant. J Pediatr Adolesc Gynecol. 2019;32:409–414.
    1. Dos Santos P.de.N.S., Madden T., Omvig K., Peipert J.F. Changes in body composition in women using long-acting reversible contraception. Contraception. 2017;95:382–389.
    1. Evidence for contraceptive options and HIV outcomes (ECHO) trial consortium. HIV incidence among women using intramuscular depot medroxyprogesterone acetate, a copper intrauterine device, or a levonorgestrel implant for contraception: a randomised, multicentre, open-label trial. Lancet. 2019;394:303–313.
    1. Gallo M.F., Legardy-Williams J., Hylton-Kong T. Association of progestin contraceptive implant and weight gain. Obstet Gynecol. 2016;127:573–576.
    1. Bonny A.E., Secic M., Cromer B. Early weight gain related to later weight gain in adolescents on depot medroxyprogesterone acetate. Obstet Gynecol. 2011;117:793–797.
    1. Batista G.A., de Souza A.L., Marin D.M. Body composition, resting energy expenditure and inflammatory markers: impact in users of depot medroxyprogesterone acetate after 12 months follow-up. Arch Endocrinol Metab. 2017;61:70–75.
    1. Venter W.D.F., Sokhela S., Simmons B. Dolutegravir with emtricitabine and tenofovir alafenamide or tenofovir disoproxil fumarate versus efavirenz, emtricitabine, and tenofovir disoproxil fumarate for initial treatment of HIV-1 infection (ADVANCE): week 96 results from a randomised, phase 3, n. Lancet HIV. 2020 doi: 10.1016/S2352-3018(20)30241-1.

Source: PubMed

3
Abonner