Effects of the levonorgestrel intrauterine system on the endometrium after long-term exposure to mifepristone: Secondary outcomes of a randomized controlled trial
article
OA: closed
CC0
AI-generated summary
This randomized controlled trial investigated the effects of the levonorgestrel intrauterine system on the endometrium following long-term mifepristone exposure.
One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works
Abstract
ObjectiveLong-term treatment with progesterone receptor modulators (PRM) is associated with a distinct histological entity termed progesterone receptor modulator associated endometrial changes (PAEC). While accumulating evidence implies that these changes are benign and reversible after cessation of treatment, there are currently no data underpinning their development. Consequently, as a precaution, endometrial shedding is recommended after long-term PRM intake. Avoiding endometrial shedding after treatment with a PRM and prior to the start of a progestin treatment would be beneficial for women in reproductive age to avoid pregnancy and bleeding. However, the endometrial morphology with such a treatment regimen is unknown. The aim of this study was to delineate the endometrial morphology following continuous long-term treatment with the PRM mifepristone and subsequent placement of a levonorgestrel intrauterine system (LNG-IUS) without prior shedding of the endometrium.Study designThis study reports the secondary outcome from a double-blinded randomized controlled trial conducted at Karolinska University Hospital, Sweden, November 2009 to January 2015. Healthy women aged 18-43 years with regular menstrual cycles were included. Eligible women were randomized to receive either 50 mg of mifepristone (n = 29) or a comparator (n = 29), every other day for two months followed by insertion of an LNG-IUS 52 mg. Endometrial biopsies were obtained at baseline and three months after placement of the device. The samples were histologically assessed. The main outcome measure of this sub-study was the endometrial morphology including presence of PAEC three months after LNG-IUS insertion.ResultsNine and eight paired biopsies from the mifepristone and comparator group, respectively, were included in the histological analysis. There were no differences in baseline characteristics between the groups and all baseline endometrial biopsies were physiological. Three months after LNG-IUS placement the endometrial morphology was still benign without PAEC in all samples treated with either mifepristone or comparator. A progestin effect on the endometrium was seen in all samples.ConclusionsPlacement of an LNG-IUS immediately following two months' treatment with the PRM mifepristone, without any prior shedding of the endometrium, may represent a feasible approach in terms of endometrial safety. However, larger studies are needed to confirm our results.
My notes (saved in your browser only)
Citation neighborhood
Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. [ expand to 2 hops ] — adds papers reached through this work's immediate citers/citees. Heavier; up to 60 extra dots.
References (37)
- Characterization of Molecular Changes in Endometrium Associated With Chronic Use of Progesterone Receptor Modulators: Ulipristal Acetate Versus Mifepristone via openalex
- Effect of long-term treatment with low-dose mifepristone on the endometrium via openalex
- Progestagens and anti-progestagens for pain associated with endometriosis via openalex
- Progestagens and anti-progestagens for pain associated with endometriosis via openalex
- Progesterone receptor modulators for endometriosis via openalex
- Safety, efficacy and patient acceptability of the contraceptive and non-contraceptive uses of the LNG-IUS via openalex
- Selective progesterone receptor modulators in reproductive medicine: pharmacology, clinical efficacy and safety via openalex
- Selective progesterone receptor modulators (SPRMs): progesterone receptor action, mode of action on the endometrium and treatment options in gynecological therapies via openalex
- Unscheduled vaginal bleeding with progestin-only contraceptive use via openalex
- doi:10.1097/pgp.0b013e318251035b via openalex
- doi:10.1038/modpathol.2008.19 via openalex
- doi:10.1056/nejmoa1103182 via openalex
- doi:10.2147/ijwh.s33125 via openalex
- doi:10.1002/14651858.cd001324.pub5 via openalex
- doi:10.1016/j.contraception.2008.08.003 via openalex
- doi:10.1093/humrep/dep100 via openalex
- doi:10.1016/j.contraception.2015.12.015 via openalex
- doi:10.1016/j.cct.2017.02.002 via openalex
- doi:10.1093/humrep/15.9.1969 via openalex
- doi:10.1056/nejmoa1103180 via openalex
- doi:10.1016/j.contraception.2018.05.020 via openalex
- doi:10.1016/j.fertnstert.2014.02.008 via openalex
- doi:10.1007/978-1-4419-0489-8 via openalex
- W6639007481 via openalex
- doi:10.1002/14651858.cd001324.pub6 via openalex
- doi:10.1016/j.fertnstert.2018.10.012 via openalex
- doi:10.1002/jcph.998 via openalex
- W6732527681 via openalex
- W6741581601 via openalex
- W7073579906 via openalex
- doi:10.1016/s0140-6736(16)31333-2 via openalex
- doi:10.1093/humrep/dey296 via openalex
- doi:10.1016/j.ijgo.2010.08.009 via openalex
- doi:10.1093/humrep/17.10.2588 via openalex
- doi:10.1016/j.contraception.2014.08.006 via openalex
- doi:10.1007/978-1-4614-3165-7 via openalex
- doi:10.1093/humrep/dew359 via openalex
SciLite annotations
chemicals 9
levonorgestrel
mifepristone
progestin
mifepristone
levonorgestrel
mifepristone
mifepristone
mifepristone
progestin
organisms 1
noordeloos 2009062
Source provenance
- openalex
- last seen: 2026-05-11T06:22:51.059792+00:00
- scilite
- last seen: 2026-05-18T04:26:01.642840+00:00
License: CC0
· commercial use OK