Progestogens
Peer reviewed by Dr Colin Tidy, MRCGPLast updated by Dr Toni Hazell, MRCGPLast updated 25 Oct 2022
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Synonyms: progestins, progestagens
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What is progesterone?
Progesterone is one of the naturally occurring sex hormones. It is secreted by the ovary as part of the menstrual cycle. It was first isolated in 1934 by Butenandt.
What are progestogens?
Progestogens are synthetic forms of progesterone.
Progestogens were developed because progesterone could not be absorbed orally, although a method of processing progesterone via micro-ionising is now available (Utrogestan®). It has been suggested that micronised progesterone may be safer than synthetic progestogens when used as part of HRT (hormone replacement therapy).1 2
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Types of progestogens3
Synthetic progestogens are divided into two main groups:
Progesterone analogues:
Dydrogesterone.
17-OH progesterone group: medroxyprogesterone acetate and cyproterone acetate.
19-nor progesterone group: nomegestrol acetate (NOMAC), trimegestone, promegestone.
Testosterone analogues:
Estranes: norethisterone.
Estrane/pregnane: dienogest.
Gonanes: norgestrel and levonorgestrel (the active isomer of norgestrel), desogestrel, norgestimate and gestodene.
Progesterone and its synthetic analogues are less androgenic than the testosterone analogues.
Dienogest is referred to as a hybrid progestogen. It is a testosterone derivative but, like drospirenone which is derived from spironolactone, has no androgenic effect but partial anti-androgenic activity.
How to administer progestogens
Tablets (often in combination with an oestrogen).
Depot: medroxyprogesterone acetate (DMPA) is available as an intramuscular (Depo-provera®) or subcutaneous (Sayana Press®) injection. Norethisterone enantate (Noristerat®) is rarely used.
Implants - etonogestrol implant (Nexplanon®).
Intrauterine systems (IUS) with slow-release levonorgestrel - Mirena® and Jaydess®.
Vaginal gel, suppositories and injections of progesterone may be used for a variety of indications, including infertility, hormone replacement therapy and heavy menstrual bleeding.4
Progesterone cream: unregulated bio-identical progesterone is marketed in cream form; it is not licensed in the UK. Serious concerns regarding the use of progesterone cream include misleading claims of effectiveness and safety, as well as variable purity and potency.5 6 7
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Contra-indications8
The BNF lists the following contra-indications for progestogens:
Acute porphyrias, breast cancer, genital cancer, idiopathic jaundice during pregnancy, pemphigoid gestationis, severe pruritus during pregnancy, history of thromboembolism, missed miscarriage, thrombophlebitis, undiagnosed vaginal bleeding.
However in day-to-day practice they are often used in women who have some of these contra-indications - for example, a progestogen-based pill may be used for contraception in a woman who cannot use oestrogen-based contraception due to a history of thromboembolism. As always, clinical judgment should be used and more detailed guidance specific to the condition being treated should be consulted.
When used for contraception or HRT, progestogens are usually contra-indicated in women with a history of breast cancer; it is a hormonally sensitive disease and prognosis may be affected by any hormonal method of contraception. A decision to initiate hormonal contraception should be made in consultation with the local oncology team and for medicolegal reasons it would be sensible to have this discussion in writing.9
What are progestogens used for?
Menstrual disorders
Women with polycystic ovary syndrome who have four or fewer periods per year may be at increased risk of endometrial cancer; inducing a withdrawal bleed every month with cyclical progestogen (or the use of combined hormonal contraception (CHC) or a levonorgestrel-releasing IUS if contraception is desired) is advised.10
In heavy menstrual bleeding, a levonorgestrel-releasing IUS is first-line if pharmaceutical treatment is appropriate.11
In dysfunctional uterine bleeding, progestogens may be used, with or without oestrogens. It may be necessary to ensure that the patient does not have atypical endometrial hyperplasia or a cervical lesion prior to having treatment for dysfunctional uterine bleeding, particularly in older women.
To delay menses: a progestogen can be taken three days before the expected start date and continued. Normal menstruation will occur 2-3 days after stopping.
Contraception12
Progestogens are used widely for contraception, as they provide an alternative form of hormonal contraception for patients deemed unsuitable for CHC. This makes them particularly suitable for women with a history of:
Obesidad.
Hipertensión.
Diabetes mellitus.
Venous thromboembolism.
Migraine.
Heavy smoking.
Progestogens are available in many forms:
In combination with oestrogens in CHC, in oral, transdermal or intravaginal contraception when oestrogen isn't contra-indicated.
Alone in oral contraception - progestogen-only pill (POP).
Levonorgestrel-releasing IUS (see also below).
Injections:
Use of DMPA requires full counselling and warning regarding menstrual disturbances and possible delay in return to full fertility. Use beyond two years needs to be evaluated carefully, particularly in women aged under 18 years, due to its potential effects on bone density.
DMPA (Depo-provera® and Sayana Press®) provides contraception for twelve weeks. See the separate Progestogen-only Injectable Contraceptives article for more information.
Implant: etonogestrel (Nexplanon®) provides contraception for up to three years when implanted subdermally.
Emergency contraception.
In addition to anovulation, progestogens also lead to thickening of the cervical mucus, making it hostile to sperm. Furthermore, prolonged progestogen exposure leads to reversible atrophy of the endometrium, which reduces the chance of implantation of a fertilised ovum.
IUS
Progestogen is delivered directly into the uterus, using a T-shaped device which slowly releases levonorgestrel over a three-year or five-year period.
In addition to its use as a contraceptive, Mirena® may be used for endometrial protection in hormone replacement therapy (HRT), when the licence is for four years (but FSRH guidance allows for five years of use), and to treat heavy menstrual bleeding. Levosert® also has a licence for heavy menstrual bleeding, but not for use as part of HRT. The other IUS devices on the market, Jaydess® and Kyleena®, only have a licence for contraception.
See the separate Intrauterine System article.
HRT13
See also the separate Hormone Replacement Therapy (including Benefits and Risks) article.
Postmenopausal women who have not had a hysterectomy and take oestrogens for HRT require progestogen, either on a cyclical or a continuous basis, to prevent hyperplasia of the endometrium and the possible development of endometrial cancer.
Continuous combined HRT is recommended for any women requiring HRT once she is postmenopausal, ie a year after her last period or after she has been on cyclical HRT for at least one year.
There have been reports of endometrial cancer in postmenopausal women who have used unregulated progesterone cream for endometrial protection, thought to be due to inadequate progesterone dose.5
Endometriosis
See also the separate Endometriosis article. A commonly used progestogen in endometriosis is medroxyprogesterone acetate but use of a levonorgestrel-releasing IUS is increasingly advocated.14
Progestogens have been shown in several studies to reduce pain from endometriosis, with minimal side-effects.
Some theories suggest that progestogens have an anti-inflammatory effect on ectopic endometrium.
Progestogens have no effect on fertility rates in endometriosis.
Acne15 16 17
Some progestogens in combined oral contraceptives (COCs) are anti-androgenic.
COCs block androgen receptors and 5-alpha reductase which converts testosterone to the more potent dihydrotestosterone.
Androgen blockade occurs in the sebaceous glands of the skin, leading to reduction in seborrhoea and improvement in acne.
They can also reduce hirsutism.
Progestogen types appear to differ in the degree to which they prevent testosterone production, conversion or bioavailability.
COC should be considered for women with acne who also want oral contraception.
Síndrome premenstrual
Progestogen alone is not recommended for women with premenstrual syndrome (PMS), due to insufficient evidence to support its effectiveness.18 19
PMS consists of mental and physical symptoms which are related to the menstrual cycle.
The aetiology is unclear.
It is not seen in anovulatory cycles.
Psychotropics or the suppression of ovulation are the main pharmacological treatments.
Anticancer hormonal therapy
Megestrol - breast cancer and endometrial cancer (advanced disease). Efficacies of progestogens are not proven and current practice is to combine progestogens with platinum or taxane chemotherapeutic agents.
Medroxyprogesterone - renal cell cancer and prostate cancer.
Cyproterone acetate - prostate cancer.
Palliative role in neoplastic disease20
Progestogens stimulate appetite and lead to weight gain in cancer-associated anorexia-cachexia. Megestrol acetate is widely used for this indication but the mechanism is largely unknown. There may be a risk of phlebitis and pulmonary embolism.
Side-effects of progestogens
The risk and types of side-effects and adverse effects vary between different progestogens, their dosage and different modes of delivery.
Unscheduled bleeding.
Estreñimiento.
Sequedad vaginal.
Sensibilidad mamaria.
Acné.
Weight gain (DMPA).
Other adverse effects
Ovarian cysts.
HDL cholesterol can be suppressed among users of DMPA.
Decreased glucose tolerance.
Cardiovascular disease - limited evidence suggests that in women with concomitant risk factors, particularly hypertension, there is a small increase in cardiovascular events.9
Hirsutism (rare).
Jaundice (rare - contra-indicated in hepatic impairment).
Nota del editor |
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Dr Krishna Vakharia, 24th March 2023 An observational study looking at progesterone and breast cancer risk has been published. It was shown that there was an elevated risk of breast cancer - 20-30% - in women who are under 50 who currently use or have recently used progesterone-only contraception. This is in all forms of progesterone-only contraception: pill, implant, injection and coil. It was shown that in those people who had progesterone-only contraception for five years, the 15-year absolute excess risk of breast cancer associated with use of oral contraceptives ranges from 8 per 100,000 users for use from age 16 to 20 to about 265 per 100,000 users for use from age 35 to 39. However, taking into account that in 20-year-olds the risk of breast cancer is extremely low, this added risk with progesterone only contraception remains very low. Factors such as excessive alcohol use (increases breast cancer risk by 20%) and obesity will have a similar degree of risk for breast cancer. Pregnancy and all the potential risks that entails, such as blood clots, gestational diabetes as well as the emotional trauma of an unwanted pregnancy or termination, need to be taken into account when counselling. The risk of breast cancer increases with age - however, it still remains low. The added risk in the 35-39 year group, is still low. All women should be told about the risks when taking hormonal contraception. For those who have a high risk of cancer - those who have the BRCA 1 or BRCA 2 genes or a strong family history - there is no evidence yet to know what the increased risks would be, and should be discussed during contraception counselling. Currently, the guidance for having progesterone-only contraception has not changed, as benefits outweigh the risks. |
An observational study looking at progesterone and breast cancer risk has been published. It was shown that there was an elevated risk of breast cancer- 20-30% - in women who are under 50 who currently use or have recently used progesterone-only contraceptions. This is in all forms of progestrone only contraception- pill, implant, injection and coil.
It was shown that in those people who had progesterone only contraception for 5 years,the 15-year absolute excess risk of breast cancer associated with use of oral contraceptives ranges from 8 per 100,000 users for use from age 16 to 20 to about 265 per 100,000 users for use from age 35 to 39.
However, taking into account that in 20 year olds the risk of breast cancer is extremely low, this added risk with progesterone only contraceptions remains very low. Factors such as excessive alcohol use (increases breast cancer risk by 20%) and obesity will have a similar degree of risk for breast cancer. Pregnancy and all the potential risks that entails such as blood clots, gestational diabetes as well as the emotional trauma of an unwanted pregnancy or termination need to be taken into account when counselling.
The risk of breast cancer increases with age- however they still remain low. The added risk in the 35-39 year group- is still low. All women should be told about the risks when taking hormonal contraception.
For those that have a high risk of cancer- those that have the BRCA 1 or BRCA 2 genes or a strong family history- there is no evidence yet to know what the increased risks would be and should be discussed during contraception counselling.
Currently, the guidance for having progesterone only contraception has not changed as benefits outweigh the risks.
Lecturas complementarias y referencias
- EndometriosisNICE CKS, noviembre de 2024 (sólo acceso en el Reino Unido)
- MenopausiaNICE CKS, noviembre de 2024 (sólo acceso en el Reino Unido)
- Píldoras de progestágeno soloFSRH Agosto 2022
- Anticoncepción intrauterina; FSRH, 2019
- Anticonceptivos hormonales combinados y de progestágeno solo y riesgo de cáncer de mama: Un estudio anidado de casos y controles y un metaanálisis en el Reino Unido; Public Library of Science (PLOS, marzo de 2023
- Stute P, Wildt L, Neulen J; The impact of micronized progesterone on breast cancer risk: a systematic review. Climacteric. 2018 Apr;21(2):111-122. doi: 10.1080/13697137.2017.1421925. Epub 2018 Jan 31.
- Abenhaim HA, Suissa S, Azoulay L, et al; Menopausal Hormone Therapy Formulation and Breast Cancer Risk. Obstet Gynecol. 2022 Jun 1;139(6):1103-1110. doi: 10.1097/AOG.0000000000004723. Epub 2022 May 3.
- Sitruk-Ware R; Pharmacological profile of progestins. Maturitas. 2008 Sep-Oct;61(1-2):151-7.
- Progestogens and endometrial protection; British Menopause Society, 2021
- Pinkerton JV, Pickar JH; Update on medical and regulatory issues pertaining to compounded and FDA-approved drugs, including hormone therapy. Menopause. 2016 Feb;23(2):215-23. doi: 10.1097/GME.0000000000000523.
- THS bioidéntica; Sociedad Británica de Menopausia, 2019 (revisado 2024)
- Health: Bio-idential Hormone Replacement Therapy; Advertising Standards Authority, 2017
- Formulario Nacional Británico (BNF)NICE Evidence Services (sólo acceso en el Reino Unido)
- Tabla resumen de los criterios médicos de elegibilidad del Reino Unido para la anticoncepción intrauterina y hormonal; Facultad de Salud Sexual y Reproductiva, 2016 - modificado septiembre 2019
- Long-term Consequences of Polycystic Ovary Syndrome; Royal College of Obstetricians and Gynaecologists (November 2014)
- Sangrado menstrual abundante: evaluación y tratamientoNICE Directriz (marzo de 2018 - actualizada en mayo de 2021)
- Anticoncepción - Métodos de progestágeno soloNICE CKS, septiembre de 2022 (sólo acceso en el Reino Unido)
- Furness S, Roberts H, Marjoribanks J, et al; Hormone therapy in postmenopausal women and risk of endometrial hyperplasia. Cochrane Database Syst Rev. 2012 Aug 15;(8):CD000402. doi: 10.1002/14651858.CD000402.pub4.
- EndometriosisNICE CKS, noviembre de 2024 (sólo acceso en el Reino Unido)
- Arowojolu AO, Gallo MF, López LM, et al.Anticonceptivos orales combinados para el tratamiento del acné (Revisión Cochrane traducida). Cochrane Database Syst Rev. 2012 Jul 11;7:CD004425. doi: 10.1002/14651858.CD004425.pub6.
- Jaisamrarn U, Chaovisitsaree S, Angsuwathana S, et al; A comparison of multiphasic oral contraceptives containing norgestimate or desogestrel in acne treatment: a randomized trial. Contraception. 2014 Nov;90(5):535-41. doi: 10.1016/j.contraception.2014.06.002. Epub 2014 Jun 12.
- Guía clínica de la FSRH: Anticoncepción hormonal combinadaFacultad de Salud Sexual y Reproductiva (enero de 2019 - modificado en octubre de 2023)
- Ford O, Lethaby A, Roberts H, et al; Progesterone for premenstrual syndrome. Cochrane Database Syst Rev. 2012 Mar 14;3:CD003415. doi: 10.1002/14651858.CD003415.pub4.
- Síndrome premenstrual; NICE CKS, 2019 (UK access only)
- Penel N, Clisant S, Dansin E, et al; Megestrol acetate versus metronomic cyclophosphamide in patients having exhausted all effective therapies under standard care. Br J Cancer. 2010 Apr 13;102(8):1207-12. doi: 10.1038/sj.bjc.6605623. Epub 2010 Mar 30.
- Anticonceptivos hormonales combinados y de progestágeno solo y riesgo de cáncer de mama: Un estudio anidado de casos y controles y un metaanálisis en el Reino Unido; Public Library of Science (PLOS, marzo de 2023
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Historia del artículo
La información de esta página ha sido redactada y revisada por médicos cualificados.
Fecha límite de la próxima revisión: 24 oct 2027
25 Oct 2022 | Latest version

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