Abstract
Levonorgestrel-releasing Intrauterine system (LNG-IUS, Mirena) is a very safe, efficient, long-acting and reversible intrauterine device, which
releases high-efficiency at a daily dose of 20ug Progesterone mainly acts on the part of the endometrium, causing the endometrial glands to shrink.
A large number of studies have fully proved that LNG-IUS is not only effective in contraception, but also widely used in non-contraceptive fields.
LNG-IUS is effective in treating gynecological diseases such as menorrhagia and dysmenorrhea. In addition, LNG-IUS is also used in endometriosis,
adenomyosis, endometrial polyps, endometrial hyperplasia, and early endometrial cancer. Reversal of cancer and endometrial protection in breast
cancer patients. This article will briefly summarize the basic knowledge of LNG-IUS and the clinical application of LNG-IUS in gynecological diseases.
Keywords
Levonorgestrel-releasing Intrauterine system; Mirena; High-efficiency progesterone; Long-acting reversible contraception
This work is licensed under Creative Commons Attribution 4.0 License WJGWH.MS.ID.000602.
ISSN: 2641-6247 DOI: 10.33552/WJGWH.2021.05.000602
World Journal of
Gynecology & Women’s Health
Review Article Copyright © All rights are reserved by Chen Jiming
Introduction
Levonorgestrel-releasing Intrauterine system (LNG-IUS),its
trade name is Mirena. It was originally designed in the 1970s,
when the main purpose was to provide safe, efficient, long-acting
and reversible contraception (LARC) for women of childbearing
age [1]. LNG-IUS is a T-shaped device with a white cylindrical
drug core rack on the longitudinal arm, which contains 52mg of
levonorgestrel (LNG). The independently designed slow-release
system releases 20ug of LNG into the uterine cavity every day.
The validity period is 5 years [2]. Currently in China, the approved
clinical indications for LNG-IUS mainly include contraception and
idiopathic menorrhagia. However, with the continuous deepening
of research in recent years, the clinical application of LNG-IUS has
become increasingly widespread, and it has already surpassed the
scope of approved clinical indications [3]. Based on this, this article
will mainly introduce the basic knowledge about LNG-IUS, and
briefly summarize the clinical application scope of LNG-IUS and the
common confusions and countermeasures of using LNG-IUS.
An Overview of the Basic Knowledge of Levonorge-
strel-Releasing Intrauterine System
Levonorgestrel-releasing Intrauterine system (LNG-IUS,
Mirena) releases a low blood concentration of levonorgestrel. The
blood concentration is reported to be 0.1-0.2ng/ml in the literature
[1]. Some key points of knowledge of the Levonorgestrel-releasing
Intrauterine system are briefly summarized: ①Levonorgestrel-
releasing Intrauterine system contains 52mg of levonorgestrel
and releases 20ug of levonorgestrel every 24 hours, the validity
period is 5 years [2]. ②What is levonorgestrel (levonorgestrel,
LNG)? LNG is a fully synthetic high-efficiency progesterone
(sterane synthetic progesterone preparation) It is the optically
active form of racemic norgestrel. The progestin activity is twice as
strong as norgestrel, which is about 100 Times of norethindrone.
Therefore, the dose can be halved compared with norgestrel, and
adverse reactions will be reduced accordingly. Levonorgestrel
mainly acts on the hypothalamus and pituitary gland, which
*Corresponding author: Chen Jiming, Department of Obstetrics and Gynecology,
The Affiliated Changzhou NO. 2 People’s Hospital of Nanjing Medical University,
Changzhou 213000, Jiangsu Province, China.
Received Date: May 24, 2021
Published Date: June 07, 2021
Citation: Junling Liu, Mengyue Chen, Zhiyong Dong, Shoufeng Zhang, Wendi Zhang, Zhenyue Qin, Chen Jiming. An Overview of the
Basic Knowledge of Levonorgestrel-Releasing Intrauterine System. W J Gynecol Women’s Health. 5(1): 2021. WJGWH.MS.ID.000602.
DOI: 10.33552/WJGWH.2021.05.000602.
Page 2 of 4
World Journal of Gynecology & Women’s Health Volume 5-Issue 1
significantly reduces or disappears the peaks of FSH and LH
levels in the middle of menstruation. The ovaries do not ovulate
and have obvious anti-estrogen activity. Its anti-estrogen activity
is stronger than norethindrone 10 times(Note: Norethindrone
is a synthetic progesterone preparation of estradiol, a synthetic
19-desmethyltestosterone derivative, which has weak estrogenic
and anti-estrogenic activity, and has mild androgen Activity and
protein assimilation, its androgenic activity is approximately
equivalent to 1/6 of testosterone). LNG has almost no estrogenic
activity. It can thicken cervical mucus and hinder sperm penetration.
It shows strong progesterone activity for the transformation of the
endometrium, which can make the endometrium thin, and the
endometrial epithelial cells are low columnar, and the secretion
function is poor, which is not conducive to the implantation of
pregnant eggs. LNG also has a certain androgenic activity and protein
assimilation, which can inhibit ovulation by oral or subcutaneous
injection [3]. ③The levonorgestrel contained in the levonorgestrel
intrauterine sustained-release system is an extremely effective
progesterone, which mainly acts locally [4-6]. ④ What is the
actual blood concentration of levonorgestrel released by the
intrauterine release system of levonorgestrel? It has been reported
in the literature that about 10% of levonorgestrel is released in the
systemic circulation. Some patients may still have hormone-related
complaints, such as breast tenderness, acne, mood changes, weight
gain, hair loss, hirsutism or general swelling. Some patients will
have functional ovarian cysts. These phenomena are more obvious
in the first few months of use and will gradually decrease with the
extension of use time. This is actually related to the patients’ extreme
sensitivity to levonorgestrel [7]. ⑤The concentration of LNG in the
blood circulation of women using LNG-IUS is very low and stable.
Pharmacokinetic studies have shown that the plasma concentration
reached by the LNG sustained-released by LNG-IUS in the uterine
cavity is maintained at 0.4-0.6nmol/L (150-200pg/ml) through
the intimal basal capillary network to reach the blood circulation.
The blood concentration of commonly used oral contraceptives is
low, and the concentration in the fallopian tube is also very low [8].
Another study reported that the median blood LNG concentration
of women who used LNG-IUS within 7 years was 125-200ng/L [9].
⑥The Levonorgestrel-releasing Intrauterine system often causes
amenorrhea in patients. Isn’t menstruation after LNG-IUS a sign of
ovarian function decline? Will the patient get older as a result? will
not. A large number of studies have confirmed [10-12] that LNG-
IUS does not affect the patient’s ovarian function, ovarian cycle, and
estrogen secretion. The amenorrhea caused by LNG-IUS is mainly
caused by the local inhibition of LNG on the endometrium. This
inhibition is caused by the local high level of LNG on the endometrial
estrogen receptor down-regulation, so that the endometrium is
against the endogenous Sexual and exogenous estrogen are not
sensitive, and inhibit the intimal hyperplasia reaction, resulting
in oligomenorrhea and even amenorrhea after LNG-IUS use. And
this inhibition is reversible. After the birth control ring is removed,
as long as the patient’s ovarian function is present, the normal
menstrual cycle can still be restored. After the LNG-IUS is taken out,
menstruation can be recovered, and the average recovery time is
23 days. Therefore, the ovaries of patients with LNG-IUS can still
secrete E2 hormones normally, and will not cause the increase of
FSH, and can have a normal ovulation cycle. ⑦So, what mechanism
does the levonorgestrel intrauterine sustained-release system use
to exert its high-efficiency contraceptive effect? It mainly includes
three aspects: a. Continuous inhibition of the endometrium, which
interferes with or is not conducive to the implantation of fertilized
eggs; b. Increases the consistency of cervical mucus and inhibits
the passage of sperm (the increase in the consistency of cervical
mucus can effectively inhibit retrograde infection and reduce the
pelvic cavity The occurrence of inflammatory diseases); c. Anti-
fertilization: inhibit the activity and function of sperm in the uterus
and fallopian tubes, and prevent fertilization [5,9].
Clinical Application of Levonorgestrel-Releasing
Intrauterine System
What are the main clinical applications of Levonorgestrel-
releasing Intrauterine system? In summary, the main points are as
follows [13-24]: ①Long-acting reversible contraception (LARC),
which has a contraceptive effect comparable to sterilization;
②Functional uterine bleeding and menorrhagia; ③Resistance
to menstruation caused by uterine fibroids More therapeutic
effects; ④Therapeutic effect on adenomyosis; ⑤Maintenance
treatment after endometriosis; ⑥The effect of LNG-IUS in relieving
dysmenorrhea; ⑦The protective effect of endometrium in HRT;
⑧Tamoxifen treatment after breast cancer surgery Endometrial
protection; ⑨impact on endometrial hyperplasia and endometrial
cancer.
The 2016 British Endometrial Hyperplasia Management
Guidelines pointed out that for the hormone treatment of
endometrial hyperplasia, the Levonorgestrel-releasing Intrauterine
system is listed as the first choice. Progesterone therapy is prioritized
to recommend the Levonorgestrel-releasing Intrauterine system,
that is, Mirena (LNG-IUS× at least 6 months, preferably × 5 years
for those without a childbirth plan), which can obtain a higher
remission rate. According to the 2016 UK Endometrial Hyperplasia
Management Guidelines and the 2017 China Endometrial
Hyperplasia Diagnosis and Treatment Consensus [25-26], for the
treatment of endometrial hyperplasia, whether it is the treatment
of no dysplasia or atypical hyperplasia, LNG-IUS seems to have
been Placed in a very important position, this is slightly different
from the previous view (the dysplasia should be converted with
high-efficiency progesterone before considering the placement of
LNG-IUS maintenance therapy [27-29]). However, whether these
new ideas can be widely and consistently adopted remains to be
confirmed by the test of time and further research.
Citation: Junling Liu, Mengyue Chen, Zhiyong Dong, Shoufeng Zhang, Wendi Zhang, Zhenyue Qin, Chen Jiming. An Overview of the
Basic Knowledge of Levonorgestrel-Releasing Intrauterine System. W J Gynecol Women’s Health. 5(1): 2021. WJGWH.MS.ID.000602.
DOI: 10.33552/WJGWH.2021.05.000602.
Page 3 of 4
World Journal of Gynecology & Women’s Health Volume 5-Issue 1
Common Confusion and Countermeasures in
the Clinical Use of Levonorgestrel-Releasing
Intrauterine System
What are the main problems and confusions in the clinical
use of Levonorgestrel-releasing Intrauterine system? In summary,
the main points are as follows: ①Irregular vaginal bleeding often
occurs during the first half of the year after using LNG-IUS. If the
amount of vaginal bleeding is small, it can be observed without
special treatment; if the patient is worried and urgently requires
treatment, you can try estrogen therapy according to the following
plan: low-dose compound oral contraceptives- compound LNG
tablets (ethinyl estradiol 30µg / LNG150µg), one tablet a day for
22 days; ethinyl estradiol 50µg once a day for 20 days; estradiol
valerate 2mg, continuous use for two months [22]; ② Patients
with adenomyosis have a large uterine cavity and should not be
placed directly. Consider three injections of GnRH-a and wait for
the uterus to shrink before placing it (uterus 8 weeks of gestation, placed
after GnRH-a is used, it is recommended to place a birth control
ring when menstruation is not regained) [23]. ③The problem of
the birth control ring moving down or falling off [30]. Lowering
the birth control ring often causes increased vaginal bleeding.
Therefore, for patients with significantly increased vaginal bleeding
after LNG-IUS placement, it is necessary to consider the possibility
of the contraceptive ring moving down or completely falling off.
For such patients, if the contraceptive ring does not protrude
out of the uterine cavity, consider pushing the contraceptive ring
up after disinfection to maintain the handle of the contraceptive
ring above the internal cervix. It does not necessarily require the
position of the contraceptive ring to be in the middle of the uterine
cavity (the uterine cavity is often very Difficult to do). If the birth
control ring completely protrudes out of the uterine cavity, it is not
recommended to re-enter the original ring into the uterine cavity
[13,22]. ④For patients with large uterine cavity, can a T-ring be
placed at the same time as LNG-IUS to prevent the contraceptive
ring from moving down or falling off? First of all, the efficacy of
this approach is not clear; secondly, it does not meet the criteria for
diagnosis and treatment. Therefore, it should be used with caution.
Summary and Outlook
In summary, the Levonorgestrel-releasing Intrauterine system
not only has a long-term and reversible effect in contraception, but
also has a wide range of non-contraceptive clinical applications
and good results. However, there are also many problems in the
clinical application of Levonorgestrel-releasing Intrauterine
system, which confuses clinicians. In order to facilitate memory,
the author compiled the essentials of the Levonorgestrel-releasing
Intrauterine system (Mirena) for your reference:
• Mirena ring is very different and contains levonorgestrel;
• In fact, high-efficiency progesterone, the local effect is
very sufficient;
• The concentration of hormones in the blood is low, and
the blood drug level is stable;
• Complications take place in the initial use;
• Often cause amenorrhea, and ovarian function does not
decline;
• The inhibitory effect is often reversible, and ovarian
hormones are still secreted;
• The contraceptive effect can be assured;
• Mirena has many effects, such as stopping bleeding,
relieving pain and protecting the endometrium;
Acknowledgement
This work was supported by grants from the Scientific Research
Support Program for Postdoctoral of Jiangsu Province(2019K064)
, the Major Science and Technology Program of Changzhou Health
and Family Planning Commission (ZD201812), and the Scientific
Research Support Program for “333 Project” of Jiangsu Province
(BRA2019161)
Conflict of Interest
Authors declare no conflict of interest.
References
1. Nilsson CG, HaukkamaaM, VierolaH, Luukkainen T (1983) Tissue
concentrations of levonorgestrel in women using a levonorgestrel-
releasing IUD. Clin Endocrinol 17(6): 529-536.
2. Bednarek PH, Jensen JT (2009) Safety, efficacy and patient acceptability
of the contraceptive and non-contraceptive uses of the LNG-IUS. Int J
Womens Health 1:45-58.
3. M Yang, H Xu, N Chu, Cao L, Gui Y, et al. (2013) Bioequivalence of
compound levonorgestrel tablets in healthy volunteers. Pharmaceutical
Care & Research 13(2): 133-135.
4. Rutanen EM (1998) Endometrial response to intrauterine release of
levonorgestrel. Gynecol Forum 3(1): 11-14.
5. Qi Jie, Fan Limei, Lu Xue (2015) Basic research on Levonorgestrel-
releasing Intrauterine system. Maternal and Child Health Care of China
30(21): 3751-3754.
6. Shan D, Jinghe L (2004) The clinical function and related basic research
of Levonorgestrel-releasing Intrauterine system.Foreign Medical
Sciences(Obstet Gynecol Fascicle) 31(5): 285-288.
7. Gardner FJ, Konje JC, Abrams KR, Brown LJ, Khanna S, et al. (2000)
Endometrial protection from tamoxifen-stimulated changes by a
levonorgestrel-releasing intrauterine system: a randomised controlled
trail. Lancet 356(9243): 1711-1717.
8. Luukkainen T ,Lähteenmäki P , Toivonen J (1990) Levonorgestrel-re -
leasing intrauterine device. Ann med 22(2): 85-90.
9. Xiao B, Zeng T, Wu S, Sun H, Xiao N (1995) Effect of levonorgestrel-re-
leasing intrauterine device on hormonal profile and menstrual pattern
after long-term use. Contraception 51(6):359-365.
10. Barbosa I, Olsson SE, Odlind V, Goncalves T , Coutinho E (1995) Ovar-
ian function after seven years’ use of a levonorgestrel IUD. Adv Contra -
cept 11(2):85-95.
11. Pakarinen PI, Lähteenmäki P , Lehtonen E, Reima I (1998) The ultra -
structure of human endometrium is altered by administration of intra -
uterine levonorgestrel. Hum Reprod 13(7): 1846-1853.
Citation: Junling Liu, Mengyue Chen, Zhiyong Dong, Shoufeng Zhang, Wendi Zhang, Zhenyue Qin, Chen Jiming. An Overview of the
Basic Knowledge of Levonorgestrel-Releasing Intrauterine System. W J Gynecol Women’s Health. 5(1): 2021. WJGWH.MS.ID.000602.
DOI: 10.33552/WJGWH.2021.05.000602.
Page 4 of 4
World Journal of Gynecology & Women’s Health Volume 5-Issue 1
12. Luukkainen T , Pakarinen P , Toivonen J (2001) Progestin-releasing intra-
uterine system. Semi Reprod Med 19(4): 355-363.
13. Huang He, Tian Qinjie (2016) The clinical application of Levonorgestrel-
releasing Intrauterine system in gynecological diseases. Journal of
Reproductive Medicine 25(6): 580-584.
14. Tian Qinjie, Wang Chunqing (2014) Application progress of
Levonorgestrel-releasing Intrauterine system in abnormal uterine
bleeding. Chinese Journal of Obstetrics and Gynecology 49(7): 553-555.
15. Xiaoyan Z, Weiyang Z, Huifang M (2016) Application progress of Mirena
in endometrial precancerous lesions. Maternal and Child Health Care of
China 31(7): 1568-1570.
16. Gallos ID , Shehmar M , Thangaratinam S, Papapostolou TK,
Coomarasamy A, et al. (2010) Oralprogestogens vs levonorgestrel- re -
leasing intrauterine system forendometrial hyperplasia: a systematic
review and meta-analysis. Am J Obstet Gynecol 203(6): 1-10.
17. Zhang P,Song K,Li L, Yukuwa K, Kong B (2013) Efficacy of combined
levonorgestrel- releasing intrauterine system with gonadotropin-releas-
ing hormone analog for the treatment of adenomyosis. Med Princ Pract
22(5):480-483.
18. Abu Hashim H, Zayed A, Ghayaty E, Rakhawy ME (2013) LNG-IUS
treatment of non- atypical endometrial hyperplasia in perimenopausal
women: a randomized controlled trial. J Gynecol Oncol 24(2): 128-134.
19. Bahamondes L, Valeria Bahamondes M, Shulman LP (2015)
Noncontraceptive benefits of hormonal and intrauterine reversible
contraceptive methods. Hum Reprod Update 21(5): 640-651.
20. Shi Q, Li J, Li M, Wu J, Yao Q, et al. (2014) The role of levonorgestrel-
releasing intrauterine system for endometrial protection in women with
breast cancer taking tamoxifen. Eur J Gynaecol Oncol 35(5): 492-498.
21. Fu Y, Zhuang Z (2014) Long-term effects of levonorgestrel-releasing
intrauterine system on tamoxifen-treated breast cancer patients: a
meta-analysis. Int J Clin Exp Pathol 7(10): 6419-6429.
22. El Behery MM, Saleh HS, Ibrahiem MA, Kamal EM, Kassem GA, et al. (2015)
Levonorgestrel-releasing intrauterine device versus dydrogesterone for
management of endometrial hyperplasia without atypia. Reprod Sci
22(3): 329-334.
23. Kim MK, Seong SJ, Kim JW, Jeon S, Choi HS, et al. (2016) Management of
Endometrial Hyperplasia with a Levonorgestrel-Releasing Intrauterine
System: A Korean Gynecologic-Oncology Group Study. Int J Gynecol
Cancer 26(4): 711-715.
24. Soini T , Hurskainen R, Grénman S (2016) Levonorgestrel-releasing
intrauterine system and the risk of breast cancer: A nationwide cohort
study.Acta Oncol 55(2): 188-192.
25. (2016) Royal College of Obstetricians and Gynecological Endoscopy
(BSGE). Management of endometrial hyperplasia green-top guideline 67
RCOG/BSGE joint guideline. London: RCOG.
26. (2017) Reproductive Endocrinology Group of the Women and Children
Health Industry Branch of the National Health Industry Enterprise
Management Association. Consensus on the diagnosis and treatment
of endometrial hyperplasia in China. Journal of Reproductive Medicine
26(10): 957-959.
27. (2009) Endocrinology Group, Chinese Medical Association Obstetrics
and Gynecology Branch. Guidelines for clinical diagnosis and treatment
of dysfunctional uterine bleeding. Chinese Journal of Obstetrics and
Gynecology 44(3): 234-236.
28. (2014) Gynecological Endocrinology Group, Chinese Medical Association
Obstetrics and Gynecology Branch. Guidelines for the diagnosis and
treatment of abnormal uterine bleeding. Chinese Journal of Obstetrics
and Gynecology 49(11): 801-806.
29. Yu Qi (2013) Interpretation of gynecological endocrine diagnosis and
treatment guidelines-case analysis. People’s Medical Publishing House.
30. Lara-Torre E Spotswood L Correia N Weiss PM (2011) Intrauterine
contraception in adolescents and young women: a descriptive study of
use, side effects, and compliance. J Pediatr Adolesc Gynecol 24(1): 39-41.