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Menstrual Cycle Proliferative And Follicular Phase

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Last Update: September 12, 2022.


The follicular phase of the female menstrual cycle includes the maturation of ovarian follicles to prepare one of them for release during ovulation. During the same period, there are concurrent changes in the endometrium, which is why the follicular phase is also known as the proliferative phase (see Image. Proliferative Phase Endometrium and the Menstrual Cycle). 

Issues of Concern

Follicular Phase

The duration of the menstrual cycle varies and occurs every 21 to 35 days, with an average span of 28 days. Oligomenorrhea describes infrequent menstrual periods and cycles lasting more than 35 days. Polymenorrhea refers to frequent menstrual periods and cycles lasting less than 21 days. It is important to note that the duration of the follicular phase can differ depending on the length of the cycle, while the luteal phase is usually stable and lasts 14 days. Based on a 28-day cycle, the follicular phase measures from the first day of menstruation (day 0) until the beginning of ovulation (day 14). When the previous menstrual cycle completes and the corpus luteum breaks down, estrogen, progesterone, and inhibin A levels decrease. This chain of events causes positive feedback to the hypothalamus and anterior pituitary and a subsequent pulsatile release of GnRH and FSH into circulation. This increase in FSH stimulates the granulosa cells of the ovaries to recruit several follicles from each ovary. These follicles complete maturation and only one Graafian follicle goes through ovulation during that cycle. The increase in FSH also stimulates the secretion of Inhibin B by the granulosa cells. Inhibin B eventually blunts the secretion of FSH toward the end of the follicular phase. Inhibin B levels are highest during the LH surge before ovulation and quickly taper off after.[1][2]

The level of FSH available can vary based on the age of the female. The functioning of the ovaries weakens with increasing age, which causes less inhibin production in the previous luteal phase. The decreased inhibin levels stimulate a larger release of FSH compared to that of a younger female. These increasing levels of FSH cause more active recruitment of ovarian follicles, which can increase the occurrence of more than one ovulation per cycle. Since the follicles get recruited at an increased rate, the overall duration of the follicular phase decreases, and the follicle released for ovulation is immature. Due to these age-related changes in the early follicular phase, physicians can assess suspected infertility by checking serum FSH and estradiol levels around day 3 of the cycle. Also, ovarian reserve can be predicted by monitoring serum levels of anti-Mullerian hormone (AMH) made by the granulosa cells, as this hormone plays an important role in folliculogenesis. AMH levels can be monitored at any point during the menstrual cycle.[3][4][5]

The mid-follicular phase begins with a rise in levels of estradiol and inhibin B produced by the ovarian follicles in response to an increase in FSH; this results in negative feedback that decreases the levels of FSH. It is during this time that the selection of the follicle intended for ovulation takes place. This follicle is called the dominant follicle. Different theories suggest how the dominant follicle is determined. One idea is that the follicle expressing the highest amount of FSH receptors is the one to promote its growth and ovulate, while the other follicles are suppressed and undergo atresia. Another theory states that the anti-Mullerian hormone (AMH) plays a role in selecting the dominant follicle.[6][7][8][9]

As a response to the rise in FSH levels during the early follicular phase, granulosa cells proliferate. This rise in granulosa cells causes a concurrent rise in FSH receptors in the cells. The increased FSH levels allow the granulosa cells to produce estradiol, which recruits LH receptors in granulosa cells as well. With LH receptors now present, the granulosa cells produce small amounts of progesterone and 17-hydroxyprogesterone. The progesterone released by the granulosa cells regulates granulosa cell proliferation and ultimately slows follicular growth.[10] 

As the follicular phase comes to an end, estradiol levels rapidly increase. With this increase in estradiol, the negative feedback loop switches to positive feedback. There is no definitive answer as to why this switch in feedback happens, but suggestions are that kisspeptin neurons play a role. The positive feedback from the estradiol stimulates the hypothalamus and the anterior pituitary, and there is a surge in LH, signaling the end of the follicular phase and the beginning of ovulation.[11]

Proliferative Phase

In addition to ovarian follicle maturation, changes occur in the endometrium during the first 14 days of the cycle, hence the term proliferative phase. The increasing concentrations of estradiol strongly influence the endometrial changes that happen before ovulation. The proliferative phase can be subdivided into the early, mid-, and late proliferative phases. The early proliferative phase occurs right after menses, usually around day 4 to day 7. The regenerating surface of the endometrium forms a thin, linear, and echogenic layer. The glands are short, straight, and narrow with microvilli and cilia forming on the epithelial cells. Inactive glands still overcoming the last menstrual cycle may appear cuboidal and ragged. During this early phase, the closely bunched stroma will display some mitotic activity, with its cells appearing spindle-shaped. The cellular nuclei will also undergo enlargement with minimal surrounding cytoplasm. The endometrium will then progress to the mid-proliferative phase, usually around day 8 to day 10 of the cycle. These glands will be composed of columnar epithelium and will be more elongated and curved. Finally, the late proliferative phase occurs from around day 11 to day 14. During the late proliferative phase, the glands coil and become closely packed. These glands will be undergoing active mitosis and nuclear pseudostratification. The stratum functional layer (also known as the inner lining) of the endometrium will reach its maximal thickness of around 0.5 to 5mm and develop a trilaminar appearance. The trilaminar endometrium will consist of a thin inner line and an outer basil layer, both echogenic. In the middle layer will be a darker rim. The spiral arteries will elongate to provide adequate blood flow to the endometrium, to compensate for this increased endometrial thickness.[2][12] 

During the proliferative phase, the cervix concurrently changes in response to the increasing estradiol levels. There are crypts or channels in the cervix that produce a watery, thin, mucoid discharge to make the vagina less acidic. The cervical canal appears more dilated and distended on ultrasonography to accommodate the increasing amounts of cervical discharge. Overall, these endometrial and cervical changes function to create a less hostile environment for entering sperm.[13]

Clinical Significance

The median age of menarche in the United States is 12.5 years. The average female has around 450 menstrual cycles after that. As clinicians, it is essential to have an understanding of all phases of the menstrual cycle. It is especially important to use this knowledge to educate younger patients on the normal menstrual cycle range and the changes they can expect their bodies to undergo at various cycle stages. By being able to differentiate between a normal and abnormal menstrual cycle early on, the clinician can diagnose and treat any unusual patterns in subsequent cycles such as dysmenorrhea, amenorrhea, menorrhagia, infertility, and various others.[14]

Review Questions

Proliferative Phase Endometrium and the Menstrual Cycle


Proliferative Phase Endometrium and the Menstrual Cycle. Public Domain via Wikimedia Commons.


Thiyagarajan DK, Basit H, Jeanmonod R. StatPearls [Internet]. StatPearls Publishing; Treasure Island (FL): Oct 24, 2022. Physiology, Menstrual Cycle. [PubMed: 29763196]
Reed BG, Carr BR. The Normal Menstrual Cycle and the Control of Ovulation. In: Feingold KR, Anawalt B, Blackman MR, Boyce A, Chrousos G, Corpas E, de Herder WW, Dhatariya K, Dungan K, Hofland J, Kalra S, Kaltsas G, Kapoor N, Koch C, Kopp P, Korbonits M, Kovacs CS, Kuohung W, Laferrère B, Levy M, McGee EA, McLachlan R, New M, Purnell J, Sahay R, Shah AS, Singer F, Sperling MA, Stratakis CA, Trence DL, Wilson DP, editors. Endotext [Internet]. MDText.com, Inc.; South Dartmouth (MA): Aug 5, 2018. [PubMed: 25905282]
Umehara T, Kawai T, Kawashima I, Tanaka K, Okuda S, Kitasaka H, Richards JS, Shimada M. The acceleration of reproductive aging in Nrg1flox/flox ;Cyp19-Cre female mice. Aging Cell. 2017 Dec;16(6):1288-1299. [PMC free article: PMC5676068] [PubMed: 28857490]
Shaw ND, Srouji SS, Welt CK, Cox KH, Fox JH, Adams JA, Sluss PM, Hall JE. Compensatory Increase in Ovarian Aromatase in Older Regularly Cycling Women. J Clin Endocrinol Metab. 2015 Sep;100(9):3539-47. [PMC free article: PMC4570155] [PubMed: 26126208]
Jamil Z, Fatima SS, Ahmed K, Malik R. Anti-Mullerian Hormone: Above and Beyond Conventional Ovarian Reserve Markers. Dis Markers. 2016;2016:5246217. [PMC free article: PMC4764725] [PubMed: 26977116]
Yding Andersen C. Inhibin-B secretion and FSH isoform distribution may play an integral part of follicular selection in the natural menstrual cycle. Mol Hum Reprod. 2017 Jan;23(1):16-24. [PubMed: 27756855]
Ilha GF, Rovani MT, Gasperin BG, Antoniazzi AQ, Gonçalves PB, Bordignon V, Duggavathi R. Lack of FSH support enhances LIF-STAT3 signaling in granulosa cells of atretic follicles in cattle. Reproduction. 2015 Oct;150(4):395-403. [PubMed: 26336147]
Durlinger AL, Kramer P, Karels B, de Jong FH, Uilenbroek JT, Grootegoed JA, Themmen AP. Control of primordial follicle recruitment by anti-Müllerian hormone in the mouse ovary. Endocrinology. 1999 Dec;140(12):5789-96. [PubMed: 10579345]
Hampl R, Šnajderová M, Mardešić T. Antimüllerian hormone (AMH) not only a marker for prediction of ovarian reserve. Physiol Res. 2011;60(2):217-23. [PubMed: 21114374]
Chaffkin LM, Luciano AA, Peluso JJ. Progesterone as an autocrine/paracrine regulator of human granulosa cell proliferation. J Clin Endocrinol Metab. 1992 Dec;75(6):1404-8. [PubMed: 1464640]
Wang L, Vanacker C, Burger LL, Barnes T, Shah YM, Myers MG, Moenter SM. Genetic dissection of the different roles of hypothalamic kisspeptin neurons in regulating female reproduction. Elife. 2019 Apr 04;8 [PMC free article: PMC6491090] [PubMed: 30946012]
Noyes RW, Hertig AT, Rock J. Dating the endometrial biopsy. Am J Obstet Gynecol. 1975 May;122(2):262-3. [PubMed: 1155504]
Chaudhari UK, Metkari SM, Manjaramkar DD, Sachdeva G, Katkam R, Bandivdekar AH, Mahajan A, Thakur MH, Kholkute SD. Echography of the cervix and uterus during the proliferative and secretory phases of the menstrual cycle in bonnet monkeys (Macaca radiata). J Am Assoc Lab Anim Sci. 2014 Jan;53(1):18-23. [PMC free article: PMC3894643] [PubMed: 24411775]
ACOG Committee Opinion No. 651: Menstruation in Girls and Adolescents: Using the Menstrual Cycle as a Vital Sign. Obstet Gynecol. 2015 Dec;126(6):e143-e146. [PubMed: 26595586]

Disclosure: Carol Monis declares no relevant financial relationships with ineligible companies.

Disclosure: Maggie Tetrokalashvili declares no relevant financial relationships with ineligible companies.

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