Reproduction I: Gonadal Function Flashcards

1
Q

Follicular phase of menstrual cycle

A

Ovarian follicles are recruited and developed, and this phase ends with the ovulation of a single mature ovum

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2
Q

Luteal phase of the menstrual cycle

A

Progesterone produced by the corpus luteum (the remnants of the ovulated follicle) differentiates the uterine endometrium to prepare it for implantation of the (hopefully) fertilized ovum.

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3
Q

Management of ovarian follicles

A

About 1-2 million ovarian follicles are present at birth, and this number decreases over the lifetime as follicles continuously undergo atresia (degeneration).

About 300,000 follicles remain by the time puberty begins, and when the supply of follicles is exhausted (roughly around age 50), menopause ensues.

Only about 400-500 follicles are ovulated in the average functional lifespan of the ovaries.

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4
Q

Menstrual cycle diagram

A
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5
Q

By definition, the follicular phase of each menstrual cycle begins . . .

A

By definition, the follicular phase of each menstrual cycle begins on the first full day of menstrual bleeding

This is set as day 1.

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6
Q

Selection of the “dominant follicle”

A

As FSH and LH levels rise in the early follicular phase, the largest developing follicle emerges as the dominant follicle, producing larger amounts of estradiol, which feeds back to slightly suppress gonadotropin secretion toward the mid-follicular phase.

The dominant follicle also secretes inhibin B, which further suppresses FSH. The lack of FSH then causes atresia of all the non-dominant follicles that were activated.

However, the dominant follicle continues to grow and mature, partly because it increases expression of the FSH receptor, which allows it to continue developing and avoid atresia even in the face of lower FSH levels.

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7
Q

Effects of estradiol on the endometrium

A

In the uterus, estradiol causes the endometrium to proliferate. As estradiol levels rise through the follicular phase, the endometrium proliferates and thickens in anticipation of implantation

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8
Q

Ovulation

A
  • Occurs about 36 hours after the beginning of the LH surge.
  • The follicle ruptures through the outer capsule of the ovary and the ovum is released into the pelvic cavity, where it is taken up into the fallopian tubes
  • Fertilization occurs in the distal 1/3 of the fallopian tube
  • If the ovum is not fertilized within 24 hours after ovulation, it degenerates
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9
Q

“Fertile period”

A

Sperm can live in the receiving reproductive organs (vagina, uterus, fallopian tubes) for 3-5 days

Thus, the 5 days preceding ovulation is the “fertile period” in which intercourse is most likely to lead to conception.

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10
Q

Progesterone in the luteal phase

A

Progesterone is required for implantation and for maintenance of a pregnancy because it causes the now-thickened endometrium to mature and differentiate, inducing the in-growth of spiral arteries to provide circulation to an implanted embryo

This comes from the corpus luteum during the luteal phase, until the corpus decays. At this point, withdrawal of progesterone will initiate the beginning of menses, unless implantation of a fertilized ovum leads to hCG production which may rescue the endometrium from shedding and initiate pregnancy.

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11
Q

The length of a menstrual cycle is counted from. . .

A

. . . the first day of bleeding of one period to the first day of bleeding of the next period

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12
Q

“Normal” menstrual cycle lengths

A
  • 24-35 days, but cycle length varies both among and within individuals
  • Because the finite life span of the corpus luteum is relatively fixed, the luteal phase is quite consistent at about 14 days in most normal cycles.
  • Variation in cycle length is mostly due to the variable duration of the follicular phase
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13
Q

Moliminal symptoms

A

Symptoms of weight gain, mood changes, and acne preceding menses due to progesterone from the corpus luteum, as well as uterine cramping, which is caused by progesterone withdrawal.

Their presence indicates an ovulatory cycle with corpus luteum formation.

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14
Q

The inclusion of progestin in combined hormonal contraception is important to avoid. . .

A

. . . prolonged exposure of the endometrium to estrogen alone.

Without the maturing effect of progestin and the periodic shedding induced by progestin withdrawal, continuous exposure to unopposed estrogen increases the risk of endometrial hyperplasia and carcinoma

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15
Q

Progrestin-only contraception

A
  • Can be given for those who have contraindications to estrogen
  • As effective as combined OCPs and are taken continuously without a placebo week
  • Can also be given as a depot injection every three months or as a subcutaneous implant
  • Risks: There is a significant incidence of breakthrough bleeding, and prolonged treatment with progestin-only contraception may result in complications of estrogen deficiency such as low bone density (due to gonadotropin suppression)
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16
Q

Levonorgestrel

A
  • Given after intercourse to prevent unwanted pregnancy
  • The most common form is the progestin levonorgestrel
  • Works by feeding back to suppress LH at the pituitary level, preventing the LH surge that is required for ovulation
  • Only effective if taken within 3 days of intercourse
  • Prevents about 50% of pregnancies that might otherwise occur, IT IS NOT A GAURANTEE
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17
Q

Emergency contraception

A
  • Levonorgestrel
  • Mifepristone
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18
Q

Mifepristone

A
  • Progesterone receptor antagonist
  • When used after pregnancy is established, mifepristone can induce abortion by blocking the action of progesterone required to maintain the pregnancy
  • When used prior to pregnancy establishment, mifepristone can also preventing ovulation and conception
  • This tends to be the more controvertial form of contraception
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19
Q

Intrauterine devices

A
  • Small devices made of either copper or progestin-eluting plastic that are placed inside the uterus to provide long-term contraception.
  • Create an inflammatory response in the uterus that suppresses the endometrium, thereby preventing fertilization and implantation
  • IUDs are >99% effective in preventing pregnancy.
  • Normal structure and function of the endometrium returns about a month after an IUD is removed
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20
Q

Menopause can essentially be thought of as a form of . . .

A

. . . primary hypogonadism

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21
Q

Onset of menopause

A
  • Occurs between ages 40 and 58, average ~51
  • Menses often become irregular in the months or years leading up
  • Falling estradiol levels lead to symptoms of estrogen deficiency: Hot flashes, vaginal atrophy causing discomfort, dryness, or pain with intercourse; bone loss leading to osteroporosis, increased risk of cardiovascular disease.
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22
Q

Treating menopause

A
  • HRT with estradiol +/- progestin (depending on if the individual still has a uterus)
    • Effective for treating hot flashes and vaginal atrophy, and for reducing bone loss and decreasing fracture risk
    • However, HRT does not decrease cardiovascular risk, and it appears to increase the risk of stroke and thromboembolism.
    • HRT may be used cautiously for up to several years to treat menopausal symptoms, but long-term HRT is generally not recommended
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23
Q

Oligomenorrhea

A
  • Menses less frequent than normal
  • Cycles longer than 35 days, or fewer than 9 cycles per year
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24
Q

Amenorrhea

A
  • Primary amenorrhea: Not beginning menstruation
  • Secondary amenorrhea: Loss of periods after previously having them
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25
Q

Most common cause of secondary amenorrhea

A

Pregnancy, of course

26
Q

Anatomic causes of amenorrhea

A
  • Abnormalities of the uterus and its outflow tract may prevent menstrual flow
  • Malformations of any part of the fetal müllerian system (including the uterus, cervix, or upper vagina), vaginal webs or septae, or an imperforate hymen
  • If the obstruction is distal, patients may present with cyclic abdominal/pelvic body due to distention of the uterus and fallopian tubes by retained menstrual blood
  • Most anatomic causes are congenital and cause primary amenorrhea
  • Asherman’s syndrome is secondary amenorrhea due to endometrial scarring and adhesions
27
Q

Anovulation

A
  • If ovulation does not occur in a given cycle, no corpus luteum forms, and therefore there is no progesterone withdrawal and no coordinated shedding of the endometrium
  • Chronic anovulation is a common cause of amenorrhea. Anovulation can cause either primary or secondary amenorrhea.
  • Anovulation may be secondary to hypogonadism, hyperandrosteronism (and thus inhibition of central LH/FSH secretion), or polycystic ovarian syndrome
28
Q

Diagnosing PCOS

A
29
Q

Polcystic ovarian syndrome

A
  • Affects 6-8% of those born w/ female biological sex
  • Clinically a syndrome of hyperandrogenism, oligo- or anovulation, and multiple ovarian cysts
  • Insulin resistance also a component, and inviduals are at higher risk for the metabolic syndrome including obesity, hypertension, and dyslipidemia.
  • Often have high estrogen, almost never have low estradiol
30
Q

Clinical syndorme of hyperandrogenism

A
  • Hirsutism (excess body hair)
  • Acne
31
Q

Workup for anovulation

A
  • Pregnancy must always be excluded
  • Evaluation of LH, FSH, estradiol
  • Evaluation of common causes of disruption to this pathway: prolactin, TSH
  • If clinical signs of hyperandrogenism, testosterone
  • Pelvic ultrasound may diagose or exclude PCOS
  • If primary, workup for congenital anatomic cause (unnecessary for secondary unless indicated by something like Crohn’s)
  • Progestin withdrawal test
32
Q

Progestin withdrawal test

A
  • Useful to distinguish causes of decreased uterine bleeding
  • Administer medroxyprogesterone for 5-10 days, then withdraw and see if menses ensues
  • This test is basically an assay for functional estradiol pathways
  • If estradiol levels are normal or high (e.g., PCOS), the proliferating endometrium is stabilized and differentiated by the progestin and withdrawal will enduce menses
  • If estradiol levels are low or estradiol is nonfunctional, there is nothing to shed when the progestin is withdrawn, so no bleeding is observed
  • Also tests the patency of the genital tract
33
Q

Treatment of amenorrhea and oligomenorrhea

A
  • Treatment of underlying cause
  • For primary hypogonadism or irremediable secondary hypogonadism (like Kallmann syndrome), treatment consists of HRT with cyclic variation, Oral contraceptive works for this purpose in those who have secondary amenorrhea
  • Treatment for PCOS is more involved and warrants its own discussion
34
Q

Treating PCOS

A
  • Goals of treatment are to decrease hyperandrogenism and to prevent the long-term risk of endometrial hyperplasia from estrogen exposure, as well as preventing development of the metabolic syndrome
  • Combined hormonal contraception works to decrease hyperandrogenism by 1) suppressing LH, 2) increasing levels of SHBG, 3) inhibition of GnRH-stimulated LH secretion, and 4) induction of cyclie menses preventing hyperplasia (1 and 2 are estradiol effects, 3 and 4 are progestin effects)
  • Exercise and weight loss critical due to insulin resistance aspect
  • Metformin
  • Spironolactone used as anti-androgen
  • Clomiphene or letrozole can induce ovulation if individual plans on becoming pregnant
35
Q

Sex hormone binding globulin (SHBG)

A
  • Stable binding partner and transport protein for sex hormones within the plasma
  • Elevation in this protein can decrease the effective activity of sex hormones
36
Q

Spironolactone as an anti-androgen

A

In addition to working as a mineralocorticoid receptor antagonist, spironolactone can work as a androgen receptor antagoist

It is usually used in conjunction with OCPs for the treatment of hyperandrogenic symptoms, particularly hirsutism

37
Q

Inducing fertility in individuals with PCOS

A
  • Fertility in those with PCOS is reduced largely because low FSH levels are insufficient to recruit and develop follicles for ovulation
  • Clomiphene (a selective estrogen receptor antagonist) or letrozole (an aromatase inhibitor) can induce ovulation in those with PCOS by decreasing the negative feedback of estradiol on FSH, raising FSH level
  • A potential side effect is an increased risk of multiple gestation if multiple follicles are ovulated and fertilized.
38
Q

Abnormal (or disordered) uterine bleeding

A
  • Menstrual bleeding that is excessive in frequency (7 days), or volume
  • May be caused by pregnancy, endometrial hyperplasia, coagulation disorders, or uterine neoplasms
  • Always remember to address the possibility that the blood is not originating from the uterus – bleeding can occur at any point in the genital tract, including the external genitalia, vagina, cervix, uterus, and fallopian tubes
39
Q

Endometrial hyperplasia

A
  • Occurs when the endometrium is exposed to excessive estradiol without adequate progesterone
  • Conditions include PCOS, use of estrogen-only hormone replacement, or estrogenomas
  • Endometrium proliferates excessively and may become structurally unstable, causing unpredictable endometrial sloughing (“overflow bleeding”)
  • Chronic endometrial hyperplasia may give rise to an endometrial carcinoma.
40
Q

Uterine neoplasms

A
  • Benign neoplasms:
    • Endometrial polyps
    • Leiomyomas (aka fibroid): Leiomyomas are benign smooth muscle tumors. Very common. Symptoms: excessive or irregular bleeding, pain with menses or with intercourse (dyspareunia), pregnancy loss, or infertility.
  • Endometrial carcinoma: Risk factors include postmenopausal menorrhagia, endometrial hyperplasia, obesity, nulliparity, late menopause, PCOS, family history, and a history of pelvic irradiation
41
Q

Diagnosing patterns of abnormal uterine bleeding

A
  • Pregnancy should always be excluded
  • Hormonal testing (especially for estrogen excess and testosterone excess)
  • Visualization of anatomic lesions by ultrasound, CT, MRI
  • Intraluminal lesions may require hysterosalpingogram
  • Endometrial neoplasia is diagnosed by endometrial biopsy
42
Q

Hysterosalpingogram

A

Injection of radio-opaque dye into the uterine cavity for visualization by fluoroscopy

43
Q

Treatment of abnormal uterine bleeding

A
  • Combined hormonal contraception is the main treatment for hormonally mediated forms of abnormal uterine bleeding
    • Estradiol component prevents shedding
    • Progestin component differentiates the endometrium into a more stable form
    • Higher doses may be needed initially to control severe acute bleeding
  • Anatomic causes (leiomyoma, carcinoma) require surgical resection
44
Q

Functional definition of interfility

A

An inability to conceive a pregnancy despite unprotected intercourse during the fertile period of the menstrual cycle for more than 12 months

This is based on data that roughly 90% of couples will conceive within 12 months under these conditions

45
Q

Male Factor Infertility

A
  • Male infertility accounts for ~50% of cases, at least in part
  • Many of these individuals (30-40%) have idiopathic infertility for which no specific cause can be determined
  • The remaining cases are caused by primary testicular insufficiency (as in Kleinfelter’s/47,XXY or testicular irradiation), secondary hypogonadism, or obstruction of the epididymus or vas deferens, or other rare causes.
  • Evaluation includes HPG axis assessment and semen analysis to assess number, mobility, and morphology
46
Q

Female Factor Infertility

A
  • Caused by almost any disorder resulting in abnormal menstrual cycling
  • Most common is chronic anovulation
  • Anatomic factors (pelvic adhesions, endometriosis, and uterine or tubal abnormalities) that prevent the normal migration of ova and/or implantation in the uterus
  • Antiphospholipid syndrome is associated with FF infertility
  • Other factors include older age, tobacco or alcohol use, obesity, excessive exercise, and psychological stress
47
Q

Evaluating female factor infertility

A

Evaluation is essentially the same as for amenorrhea, often with the addition of a hysterosalpingogram to assess uterine and tubal anatomy and patency.

48
Q

Standard of care in adolescents who identify as transgender

A

The physical changes of puberty often cause great distress to transgender individuals, and many of these changes are permanent and not reversible with medical treatment, or even surgery

Therefore, the standard is to suppress their innate puberty at an early stage, then at a later stage to initiate gender-affirming hormone therapy.

49
Q

Pubertal suppression

A
  • Indicated only following diagnosis of gender incongruence by a mental health professional
  • Long-acting analogs of GnRH (like leuprolide) are given to suppress FSH/LH secretion
  • Pubertal suppression should begin when the patient first exhibit signs of puberty (Tanner stage 2 or 3), or following detection of LSH/FSH/estradiol/testosterone elevation on bloodwork
    • These early physical changes are often associated with emotional distress, which is an element of gender dysphoria
50
Q

Gender-affirming hormone therapy

A
  • Gender-affirming hormone therapy for transgender adolescents treated with pubertal suppression usually begins around age 16
  • . Suppression of innate puberty with a GnRH analog is continued while the patient receives gender-affirming hormone therapy
  • In transgender adults presenting after puberty is complete, a GnRH analog can be used to suppress endogenous sex hormone production and gender-affirming hormone therapy can be initiated immediately.
51
Q

Feminizing therapy

A
  • Estrogens (most commonly 17β-estradiol) are given to achieve normal female serum levels of estradiol.
    • This also suppresses endogenous FSH/LH
    • Testosterone levels usually do not drop into the normal female range
    • It should be known that certain preparations increase the risk of thrombosis
  • Anti-androgens (spironolactone) suppress testosterone production and/or block its effects
  • GnRH agonists (inhibit gonadotropin secretion, can be used in place of spironolactone)
  • Gonadectomy (eliminates endogenous hormone production, so anti-androgens and GnRH agonists are no longer needed)
52
Q

Masculinizing therapy

A
  • Testosterone
    • Since testosterone disrupts endogenous HPG axis in these individuals, an anti-androgen or GnRH agonist is not necessary
    • Testosterone increases erythropoiesis, so hematocrit should be monitored, along with weight and blood pressure
  • Estradiol levels remain within the normal range in medically treated transgender men and do not rise.
  • As long as individuals assigned female at birth have breasts and a cervix, they should undergo routine screening for malignancy with mammograms and pap smears, respectively.
  • Gonadectomy
53
Q

Does gender-affirming hormone therapy result in infertility?

A

NO! Not always!

So, all patients with gonads and who engage in sexual intercourse should be counseled about fertility and the need for contraception before starting gender-affirming hormone therapy or undergoing surgery.

54
Q

Feminizing or masculinizing surgery

A
  • Aka sex reassignment surgery [SRS], gender-affirming surgery
  • Alters a transgender person’s appearance beyond that which is possible with hormones alone
  • Feminizing procedures in transgender women include breast augmentation, facial feminization surgery, and laser hair removal, as well as orchiectomy, penectomy, and vaginoplasty.
  • Masculinizing procedures include mastectomy and construction of a penis through phalloplasty or metoidioplasty, although reconstructive genital surgery is complex in transgender men
55
Q

Reproductive health for transgender women

A
  • Estrogen reduces spermatogenesis by directly suppressing gonadotropins, and also decreases sperm count and sperm motility by decreasing testosterone levels.
    • These changes may or may not be reversible if estrogen is stopped. Orchiectomy results in permanent infertility.
  • Fertility preservation can be accomplished in adult individuals assigned male sex at birth by sperm cryopreservation, testicular sperm extraction, or testicular tissue preservation
    • However, transgender adolescents who have not undergone typical male puberty do not have sperm to preserve
    • Cryopreservation is expensive
56
Q

Reproductive health for transgender men

A
  • Testosterone usually leads to anovulation and amenorrhea, which may or may not be reversible if testosterone is stopped
  • Testosterone is a teratogen and is contraindicated during pregnancy.
  • Oocyte cryopreservation can be offered to peri- or postmenarchal individuals using hormone-induced ovulation and ultrasound-guided oocyte retrieval
    • If eggs are immediately fertilized with sperm from a partner or donor, embryo banking is another possibility
    • These procedures are costly
57
Q

Alternative methods for starting a family for transgender individuals

A

Adoption, assisted reproductive treatment with donor sperm/egg, cryopreserved sperm/egg, and surrogacy are additional parenthood options for transgender individuals.

58
Q

What are the “cysts” in polycystic ovarian syndrome?

A

Arrested follicles which have halted maturation due to insufficient FSH. Found on ultrasound.

59
Q

PCOS summary

A
60
Q

PCOs treatment summary

A