Endocrine Control Female Reproduction 7 Flashcards
Summarize the hormonal changes characteristics of different categories of reproductive disorders.
List the types of gonadotropin profiles in reproductive disorders.
- Hypogonadotropic hypogonadism
- Hypergonadostropic hypogonadism
Describe the common features of hypogonadotropic hypogonadism.
-
Findings:
- anovulation
- oligomenorrhea or amenorrhea
- low or “inappropriately” normal circulating LH and FSH levels
-
A single blood level does not reflect LH secretion
- circulating levels must be asses because of pulsatile nature
- done in context of reproductive function
- ex. if LH levels are normal but there is anovulation, then LH secretion is inadequate
- circulating E2 levels may be normal or low depending ont he diagnosis and duration of the condition
- common organs affected:
- hypothalamus
- pituitary
Describe the common features of hypergonadotropic hypogonadism.
-
Findings:
- anovulation
- oligomenorrhea or amenorrhea
- high circulating FSH and variably elevated LH levels
- Elevated FSH levels are a reliable indicator of ovarian follicular damage
- Circulating E2 levels are usually low
- Damage or loss of ovarian follicles results in this
List the common hypothalamus disorders that affect reproduction.
- Absence/destruction of GnRH secretory neurons
- GnRH deficiency - Functional Hypothalamic Amenorrhea (FHA)
What are the common causes of absence/destruction of GnRH secretory neurons?
-
Idiopathic hypogonadotropic hypogonadism (IHH)
- more common in men than women
- usually presents with delayed puberty
- can be caused by several genetic defects
- can be acquired and result in secondary amenorrhea
-
Structural lesions
- ex. craniopharyngiomas
-
Infiltrative disorders
- ex. sarcoidosis
What is functional hypothalamic amenorrhea (FHA) and what are the common causes? What is the treatment?
-
GnRH deficiency
- due to disruption of GnRH release in the absence of structural lesions (hence “functional”)
- ovulation depends on the precisely coordinated pulsatile secretion of GnRH
- disruption can result in failure of ovulation and irregular or absent menses
- GnRH secretion is often present but disrupted
- LH and FSH are usually within the normal range but inappropriately low due to anovulation
-
Treatment
-
opiate antagonists or leptin
- restores ovulator cycles
-
opiate antagonists or leptin
-
Causes
- weight loss
- anorexia nervosa
- simple weight loss
- exercise
- elite runners
- gymnasts
- ballet dancers
- stress
- change in environment
- systemic disease
- weight loss
What are the common disorders of the pituitary that lead to reproductive problems in females?
-
Prolactinomas
- hyperprolactinemia
- results in alterations in dopaminergic thone
- disrupts GnRH release
- ovulatory cycles can be restored by lowering prolactin levels
- macroadenomas can cause mass effect as well
-
Other secretory pituitary tumors
- elevated cortisol levels of Cushing’s syndrome can suppress GnRH release
-
Gonadotrope destruction
- non-functional tumors
- postpartum necrosis (Sheehan’s)
- primary and secondary hemachromatosis
What happens in dysfunction of the ovary? How is this detected?
-
Primary gonadal failure with loss of gonadal steroid and inhibin feedback
- results in increased LH and FSH levels
-
FSH most sensitive marker of gonadal failure
- inhibin secretion can be diminished before steroid secretion
- loss of inhibin results in a selective increase in circulating FSH levels
What is premature ovarian insufficiency (POI)?
-
Defined as the onset of menopause or evidence of follicular loss
- ex. increased FSH levels before 40
-
Common causes:
- idiopathic
- 45 XO mosaics
- presenting as secondary amenorrhea
- cytotoxic drugs
- ex. cytoxan
- radiation
- autoimmune polyendocrine syndromes (APSs)
- Some causes can wax and wane so there may onl be intermittent elevations of FSH
Aside from PCOS, what is the other cause of androgen excess?
-
Hyperandrogenic chronic anovulation differential
- PCOS
- Classic congenital adrenal hyperplasia
- presents in infancy
- Non-classic congenital adrenal hyperplasia
- 21-hydroxylase deficiency
- presents after menarche with hyperandrogenism and chronic anovulation
- Extreme insulin resistance syndromes
- Type A syndrome
- Familial partial lipodystrophy syndromes
- Hyperprolactinemia
- Androgen secreting tumors
- Cushing’s
- Iatrogenic - anabolic steroids