Hyperprolactinemia
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Basics
Description
Hyperprolactinemia is an abnormal elevation in the serum prolactin level, from either physiologic or pathologic influences of the lactotroph cells of the pituitary gland
Epidemiology
Prevalence- Predominant age: reproductive age
- Predominant sex: female > male
- More readily detected in females because a slight elevation in prolactin causes changes in menstruation and galactorrhea
Etiology and Pathophysiology
- Prolactin, which is produced by lactotrophs in the anterior pituitary, is regulated by:
- Inhibitory factors, primarily dopamine, produced in the hypothalamus and delivered via the hypothalamic-pituitary vessels in the pituitary stalk
- Stimulatory factors, primarily thyrotropin-releasing hormone (TRH)
- Causes of hyperprolactinemia include the following:
- Physiologic
- Pregnancy due to increased estrogen
- Breastfeeding
- Nipple stimulation
- Stress, including postoperative state
- Medications-concentrations are typically in the 25–100 ng/mL range (1)[A]
- Dopamine (D2) blockers: prochlorperazine, metoclopramide
- Dopamine depleters: α-methyldopa, reserpine
- Antidepressants: selective serotonin reuptake inhibitors (SSRIs), tricyclic antidepressants (SSRIs do not appear to cause clinically significant hyperprolactinemia.)
- Verapamil (but no other calcium channel blockers; thought to decrease hypothalamic synthesis of dopamine)
- Antipsychotics: (category is the most common cause of medication induced) haloperidol, fluphenazine, risperidone
- Hypothyroidism (due to elevated TRH)
- Chest wall conditions:
- Herpes zoster
- After thoracotomy
- Trauma
- Prolactin-secreting adenoma (anterior pituitary), categorized:
- Microadenoma: <1 cm
- Macroadenoma: >1 cm
- Pituitary stalk compression/disruption:
- Craniopharyngioma
- Rathke cleft cyst
- Meningioma
- Astrocytoma
- Metastases
- Head trauma
- Infiltrative/inflammatory disorders
- Diminished prolactin clearance:
- Chronic renal failure
- Cirrhosis
- Cocaine
- Idiopathic hyperprolactinemia—when the serum levels are between 20–100 ng/mL but etiology cannot be found (2)[A]
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Basics
Description
Hyperprolactinemia is an abnormal elevation in the serum prolactin level, from either physiologic or pathologic influences of the lactotroph cells of the pituitary gland
Epidemiology
Prevalence- Predominant age: reproductive age
- Predominant sex: female > male
- More readily detected in females because a slight elevation in prolactin causes changes in menstruation and galactorrhea
Etiology and Pathophysiology
- Prolactin, which is produced by lactotrophs in the anterior pituitary, is regulated by:
- Inhibitory factors, primarily dopamine, produced in the hypothalamus and delivered via the hypothalamic-pituitary vessels in the pituitary stalk
- Stimulatory factors, primarily thyrotropin-releasing hormone (TRH)
- Causes of hyperprolactinemia include the following:
- Physiologic
- Pregnancy due to increased estrogen
- Breastfeeding
- Nipple stimulation
- Stress, including postoperative state
- Medications-concentrations are typically in the 25–100 ng/mL range (1)[A]
- Dopamine (D2) blockers: prochlorperazine, metoclopramide
- Dopamine depleters: α-methyldopa, reserpine
- Antidepressants: selective serotonin reuptake inhibitors (SSRIs), tricyclic antidepressants (SSRIs do not appear to cause clinically significant hyperprolactinemia.)
- Verapamil (but no other calcium channel blockers; thought to decrease hypothalamic synthesis of dopamine)
- Antipsychotics: (category is the most common cause of medication induced) haloperidol, fluphenazine, risperidone
- Hypothyroidism (due to elevated TRH)
- Chest wall conditions:
- Herpes zoster
- After thoracotomy
- Trauma
- Prolactin-secreting adenoma (anterior pituitary), categorized:
- Microadenoma: <1 cm
- Macroadenoma: >1 cm
- Pituitary stalk compression/disruption:
- Craniopharyngioma
- Rathke cleft cyst
- Meningioma
- Astrocytoma
- Metastases
- Head trauma
- Infiltrative/inflammatory disorders
- Diminished prolactin clearance:
- Chronic renal failure
- Cirrhosis
- Cocaine
- Idiopathic hyperprolactinemia—when the serum levels are between 20–100 ng/mL but etiology cannot be found (2)[A]
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