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History and physical examination can distinguish among most physiologic, pharmacologic, or pathologic causes of an elevated serum prolactin level (SPL) (strength of recommendation [SOR]: C, expert opinion). Patients with unexplained elevations of serum prolactin or with a level above 200 ng/mL should undergo imaging of the sella turcica (SOR: C, expert opinion). Mildly elevated SPL due to physiologic causes may be managed expectantly (SOR: B, cohort studies) and pharmacologic elevations may be treated by discontinuing the causative medication (SOR: C, expert opinion). Elevated SPL due to pathologic causes requires both monitoring for complications and treatment of the underlying condition (SOR: C, expert opinion).
Dopamine agonists are effective for patients requiring drug treatment (SOR: B, systematic review of cohort studies), and cabergoline is more effective and better tolerated than bromocriptine (SOR: B, randomized controlled trial [RCT]). Surgery is reserved for symptomatic patients not controlled medically (SOR: C, expert opinion).
Patients with mildly elevated SPLs can be safely watched with testing and symptom monitoring
Allen Daugird, MD
University of North Carolina at Chapel Hill
Most elevated prolactin levels in my practice have been mild and often secondary to medication, though there are a host of causes, as listed in the TABLE. This Clinical Inquiry reassures us that patients with mildly elevated SPLs can be safely watched with serial testing and monitoring symptoms. Obtaining SPLs only on fasting specimens can help improve test accuracy. The feared risk of vision loss due to a macroadenoma seems to be quite small. Patients with significantly elevated SPLs with amenorrhea or infertility deserve referral to clinicians comfortable with using dopamine agonists because of the high rate of success with this treatment.
Evidence summary
An expert guideline recommends a history and physical examination to determine whether an elevated SPL is due to physiologic, pharmacologic, or pathologic causes (TABLE).1 The fasting morning SPL is least variable and correlates best with a disease state.1 Clinical correlation is necessary to reveal false positives (due to biologically inactive forms of prolactin) or false negatives (due to very high SPLs that exceed the ability of the assay). If an elevated SPL is suspected despite a normal laboratory report, retesting with serum diluted 1:100 can identify a false-negative value.2
A detailed drug history is important since drug-induced elevated SPL is common.1 Laboratory evaluation includes thyroid-stimulating hormone, blood urea nitrogen, and creatinine, as well as pregnancy testing when applicable. If no cause of elevated SPL is identified by initial clinical evaluation or if the SPL is greater than 200 ng/mL, experts recommend imaging of the sella turcica with computed tomography or magnetic resonance imaging.1
Physiologic causes. For patients with a mildly elevated SPL due to a physiologic cause, experts recommend expectant management. Patients should be monitored for symptoms of hypogonadism (amenorrhea, infertility, or sexual dysfunction) and have SPL measured at 6- to 12-month intervals.1 In cohort studies, treatment of the underlying cause of elevated SPL reverses secondary physiologic changes of low estrogen or testosterone, and hypogonadism.3-5
Pharmacologic causes. Eliminating a pharmacologic cause may lead to normalization of SPL, although experts recommend psychiatric consultation before discontinuing neuroleptic medications.1
Pathologic causes. Experts advise treating the underlying cause of a pathologic elevation of SPL. Patients with microadenoma should have SPLs monitored to prevent complications of decreased bone mineral density and sexual dysfunction due to persistently elevated SPL. Patients with a macroadenoma (>1 cm) are at risk for tumor growth and require serial imaging studies in addition to treatment of SPL, according to expert opinion.1-3
Medical therapy. Medical therapy with a dopamine agonist is indicated for patients with either symptoms of hypogonadism due to elevated SPL, or neurologic symptoms due to the size of a macroadenoma.1 In a review of 13 cohort studies, bromocriptine improved symptoms and reduced SPLs to normal for 229 of 280 women (82%).6 A cohort study of 27 patients with macroadenomas treated with bromocriptine found 10% to 50% reductions of tumor size.7 A randomized controlled trial treating 459 women having hyperprolactinemic amenorrhea with either cabergoline or bromocriptine achieved a stable normal SPL in 83% and 59%, respectively (P<.001). Adverse effects were common but were less common with cabergoline (68% vs 78%) and resulted in fewer discontinuations (3% vs 12%).8
Surgical therapy. Surgery is indicated for patients unresponsive to or intolerant of medical therapy, or who have visual field loss, cranial nerve palsy, or headache due to macroadenoma.1 A retrospective review of patients who underwent surgical resection found a 40% recurrence rate.9
Recommendations from others
Williams Textbook of Endocrinology includes the recommendations above and advises seeking consultation for patients with mass effects of macroadenomas such as visual field loss, cranial nerve palsy, or headaches; for patients with progressive elevation of SPL despite medical treatment; and for pregnant women.4 Conventional antipsychotic agents are commonly associated with elevated prolactin due to dopamine agonist activity. Some atypical antipsychotics may lead to lower levels of elevated prolactin, transient elevations or marked elevations.10 Experts recommend following serial SPLs, if antipsychotics are truly needed. Psychiatric consultation may assist in making decisions about medication selection. Patients with symptoms (galactorrhea, amenorrhea, headaches, visual disturbances, sexual dysfunction) or levels of 200 or more, should undergo an MRI or CT. Experts recommend monitoring levels every 1 to 3 months.1
TABLE
Physiologic, pharmacologic, and pathologic causes of an elevated serum prolactin level1
| PHYSIOLOGIC |
| Pregnancy |
| Ectopic pregnancy |
| Lactation |
| Nipple stimulation |
| Stress |
| Sleep disorder |
| PHARMACOLGIC |
| Dopamine receptor antagonists: phenothiazines, butyrophenones, thioxanthene, risperidone, metoclopramide, sulpiride, pimozide |
| Dopamine-depleting agents: α-methyldopa, reserpine |
| Hormones: estrogens, antiandrogens |
| Others: danazol, isoniazid, verapamil, cyproheptadine, opiates, H2-blockers (cimetidine), cocaine and marijuana, tricyclic antidepressants |
| PATHOLOGIC |
| Acromegaly |
| Alcoholic cirrhosis |
| Chest wall trauma or tumor |
| Herpes zoster |
| Hypothalamic and pituitary stalk disease |
| Hypothyroidism |
| Pituitary tumors: prolactinomas, adenomas |
| Polycystic ovarian syndrome |
| Renal failure |
| Sarcoidosis |
1. Biller BM, Luciano A, Crosignani PG, et al. Guidelines for the diagnosis and treatment of hyperprolactinemia. J Reprod Med 1999;44(12 Suppl):1075-1084.
2. Barkan AL, Chandler WF. Giant pituitary prolactinoma with falsely low serum prolactin: the pitfall of the “high hook effect”: Case report. Neurosurgery 1998;42:913-915.
3. Sanfilippo JS. Implications of not treating hyperprolactinemia. J Reprod Med 1999;44(12 Suppl):1111-1115.
4. Melmed S, Kleinberg D. Physiology and disorders of the pituitary hormone axes. In: Williams RH, Larsen PR. Williams Textbook of Endocrinology. 10th ed. Philadelphia, Pa: Saunders; 2003;200-212.
5. Schlechte J, Dolan K, Sherman B, Chapler F, Luciano A. The natural history of untreated hyperprolactinemia: a prospective analysis. J Clin Endocrinol Metab 1989;68:412-418
6. Vance ML, Evans WS, Thorner MO. Drugs five years later. Bromocriptine. Ann Intern Med 1984;100:78-91.
7. Molitch ME, Elton RL, Blackwell RE, Caldwell B, Chang RJ, Jaffe R, et al. Bromocriptine as primary therapy for prolactin-secreting macroadenomas: results of a prospective multicenter study. J Clin Endocrinol Metab 1985;60:698-705.
8. Webster J, Piscitelli G, Polli A, Ferrari C, Ismail I, Scanlon MF. A comparison of cabergoline and bromocriptine in the treatment of hyperprolactinemic amenorrhea. N Engl J Med 1994;331:904-909.
9. Abrahamson M, Snyder P. Treatment of hyperprolactin due to lactotroph adenomas and other causes. UpToDate [database]. Waltham, Mass: UpToDate; 2004.
10. Smith S. Effects of antipsychotics on sexual and endocrine function in women: implications in clinical practice. J Clin Psychopharmacol 2003;23(3 Suppl 1):S27-S32.
History and physical examination can distinguish among most physiologic, pharmacologic, or pathologic causes of an elevated serum prolactin level (SPL) (strength of recommendation [SOR]: C, expert opinion). Patients with unexplained elevations of serum prolactin or with a level above 200 ng/mL should undergo imaging of the sella turcica (SOR: C, expert opinion). Mildly elevated SPL due to physiologic causes may be managed expectantly (SOR: B, cohort studies) and pharmacologic elevations may be treated by discontinuing the causative medication (SOR: C, expert opinion). Elevated SPL due to pathologic causes requires both monitoring for complications and treatment of the underlying condition (SOR: C, expert opinion).
Dopamine agonists are effective for patients requiring drug treatment (SOR: B, systematic review of cohort studies), and cabergoline is more effective and better tolerated than bromocriptine (SOR: B, randomized controlled trial [RCT]). Surgery is reserved for symptomatic patients not controlled medically (SOR: C, expert opinion).
Patients with mildly elevated SPLs can be safely watched with testing and symptom monitoring
Allen Daugird, MD
University of North Carolina at Chapel Hill
Most elevated prolactin levels in my practice have been mild and often secondary to medication, though there are a host of causes, as listed in the TABLE. This Clinical Inquiry reassures us that patients with mildly elevated SPLs can be safely watched with serial testing and monitoring symptoms. Obtaining SPLs only on fasting specimens can help improve test accuracy. The feared risk of vision loss due to a macroadenoma seems to be quite small. Patients with significantly elevated SPLs with amenorrhea or infertility deserve referral to clinicians comfortable with using dopamine agonists because of the high rate of success with this treatment.
Evidence summary
An expert guideline recommends a history and physical examination to determine whether an elevated SPL is due to physiologic, pharmacologic, or pathologic causes (TABLE).1 The fasting morning SPL is least variable and correlates best with a disease state.1 Clinical correlation is necessary to reveal false positives (due to biologically inactive forms of prolactin) or false negatives (due to very high SPLs that exceed the ability of the assay). If an elevated SPL is suspected despite a normal laboratory report, retesting with serum diluted 1:100 can identify a false-negative value.2
A detailed drug history is important since drug-induced elevated SPL is common.1 Laboratory evaluation includes thyroid-stimulating hormone, blood urea nitrogen, and creatinine, as well as pregnancy testing when applicable. If no cause of elevated SPL is identified by initial clinical evaluation or if the SPL is greater than 200 ng/mL, experts recommend imaging of the sella turcica with computed tomography or magnetic resonance imaging.1
Physiologic causes. For patients with a mildly elevated SPL due to a physiologic cause, experts recommend expectant management. Patients should be monitored for symptoms of hypogonadism (amenorrhea, infertility, or sexual dysfunction) and have SPL measured at 6- to 12-month intervals.1 In cohort studies, treatment of the underlying cause of elevated SPL reverses secondary physiologic changes of low estrogen or testosterone, and hypogonadism.3-5
Pharmacologic causes. Eliminating a pharmacologic cause may lead to normalization of SPL, although experts recommend psychiatric consultation before discontinuing neuroleptic medications.1
Pathologic causes. Experts advise treating the underlying cause of a pathologic elevation of SPL. Patients with microadenoma should have SPLs monitored to prevent complications of decreased bone mineral density and sexual dysfunction due to persistently elevated SPL. Patients with a macroadenoma (>1 cm) are at risk for tumor growth and require serial imaging studies in addition to treatment of SPL, according to expert opinion.1-3
Medical therapy. Medical therapy with a dopamine agonist is indicated for patients with either symptoms of hypogonadism due to elevated SPL, or neurologic symptoms due to the size of a macroadenoma.1 In a review of 13 cohort studies, bromocriptine improved symptoms and reduced SPLs to normal for 229 of 280 women (82%).6 A cohort study of 27 patients with macroadenomas treated with bromocriptine found 10% to 50% reductions of tumor size.7 A randomized controlled trial treating 459 women having hyperprolactinemic amenorrhea with either cabergoline or bromocriptine achieved a stable normal SPL in 83% and 59%, respectively (P<.001). Adverse effects were common but were less common with cabergoline (68% vs 78%) and resulted in fewer discontinuations (3% vs 12%).8
Surgical therapy. Surgery is indicated for patients unresponsive to or intolerant of medical therapy, or who have visual field loss, cranial nerve palsy, or headache due to macroadenoma.1 A retrospective review of patients who underwent surgical resection found a 40% recurrence rate.9
Recommendations from others
Williams Textbook of Endocrinology includes the recommendations above and advises seeking consultation for patients with mass effects of macroadenomas such as visual field loss, cranial nerve palsy, or headaches; for patients with progressive elevation of SPL despite medical treatment; and for pregnant women.4 Conventional antipsychotic agents are commonly associated with elevated prolactin due to dopamine agonist activity. Some atypical antipsychotics may lead to lower levels of elevated prolactin, transient elevations or marked elevations.10 Experts recommend following serial SPLs, if antipsychotics are truly needed. Psychiatric consultation may assist in making decisions about medication selection. Patients with symptoms (galactorrhea, amenorrhea, headaches, visual disturbances, sexual dysfunction) or levels of 200 or more, should undergo an MRI or CT. Experts recommend monitoring levels every 1 to 3 months.1
TABLE
Physiologic, pharmacologic, and pathologic causes of an elevated serum prolactin level1
| PHYSIOLOGIC |
| Pregnancy |
| Ectopic pregnancy |
| Lactation |
| Nipple stimulation |
| Stress |
| Sleep disorder |
| PHARMACOLGIC |
| Dopamine receptor antagonists: phenothiazines, butyrophenones, thioxanthene, risperidone, metoclopramide, sulpiride, pimozide |
| Dopamine-depleting agents: α-methyldopa, reserpine |
| Hormones: estrogens, antiandrogens |
| Others: danazol, isoniazid, verapamil, cyproheptadine, opiates, H2-blockers (cimetidine), cocaine and marijuana, tricyclic antidepressants |
| PATHOLOGIC |
| Acromegaly |
| Alcoholic cirrhosis |
| Chest wall trauma or tumor |
| Herpes zoster |
| Hypothalamic and pituitary stalk disease |
| Hypothyroidism |
| Pituitary tumors: prolactinomas, adenomas |
| Polycystic ovarian syndrome |
| Renal failure |
| Sarcoidosis |
History and physical examination can distinguish among most physiologic, pharmacologic, or pathologic causes of an elevated serum prolactin level (SPL) (strength of recommendation [SOR]: C, expert opinion). Patients with unexplained elevations of serum prolactin or with a level above 200 ng/mL should undergo imaging of the sella turcica (SOR: C, expert opinion). Mildly elevated SPL due to physiologic causes may be managed expectantly (SOR: B, cohort studies) and pharmacologic elevations may be treated by discontinuing the causative medication (SOR: C, expert opinion). Elevated SPL due to pathologic causes requires both monitoring for complications and treatment of the underlying condition (SOR: C, expert opinion).
Dopamine agonists are effective for patients requiring drug treatment (SOR: B, systematic review of cohort studies), and cabergoline is more effective and better tolerated than bromocriptine (SOR: B, randomized controlled trial [RCT]). Surgery is reserved for symptomatic patients not controlled medically (SOR: C, expert opinion).
Patients with mildly elevated SPLs can be safely watched with testing and symptom monitoring
Allen Daugird, MD
University of North Carolina at Chapel Hill
Most elevated prolactin levels in my practice have been mild and often secondary to medication, though there are a host of causes, as listed in the TABLE. This Clinical Inquiry reassures us that patients with mildly elevated SPLs can be safely watched with serial testing and monitoring symptoms. Obtaining SPLs only on fasting specimens can help improve test accuracy. The feared risk of vision loss due to a macroadenoma seems to be quite small. Patients with significantly elevated SPLs with amenorrhea or infertility deserve referral to clinicians comfortable with using dopamine agonists because of the high rate of success with this treatment.
Evidence summary
An expert guideline recommends a history and physical examination to determine whether an elevated SPL is due to physiologic, pharmacologic, or pathologic causes (TABLE).1 The fasting morning SPL is least variable and correlates best with a disease state.1 Clinical correlation is necessary to reveal false positives (due to biologically inactive forms of prolactin) or false negatives (due to very high SPLs that exceed the ability of the assay). If an elevated SPL is suspected despite a normal laboratory report, retesting with serum diluted 1:100 can identify a false-negative value.2
A detailed drug history is important since drug-induced elevated SPL is common.1 Laboratory evaluation includes thyroid-stimulating hormone, blood urea nitrogen, and creatinine, as well as pregnancy testing when applicable. If no cause of elevated SPL is identified by initial clinical evaluation or if the SPL is greater than 200 ng/mL, experts recommend imaging of the sella turcica with computed tomography or magnetic resonance imaging.1
Physiologic causes. For patients with a mildly elevated SPL due to a physiologic cause, experts recommend expectant management. Patients should be monitored for symptoms of hypogonadism (amenorrhea, infertility, or sexual dysfunction) and have SPL measured at 6- to 12-month intervals.1 In cohort studies, treatment of the underlying cause of elevated SPL reverses secondary physiologic changes of low estrogen or testosterone, and hypogonadism.3-5
Pharmacologic causes. Eliminating a pharmacologic cause may lead to normalization of SPL, although experts recommend psychiatric consultation before discontinuing neuroleptic medications.1
Pathologic causes. Experts advise treating the underlying cause of a pathologic elevation of SPL. Patients with microadenoma should have SPLs monitored to prevent complications of decreased bone mineral density and sexual dysfunction due to persistently elevated SPL. Patients with a macroadenoma (>1 cm) are at risk for tumor growth and require serial imaging studies in addition to treatment of SPL, according to expert opinion.1-3
Medical therapy. Medical therapy with a dopamine agonist is indicated for patients with either symptoms of hypogonadism due to elevated SPL, or neurologic symptoms due to the size of a macroadenoma.1 In a review of 13 cohort studies, bromocriptine improved symptoms and reduced SPLs to normal for 229 of 280 women (82%).6 A cohort study of 27 patients with macroadenomas treated with bromocriptine found 10% to 50% reductions of tumor size.7 A randomized controlled trial treating 459 women having hyperprolactinemic amenorrhea with either cabergoline or bromocriptine achieved a stable normal SPL in 83% and 59%, respectively (P<.001). Adverse effects were common but were less common with cabergoline (68% vs 78%) and resulted in fewer discontinuations (3% vs 12%).8
Surgical therapy. Surgery is indicated for patients unresponsive to or intolerant of medical therapy, or who have visual field loss, cranial nerve palsy, or headache due to macroadenoma.1 A retrospective review of patients who underwent surgical resection found a 40% recurrence rate.9
Recommendations from others
Williams Textbook of Endocrinology includes the recommendations above and advises seeking consultation for patients with mass effects of macroadenomas such as visual field loss, cranial nerve palsy, or headaches; for patients with progressive elevation of SPL despite medical treatment; and for pregnant women.4 Conventional antipsychotic agents are commonly associated with elevated prolactin due to dopamine agonist activity. Some atypical antipsychotics may lead to lower levels of elevated prolactin, transient elevations or marked elevations.10 Experts recommend following serial SPLs, if antipsychotics are truly needed. Psychiatric consultation may assist in making decisions about medication selection. Patients with symptoms (galactorrhea, amenorrhea, headaches, visual disturbances, sexual dysfunction) or levels of 200 or more, should undergo an MRI or CT. Experts recommend monitoring levels every 1 to 3 months.1
TABLE
Physiologic, pharmacologic, and pathologic causes of an elevated serum prolactin level1
| PHYSIOLOGIC |
| Pregnancy |
| Ectopic pregnancy |
| Lactation |
| Nipple stimulation |
| Stress |
| Sleep disorder |
| PHARMACOLGIC |
| Dopamine receptor antagonists: phenothiazines, butyrophenones, thioxanthene, risperidone, metoclopramide, sulpiride, pimozide |
| Dopamine-depleting agents: α-methyldopa, reserpine |
| Hormones: estrogens, antiandrogens |
| Others: danazol, isoniazid, verapamil, cyproheptadine, opiates, H2-blockers (cimetidine), cocaine and marijuana, tricyclic antidepressants |
| PATHOLOGIC |
| Acromegaly |
| Alcoholic cirrhosis |
| Chest wall trauma or tumor |
| Herpes zoster |
| Hypothalamic and pituitary stalk disease |
| Hypothyroidism |
| Pituitary tumors: prolactinomas, adenomas |
| Polycystic ovarian syndrome |
| Renal failure |
| Sarcoidosis |
1. Biller BM, Luciano A, Crosignani PG, et al. Guidelines for the diagnosis and treatment of hyperprolactinemia. J Reprod Med 1999;44(12 Suppl):1075-1084.
2. Barkan AL, Chandler WF. Giant pituitary prolactinoma with falsely low serum prolactin: the pitfall of the “high hook effect”: Case report. Neurosurgery 1998;42:913-915.
3. Sanfilippo JS. Implications of not treating hyperprolactinemia. J Reprod Med 1999;44(12 Suppl):1111-1115.
4. Melmed S, Kleinberg D. Physiology and disorders of the pituitary hormone axes. In: Williams RH, Larsen PR. Williams Textbook of Endocrinology. 10th ed. Philadelphia, Pa: Saunders; 2003;200-212.
5. Schlechte J, Dolan K, Sherman B, Chapler F, Luciano A. The natural history of untreated hyperprolactinemia: a prospective analysis. J Clin Endocrinol Metab 1989;68:412-418
6. Vance ML, Evans WS, Thorner MO. Drugs five years later. Bromocriptine. Ann Intern Med 1984;100:78-91.
7. Molitch ME, Elton RL, Blackwell RE, Caldwell B, Chang RJ, Jaffe R, et al. Bromocriptine as primary therapy for prolactin-secreting macroadenomas: results of a prospective multicenter study. J Clin Endocrinol Metab 1985;60:698-705.
8. Webster J, Piscitelli G, Polli A, Ferrari C, Ismail I, Scanlon MF. A comparison of cabergoline and bromocriptine in the treatment of hyperprolactinemic amenorrhea. N Engl J Med 1994;331:904-909.
9. Abrahamson M, Snyder P. Treatment of hyperprolactin due to lactotroph adenomas and other causes. UpToDate [database]. Waltham, Mass: UpToDate; 2004.
10. Smith S. Effects of antipsychotics on sexual and endocrine function in women: implications in clinical practice. J Clin Psychopharmacol 2003;23(3 Suppl 1):S27-S32.
1. Biller BM, Luciano A, Crosignani PG, et al. Guidelines for the diagnosis and treatment of hyperprolactinemia. J Reprod Med 1999;44(12 Suppl):1075-1084.
2. Barkan AL, Chandler WF. Giant pituitary prolactinoma with falsely low serum prolactin: the pitfall of the “high hook effect”: Case report. Neurosurgery 1998;42:913-915.
3. Sanfilippo JS. Implications of not treating hyperprolactinemia. J Reprod Med 1999;44(12 Suppl):1111-1115.
4. Melmed S, Kleinberg D. Physiology and disorders of the pituitary hormone axes. In: Williams RH, Larsen PR. Williams Textbook of Endocrinology. 10th ed. Philadelphia, Pa: Saunders; 2003;200-212.
5. Schlechte J, Dolan K, Sherman B, Chapler F, Luciano A. The natural history of untreated hyperprolactinemia: a prospective analysis. J Clin Endocrinol Metab 1989;68:412-418
6. Vance ML, Evans WS, Thorner MO. Drugs five years later. Bromocriptine. Ann Intern Med 1984;100:78-91.
7. Molitch ME, Elton RL, Blackwell RE, Caldwell B, Chang RJ, Jaffe R, et al. Bromocriptine as primary therapy for prolactin-secreting macroadenomas: results of a prospective multicenter study. J Clin Endocrinol Metab 1985;60:698-705.
8. Webster J, Piscitelli G, Polli A, Ferrari C, Ismail I, Scanlon MF. A comparison of cabergoline and bromocriptine in the treatment of hyperprolactinemic amenorrhea. N Engl J Med 1994;331:904-909.
9. Abrahamson M, Snyder P. Treatment of hyperprolactin due to lactotroph adenomas and other causes. UpToDate [database]. Waltham, Mass: UpToDate; 2004.
10. Smith S. Effects of antipsychotics on sexual and endocrine function in women: implications in clinical practice. J Clin Psychopharmacol 2003;23(3 Suppl 1):S27-S32.
Evidence-based answers from the Family Physicians Inquiries Network