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Unidaddocentemfyclaspalmas.org.esAmenorrhea: Evaluation and Treatment
TARANNUM MASTER-HUNTER, M.D., University of Michigan Medical School, Ann Arbor, Michigan
DIANA L. HEIMAN, M.D., University of Connecticut School of Medicine, Hartford, Connecticut
A thorough history and physical examination as well as laboratory
testing can help narrow the differential diagnosis of amenorrhea.
In patients with primary amenorrhea, the presence or absence of
sexual development should direct the evaluation. Constitutional
delay of growth and puberty commonly causes primary amenorrhea
in patients with no sexual development. If the patient has normal
pubertal development and a uterus, the most common etiology is con-
genital outflow tract obstruction with a transverse vaginal septum or
imperforate hymen. If the patient has abnormal uterine development,
müllerian agenesis is the likely cause and a karyotype analysis should
confirm that the patient is 46,XX. If a patient has secondary amenor-
rhea, pregnancy should be ruled out. The treatment of primary and
secondary amenorrhea is based on the causative factor. Treatment
goals include prevention of complications such as osteoporosis, endo-
metrial hyperplasia, and heart disease; preservation of fertility; and, in
primary amenorrhea, progression of normal pubertal development.
(Am Fam Physician 2006;73:1374-82, 1387. Copyright 2006 Ameri-
can Academy of Family Physicians.)
A handout on amenor-rhea, written by the authors of this article, is provided on page 1387.
Primary amenorrhea can be diag- ination of patients with amenorrhea (Table 22,6-8). Many algorithms exist for the evalu- ondary sexual characteristics but ation of primary amenorrhea; Figure 11,7,9,10 no menarche by 16 years of age. If is one example. Laboratory tests and radi- a patient has no secondary sexual character- ography, if indicated, should be performed to evaluate for suspected systemic disease. If rhea can be diagnosed as early as 14 years of secondary sexual characteristics are present, age. Secondary amenorrhea is the absence pregnancy should be ruled out. Routine radi-of menses for three months in women with ography is not recommended, however.7 previously normal menstruation and for nine Figure 21-3,6 is an algorithm for the evalu- orrhea. Secondary amenorrhea is more com- is pregnancy. After pregnancy is ruled out, Pubertal changes typically occur over a the initial work-up should be based on three-year period and can be measured using patient history and physical examination Tanner staging.4 The normal progression of findings. Prolactin levels should be checked female puberty is illustrated in Table 1.4,5 in most patients. The risk of amenorrhea is The normal menstrual cycle involves a com- lower with subclinical hypothyroidism than plex interaction between the hypothalamic- with overt disease. However, the effects of pituitary-ovarian axis and the outflow tract. subclinical hypothyroidism on menstrua-Any disruption in this interaction can cause tion and fertility are unclear, and abnormal amenorrhea. thyroid hormone levels can affect prolactin levels; therefore, physicians should consider Evaluation
Physicians should conduct a comprehensive (TSH) levels.3,11,12 A study13 of 127 women patient history and a thorough physical exam- Downloaded from the American Family Physician Web site at www.aafp.org/afp. Copyright 2006 American Academy of Family Physicians. For the private, noncom- me rcA
r ioaf n
t he Web site. All other rights res w Amenorrhea
SORT: KEY RECOMMENDATIONS FOR PRACTICE
A female patient with primary amenorrhea and sexual development, including pubic hair, should be evaluated for the presence of a uterus and vagina. Women with secondary amenorrhea should receive pregnancy tests.
Women with polycystic ovary syndrome should be tested for glucose intolerance. A = consistent, good-quality patient-oriented evidence; B = inconsistent or limited-quality patient-oriented evidence; C = consensus, disease-oriented evidence, usual practice, expert opinion, or case series. For information about the SORT evidence rating system, see page 1313 or http://www.aafp.org/afpsort.xml. Table 1
Normal Female Pubertal Development
Elevation of papil a only; no pubic hair The rights holder did not grant the American Academy of Family Physicians the right to sublicense this material to a third party. For the missing item, see the original print version of this publication.
Information from references 4 and 5. April 15, 2006 ◆ Volume 73, Number 8 American Family Physician 1375
7.5 percent of participants had abnormal prolactin levels tive progestogen challenge test signifies an outflow tract and 4.2 percent had abnormal TSH levels. abnormality or inadequate estrogenization. An estrogen/ If TSH and prolactin levels are normal, a progestogen progestogen challenge test (Table 33,14) can differentiate challenge test (Table 33,14) can help evaluate for a patent the two diagnoses. A negative estrogen/progestogen chal-outflow tract and detect endogenous estrogen that is lenge test typically indicates an outflow tract obstruc-affecting the endometrium. A withdrawal bleed usually tion. A positive test indicates an abnormality within the occurs two to seven days after the challenge test.3 A nega- hypothalamic-pituitary axis or the ovaries. Table 2
History and Physical Examination Findings Associated with Amenorrhea
Exercise, weight loss, current or previous chronic il ness,
Previous central nervous system chemotherapy or radiation Psychosocial stressors; nutritional and exercise history Family history
Menarche and menstrual history (mother and sisters) Constitutional delay of growth and puberty Constitutional delay of growth and puberty Physical examination
Anthropomorphic measurements; growth chart
Constitutional delay of growth and puberty Dysmorphic features (e.g., webbed neck, short stature, Striae, buffalo hump, significant central obesity, easy bruising, hypertension, or proximal muscle weakness Transverse vaginal septum; imperforate hymen Undescended testes; external genital appearance; pubic hair Review of systems
Outflow tract obstruction or mül erian agenesis Galactorrhea; headache and visual disturbances Signs and symptoms of hypothyroidism or hyperthyroidism Information from references 2 and 6 through 8. 1376 American Family Physician
Volume 73, Number 8 ◆ April 15, 2006 Amenorrhea
Evaluation of Primary Amenorrhea
History and physical examination completed for a patient with primary amenorrhea Figure 1. algorithm for the evaluation of primary amenorrhea. (FSH = follicle-stimulating hormone; lH = luteinizing
Information from references 1, 7, 9, and 10. Gonadotropin levels can further help determine the are present, they should be removed because of the high source of the abnormality. Elevated follicle-stimulat- risk of malignant transformation after puberty.1 ing hormone (FSH) or luteinizing hormone (LH) levels If a patient has normal secondary sexual characteris- suggest an ovarian abnormality (hypergonadotropic tics, including pubic hair, the physician should perform hypogonadism). Normal or low FSH or LH levels suggest MRI or ultrasonography to determine if a uterus is a pituitary or hypothalamic abnormality (hypogonado- present. Müllerian agenesis (the congenital absence of tropic hypogonadism). Magnetic resonance imaging a vagina and abnormal uterine development [usually (MRI) of the sella turcica can rule out a pituitary rudimentary]) causes approximately 15 percent of pri-tumor. Normal MRI indicates a hypothalamic cause of mary amenorrhea.16 The etiology is thought to involve amenorrhea.3 embryonic activation of the antimüllerian hormone, causing malformation of the female genital tract.7,17 Differential Diagnosis of Primary Amenorrhea
Patients may have cyclic abdominal pain if there is endo- Causes of primary amenorrhea should be evaluated in the metrial tissue in the rudimentary uterus, mittelschmerz, context of the presence or absence of secondary sexual or breast tenderness. An absent or truncated vagina and characteristics. Table 43,6,15 includes the differential diag- an abnormal adult uterus confirm müllerian agenesis. Karyotype analysis should be performed to determine if the patient is genetically female.8 PRESENCE OF SECONDARY SExuAl CHARACTERISTICS
If the patient has a normal uterus, outflow tract If a patient with amenorrhea has breast development and obstruction should be considered. An imperforate hymen minimal or no pubic hair, the usual diagnosis is androgen or a transverse vaginal septum can cause congenital out-insensitivity syndrome (i.e., patient is phenotypically female flow tract obstruction, which typically is associated with but genetically male with undescended testes). A karyotype cyclic abdominal pain from blood accumulation in the analysis is needed to determine proper treatment. If testes uterus and vagina.1 If the outflow tract is patent, the April 15, 2006 ◆ Volume 73, Number 8 American Family Physician 1377
Evaluation of Secondary Amenorrhea
Patient presenting with secondary amenorrhea; negative pregnancy test Normal MRI: hypogonadotropic hypogonadism (Table 4) Figure 2. algorithm for the evaluation of secondary amenorrhea. (TSH = thyroid-stimulating hormone; MRI = magnetic
resonance imaging; FSH = follicle-stimulating hormone; lH = luteinizing hormone.) Information from references 1 through 3 and 6. physician should continue an evaluation similar to that stitutional delay of growth and puberty is indistinguish-for secondary amenorrhea (Figure 21-3,6).1 able from that associated with hypothalamic or pituitary failure.10 Watchful waiting is appropriate for constitu- AbSENCE OF SECONDARY SExuAl CHARACTERISTICS
tional delay of growth and puberty. Kallmann syndrome, Diagnosis of patients with amenorrhea and no second- which is associated with anosmia, also can cause hypogo- ary sexual characteristics is based on laboratory test nadotropic hypogonadism.18results and karyotype analysis. The most common cause Hypergonadotropic hypogonadism (elevated FSH and of hypogonadotropic hypogonadism (low FSH and LH LH levels) in patients with primary amenorrhea is caused levels) in primary amenorrhea is constitutional delay of by gonadal dysgenesis or premature ovarian failure. growth and puberty.16,17 A detailed family history also Turner’s syndrome (45,XO karyotype) is the most com-may help detect this etiology, because it often is familial. mon form of female gonadal dysgenesis. Characteristic Hypogonadotropic hypogonadism associated with con- physical findings include webbing of the neck, widely 1378 American Family Physician
Volume 73, Number 8 ◆ April 15, 2006 Amenorrhea
guidelines for Progestogen and Estrogen/Progestogen Challenge Tests
Progestogen challenge test
Medroxyprogesterone acetate (Provera)
Estrogen/progestogen challenge test
Conjugated equine estrogen (Premarin)
Information from references 3 and 14. spaced nipples, and short stature. Mosaicism occurs prolactinemia. Medications usually raise prolactin levels in approximately 25 percent of patients with Turner’s to less than 100 ng per mL.15 When hyperprolactinemia syndrome.19 These patients often have a more normal is not related to tumor, physicians should identify and phenotype with spontaneous onset of puberty and men- treat or eliminate the underlying cause. Table 43,6,15 lists arche. Other rare causes of pure gonadal dysgenesis can common etiologies of hyperprolactinemia.
occur with a 46,XY or XX karyotype.7 If asymptomatic microadenomas (smaller than 10 mm) are found on MRI, repeat prolactin measurements Differential Diagnosis of Secondary Amenorrhea
and imaging should be performed to monitor for pro- After pregnancy, thyroid disease, and hyperprolactinemia gression. Microadenomas are slow growing and rarely are eliminated as potential diagnoses, the remaining malignant. Treatment of microadenomas should focus causes of secondary amenorrhea are classified as nor- on management of infertility, galactorrhea, and breast mogonadotropic amenorrhea, hypogonadotropic hypo- discomfort. A dopamine agonist can help improve gonadism, and hypergonadotropic hypogonadism; each symptoms and fertility. Bromocriptine (Parlodel) is is associated with specific etiologies (Table 43,6,15). effective, but cabergoline (Dostinex) has been shown to be superior in effectiveness and tolerability.20 Mac- HYPOTHYROIDISM
roadenomas may be treated with dopamine agonists or Other clinical signs of thyroid disease are usually noted removed with transsphenoidal resection or craniotomy, before amenorrhea presents. Mild hypothyroidism is if necessary. more often associated with hypermenorrhea or oligo-menorrhea than with amenorrhea. Treatment of hypo- NORMOgONADOTROPIC AMENORRHEA
thyroidism should restore menses, but this may take Two common causes of normogonadotropic amenor-several months.12 rhea are outflow tract obstruction and hyperandrogenic chronic anovulation. The most common cause of out- HYPERPROlACTINEMIA
flow obstruction in secondary amenorrhea is Asherman’s A patient with markedly elevated prolactin levels, galac- syndrome (intrauterine synechiae and scarring, usually torrhea, headaches, or visual disturbances should receive from curettage or infection).3 Hysterosalpingography, imaging tests to rule out a pituitary tumor. Adenomas hysteroscopy, or sonohysterography can help diagnose are the most common cause of anterior pituitary dys- Asherman’s syndrome. Other causes of outflow tract function.15 A prolactin level more than 100 ng per mL obstruction include cervical stenosis and obstructive (100 mcg per L) suggests a prolactinoma, and MRI fibroids or polyps.
should be performed. If tumor is excluded as the cause, Polycystic ovary syndrome (PCOS) is the most com- medications (e.g., oral contraceptive pills, antipsychotics, mon cause of hyperandrogenic chronic anovulation. antidepressants, antihypertensives, histamine H2 block- The National Institutes of Health diagnostic criterion for ers, opiates) are the next most common cause of hyper- PCOS21 is chronic anovulation and hyperandrogenism April 15, 2006 ◆ Volume 73, Number 8 American Family Physician 1379
Causes of Amenorrhea
Nonclassic congenital adrenal hyperplasia Constitutional delay of growth and puberty* Severe depression or psychosocial stressors *—Causes of primary amenorrhea only. Information from references 3, 6, and 15. with no other identified secondary cause. The primary fivefold; therefore, testing for glucose intolerance should etiology of PCOS is unknown, but resistance to insulin be considered.21-24is thought to be a fundamental component.21 The primary treatment for PCOS is weight loss The diagnosis of PCOS is primarily clinical, although through diet and exercise. Modest weight loss can lower laboratory studies may be needed to rule out other causes androgen levels, improve hirsutism, normalize menses, of hyperandrogenism (Table 56,21). Significantly elevated and decrease insulin resistance. It may take months to testosterone or dehydroepiandrosterone sulfate levels see these results, however.21 Use of oral contraceptive indicate a possible androgen-secreting tumor (ovarian pills or cyclic progestational agents can help maintain or adrenal). Levels of 17-hydroxyprogesterone can help a normal endometrium. The optimal cyclic progestin diagnose adult-onset congenital adrenal hyperplasia. regimen to prevent endometrial cancer is unknown, Cushing’s disease is rare; therefore, patients should only but a monthly 10- to 14-day regimen is recommended.21 be screened when characteristic signs and symptoms Insulin sensitizing agents such as metformin (Gluco-(e.g., striae, buffalo hump, significant central obesity, phage) can reduce insulin resistance and improve ovula-easy bruising, hypertension, proximal muscle weakness) tory function.21,25,26 are present.21,22 Patients with PCOS have excess unopposed circulat- HYPERgONADOTROPIC HYPOgONADISM
ing estrogen, increasing their risk of endometrial cancer Ovarian failure can cause menopause or can occur pre-threefold.21 The insulin resistance associated with PCOS maturely. On average, menopause occurs at 50 years of increases a patient’s risk of diabetes mellitus two- to age and is caused by ovarian follicle depletion. Premature 1380 American Family Physician
Volume 73, Number 8 ◆ April 15, 2006 Amenorrhea
laboratory Evaluation of Hyperandrogenism
Serum testosterone (normal: 20 to 80 ng per dl [0.7 to 2.8 nmol per l])
≤ 200 ng per dL (6.9 nmol per L)
Consider hyperandrogenic chronic anovulation* Serum dehydroepiandrosterone sulfate (normal: 250 to 300 ng per dl [0.7 to 0.8 µmol per l])
≤ 700 ng per dL (1.9 µmol per L)
Consider hyperandrogenic chronic anovulation* Serum 17-hydroxyprogesterone (normal: < 2 ng per ml (6.1 nmol per l])†
> 4 ng per mL (12.1 nmol per L)
Consider adrenocorticotropic stimulation test to diagnose Dexamethasone suppression test (if clinically indicated)††
Morning cortisol level > 5 µg per dL (138 nmol per L)§
*— These values are not specific for diagnosis of hyperandrogenic chronic anovulation.
†—Morning level during fol icular phase of menstrual cycle.
††—For an overnight dexamethasone suppression test, the physician should administer a 1-mg dose of dexamethasone oral y between 11 p.m. and midnight and draw a single blood sample for serum cortisol testing at 8 a.m. the fol owing day. §—Morning cortisol level in a healthy patient with an intact hypothalamic-pituitary axis. There is some variability in the cutoff values that can affect sensitivity and specificity of the test. Patients should receive further testing to confirm Cushing’s disease. Information from references 6 and 21. ovarian failure is characterized by amenorrhea, hypoes- secretion and disruption of the hypothalamic-pituitary- trogenism, and increased gonadotropin levels occurring ovarian axis. The condition often is caused by excessive before 40 years of age and is not always irreversible27 weight loss, exercise, or stress. Other causes are listed (0.1 percent of women are affected by 30 years of age in Table 4.3,6,15 The mechanism of how stress or weight and one percent by 40 years of age).28 Approximately loss affects GnRH secretion is unknown.33-35 Treatment 50 percent of women with premature ovarian failure have of hypothalamic amenorrhea depends on the etiology. intermittent ovarian functioning29 with a 5 to 10 percent Women with excessive weight loss should be screened chance of achieving natural conception. for eating disorders and treated if anorexia nervosa or Women with premature ovarian failure have an bulimia nervosa is diagnosed. Menses usually will return increased risk of osteoporosis and heart disease.29-31 after a healthy body weight is acheived.35 The condition also can be associated with autoim- Young athletes may develop a combination of health mune endocrine disorders such as hypothyroidism, conditions called the female athlete triad that includes Addison’s disease, and diabetes mellitus.27,29 Therefore, an eating disorder, amenorrhea, and osteoporosis. Men-fasting glucose, thyroid-stimulating hormone (TSH), ses may return after a modest increase in caloric intake and, if clinically appropriate, morning cortisol levels or a decrease in athletic training. Similar to patients should be measured. Other laboratory testing should be with eating disorders, athletes with continued amenor-determined based on the individual patient.32 Approxi- rhea are at risk of bone loss. In adolescent athletes, the mately 20 to 40 percent of women with premature ovar- bone loss occurs during peak bone mass development ian failure will develop another autoimmune disorder; and may not be reversible.36,37 Weight-bearing exercise therefore, if initial laboratory tests are normal, periodic may partially protect against bone loss.38 screening should be considered. Patients younger than In patients with amenorrhea caused by eating disor- 30 years should receive a karyotype analysis to rule ders or excessive exercise, the use of oral contraceptive out the presence of a Y chromosome and the need for pills or menopausal hormone therapy may decrease removal of gonadal tissue.29 Ovarian biopsy and anti- bone turnover and partially reverse bone loss; however, ovarian antibody testing have not been shown to have neither therapy has been shown to significantly increase clinical benefit.27,29 bone mass.38 Bisphosphonates, traditionally used to treat postmenopausal osteoporosis, are possible terato- HYPOgONADOTROPIC HYPOgONADISM
gens and have not been studied as a therapy in women Hypothalamic amenorrhea is associated with abnor- of reproductive age. Adequate calcium and vitamin D malities in gonadotropin-releasing hormone (GnRH) intake are recommended for these patients. April 15, 2006 ◆ Volume 73, Number 8 American Family Physician 1381
The authors thank Barbara S. Apgar, M.D., M.S., for her assistance in the 15. Pickett CA. Diagnosis and management of pituitary tumors: recent 16. Folch M, Pigem I, Konje JC. Mül erian agenesis: etiology, diagnosis, and management. Obstet Gynecol Surv 2000;55:644-9.
17. Seldmeyer IL, Palmert MR. Delayed puberty: analysis of a large case TARANNUM MASTER-HUNTER, M.D., C.A.Q., is lecturer in the Department series from an academic center. J Clin Endo Metab 2002;87:1613-20.
of Family Medicine at the University of Michigan Medical School, Ann 18. Traggiai C, Stanhope R. Delayed puberty. Best Pract Res Clin Endocrinol Arbor. She received a medical degree from the University of Medicine and Dentistry of New Jersey-New Jersey Medical School in Newark. Dr. 19. Simpson J, Rajkovic A. Ovarian differentiation and gonadal failure. Am Master-Hunter completed a family practice residency at the University of 20. Webster J, Piscitel i G, Pol i A, Ferrari CI, Ismail I, Scanlon MF, et al. A comparison of cabergoline and bromocriptine in the treatment of DIANA L. HEIMAN, M.D., C.A.Q., is assistant professor in the Department hyperprolactinemic amenorrhea. N Engl J Med 1994;331:904-9.
of Family Medicine at the University of Connecticut School of Medicine, Hartford. She received a medical degree from Case Western Reserve 21. American Col ege of Obstetricians and Gynecologists. ACOG Practice Bul etin. Clinical management guidelines for obstetrician-gynecologists: University School of Medicine in Cleveland, Ohio. Dr. Heiman completed a number 41, December 2002. Obstet Gynecol 2002;100:1389-402.
family practice residency at the University of Virginia School of Medicine, Charlottesvil e.
22. Solomon CG. The epidemiology of polycystic ovary syndrome. Preva- lence and associated disease risks. Endocrinol Metab Clin North Am Address correspondence to Tarannum Master-Hunter, M.D., C.A.Q., Chelsea Family Practice, 14700 Old U.S. Hwy. 12, Chelsea, MI 48118 23. Chang RJ, Katz SE. Diagnosis of polycystic ovarian syndrome. Endocri- (e-mail: firstname.lastname@example.org). Reprints are not available from the nol Metab Clin North Am 1999;28:397-408, vi .
24. Mather KJ, Kwan F, Corenblum B. Hyperinsulinemia in polycystic ovary syndrome correlates with increased cardiovascular risk independent of Author disclosure: Nothing to disclose.
obesity. Fertil Steril 2000;73:150-6.
25. Velazquez E, Acosta A, Mendoza SG. Menstrual cyclicity after metformin REFERENCES
therapy in polycystic ovary syndrome. Obstet Gynecol 1997;90:392-5.
26. Kolodziejczyk B, Duleba AJ, Spaczynski RZ, Pawelczyk L. Metformin 1. The Practice Committee of the American Society for Reproductive Med- therapy decreases hyperandrogenism and hyperinsulinemia in women icine. Current evaluation of amenorrhea. Fertil Steril 2004;82(suppl 1): with polycystic ovary syndrome. Fertil Steril 2000;73:1149-54.
27. Anasti JN. Premature ovarian failure: an update. Fertil Steril 1998;70:1-15.
2. American Col ege of Obstetricians and Gynecologists. Amenorrhea 28. Kalantaridou S, Naka KK, Papanikolaou E, Kazakos N, Kravariti M, (ACOG Technical Bul etin 128). Washington, D.C.: ACOG, 1989. Calis KA, et al. Impaired endothelial function in young women with 3. Speroff L, Fritz MA. Amenorrhea. In: Clinical gynecologic endocrinol- premature ovarian failure: normalization with hormone therapy. J Clin ogy and infertility. 7th ed. Philadelphia, Pa.: Lippincott Wil iams & 29. Kalantaridou S, Davis SR, Nelson LM. Premature ovarian failure. Endo- 4. Marshall WA, Tanner JM. Variations in patterns of pubertal changes in crinol Metab Clin North Am 1998;27:989-1006.
girls. Arch Dis Child 1969;44:291-303.
30. van der Schouw Y, van der Graaf Y, Steyerberg EW, Eijkemans JC, Banga 5. Speroff L, Glass RH, Kase NG. Normal and abnormal sexual develop- JD. Age at menopause as a risk factor for cardiovascular mortality. Lan- ment. In: Clinical gynecologic endocrinology and infertility. 6th ed. Baltimore, Md.: Lippincott Wil iams & Wilkins, 1999:339-79. 31. Jacobsen BK, Nilssen S, Heuch I, Kvale G. Does age at natural meno- 6. Kiningham RB, Apgar BS, Schwenk TL. Evaluation of amenorrhea. Am pause affect mortality from ischemic heart disease? J Clin Epidemiol 7. Pletcher JR, Slap GB. Menstrual disorders. Pediatr Clin North Am 32. Kim TJ, Anasti JN, Flack MR, Kimzey LM, Defensor RA, Nelson LM. Rou- tine endocrine screening for patients with karyotypically normal sponta- 8. Reindol ar RH, Byrd JR, McDonough PG. Delayed sexual development: neous premature ovarian failure. Obstet Gynecol 1997;89(5 pt 1):777-9.
a study of 252 patients. Am J Obstet Gynecol 1981;140:371-80.
33. Mil er KK, Parulekar MS, Schoenfeld E, Anderson E, Hubbard J, Kliban- 9. McIver B, Romanski SA, Nippoldt TB. Evaluation and management of ski A, et al. Decreased leptin levels in normal weight women with hypo- amenorrhea. Mayo Clin Proc 1997;72:1161-9.
thalamic amenorrhea: the effects of body composition and nutritional 10. Albanese A, Stanhope R. Investigation of delayed puberty. Clin Endo- intake. J Clin Endocrinol Metab 1998;83:2309-12. 34. Welt CK, Chan JL, Bul en J, Murphy R, Smith P, DePaoli AM, et al. 11. Arojoki M, Jokimaa V, Juuti A, Koshinen P, Irajala K, Anttila L. Hypothy- Recombinant human leptin in women with hypothalamic amenorrhea. roidism among infertile women in Finland. Gynecol Endocrinol 2000; 35. Mitan LA. Menstrual dysfunction in anorexia nervosa. J Pediatr Adolesc 12. Kalro B. Impaired fertility caused by endocrine dysfunction in women. Endocrinol Metab Clin North Am 2003;32:573-92.
36. Drinkwater BL, Nilson K, Ott S, Chesnut CH III. Bone mineral density after 13. Laufer MR, Floor AE, Parsons KE, Kuntz KM, Barbieri RL. Hormone resumption of menses in amenorrheic athletes. JAMA 1986;256:380-2.
testing in women with adult onset amenorrhea. Gynecol Obstet Invest 37. Robinson TL, Snow-Harter C, Taaffe DR, Gil is D, Shaw J, Marcus R. Gym- nasts exhibit higher bone mass than runners despite similar prevalence 14. Warren MP, Bil er BM, Shangold MM. A new clinical option for hormone of amenorrhea and oligomenorrhea. J Bone Miner Res 1995;10:26-35.
replacement therapy in women with secondary amenorrhea: effects of 38. Hergenroeder AC, Smith EO, Shypailo R, Jones LA, Klish WJ, El is K. cyclic administration of progesterone from the sustained–release vagi- Bone mineral changes in young women with hypothalamic amenorrhea nal gel Crinone (4% and 8%) on endometrial morphologic features and treated with oral contraceptives, medroxyprogesterone, or placebo withdrawal bleeding. Am J Obstet Gynecol 1999;180(pt 1):42-8.
over 12 months. Am J Obstet Gynecol 1997;176:1017-25.
1382 American Family Physician
Volume 73, Number 8 ◆ April 15, 2006
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