Eating Disorders:
The Female Athlete Triad

According to Title IX of the Educational Assistance Act, any college that accepts federal funding must provide equal opportunities for women and men to participate in athletic programs. Last year marked the 25th anniversary of the passage of Title IX legislation, which dramatically increased the number of women who participate in sports at all competitive levels. Increased participation in exercise can result in a myriad of proven short- and long-term benefits. However, potential adverse health consequences are associated specifically with the overzealous female athlete. The family physician, who may recognize pathologic conditions that are related to exercise, usually has multiple opportunities to intervene.

Definitions and Prevalence

The female athlete triad is a combination of three interrelated conditions that are associated with athletic training: disordered eating, amenorrhea and osteoporosis. Patients with disordered eating may engage in a wide range of harmful behaviors, from food restriction to bingeing and purging, to lose weight or maintain a thin physique. Many athletes do not meet the strict criteria for anorexia nervosa or bulimia nervosa that are listed in the Diagnostic and Statistical Manual of Mental Disorders, 4th ed. (Table 1), but will manifest similar disordered eating behaviors as part of the triad syndrome.1

 Amenorrhea that is related to athletic training and weight fluctuation is caused by changes in the hypothalamus. These changes result in decreased levels of estrogen. Amenorrhea in the female athlete triad may be classified as primary or secondary. In patients with primary amenorrhea, there is no spontaneous uterine bleeding in the following situations: (1) by the age of 14 years without the development of secondary sexual characteristics, or (2) by the age of 16 years with otherwise normal development. Secondary amenorrhea is defined as the six-month absence of menstrual bleeding in a woman with primary regular menses or a 12-month absence with previous oligomenorrhea.

Osteoporosis is defined as the loss of bone mineral density and the inadequate formation of bone, which can lead to increased bone fragility and risk of fracture. Premature osteoporosis puts the athlete at risk for stress fractures as well as more devastating fractures of the hip or vertebral column. The morbidity associated with osteoporosis is significant, and lost bone density may be irreplaceable.

Although the exact prevalence of the female athlete triad is unknown, studies have reported disordered eating behavior in 15 to 62 percent of female college athletes. Amenorrhea occurs in 3.4 to 66 percent of female athletes, compared with only 2 to 5 percent of women in the general population.2-7 Some components of the female athlete triad are often undetected because of the secretive nature of disordered eating behavior and the commonly held belief that amenorrhea is a normal consequence of training.

Recognition of Risk Factors

The development of poor self-image and pathogenic weight control behaviors in the female athlete may be caused by many factors. Frequent weigh-ins, punitive consequences for weight gain, pressure to "win at all costs," an overly controlling parent or coach, and social isolation caused by intensive involvement in sports may increase an athlete's risk. Societal perpetuation of the ideal body image may intensify the endeavor for a thin physique. Athletic endeavors such as gymnastics, figure skating, ballet, distance running, diving and swimming that emphasize low body weight and a lean physique can also increase the risk of developing the female athlete triad.2,4

Prevention

Prevention of the female athlete triad through education is crucial. Coaches, parents and teachers are often unaware of the impact they have on athletes. During adolescence and young adulthood, these athletes may receive comments or instructions that seem to encourage or demand maladaptive patterns of diet and exercise. According to one small study,2 75 percent of female college gymnasts who were told by their coaches that they were overweight used pathogenic behaviors to control their weight. The physician may recognize such patterns and be able to intervene before the development of the female athlete triad.

Screening

The optimal time to screen athletes for the female athlete triad is during the preparticipation sports physical examination. The physician might also screen for the triad during acute visits for fractures, weight change, disordered eating, amenorrhea, bradycardia, arrhythmia and depression, and also during visits for routine Papanicolaou smears.8

A history of amenorrhea is one of the easiest ways to detect the female athlete triad in its earliest stages. Evidence suggests that menstrual history may predict current bone density in female athletes.9 In a study of young female athletes, longer, more consistent patterns of amenorrhea were found to have a linear correlation with measures of bone density. Amenorrhea should not be discounted by the family physician as a benign consequence of athletic training. During preparticipation physical examinations at the University of California, Los Angeles, most women whose menstruation had stopped for three months or more had been told by their family physicians that amenorrhea was normal in athletes.10

While taking a patient's history, especially when asking about disordered eating practices, the physician should focus initially on the past. The patient may feel less threatened when discussing past eating behaviors. Patients are more likely to confirm that they have previously induced vomiting or used laxatives than to admit to current disordered eating patterns. A screening history for the female athlete triad is outlined in Table 2.

Diagnosis

In the beginning, the symptoms of the female athlete triad may be subtle. On physical and laboratory examination, however, the presence of symptoms such as fatigue, anemia, electrolyte abnormalities or depression caused by dieting may alert the physician to the diagnosis.5 Some of the most common signs and symptoms of disordered eating in the female athlete triad are listed in Table 3.

Amenorrhea secondary to excessive exercise is not a clinical diagnosis, nor one that can be made by laboratory testing. It is a diagnosis of exclusion. A history and physical examination should be completed for every female athlete with amenorrhea to rule out other treatable causes. The differential diagnosis of amenorrhea is listed in Table 4. Recently published review articles discuss the differential diagnosis and evaluation of amenorrhea in further detail.11

There is a lack of published evidence to guide the physician in the cost-effective use of bone density testing for female athletes who are at risk for osteoporosis. Osteoporosis is defined as bone density 2.5 standard deviations below normal for the patient's age.8 Early studies of osteoporosis in female athletes focused on the loss of bone mineral density in the vertebral column.12 In recent studies, prolonged amenorrhea was found to affect multiple axial and appendicular skeletal sites, including those that were subjected to impact loading during exercise.12,13 Because the risk of bone loss increases with the duration of amenorrhea, a dual energy x-ray absorptiometry (DEXA) scan or similar study should be considered in athletes with amenorrhea lasting at least six months.

A position paper published by the American College of Sports Medicine recommends that short-term amenorrhea be considered a warning symptom for the female athlete triad and suggests medical evaluation within the first three months.8 At the time of examination, the patient should be educated about the risks of irreplaceable bone loss that can occur after only three years of amenorrhea. Documentation of the loss of bone density may enhance patient compliance with recommendations for changes in eating behaviors and training regimens, and may convince the patient to start estrogen replacement therapy.14

Prognosis

Preservation of bone mineral density is one of the many reasons to screen female athletes and diagnose the female athlete triad early in its course. Postmenopausal women lose most of their bone mass and density in the first four to six years after menopause. If this is also true of amenorrheic athletes, intervention is needed before bone mass is irreversibly lost.9

Recent studies indicate that peak bone mass occurs at a younger age than was previously believed. Several studies have shown that the average age of peak bone mass is closer to 18 to 25 years rather than the currently accepted age of 30 years.15-18 If this is true, efforts to affect females with delayed or interrupted menses should begin during adolescence.

One study evaluated previously amenorrheic women who had resumed normal menses. After the first 14 months, their bone mineral density increased by an average of 6 percent. However, this trend did not continue. The rate of increase slowed to 3 percent the following year and reached a plateau at a bone mineral density that was well below the normal level for their age.9 Again, this finding shows the paramount importance of early intervention in preventing irreversible loss of bone mineral density.

Severe disordered eating patterns may put the athlete at risk for more significant morbidity or even death. In nonathletes, the mortality rate in treated anorexia nervosa can range from 10 to 18 percent.7 Even though most women with the triad do not meet strict criteria for anorexia or bulimia, they still appear to have a greater risk of mortality than that of the general population.7

Treatment

In addition to having a fundamental role in the diagnosis of the female athlete triad, the family physician has an integral part in coordinating the management of this condition. While a multidisciplinary approach to treatment has not been studied, many patients may benefit from a treatment plan that involves consultation with subspecialists. Involvement of a psychiatrist or psychologist and a dietician who specialize in the management of the female athlete triad may facilitate prompt improvement. Often, athletic trainers or coaches are the persons closest to the athlete. Their insights and support may be crucial to the success of any treatment plan.

Lifestyle Changes
Optimal treatment of the female athlete triad includes instruction from a dietician to educate and monitor the patient for adequate nutrition and to help the patient attain and maintain a goal weight. The patient, dietician and physician should agree on a goal weight, with consideration for the weight requirements for participation in the patient's chosen sport. A weight gain of 0.23 to 0.45 kg (0.5 to 1 lb) per week until the goal weight is achieved is a reasonable expectation. Helping the patient focus on optimal health and performance instead of weight is important. The patient need not stop exercising completely. Exercise activity should be decreased by 10 to 20 percent, and weight should be monitored closely for two to three months. 5

Hormone Replacement Therapy
No published longitudinal studies are available on the long-term benefits of hormone replacement therapy (HRT) to slow or reverse the loss of bone mineral density in these young women. Most of the evidence for the use of HRT has been extrapolated from data that support its use in postmenopausal women. Both oral contraceptives and cyclic estrogen/ progesterone have been used to treat amenorrhea of the triad. While hormonal therapy will treat the amenorrhea, the ultimate goal is the return of regular menses through proper nutrition, revised training regimens and maintenance of reasonable body weight.

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One retrospective study of amenorrheic runners compared hormonal therapy with placebo over 24 to 30 months. The regimen included either conjugated estrogen in a dosage of 0.625 mg per day or an estradiol transdermal patch in a dosage of 50 µg per day. Both were given in combination with medroxyprogesterone in a dosage of 10 mg per day for 14 days per month. Patients receiving hormonal therapy showed a significant increase in bone mineral density, while those in the control group showed nonsignificant decreases of less than 2.5 percent.19 Small studies have also supported the use of oral contraceptives in persons with athletic amenorrhea.20 Retrospective studies have shown that athletes with a history of oral contraceptive use may have a decreased risk of stress fracture.13,21

While little direct evidence is available on the appropriate timing for initiation of HRT, considering hormone therapy after six months of amenorrhea seems prudent. Irreversible bone loss can occur after only three years of amenorrhea.6 Patients who already have evidence of early bone mineral density loss (osteopenia) on the basis of bone densitometry/DEXA scanning should be strongly encouraged to start hormonal therapy.

Estrogen may be replaced in a variety of ways. Oral contraceptives are frequently used and are advantageous if birth control is also desired. Hormone replacement regimens as prescribed for postmenopausal women are also feasible options. No single treatment regimen has been proved to be the most beneficial for the female athlete triad. Some options for estrogen replacement therapy are listed in Table 5.5,22 Progesterone should be included in any treatment regimen to prevent the endometrial hyperplasia that can result from use of unopposed estrogen.

Additional Pharmacotherapy
Research has shown that athletes who had a higher incidence of stress fractures also had lower calcium intakes and less frequent use of oral contraceptives.11 The recommended dietary allowance of calcium is 1,200 to 1,500 mg per day for females between 11 and 24 years of age.23 Surveys of females between 12 and 19 years of age have shown an inadequate average daily calcium intake of less than 900 mg per day.23 Additional daily supplementation of 400 to 800 IU of vitamin D will also facilitate the absorption of calcium. Treatments for osteoporosis, such as bisphosphonates and calcitonin, have not been tested specifically in younger patients with the female athlete triad. However, the physician should consider all available treatment options for athletes with frank osteoporosis on the basis of DEXA scanning (more than 2.5 standard deviations below age-specific norms). Options for the treatment of osteoporosis have been discussed in detail in a number of recent review articles.24,25

Depending on the severity of the eating disorder, a selective serotonin reuptake inhibitor (SSRI) may be indicated for treatment of a specific disorder. Benzodiazepines have also been suggested by one author for the treatment of a patient with severe mealtime anxiety.26 A psychiatric evaluation may help with the assessment of depression or eating disorders, and with the selection of medications.

Family Involvement Involvement of the family is crucial to the success of treatment. Family members should be included in treatment plans from the beginning, particularly with adolescent patients. Although at first the physician's intervention may appear to be detrimental to the child's athletic career, education about the significance of the female athlete triad may motivate parents to participate in a treatment program.

The Authors

JULIE A. HOBART, M.D., is residency faculty and assistant professor of family medicine at the University of Cincinnati/Mercy­Franciscan Hospitals Family Medicine Residency Program, Cincinnati, Ohio. Dr. Hobart received her medical degree from Ohio State University College of Medicine, Columbus, and completed a residency in family medicine and a faculty development fellowship at the University of Cincinnati/Franciscan Hospitals.

DOUGLAS R. SMUCKER, M.D., M.P.H., is assistant professor and codirector of research in the Department of Family Medicine at the University of Cincinnati College of Medicine. Dr. Smucker completed his medical degree and served a residency in family practice at the Medical College of Ohio in Toledo. He also completed a primary care research fellowship and a residency in preventive medicine at the University of North Carolina at Chapel Hill School of Medicine.

REFERENCES

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Julie A. Hobart, M.D., and Douglas R. Smicker, M.D., M.P.H.

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