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Diagnostic Evaluation of Polycystic Ovary Syndrome in Adolescents - UpToDate
Diagnostic Evaluation of Polycystic Ovary Syndrome in Adolescents - UpToDate
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All topics are updated as new evidence becomes available and our peer review process is complete.
Literature review current through: Sep 2020. | This topic last updated: Jul 27, 2020.
INTRODUCTION
Polycystic ovary syndrome (PCOS) is the most common cause of infertility in women [1],
frequently becomes manifest during adolescence, and is primarily characterized by ovulatory
dysfunction and androgen excess (hyperandrogenism). The syndrome is heterogeneous
clinically and biochemically. The diagnosis of PCOS has lifelong implications with increased
risk for metabolic syndrome, type 2 diabetes mellitus, and possibly cardiovascular disease and
endometrial carcinoma. PCOS should be considered in any adolescent girl presenting with a
chief complaint of hirsutism, treatment-resistant acne, menstrual irregularity, acanthosis
nigricans, and/or obesity.
The diagnostic evaluation of an adolescent with suspected PCOS is described here. Other
aspects of PCOS in adolescents are reviewed separately:
● (See "Definition, clinical features, and differential diagnosis of polycystic ovary syndrome
in adolescents".)
● (See "Treatment of polycystic ovary syndrome in adolescents".)
● (See "Etiology and pathophysiology of polycystic ovary syndrome in adolescents".)
Work-up for PCOS is recommended for adolescent girls with one or more of the following
characteristics:
● Focal hirsutism (localized areas of excessive sexual hair growth), if this is accompanied by
menstrual abnormality
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Acanthosis nigricans and/or obesity are manifestations of insulin resistance and metabolic
syndrome and may be the presenting complaint of PCOS. Examination will usually reveal
some of the above classical symptoms or signs, but occasionally these may not develop for
some time. Thus, in the absence of risk factors for PCOS, such as a family history of PCOS, one
may choose to defer a work-up of these latter patients for PCOS and instead observe them for
the emergence of clinical evidence of PCOS over time. (See "Definition, clinical features, and
differential diagnosis of polycystic ovary syndrome in adolescents", section on 'Clinical
features'.)
EVALUATION OVERVIEW
We suggest a stepwise approach to the evaluation that addresses the diagnostic criteria (
table 2) [2]. This approach is first outlined here and then detailed in the sections below (
algorithm 1).
● Basic evaluation – The evaluation begins with a focused clinical evaluation for symptoms
and signs suggestive of PCOS: menstrual irregularity, hirsutism (or hirsutism equivalents,
such as acne), and acanthosis nigricans. This is followed by laboratory testing for
hyperandrogenemia, starting with measurement of total or free testosterone as outlined
in the algorithm ( algorithm 1). Elevated total or free testosterone levels are very
suggestive of PCOS. (See 'History and physical examination' below and 'Screening tests to
detect common causes of abnormal menses' below.)
Patients with elevated testosterone should be further evaluated with a screening panel of
laboratory tests to rule out other common non-PCOS causes of hyperandrogenemia (
algorithm 2) [3]. This evaluation excludes the vast majority of disorders that mimic
PCOS.
I also generally include ultrasonography of the ovaries and adrenal glands in the work-up
of hyperandrogenic females, primarily to evaluate for rare tumors of these organs. Some
other experts reserve the ultrasonographic screening for those patients with atypical
features suggestive of virilization, such as rapidly progressive hirsutism, clitoromegaly, or
hirsutism or menstrual abnormality that fails to respond to therapy. (See 'Screening tests
to exclude common non-PCOS causes of hyperandrogenemia' below.)
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● Further endocrine evaluation – The basic evaluation described above does not exclude
rare virilizing disorders ( table 3) [10-12]. In the presence of concern about the
possibility of a rare virilizing disorder, such as a tumor or rare congenital disorder, a more
comprehensive evaluation is suggested, including dexamethasone suppression testing
and cosyntropin testing, which determine the source of androgen ( algorithm 3). These
tests also help to exclude the possibility that a mild PCOS picture is due to obesity and
would be expected to respond to simple weight-control measures alone. This approach is
consistent with the hirsutism clinical practice guidelines from the Endocrine Society [12].
(See 'Further endocrine evaluation for rare disorders mimicking PCOS' below.)
● Additional evaluation after the diagnosis of PCOS – Girls diagnosed with PCOS should
have additional evaluations for glucose intolerance and other features of the metabolic
syndrome, particularly if they are obese. Primary relatives of PCOS patients may also
benefit from screening for these disorders. (See 'Additional evaluation of PCOS patients'
below and 'Evaluation of family members' below.)
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● Hirsutism – The degree and distribution of sexual hair growth should be documented
using the Ferriman-Gallwey score ( figure 1). An adult level of hirsutism ordinarily is
reached by two years after menarche [5]. Hirsutism should be interpreted in the context
of norms for the patient's ethnicity. Moderate or severe hirsutism (hirsutism score >15)
constitutes clinical evidence of hyperandrogenism in an adolescent [4-6]. The history
should specifically explore whether the patient shaves excess hair or uses depilatory
agents, which may obscure the physical findings, and whether the patient is taking
medications that cause hirsutism (eg, anabolic-androgenic steroids, valproic acid). (See
"Definition, clinical features, and differential diagnosis of polycystic ovary syndrome in
adolescents", section on 'Hirsutism'.)
● Acne – The degree of acne should be evaluated in the context of the patient's gynecologic
age. The possibility of hyperandrogenism is suggested by moderate or severe
inflammatory acne (>10 lesions in any area, eg, face, chest, back ( table 4)) through the
perimenarcheal years or acne that is persistent and poorly responsive to topical or oral
antibiotic dermatologic therapy [4-6]. (See "Definition, clinical features, and differential
diagnosis of polycystic ovary syndrome in adolescents", section on 'Acne'.)
● Menses – The age of menarche and subsequent menstrual patterns should be described
and interpreted in the context of the patient's gynecologic age. The types of menstrual
dysfunction that suggest abnormal degrees of anovulation in adolescence are detailed in
the table ( table 1) [2]. A menstrual pattern that is outside of these bounds for two
years (or one year with supporting evidence for PCOS) can be considered a "persistent"
abnormality and fulfills one of the two criteria for the diagnosis of PCOS [2,4-6]. Note that
normal menstrual regularity does not necessarily mean that ovulatory function is normal.
(See "Definition, clinical features, and differential diagnosis of polycystic ovary syndrome
in adolescents", section on 'Anovulation'.)
● Obesity and acanthosis nigricans – Obesity or acanthosis nigricans are often the initial
complaint, though not the only PCOS symptom elucidated upon review of systems and
examination. (See "Definition, clinical features, and differential diagnosis of polycystic
ovary syndrome in adolescents".)
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● Other – Assessment should include a history of medications that may either mask the
symptoms (eg, oral contraceptives and topical or systemic acne medications) or cause the
symptoms (eg, anabolic-androgenic steroids, valproic acid for epilepsy). Assessment
should also include evaluation for features that suggest a hyperandrogenic disorder other
than PCOS, including virilization (eg, rapidly progressive hirsutism), galactorrhea,
Cushingoid or acromegaloid changes, evidence of thyroid dysfunction, or a family history
of hyperandrogenic disorders ( algorithm 1). (See "Definition, clinical features, and
differential diagnosis of polycystic ovary syndrome in adolescents", section on 'Differential
diagnosis'.)
If a reliable testosterone assay is not available, the presence of moderate or severe hirsutism
is approximately 85 percent specific for hyperandrogenism and may be used as clinical
evidence for hyperandrogenism [4-6]. Mild hirsutism is a less reliable criterion for
hyperandrogenism because only approximately one-half of patients with mild hirsutism have
hyperandrogenemia, three-quarters of whom have a coincident menstrual abnormality [12].
Patients who have clinical features consistent with PCOS but have an initial normal total
testosterone level, should have repeat testing measuring an early-morning (8 AM) serum free
testosterone level in a reliable specialty laboratory by dialysis, or calculated from total
testosterone and sex hormone-binding globulin (SHBG).
The choice between testing for the presence of hyperandrogenemia with assay of total or free
testosterone depends on assay reliability and cost-effectiveness considerations [12]. If a
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reliable measurement of total testosterone is easily available, this can be used as an initial test
but should be followed by measurement of free testosterone if the results are not consistent
with the patient's clinical course. If a reliable method for measuring serum free (or
bioavailable) testosterone is available to the practitioner, and cost is not a significant issue,
this test is the preferred choice for initial testing.
There are many pitfalls in testosterone assays at the low levels found in women, and reliable
testosterone assays are not available to many clinicians. For these and other reasons
discussed below, assessment may be best deferred to a specialist.
● Total testosterone – Reliable total testosterone assays are critical to accurate assessment
for biochemical evidence of hyperandrogenism. This is important to obtain specificity for
testosterone versus other steroids that cross-react in assays at the relatively low levels
present in women and children. Their availability is limited to major specialty laboratories.
Liquid chromatography-mass spectrometry methods are becoming the preferred method
[13]. Where this technology is not available, high-quality postchromatographic
radioimmunoassays yield comparable results and are the method of choice [6].
The automated assays that are used to measure serum total testosterone in most
laboratories are not suitable to accurately measure levels in females [14,15]. Results by
the best available assays vary by an average of approximately 6 to 26 percent [11,16]. The
interpretation of the laboratory results is further complicated by systematic differences
between assays and excessively broad normal ranges derived from populations of
apparently normal women with unrecognized androgen excess.
● Free testosterone – An elevation of serum (or plasma) free testosterone is the single most
sensitive test to establish the presence of hyperandrogenemia [4,12,15,17,18].
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excess glucose and fructose intake themselves and inflammatory cytokines mediate
the SHBG reduction in patients with obesity [23].
• The most accurate free testosterone determinations come from specialty laboratories
using established, validated assays in well-characterized control women. This is
because lack of uniform assay methodology and standards introduces systematic
differences between assays.
• Direct assays of the serum free testosterone concentration are inaccurate and should
be avoided [12].
• The only reliable methods report free testosterone that is calculated as the product of
the total testosterone and a function of SHBG (free testosterone = total testosterone
× percent free testosterone) [12,24]. The most accurate methods calculate percent
free testosterone as determined by equilibrium dialysis or, alternatively, as calculated
from the SHBG concentration [25]. An alternative reliable method is to calculate
"bioavailable testosterone" by determining the percent of serum testosterone not
precipitated with globulins by ammonium sulfate (the supernatant includes both the
fraction free and that weakly bound to albumin, the latter being bioactive to the
extent that it dissociates to free in a given tissue space dependent upon the local
interstitial albumin concentration) [24].
For practical purposes, an elevated serum total and/or free testosterone at any time of day
provides evidence of hyperandrogenism in an anovulatory cycle. However, a normal level in
the afternoon does not exclude hyperandrogenemia. This is partly because serum
testosterone undergoes episodic changes of approximately twofold (trough-to-peak). It is also
partly because norms are standardized for early morning (8 AM) on days 4 through 10 of the
menstrual cycle in regularly cycling women as normal testosterone levels fall 10 percent from
8 AM to 4 PM and double during midcycle [27,28].
The estrogen and progestin contents of COCs interfere with the assessment of androgens.
They suppress gonadotropins, elevate SHBG, and directly inhibit steroidogenic enzymes such
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● Thyroid-stimulating hormone (TSH) – Normal serum TSH levels are ordinarily adequate
to rule out thyroid dysfunction, which causes menstrual dysfunction. Hypothyroidism may
cause confusion with hyperandrogenism by causing coarsening of hair (which can be
mistaken for hirsutism [5]), lowering SHBG, and causing multicystic ovaries.
Hyperthyroidism may confound the diagnosis of hyperandrogenism by raising SHBG,
which may elevate the total testosterone. Note that mildly elevated levels of TSH are often
found in obese individuals, but this is a consequence rather than a cause of the obesity
and is reversible if weight loss can be achieved. (See "Acquired hypothyroidism in
childhood and adolescence".)
tests should be considered only in those patients with suggestive clinical features of disorders
that may mimic PCOS [4,30-33]. Consequently, expert practice varies regarding the extent and
timing of further laboratory evaluation. In my practice, I routinely perform a simple screening
battery of endocrine tests and ultrasonography at this stage ( algorithm 2 and table 3).
Other experts perform these tests in selected patients with atypical features, such as
virilization (to rule out virilizing neoplasm), central obesity (to rule out Cushing syndrome), or
acromegaloid features.
Endocrine screening panel — In patients with PCOS, the following endocrine studies will
be normal. An abnormal result, however, for any of these tests suggests another cause of
hyperandrogenism (see "Definition, clinical features, and differential diagnosis of polycystic
ovary syndrome in adolescents", section on 'Differential diagnosis') and should be further
evaluated as suggested in the linked topic reviews.
• I also measure serum progesterone at the same time as the 17OHP measurement to
rule out the possibility that the patient has unexpectedly ovulated (which occurs in
approximately 10 percent of oligo-amenorrheic PCOS patients) and is unknowingly
being tested in the luteal phase of her cycle. The luteal phase is indicated by a serum
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progesterone >175 ng/dL (5.5 nmol/L) and can be accompanied by 17OHP levels up to
350 ng/dL (10.5 nmol/L).
• In those patients with known CAH that is complicated by PCOS (see "Etiology and
pathophysiology of polycystic ovary syndrome in adolescents", section on 'Congenital
virilization'), full glucocorticoid replacement treatment will suppress the 17OHP level
to normal, but androgen levels will remain slightly elevated. (See "Etiology and
pathophysiology of polycystic ovary syndrome in adolescents", section on 'Congenital
virilization'.)
● Other androgens – DHEAS is included primarily to screen for an adrenal tumor. Routine
testing for other androgenic steroids, such as androstenedione, has been of little
diagnostic utility in most populations [12]. It is a marker for adrenal hyperandrogenism
and has little diurnal variation. While the most common cause of DHEAS elevation is the
functional adrenal hyperandrogenism of PCOS [39], the main purpose of measuring
DHEAS levels is to rapidly identify an unusual virilizing adrenal disorder, such as cortisone
reductase deficiency [40,41] or an adrenal tumor. Girls with a virilizing tumor usually
present with a rapid onset of virilizing features, and DHEAS levels are often, but not
necessarily, markedly elevated (>700 mcg/dL, 19 micromol/L) if the tumor is of adrenal
origin. CAH seldom causes severe DHEAS elevation [39]. However, in a substantial
minority of patients with virilizing tumors, the symptoms are indolent in onset and mimic
PCOS in presentation (see "Definition, clinical features, and differential diagnosis of
polycystic ovary syndrome in adolescents", section on 'Differential diagnosis' and "Adrenal
hyperandrogenism"). COCs have equivocal effects on the DHEAS level. (See "Normal
adrenarche".)
● Prolactin – Prolactin should be measured at this stage if it was not done in the initial
panel of screening tests for abnormal menses. Androgen excess occurs in 40 percent of
hyperprolactinemic women due to multiple effects of prolactin excess on adrenal
androgen production and androgen metabolism, and the great majority (approximately
85 percent) of these women have galactorrhea [42]. The combination of hirsutism,
galactorrhea, and amenorrhea is sometimes described as Forbes-Albright syndrome.
Prolactin elevation is unusual in PCOS itself, occurring in less than 1 percent of subjects,
and marginal elevation in the absence of specific clinical evidence does not necessitate a
prolactinoma work-up [33,43]. Serum prolactin values more than 25 ng/mL usually have
an identifiable cause rather than PCOS [43]. Estrogenic medications increase prolactin
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secretion, but the amount of estrogen in low-dose COCs generally does not cause
hyperprolactinemia. (See "Definition, clinical features, and differential diagnosis of
polycystic ovary syndrome in adolescents", section on 'Differential diagnosis' and "Clinical
manifestations and evaluation of hyperprolactinemia".)
● Serum cortisol – Serum cortisol is an optional test that many experts perform only for
hyperandrogenic patients with central obesity. The purpose is to screen for endogenous
Cushing syndrome (due to adrenal hyperplasia or adrenal tumors), which is sometimes
associated with adrenal overproduction of testosterone. Although the normal range for
serum cortisol is wide (5 to 25 mcg/dL), a serum cortisol concentration of <10 mcg/dL (276
nmol/L) is reassuring evidence against endogenous Cushing syndrome. A midday or
afternoon sample is more optimal for this screening than an early-morning sample.
Patients with markedly elevated serum cortisol levels or those with clinical features
suggestive of Cushing disease warrant further evaluation (eg, with 24-hour urine
collection for free cortisol and creatinine). Estrogen raises total serum cortisol levels by
increasing cortisol-binding globulin, but low-dose COCs do not generally cause falsely
abnormal results. (See "Establishing the diagnosis of Cushing's syndrome".)
● Insulin-like growth factor 1 (IGF-1) – This is an optional test that many experts perform
only for hyperandrogenic patients with gigantism or acromegaloid features. Elevated IGF-
1 distinguishes growth hormone (GH) excess as a cause of hyperandrogenism [44] from
the pseudoacromegalic hyperandrogenism of severe insulin resistance syndromes [45].
GH excess usually can be identified by clinical symptoms (gigantism in growing children
or acromegaly after epiphyseal fusion) in teenagers and adults. However, the author has
seen acromegaly first present with PCOS-like symptoms. The oral estrogen of COCs may
lower IGF-1 levels sufficiently to obscure the diagnosis of acromegaly. (See "Diagnosis of
acromegaly".)
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endocrinology practice, I have recommended ovarian and adrenal ultrasonography for all
patients with anovulatory symptoms and documented hyperandrogenemia to exclude
rare but serious androgen-producing tumors, as described below. Other experts perform
ultrasonography only for selected patients with features that are atypical for PCOS, such
as very high testosterone levels (eg, >150 ng/dL), clitoromegaly, rapidly progressive
hirsutism, or poor response to treatment [47].
The primary purpose of ultrasonography is to screen for the rare but serious ovarian
tumor ( algorithm 2). In addition, other pelvic pathology, including an ovotesticular
disorder of sex development and the functional hyperandrogenism of pregnancy, may be
detected by ultrasonography. On rare occasions, ultrasonography has been insensitive in
detecting a virilizing ovarian tumor in adults [48,49]. It may also reveal a virilizing
adrenocortical tumor and, if there is reason to suspect this, more specialized imaging
studies are indicated (see "Clinical presentation and evaluation of adrenocortical
tumors"). Girls who have an ultrasound that shows an ovarian tumor or other explanation
for hyperandrogenism should be referred for further evaluation and treatment of the
underlying disorder. Otherwise, hyperandrogenic girls need further endocrine studies
irrespective of whether the ovaries are polycystic, as discussed in the section above. (See
'Endocrine screening panel' above.)
Ultrasonography also provides the opportunity for patient reassurance and education.
For many women, the diagnosis of ovarian "cysts" raises a concern about tumors, so it is
reassuring to know that a tumor has been ruled out by the ultrasound. The clinician can
explain to the PCOS patient with a polycystic ovary that these are numerous small egg
sacs that are not ovulating properly. Conversely, if a polycystic ovary is not visualized in a
PCOS patient, the clinician can explain that the ovarian dysfunction is "too mild to be seen
on the ultrasound."
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International consensus criteria for adults define PCOM on the basis of either excessive
size or follicle number (or both) in the absence of a dominant-sized follicle (>1 mL) or a
corpus luteum, as evaluated by transvaginal ultrasonography ( image 1) [32,51] (see
"Diagnosis of polycystic ovary syndrome in adults", section on 'Transvaginal ultrasound').
On the one hand, there is a high prevalence of PCOM in the most clinically severe PCOS
cases [50]. On the other hand, PCOM is a common normal variant in asymptomatic
women that may predict a slightly longer period of fertility [50]. Furthermore, it has
become apparent that these criteria are problematic in young adults because they
naturally have slightly larger ovaries [52], and the newer high-definition vaginal imaging
techniques show that small antral follicle counts up to 24 are normal [53].
Adult PCOM criteria are especially problematic when applied to adolescents [4,5]. For one
thing, an accurate antral follicle count cannot be defined by the abdominal
ultrasonographic approach necessary in virginal adolescents [53,54]. For another, even if
an accurate follicle count is obtained by magnetic resonance imaging (MRI), the adult
criteria for PCOM overlap with criteria for a multifollicular ovary. A multifollicular ovary is
defined by the presence of ≥6 follicles of 4 to 10 mm diameter without increase in ovarian
volume, and is known to be a normal variant unrelated to hyperandrogenism [4].
Additionally, studies suggest that ovarian volume is slightly larger in adolescents than in
adults, though data vary considerably [4,50,54]. Consequently, one-quarter to one-half of
normal adolescents meet adult criteria for PCOM [54,55]. In 2015, an international
consensus group proposed using an ovarian volume >12 mL to constitute PCOM in
adolescence [4]. However, this threshold may be too low since a study of 102 adolescents
with normal cycles found that 13 percent had PCOM by this criterion [56]. These findings
are consistent with the evidence that a mean ovarian volume (average of both ovaries) up
to 12 mL or a single ovarian volume up to 14 to 15 mL may be normal in adolescents
[5,50,54,55].
DIAGNOSIS
PCOS can be diagnosed in a patient with a persistently abnormal uterine bleeding pattern
and evidence of hyperandrogenism ( table 2) after exclusion of other causes of most non-
PCOS causes of hyperandrogenemia ( table 3). Most clinical guidelines recommend
screening for nonclassic congenital adrenal hyperplasia (NCCAH), Cushing's syndrome,
prolactin excess, thyroid dysfunction, and acromegaly. However, the guidelines vary as to
which tests are recommended for universal screening and which are recommended only for
patients with symptoms suggestive of one of these disorders. These guidelines are based on
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expert opinion. Therefore, the actual range of practice varies considerably among expert
clinicians in this field.
Adolescents with PCOS or with features of PCOS that do not fulfill diagnostic criteria should be
followed to determine that hyperandrogenemia and symptoms persist since data are limited
on the natural history of adolescent PCOS. The diagnosis of PCOS should not be fully
dismissed until menses normalize and androgen levels remain persistently normal.
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● A short (four-hour) DAST can be used to screen for an ovarian source of androgen in
obese women [11]. This consists of a noontime 0.5 mg oral dose of dexamethasone
followed by blood sampling four hours later for cortisol, DHEAS, and testosterone. A short
DAST is 95 percent sensitive for detecting the functional ovarian hyperandrogenism of
PCOS. Therefore, normal suppression of plasma testosterone by a short DAST rules out
PCOS with high probability. However, subnormal testosterone suppression in response to
a short DAST cannot be expected to distinguish virilizing disorders or Cushing's syndrome
from PCOS.
● A long (four-day) DAST is the definitive form of dexamethasone suppression testing for
the differential diagnosis of hyperandrogenic disorders.
virilizing tumor and adrenal rests must still be considered in the presence of
suggestive clinical factors.
● The cosyntropin (ACTH) stimulation test (using a 250 mcg dose, with samples drawn 30 to
60 minutes later) is interpreted as follows:
• A 17OHP value >1000 ng/dL (30 nmol/L) is highly suggestive, and >1500 ng/dL is
definitive for the 21-hydroxylase deficiency form of nonclassic congenital adrenal
hyperplasia (NCCAH) [57]. Intermediate 17OHP levels (1000 to 1500 ng/dL) require
genetic confirmation to make a definitive diagnosis of NCCAH [37,58]. (See "Diagnosis
and treatment of nonclassic (late-onset) congenital adrenal hyperplasia due to 21-
hydroxylase deficiency".)
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If both the DAST and the ACTH stimulation test are normal, obesity or idiopathic
hyperandrogenism is most likely. The most common cause of this may be the pseudo-PCOS of
obesity [11] (see "Definition, clinical features, and differential diagnosis of polycystic ovary
syndrome in adolescents", section on 'Differential diagnosis'). The rare possibility of cortisone
reductase deficiency should be considered on the basis of the clinical picture. (See
"Dexamethasone suppression tests" and "Initial testing for adrenal insufficiency: Basal cortisol
and the ACTH stimulation test".)
Ancillary tests
● Serum levels of anti-müllerian hormone (AMH) are mildly increased in subjects with
polycystic ovary morphology (PCOM; a category that includes both normal adolescents
and PCOS subjects) [55,62,63], while AMH elevations of twofold or more above the upper
normal limit are highly specific for PCOS [62]. AMH is a product of the granulosa cells of
small growing follicles that normally restrains follicular growth and sex steroid secretion
[64,65]; thus, it acts as an intraovarian paracrine gatekeeper to control the recruitment of
resting primordial follicles into the growth phase [55,62,63]. Androgen excess in the ovary
stimulates primordial follicle growth, causing an increase in antral follicle count that
contributes to PCOM. Thus, AMH levels are independently related on the one hand to the
size of the follicle pool ("follicle reserve" [62,66]) and PCOM (for which AMH has been
suggested as a surrogate for ultrasonographic criteria to define PCOM), and on the other
hand hyperandrogenism. (See "Etiology and pathophysiology of polycystic ovary
syndrome in adolescents", section on 'Primary functional ovarian hyperandrogenism'.)
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may facilitate the early diagnosis of PCOS in adolescents [69]. It also helps in determining
if mild PCOS is simply due to obesity, which is suggested when hyperandrogenemia is
mild, and serum luteinizing hormone (LH), AMH, and DHEAS, along with ovarian
morphology, are normal [11]. (See "Definition, clinical features, and differential diagnosis
of polycystic ovary syndrome in adolescents", section on 'Differential diagnosis' and
"Uncommon congenital adrenal hyperplasias", section on '3-beta-hydroxysteroid
dehydrogenase type 2 deficiency'.)
We advise screening for type 2 diabetes mellitus in adolescents with PCOS and obesity, or
other risk factors for diabetes mellitus. At the least, a fasting plasma glucose or hemoglobin
A1c should be measured. However, an oral glucose tolerance test (OGTT) is preferable
because it is the most sensitive and specific measure of glucose tolerance (see "Epidemiology,
presentation, and diagnosis of type 2 diabetes mellitus in children and adolescents", section
on 'Screening'). This recommendation is consistent with those made in an international
reproductive endocrinology consensus publication [72], the American Association of Clinical
Endocrinologists (AACE), and the minority position of the Androgen Excess and PCOS Society
(AE-PCOS) in adult women with PCOS [73,74]. The prevalence of diabetes was reported to be 2
percent based on the fasting blood sugar in one series, and 8 percent when based on OGTT
criteria in another series of adolescents [75,76]. In both series, almost all of the adolescents
had no symptoms of diabetes. Impaired glucose tolerance suggests insulin resistance and is a
risk factor for type 2 diabetes mellitus and cardiovascular disease. Thus, an abnormal OGTT
has important therapeutic implications. (See "Treatment of polycystic ovary syndrome in
adolescents", section on 'Obesity and insulin resistance'.)
adolescent and young women followed for a mean of 34 months, the two-hour plasma
glucose during an OGTT increased at an average rate of 9 mg/dL (0.5 mmol/L) per year [77].
Among the 14 women with PCOS and normal glucose tolerance at baseline, 55 percent
experienced deterioration of glucose tolerance when they were retested with an OGTT.
Among the 14 women with PCOS and impaired glucose tolerance at baseline, 29 percent
progressed to diabetes.
Patients should also be evaluated for quality-of-life issues. (See "Definition, clinical features,
and differential diagnosis of polycystic ovary syndrome in adolescents", section on
'Psychological issues'.)
PCOS is a risk factor for endometrial carcinoma in young women [78]. The basis of the risk is
multifactorial: it is related to the endometrial hyperplasia that arises from persistent estrogen
stimulation without the progesterone-induced inhibition of proliferation and differentiation to
secretory endometrium that occurs after ovulation. Hyperandrogenism, insulin-resistant
hyperinsulinemia, and the inflammatory changes of obesity appear to be aggravating factors
for endometrial carcinoma in women with PCOS; risk also seems related to body mass index
(BMI)-independent proto-oncogenic changes in endometrial cells [79]. (See "Clinical
manifestations of polycystic ovary syndrome in adults", section on 'Endometrial cancer risk'.)
Parents and siblings of PCOS patients are at increased risk for metabolic syndrome and
diabetes mellitus, particularly if they are obese. Screening can be accomplished by
measurement of hemoglobin A1c or oral glucose tolerance testing (OGTT) in first-degree
relatives of either sex. Premenopausal mothers and sisters are at risk for PCOS and should be
screened for those features.
These recommendations are prompted by the high prevalence of PCOS and metabolic
syndrome among immediate relatives of individuals with PCOS (see "Etiology and
pathophysiology of polycystic ovary syndrome in adolescents", section on 'Heritable traits').
According to one study, approximately one-half of sisters of PCOS probands have an elevated
serum testosterone level, and one-half of these (one-quarter of the total) in turn have
menstrual irregularity and thus meet National Institutes of Health (NIH) criteria for PCOS [80].
In another study, approximately one-quarter of sisters met the Androgen Excess and PCOS
Society (AE-PCOS) criteria for PCOS, having hyperandrogenism and a polycystic ovary,
although menses were ovulatory [81]. The likelihood of a mother having PCOS seems similar:
22 percent in our series [75].
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The prevalence of metabolic syndrome or diabetes mellitus in parents of women with PCOS is
higher than in parents of women without PCOS. In our series, one-third or more of mothers
and the great majority of fathers had metabolic syndrome and diabetes mellitus [75]. Notably,
the diabetes was asymptomatic in one-half and was uncovered by glucose tolerance testing.
Meta-analysis has demonstrated a significantly greater prevalence of type 2 diabetes mellitus
and insulin resistance in the parents of PCOS patients and a trend to diabetes and insulin
resistance in siblings [82].
OTHER RESOURCES
The following online resources are available to patients with PCOS and their families:
● PCOS resources for a healthier you – From the Center for Young Women's Health of
Boston Children's Hospital [83]
● Polycystic Ovary Syndrome: A Guide for Families – From the Pediatric Endocrine Society
(PES) and the American Academy of Pediatrics (AAP) [84]
Links to society and government-sponsored guidelines from selected countries and regions
around the world are provided separately. (See "Society guideline links: Polycystic ovary
syndrome" and "Society guideline links: Hirsutism".)
UpToDate offers two types of patient education materials, "The Basics" and "Beyond the
Basics." The Basics patient education pieces are written in plain language, at the 5th to 6th
grade reading level, and they answer the four or five key questions a patient might have
about a given condition. These articles are best for patients who want a general overview and
who prefer short, easy-to-read materials. Beyond the Basics patient education pieces are
longer, more sophisticated, and more detailed. These articles are written at the 10th to 12th
grade reading level and are best for patients who want in-depth information and are
comfortable with some medical jargon.
Here are the patient education articles that are relevant to this topic. We encourage you to
print or e-mail these topics to your patients. (You can also locate patient education articles on
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● Basics topic (see "Patient education: Polycystic ovary syndrome (The Basics)")
● Beyond the Basics topic (see "Patient education: Polycystic ovary syndrome (PCOS)
(Beyond the Basics)")
SUMMARY
● The evaluation for polycystic ovary syndrome (PCOS) begins with a focused clinical
evaluation for the presence of hirsutism (or hirsutism equivalents, such as acne that is
resistant to topical or oral antibiotic therapy) and menstrual abnormality ( table 1).
Some patients may present with a chief complaint of acanthosis nigricans or obesity
before the more classical manifestations develop. (See 'Indications for evaluation' above.)
● The clinical evaluation is followed by laboratory testing for common causes of abnormal
menses, including testing for androgen excess with total or free testosterone (
algorithm 1). (See 'History and physical examination' above and 'Screening tests to
detect common causes of abnormal menses' above.)
● If serum free testosterone levels are normal (in the absence of oral contraceptives), the
diagnosis of PCOS is unlikely. However, the possibility of PCOS in an adolescent should not
be fully dismissed until menses normalize and androgen levels are persistently normal.
(See 'Testing for hyperandrogenemia' above.)
● If serum levels of total and free testosterone are elevated, a focused history and physical
examination should be performed to exclude other hyperandrogenic disorders. Expert
practice varies regarding the extent and timing of further laboratory evaluation. In my
practice, I perform a simple screening battery of endocrine tests and ultrasonography at
this stage ( algorithm 2 and table 3). Other experts measure 17-
hydroxyprogesterone (at 8 AM) in many or all patients but perform the other screening
tests only in patients with atypical features, such as Cushingoid features, galactorrhea, or
virilization. (See 'Screening tests to exclude common non-PCOS causes of
hyperandrogenemia' above.)
• If the results of the endocrine screening panel are normal, the diagnosis of PCOS is
confirmed with a high level of certainty ( table 2). Any abnormal results suggest
that the hyperandrogenism is caused by a disorder other than PCOS. (See 'Endocrine
screening panel' above and 'Diagnosis' above.)
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• The primary purpose of ultrasonography is to exclude the rare but serious virilizing
ovarian tumor that can mimic PCOS. Determining whether the ovaries are polycystic
is not helpful for the diagnosis of PCOS, because of the high frequency of polycystic-
appearing ovaries in adolescents with or without PCOS. (See 'Ultrasonography'
above.)
● Once a diagnosis of PCOS has been established, it is important to identify and monitor for
abnormal glucose tolerance, type 2 diabetes, and other features of the metabolic
syndrome. This is because PCOS is a risk factor for the early development of these
disorders. Immediate family members are also at risk for these metabolic dysfunctions,
and premenopausal mothers and sisters are at risk for PCOS. (See 'Additional evaluation
of PCOS patients' above and 'Evaluation of family members' above.)
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