This document discusses hyperandrogenism and its diagnosis. It defines hyperandrogenism as androgen excess, which affects 5-10% of women. The most common cause is polycystic ovarian syndrome (PCOS), accounting for 80-85% of cases. Clinical signs of hyperandrogenism include hirsutism, acne, seborrhea and androgenic alopecia. The document outlines methods for diagnosing and evaluating hyperandrogenism, including the modified Ferriman-Gallwey scale for assessing hirsutism and various hormone tests and ultrasound criteria for diagnosing PCOS. Exclusion of related disorders like thyroid disease, Cushing's syndrome, and congenital adren
3. Hyperandrogenism
• Androgen excess
– Affects between 5 - 10% of women
in the reproductive age
• Poly-cystic Ovarian Syndrome (PCOS)
– Prevalence @ 80-85%
among women with androgen excess
O Bulent et al. Diagnosis of hyperandrogenism: clinical criteria. Best Practice & Research Clinical Endocrinology & Metabolism Vol. 20, No. 2, pp. 167–176, 2006
4. Hyperandrogenism
• There is considerable heterogeneity in clinical
findings among women with hyperandrogenism
• Clinical Phenotype could change over time even
in a single patient
O Bulent et al. Diagnosis of hyperandrogenism: clinical criteria. Best Practice & Research Clinical Endocrinology & Metabolism Vol. 20, No. 2, pp. 167–176, 2006
5. Clinical Manifestation of
Hyperendrogenism
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IRREGULAR
MENSES/
infertility
IRREGULAR HHAAIRIR L LOOSSSS
MENSES/
infertility
6. Clinical Signs of hyperandrogenism
• Hirsutism is a
common
manifestation of
hyperandrogenism
• Other clinical signs of
androgen excess include
* Acne,
* Seborrhea, and
* Androgenic alopecia. SAHA
O Bulent et al. Diagnosis of hyperandrogenism: clinical criteria. Best Practice & Research Clinical Endocrinology & Metabolism Vol. 20, No. 2, pp. 167–176, 2006
7. Clinical Signs of hyperandrogenism
• Depending on the
degree of
androgenization,
signs of
VIRILIZATION might
be observed in the
evaluation of a
patient with
hyperandrogenism
8. HIRSUTISM
• Excessive male-pattern - terminal
hair growth in women
• Affects up to 15% of women
• Results from androgen production
and/or sensitivity of the pilo-sebaceous
unit to androgens
O Bulent et al. Diagnosis of hyperandrogenism: clinical criteria. Best Practice & Research Clinical Endocrinology & Metabolism Vol. 20, No. 2, pp. 167–176, 2006
9. HIRSUTISM
• Observed in 70-80% of patients
with hyperandrogenism
• Leads to significant psychologic
morbidity and can negatively
influence the quality of life.
O Bulent et al. Diagnosis of hyperandrogenism: clinical criteria. Best Practice & Research Clinical Endocrinology & Metabolism Vol. 20, No. 2, pp. 167–176, 2006
12. Ferriman- Gallwey Scale
Modified Ferriman–Gallwey (F–G) hirsutism scoring system. Each of the nine body areas is rated from 0 (absence of
terminal hairs) to 4 (extensive terminal hair growth), and the numbers in each area are added for a total score. A
modified F–G score ≥ 6 generally defines hirsutism
O Bulent et al. Diagnosis of hyperandrogenism: clinical criteria. Best Practice & Research Clinical Endocrinology & Metabolism Vol. 20, No. 2, pp. 167–176, 2006
13. ACNE
• A common disorder of the Pilo-sebaceous
unit
• Commonly used classification - American
Academy of Dermatology, defines it as mild,
moderate and severe.
Yildiz BO: Diagnosis of hyperandrogenism: clinical criteria. Best Pract Res
Clin Endocrinol Metab 2006, 20(2):167-176
14. ACNE
• Evidence demonstrates a CLOSE ASSOCIATION
between Androgen & development of acne
• Has a MULTIFACTORIAL ETIOLOGY in which
androgens, skin lipids, inflammatory signals,
appear to be involved
Acne as an isolated symptom might not be
considered a sign of hyperandrogenism
Yildiz BO: Diagnosis of hyperandrogenism: clinical criteria. Best Pract Res Clin Endocrinol Metab
2006, 20(2):167-176
15. Types of Acne
Comedonal
(non-inflammatory)
Whitehead (closed): a
dilated hair follicle filled
with keratin, sebum, and
bacteria, with an
obstructed opening to the
skin.
Blackhead (open): a
dilated hair follicle filled
with keratin, sebum, and
bacteria, with a wide
opening to the skin capped
with a blackened mass of
skin debris.
Papulo-pustular
(inflammatory)
Papule:
Pustule:
Nodular
(inflammatory)
Nodule: bump
greater than
5mm in diameter.
17. Investigation Protocol
• Patients with severe
hirsutism and REGULAR
MENSES
– Testosterone
– DHEA-S
– Early morning 17-OH
progesterone
• Patients with severe
hirsutism and
IRREGULAR MENSES
– Testosterone
– DHEA-S
– Early morning 17-oH
progesterone
– FSH, LH & PRL
PELVIC USG TO BE IDEALLY PERFORMED
Davis S. Austr Fam Physician 1999;28:447-451
18. Summary
of Suggested Lab Test by
ACOG
Prolactin level
Testosterone level
LH and FSH
TSH
Fasting glucose level or 2 hr OGTT
Lipid profile, including total, LDL,HDL
17-hydroxyprogesterone level*
*--Fasting level to r/o CAH
19. Bio chemical and Diagnostic Markers of
PCOD
Accepted everywhere
– Elevated androgen (i.e. testosterone > 60 or free
testosterone >0.75) levels
– Elevated LH:FSH ratio > 2:1
– Increased Insulin levels ( Not needed)
– Insulin resistance , (Clinical / Lab)
Lab diagnosis of insulin resistance is not needed
–Ultrasound appearance of PCO
20. Ultrasound
Rotterdam Criteria
• In one or both ovaries
Ovarian volume
> 10 ml
• 12 follicles, 2-9 mm in diameter
• Echo dense stroma
Typical “Black Pearl” Necklace
21. Screening Tests For PCOD
ACOG Recommendation
• ACOG recommends that all women with a
suspected diagnosis of PCOD should be
screened with
17-hydroxyprogesterone
level to R/O late onset CAH (Level C).
• PCOD and late onset CAH are
distinguished from each other only by
laboratory testing.
22. A Lab Tests suggested for
SUDDEN onset of Hyperandrogenism
Test Result
Total testosterone level Slightly elevated in PCOS
Total testosterone > 200 ng/dL -- suspicious for adrenal or ovarian tumor
therefore additional evaluation with pelvic US, CT or MRI indicated
Serum DHEAS level Slightly elevated in PCOS
DHEAS level > 8 ng/ml -- suspicious for adrenal tumor therefore additional
evaluation should include adrenal gland imaging with CT or MRI
24 hour urine cortisol or overnight dexamethasone
Urine free cortisol >20 ug/d is suggestive of
Cushing’s Syndrome
23. PCOS – Diagnostic Criteria
NIH 19901 Rotterdam 20031 AE*-PCOS Society
20061,2
If both the criteria are
met:
•Chronic anovulation
•Clinical and/or
biochemical signs of
hyper-androgenism
(with exclusion of
other etiologies, e.g.,
congenital adrenal
hyperplasia)
If two of three
criteria are met:
•Oligo- and/or
anovulation
•Clinical and/or
biochemical signs of
hyperandrogenism
•Polycystic ovaries
*AE: Androgen Excess
If both the criteria are
met (after excluding
other androgen excess
or related disorders a):
•Clinical and/or
biochemical signs of
hyperandorgenism
•Ovarian dysfunction
(Oligo-anovulation
and/or polycystic
ovarian morphology)
NIH: National Institute of Health, AE-PCOS:
Androgen Excess- Polycystic Ovarian Syndrome
1. National institutes of health evidence-based methodology workshop on polycystic ovary syndrome december 3–5, 2012
2. Azziz et.al. The Androgen Excess and PCOS Society criteria for the polycystic ovary syndrome: the complete task force report , Fert. Stert.; 91(2): 456-
24. EExxcclluussiioonn ooff RReellaatteedd DDiissoorrddeerrss
• Thyroid disorders
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• Hyperprolactinemia
• Cushing’s syndrome
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• Late onset congenital adrenal hyperplasia (CAH)
• Basal morning 17-OHP,(2-3 ng/ml))
• Ovarian and adrenal tumors DHEAS
• WHO I &III –FSH,LH,E2
• Syndromes of severe insulin resistance(HAIRAN
syn)
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Editor's Notes
Presence of hirsutism is generally determined by the Ferriman–Gallwey hirsutism score. Ferriman and Gallwey described this subjective assessment, which scores the presence of hair growth between 0 (absence of terminal hairs) and 4 (extensive terminal hair growth) at 11 different body sites (upper lip, chin, chest, upper and lower back, upper and lower abdomen, arm, forearm, thigh, and lower leg).
Hatch et al18 suggested a method scoring 9 of the 11 body areas originally assessed by Ferriman and Gallwey, excluding the less androgen sensitive areas of lower legs and lower arms. A modified F–G score ≥ 6 generally defines hirsutism.
O Bulent et al. Diagnosis of hyperandrogenism: clinical criteria. Best Practice & Research Clinical Endocrinology & Metabolism Vol. 20, No. 2, pp. 167–176, 2006
Testosterone needed if considering treatment with antiandrogen for hisuitism as levels can then be followed.
DHEAS not needed.
Fasting morning 17-hydroxyprogesterone
Levels > 800 ng/dL (8ng/ml) highly suspicious for late-onset congenital adrenal hyperplasia (CAH)
Levels between 200-800 ng/dL (2-8ng/ml) unclear
Levels < 200 ng/dL (2ng/ml) usually no CAH
A ratio of less than 4.5 of fasting glucose to insulin levels correlates significantly with insulin resistance and has been studied for use as a screening test in obese patients with PCOS. Suggested only in selected patients. Information from Legro RS. Polycystic ovary syndrome: current and future treatment paradigms. Am J Obstet Gynecol 1998;179:S101-8.
A ratio of less than 4.5 of fasting glucose to insulin levels correlates significantly with insulin resistance and has been studied for use as a screening test in obese patients with PCOS
PCOS diagnostic criteria:
As per NIH (National Institute of Health) 19901: Chronic anovulation with clinical and/or biochemical signs of hyperandrogenism
As per Rotterdam 2003 classification1: two out of three of the following criteria?: Oligo/anovlaion, clinical and biochemical signs of hyperandrogensim and polycystic ovaries
As per Androgen-excess1,2: Clinical and or biochemical signs of hyperandrogenism with ovarian dysfunction however after excluding other androgen excess disorders.
National institutes of health evidence-based methodology workshop on polycystic ovary syndrome december 3–5, 2012
Azziz et.al. The Androgen Excess and PCOS Society criteria for the polycystic ovary syndrome: the complete task force report , Fert. Stert.; 91(2): 456-488