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HYPER-ANDROGENISM: 
UPDATE OF DIAGNOSIS 
ACNE Hirsutism Alopecia 
Dr. Sharda Jain 
Dr. Jyoti Agarwal 
Dr. Jyoti Bhaskar 
Dr. Abhishek Parihar
HYPER-ANDROGENISM: 
UPDATE OF DIAGNOSIS 
Review this Lecture at: 
Slideshare.net :
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
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
Clinical Manifestation of 
Hyperendrogenism 
AAccnnee 
AAccaannttoossisis HHirirssuuttisismm 
IRREGULAR 
MENSES/ 
infertility 
IRREGULAR HHAAIRIR L LOOSSSS 
MENSES/ 
infertility
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
Clinical Signs of hyperandrogenism 
• Depending on the 
degree of 
androgenization, 
signs of 
VIRILIZATION might 
be observed in the 
evaluation of a 
patient with 
hyperandrogenism
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
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
HIRSUITISM 
10% young girls have hirsutism 
In 60-70% - PCOS is the cause
HISUTISM
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
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
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
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.
Acne – 30% 
Severe -80% 
Moderate – 50% 
Mild - 30%
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
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
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
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
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.
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
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-
EExxcclluussiioonn ooff RReellaatteedd DDiissoorrddeerrss 
• Thyroid disorders 
SSrr..TTSSHH,,SSrr..PPrrll 
• Hyperprolactinemia 
• Cushing’s syndrome 
DDeexxaa ssuupprreessssiioonn tteesstt 
• 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)
ADDRESS 
11 Gagan Vihar, Near Karkari 
Morh Flyover, Delhi - 51 
CONTACT US 
9650588339, 011-22414049, 
WEBSITE : 
www.lifecarecentre.in 
www.drshardajain.com 
www.lifecareivf.com 
E-MAIL ID 
Sharda.lifecare@gmail.com 
Lifecarecentre21@gmail.com 
info@lifecareivf.com 
&

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HYPER - ANDROGENISM: UPDATE OF DIAGNOSIS , Dr. Sharda Jain Dr. Jyoti Agarwal Dr. Jyoti Bhaskar Dr. Abhishek Parihar

  • 1. HYPER-ANDROGENISM: UPDATE OF DIAGNOSIS ACNE Hirsutism Alopecia Dr. Sharda Jain Dr. Jyoti Agarwal Dr. Jyoti Bhaskar Dr. Abhishek Parihar
  • 2. HYPER-ANDROGENISM: UPDATE OF DIAGNOSIS Review this Lecture at: Slideshare.net :
  • 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 AAccnnee AAccaannttoossisis HHirirssuuttisismm 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
  • 10. HIRSUITISM 10% young girls have hirsutism In 60-70% - PCOS is the cause
  • 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.
  • 16. Acne – 30% Severe -80% Moderate – 50% Mild - 30%
  • 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 SSrr..TTSSHH,,SSrr..PPrrll • Hyperprolactinemia • Cushing’s syndrome DDeexxaa ssuupprreessssiioonn tteesstt • 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)
  • 25. ADDRESS 11 Gagan Vihar, Near Karkari Morh Flyover, Delhi - 51 CONTACT US 9650588339, 011-22414049, WEBSITE : www.lifecarecentre.in www.drshardajain.com www.lifecareivf.com E-MAIL ID Sharda.lifecare@gmail.com Lifecarecentre21@gmail.com info@lifecareivf.com &

Editor's Notes

  1. 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
  2. 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.
  3. 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
  4. 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