Polycystic ovarian syndrome (PCOS) is one of the most common endocrine disorders in women of reproductive age, affecting 5-10% of women. It is characterized by hyperandrogenism, chronic anovulation, and polycystic ovaries. PCOS increases the risk of metabolic syndrome, diabetes, cardiovascular disease, and endometrial cancer. Treatment involves lifestyle modifications like weight loss and exercise. Pharmacological treatments include combined oral contraceptives to regulate menstrual cycles and metformin to reduce insulin resistance. PCOS management may involve specialists like gynecologists, endocrinologists, and dietitians.
2. Dermatologist
Disorder of
hair growth,
Acne
Fertility problem
Menstrual
dysfunctionGynecologist
Obesity problem
Risk of DM II
Risk of CVS
disorderInternist
General
practitioner
?
PREVALANCE:
5-10% IN 20-40 YR
FEMALES
3. • 1st described by Irving Stein and Michael Leventhal
(1935) as a triad of amenorrhea, obesity and hirsutism
• One of the most common endocrine disorders
occurring in women
4. Definition of PCOS
ESHRE (European Society for Human Reproduction) &
ASRM (American Society of Reproductive Medicine) 2003
2 of the 3 elements:
– Hyperandrogenism
(clinical or biochemical)
– Chronic anovulation
– Polycystic ovaries
(with exclusion of other etiologies)
5. OTHER ETIOLOGIES
• Hypothyroidism
• Hyperprolactinemia
• Nonclassic congenital adrenal hyperplasia
• Cushing’s syndrome
• Androgen-secreting neoplasm
• Acromegaly
• Drugs-related (androgens, valproic acid, cyclosporine, or other drugs).
11. Hirsutism
(excessive growth of thick, dark terminal hair in women where hair growth is normally
absent)
Modified Ferriman-Gallwey scoring system
0-36
Mild <4
Moderate 4-7
Severe ≥8
1.Upper Lip
2.Chin
3.Chest
4.Upper Back
5.Lower Back
6.Upper
Abdomen
7.Upper Arm
8.Forearm
9.Thigh /Leg
16. Infertility
• >75% of women with anovulatory infertility
•Follicular arrest
– Impaired selection of dominant follicle
Ovulation
PCOS
No ovulation
Infrequent ovulation
24. The Metabolic Syndrome and
PCOS
• 43-46%
NCEPATP III
Hypertension Current antihypertensive therapy
and/or BP>130/85mmHg
Dyslipidemia Plasma Triglyceride level
>150mg/dl and/or HDL level <50
mg/dl
Obesity Waist Circumference >88cm
Glucose Fasting Blood Glucose level
>110mg/dl
Requirements for Diagnosis Any 3 of the above disorders
25. Body Image and Quality of Life
Obesity and infertility cause the greatest degree o
stress
• Anorexia nervosa
• Bulimia
• Pelvic pain
• Depression
• Psychosexual dysfunction
29. Diagnostic tests for exclusion
• Thyroid function test
• Serum Prolactin
• 17- alpha OH Progesterone
(CAH)
30. Screening test
repeat at 6 months for borderline risk and two year for normal profiles
Lipid profile
Fasting glucose / OGTT
31. Other
• Insulin resistance (IR)
– Fasting insulin >25 µIU/ml
– Fasting glucose: insulin
< 4.5 indicate IR in adult obese PCOS
<7 useful index of IR in adolescents
Test for IR not necessary to diagnose PCOS or to select any treatment
33. Adolescents
• Menstrual irregularity persists beyond two years of menarche
• Minimal diagnosis of PCOS
Include 5 tests
1. Serum total testosterone (cut off 60 ng/dL)
2. OGTT (at zero and two hours after 75 g glucose load)
3. Serum 17– hydroxy progesterone (assessed at 8 am)
4. Serum TSH
5. Serum prolactin levels
• Serum LH, FSH and cortisol as indicated
38. • inducing withdrawal bleed every 3 to 4 months
with progestogens - reduce the risk
• hyperinsulinemia is the primary cause of
endometrial hyperplasia - use of insulin
sensitizers can reduce the hyperplasia
39. withdrawal bleed every 3 to 4 months
reduce the risk of endometrial cancer
hyperinsulinemia is the primary cause of endometrial
hyperplasia
insulin sensitizers can reduce the hyperplasia
40. COMBINED ORAL CONTRACEPTIVES
first-line agents in women not willing to conceive
Menstrual irregularities
Hirsutism
Acne (androgenic/refractory/nodulocystic)
42. US FDA 2012
• OCPs containing drospironone associated with 3 times higher risk of
VTE compared with COCs containing levonorgestrel (Mala N, Mala
D, Loette )
• Assess risk of VTE before starting drospironone containing COC
• Do not use if history of thromboembolism (in family or self)
43. METFORMIN
• Mechanism - Inhibits hepatic glucose production.
Reduces insulin resistance and secretion
Directly inhibits ovarian steroidogenesis
Reduces T, free T, A4, DHEAS, LH,
Waist to hip ratio, BMI, BP
Increases FSH, SHBG
• Use – IGT
IR
DM
• 1500mg-2500mg/day, at least 3 months.
44. Adolescents
• lifestyle modification - first-line therapy
• Low dose COCs (with or without anti-androgenic progestins drospirenone
and desogestrel) for the management of MI
• metformin is second-line therapy with a wait period of 2 years post-
menarche in children
• In adolescents with hyperandrogenism, if glucose intolerance is not
established by OGTT, metformin should not be started
• Menstrual regularity: 4 cycles/year in adolescents of 12-16 years
48. Pregnancy
• Preconceptional care
- explain the risks
- screen for markers of obesity, hypertension and IR
- RPL - serum homocysteine
• Do not to use metformin therapy during pregnancy
until specific evidence on beneficial effects is
demonstrated