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www.pcosindia.org | www.pcosindia.com THE PCOS SOCIETY NEWSLETTER PANDORA Issue 2 | Pages 12 | June-September 2016 WHAT’S INSIDE ■ New Patrons & Life Members Page 02 ■ Presidential Message Page 03 ■ Report of the International Conference Page 04-06 ■ Scientific Article – Current Controversies & Consensus for Adjuvants in PCOS Page 07 ■ Scientific Article – Management of Acne in patients of Polycystic Ovary Syndrome (PCOS) Page 08 ■ Systematic Reviews in PCOS – Abstracts & PCOS Quiz Page 10 Registered Address Kwality House, 1st Floor, August Kranti Marg, Kemps Corner, Mumbai 400 026 Phone: 022 23802584, 022 23803965 Fax: 022 23804839 Email: [email protected] Welcoming.... Our New Patrons Dr. Sadhana Desai Dr. Gauri Karandikar Dr. Gayatri Suresh Thakkar Dr. K. S. Jeyarani Kamaraj Dr. Krishnendu Gupta Dr. Navneet Magon Dr. Nirmala Patil Dr. Percy B. Kharas Dr. Ragini Agarwal Dr. Sasikala Kola Dr. Manjula Agnal Our Life Members Dr. A. Bhagauathi Ammal Dr. A. Charmila Dr. A. 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Vijaya Prabha Dr. Kalpana Jatin Shah Dr. Kalyani Ghawate Dr. Kanagapriya Dr. Kanchan Dhara Dr. Kanchan Malik Dr. Kaneez Fatma Shaikh Dr. Karuna Goyal Dr. Ketan Nalin Shah Our Associate Members Dr. Shilpa Joshi 2 Dr. R. KumaraSwamy Dr. Kinjal Atul Shah Dr. Kiran Chabbra Dr. Kiran R. Barkar Dr. Kirtan Krishna Dr. Kishori D. Kadam Dr. Kshetrimayum A. Singh Dr. Kunjal N. Bathija Dr. Kushagradhi Ghosh Dr. L. Jayanthi Reddy Dr. Mrs. Laila Dave Dr. Lakshmikutty Dr. Lalita Deodhar Dr. Lavangi Sudhakar Dr. Laxmi Shrikhande Dr. Lila S. Agarwal Dr. Lila Vyas Dr. Lovee Mehnotra Dr. M. Bramavathy Dr. M. G. Hiremath Dr. M. Rajani Dr. M. Sharada Dr. M. Subbulakshmi Dr. Madhu Mayoori Dr. Madhulka Singh Dr. Madhumita Deb Dr. Mahesh Asher Dr. Mahesh Gupta Dr. Mala Biswas Dr. Mala Raj Dr. Mandira Dasgupta Dr. Mani Shanthini Dr. Manish Baheti Dr. Manisha Garg Dr. Manjiri A. Kaba Dr. Manju Mishra Dr. Manjula Rohajgi Dr. Manmeet Kaur Dr. Manzer A. 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Kedare Dr. Vijaya Lakshmi Kodali Dr. Vijayaram Rajendran Dr. Vikrant P. Wagh Dr. Vimlesh Sharma Dr. Vinisha Abhale Dr. Y. Savitha Devi Dr. Yamini Mehta Dr. Yamini V. Khatri Dr. Yendru Katyayani Swapna Presidential Address at First International Conference Jointly Organized by The PCOS Society (India) & The Androgen Excess & PCOS Society (International) Editorial Team Dr. Duru Shah President The PCOS Society (India) The first question asked by everyone around me was "Why another Society? Do we not have enough professional Societies for Gynaecologists? The symptoms of PCOS first show their ugly head in a young girl after she attains puberty and ameliorate as she reaches menopause, suggesting that these symptoms go hand in hand with her ovarian function. And during this period she faces various health related problems which make her visit different specialists, depending on the problem she has – so she sees her Gynaec for her irregular and heavy periods or infertility, her dermatologist for cosmetic issues such as pigmentation, acne, facial hair, and the endocrinologist for her obesity, not really knowing that all her symptoms are woven together by a condition called "Polycystic Ovarian Syndrome" or "PCOS". Globally 2.2 to 26% of reproductive aged women have PCOS!. An Indian prevalence study from the National Institute of Research in Reproductive Health (NIRRH) has recently reported a prevalence of 22.5% based on a community based study in the age group of young girls between 15-24 years in Mumbai! That means, 1 out of every 5 young girls in the city of Mumbai has PCOS! They reported that 50% of the girls had irregular periods, 30% were either overweight or obese, with higher chances of having raised male hormone levels, higher insulin and blood sugar levels. Hence these young girls are at a future risk of developing delayed periods followed by heavy bleeding and anaemia, infertility, diabetes, obesity, hypertension leading to an increased risk of cardiac problems and uterine cancer. Can we stop this progress? Yes we can, there is no specific cure for PCOS but simple life style changes with exercise and healthy eating, in order to maintain a normal/ low body weight, to keep this problem under control and prevent it from reaching alarming proportions! Dr. Sabahat Rasool Associate Editor Ms. Rochelle Lobo Administrative Assistant Our country has been labeled as one of the leading Diabetes Centers of the World with 62 million diabetics existing today! with a prevalence of 15% of the PCOS group becoming diabetic in future, i.e. 1 out of 6 PCOS women will turn diabetic and these girls will raise these statistics further if we do not create this awareness today! Almost 25% of Indian PCOS are obese and the combination of diabetes and obesity dramatically increases the risk of cardiac complications leading to fatal heart attacks between the ages of 50-60 yrs in such women. So PCOS is one of the conditions which could be the beginning of long term non- communicable diseases such as diabetes, hypertension, obesity and cancer in our country. By raising this awareness amongst the medical fraternity, amongst the lay population and amongst the girls themselves, and by highlighting its complications, we could prevent such morbidities in future. We needed to have a Professional Organization which would focus on this subject and involve all the specialists who deal with it and its problems, and have a single point agenda of creating this awareness. The Gynecologist, who is the primary care physician of women, is usually the first point of contact for these young girls. We need to make an early diagnosis in every girl who comes to us with a history of irregular periods and its associated symptoms. It is not enough to only regularize her periods, or to treat her acne or to manage her obesity, it is important for us to put a finger on what's ticking behind these symptoms. Our Government is focusing on simple solutions such as sanitation and hygiene which will ultimately drastically reduce deaths due to infectious diseases. Similarly a focus on PCOS will alert many young girls early in life, and with simple solutions such as exercise, yoga and healthy eating, we will prevent unnecessary complications in their later years. Today,the PCOS Society has brought together all specialists who treat such women under one umbrella to share their experiences, which will ultimately assist us to look after our PCOS girls better! We have with us the most reputed specialists from the best Universities in the World to offer their expertise; we have our national experts consisting of cardiologists, bariatric surgeons, nutritionists, cosmetic surgeons, sleep apnoea specialists, besides many experts from the field of Endocrinology and Dermatology. I do hope you all enjoy the academic exchange which will follow in this 3 days meeting, as much as the team at the PCOS Society has enjoyed putting it together! I would personally like to convey my thanks to all the members of my team who have worked very hard to put this meeting together with a special thanks to Rochelle, a special thanks to ManjuBhargav for bringing in our Celebrity Chief Guest, Mrs. Amruta Fadnavis,our everygreen Guest of Honor Dr. Rustom Soonawala admired and loved by women all over our country, the experts from the Androgen Excess & PCOS Society, our national experts, all our esteemed sponsors who have come forward and contributed generously and our invited guests from the media and Society and last but not the least all the 650 delegates present here today. Dr. Duru Shah Founder President, The PCOS Society, India Email: [email protected] Disclaimer – Published by the The PCOS SOCIETY (INDIA). Contributions to the editor are assumed intended for this publication and are subject to editorial review and acceptance. PANDORA is not responsible for articles submitted by any contributor. These contributions are presented for review and comment and not as a statement on the standard of care. All advertising material is expected to conform to ethical medical standards, acceptance does not imply endorsement by PANDORA. www.pcosindia.org | www.pcosindia.com 3 Report of the International Conference Dr. Duru Shah Founder President The PCOS Society (India) The first International Conference of the PCOS Society (India) entitled "PCOS – Understanding the Science and Practice" was held from the 17th- 19th June, 2016 at The Leela Hotel, Mumbai. It was jointly organized by the PCOS Society (India) and the Androgen Excess and PCOS Society (AE-PCOS Society) an International Society of Androgen Excess and PCOS, and endorsed by the Federation of International Societies of Gynecological Endocrinology (FISGE). We had a galaxy of international speakers, which included Anuja Dokras, President of the AE-PCOS Society, Enrico Carmina, Executive Director and CEO of AE-PCOS Society along with Richard Legro, Kathy Hoeger and Maurizio Nordio. The consequences of PCOS are seen across the entire lifespan of women requiring a multidisciplinary approach, hence faculty from various specialties such as endocrinologists, obstetricians, gynecologists, fertility specialists, dermatologists, sonologists, pulmonologists, physicians, obesity surgeons, nutritionists were all invited on the same platform to share their expertise. The Conference Sessions discussed all areas of PCOS from puberty to menopause, covering the entire lifespan of the women. There were two Precongress Workshops, one on "Impact of PCOS on pregnancy" and the other on "Management of cosmetic concerns in PCOS". The Cosmetic Workshop was followed by a live demonstration of laser therapies. Both the Workshops were well attended and there was more than sufficient time for interaction between the egnancy– Impact of PCOS in pr p pre-congress Worksho 4 Dr. Madhuri Patil Scientific Co-ordinator The PCOS Society (India) delegates and the faculty at the end of the Session. The Inaugural Function was preceded by two excellent Inaugural Lectures followed by a very elegant Inaugural Function where the Chief Guest was Mrs. Amruta Fadnavis the better half of the Maharashtra Chief Minister Shri. Devendra Fadnavis and a woman of substance in her own right. Our Guest of Honour was Padmashree Rustom Soonawalla, our respected senior gynaecologist, and both lent charm and grace to the function, which was attended by a full house followed by the Banquet. The total number of delegates who had registered for our meeting were 650 and it was good to see that the majority of the delegates were present in the "Single Hall only". This goes to show the high academic standards maintained at this congress, which allowed a good 30 minutes interaction between the delegates and the faculty after every session. Overall this International Congress was well appreciated by all the delegates who gave a very positive feedback. The evening Cocktails followed by Dinner was very enjoyable with music and a wonderful "Standup Comedy" show by Sahil Shah of the Canvas Club. Everyone had a totally relaxing time as they were in splits of laughter. We also had a guitarist and a violinist and all sang along with the musicians. There were four Round Tables, which assisted in developing Algorithms on "Management of Ovarian Hyper Stimulation Syndrome (OHSS), Obesity, Menstrual disorders and Metabolic syndrome". Each The lectures slides, which have the consent of the authors will be available free of cost to all as Continuing Medical Education on the PCOS Society Website. table had an international expert and 10 national experts. They brainstormed to arrive at a consensus on these topics, which will be published as algorithms on the PCOS Society Website and Newsletter. There was an excellent session by our scientists from the National Institute for Research in Reproductive Health (NIRRH) to showcase their research in this field and appraise the delegates on the excellent work happening in India. Their research involved community based studies giving us the prevalence of PCOS amongst young girls in Mumbai, along with a holistic approach of treating PCOS through womens lives. They also showcased the research work done in their laboratory involving the pathophysiology of Folliculogenesis. The Conference ended on Sunday afternoon after a Valedictory function followed by lunch. During the Valedictory Function, Life Membership Awards of the PCOS Society were given to young delegates who presented free papers. The President also thanked the sponsors of this Conference for their magnanimous support, without which this conference would not have been possible. We offer our gratitude to the following Sponsors – Diamond Sponsor – USV Private Limited. Ruby Sponsors – Abbott India Limited, Alembic Pharmaceutical Limited. Sapphire Sponsors – Metropolis Healthcare Limited, Lupin Limited, Torrent Pharmaceuticals Limited, Glaxosmithkline Pharmaceuticals Limited. Crystal Sponsors – Sanofi India Limited, Sun Pharma Limited (Spectra), Bayer Zydus Pharma Private Limited. Management of Co smetic Concer ns in PCOS – Workshop Live Worksh op Inaugural lectures Book release Selfie please... Evening Banquet... ogress – Round Tables Scientific session in pr Stand up comedian Some laughter and m usic.... orrow... Concerns of tom NIRRH session 6 Valedictory See page 9 for more pictures Scientific Article – Current Controversies & Consensus for Adjuvants in PCOS Dr. Sujata Kar KCHPL, Bhubaneswar PCOS is the commonest multi-organ endocrinopathy affecting women of reproductive age group. This reproductive and cardiometabolic syndrome greatly increasing a woman's life time risk of infertility, menstrual abnormalities, type II Diabetes Mellitus and cardio vascular diseases. A cure is being highly sought after by researchers. But in the absence of a known pathophysiologic mechanism, this appears to be elusive. Currently, various investigational therapies, targeting the many symptoms of PCOS are being tried. Present article attempts to enumerate such therapies and explore their current status. Insulin sensitizing agents PCOS women, both obese and normal weight, have a very high prevalence of insulin resistance and hyperinsulinemia. Thus, the rationale to use insulin sensitizing agents in PCOS women is very strong. Biguanides and Thiazolidiones have been used extensively and large body of data exists on this subject. Some other novel agents which likely affect insulin resistance and metabolic profile of the PCOS woman have been discussed in this article. Somatostatin analogs Somatostatin is an endogenous hypothalamic peptide with 14 amino acids and a short half life. It inhibits pancreatic insulin release, pituitary growth hormone secretion and also LH release in response of gonadotropin releasing hormone (GnRH)1,2,3. This property therefore should be useful in PCOS management. Somatostatin analogue, octreotide, has been shown in few studies to improve pulsatile gonadotropin patterns, reduce LH, androgen and IGF- I levels and improve ovulation 4-13. Octreotide (LAR) long acting Somatostatin analog formulation, has also to been tried and shown to directly influence insulin secretion 3,14,15,16. Thus, this drug has potential role as insulin sensitizing agent, improve hyperinsulinemia, as well as have direct effect on the ovaries, as suggested by recent discovery of somatostatin receptors at ovarian levels17. Inositols "Inositol" is a group of naturally occurring carbohydrate compounds, which plays a small but significant role in "insulin" signaling. Many studies have reported defective inositol signaling as likely pathologic mechanism for insulin resistance of PCOS women. Three inositol family members have been tried in PCOS. D-Chiro-inositol, Myoinositol and D-Pinitol. These new molecules are thought to be having insulin sensitizing properties, likely to improve metabolic, cardiovascular and reproductive profile of PCOS women. There are many studies reporting the use of inositols in reducing insulin resistance and dyslipidemias in PCOS women18. In a recent paper, combination of myoinositol and D-Chiro inositol, in a physiologic ratio of 40:1, was shown to improve metabolic profile of PCOS women19. Also, in another study this combination therapy was shown to improve oocyte, embryo quality and pregnancy rates in PCOS women undergoing IVF-ET 20. Artini et al studied 50 overweight PCOS women before and after a 12 weeks course of myo-inositol 2 gms with folic acid 200 mg daily. Patients were randomized to either the above combination or to only folic acid 200 mg daily 21. They reported that after 12 weeks of myo-inositol administration, plasma LH, prolactin, testosterone, insulin levels and LH / FSH were significantly reduced. Insulin sensitivity, expressed as glucose to insulin ratio and HOMA index, significantly improved. Menstrual cyclicity was restored in all amenorrheic and oligomenorrheic subjects. No such improvement was seen in "Folic acid only" group. A systematic review published in 2011, looked into the effects of D-chiro-inositol on ovulation and insulin resistance in women with PCOS22. All studies published on PCOS and D-Chiro inositol (DCI) upto 2010 were included. Patients were women with PCOS receiving D-chiro inositol or where the relationship between insulin resistance and DCI had been investigated. Ovulation rates and insulin resistance were the main out come measures. They concluded that heterogeneity in study methodologies and small sample size used prohibit reliable conclusions to be drawn. More studies are needed to evaluate accurately the effects of DCI in PCOS. The inositols have potential to improve reproductive axis functioning by reducing hyperinsulinemia. N Acetyl-Cysteine (NAC) N-acetyl cysteine is a pharmaceutical drug and also a nutritional supplement. Acetyl-cysteine is the Nacetyl derivative of amino acid L-Cysteine which forms antioxidant glutathione in the body. This compound is sold commonly as a dietary supplement, claiming antioxidant and liver protecting effects. Recent studies have shown beneficial effects from the use of NAC for patients with PCOS. Oner et al, reported clinical, endocrine and metabolic effects of metformin and NAC in PCOS women23. In this prospective trial, 100 women with PCOS were randomly divided to receive metformin (1500 mg/ day) or NAC (1800 mg/day) for 24 weeks. Both treatments resulted in a significant decrease in body mass index, hirsutism score, fasting insulin, HOMA index, free testosterone and menstrual irregularity, compared with baseline values. Also both treatments had equal efficacy. NAC reduced both total and low density lipo-proteins, where as metformin only led to a decrease in total cholesterol. Badawy et al24 studied NAC as a novel adjuvant to clomiphene citrate (CC) in clomiphene citrate resistant PCOS women. One hundred and fifty women diagnosed with CC resistant PCOS, aged 1839 years, undergoing infertility treatment were included. The women were randomized to receive either NAC (1.2 gm/day) or placebo with CC 100 mg/day. Ovulation rates and pregnancy rates were reported. They concluded that NAC as an adjuvant was more effective than placebo for CC resistant PCOS women. Nasr, studied effect of NAC after ovarian drilling in CC-resistant PCOS women. Sixty CC-resistant women who had undergone unilateral laparoscopic ovarian drilling were randomized to receive placebo or NAC (1.2 gm/day) for 12 consecutive cycles. Ovulation rate, pregnancy rate and live birth rate were all significantly higher in the NAC group25. Thus, there is now a large body of evidence to support use of NAC in women with PCOS. It is likely to help to improve insulin sensitivity, to restore fertility and also to tackle homocysteine levels. It has been shown that many women with PCOS have high homocysteine levels24. Elevated homocysteine is associated with coronary artery disease, heart attack, chronic fatigue, fibromyalgia and cervical cancer. A 2009 study showed that people taking NAC for two months had a significant decrease in homocysteine levels26. 25-OH Vitamin D Vitamin D deficiency has been shown to be prevalent in PCOS women27. About 65-85% of women with PCOS have serum concentration of 25-hydroxy vitamin-D (25-0H vit D) < 20 ng/ml. Some observational studies have shown that lower 25-0H vitD levels are associated with insulin resistance, ovulatory and menstrual irregularities, hirsutism, hyper-androgenism, obesity and elevated cardio vascular risk factors. Pal et al28 studied 12 overweight, Vitamin-D deficient, PCOS women. Blood pressure, plasma glucose, total testosterone, serum sex hormone binding globulin, 2 hr oral glucose tolerance test, were assessed at base line and after 3 months therapy with VitaminD and elemental calcium. Their results showed improved androgen and blood pressure profile. However, glucose and insulin resistance parameters remained unchanged. Wehr et al studied 57 PCOS women, who received 20,000 IU of cholecalciferol weekly for 24 weeks. Anthropometric measures, oral glucose tolerance test and blood analyses of endocrine parameters were performed at baseline, after 12 weeks and after 24 weeks. 7 Scientific Article – Management of Acne in patients of Polycystic Ovary Syndrome (PCOS) Dr. Akshitha Shetty Dermatologist Introduction Acne vulgaris is a common skin condition with 85% lifetime prevalence. While acne is commonly viewed as a disorder of adolescence, it may persist into adulthood and often may present for the first time in adulthood1. Adult acne is a common reason for patients to present for dermatological evaluation, and adults, in fact, make up a large portion of the patient population seen by dermatologists for acne. Pathogenesis of acne Pathogenesis of acne in adult women is complex, involving androgens in addition to other important factors well accepted for their role in the pathogenesis of acne: sebum production, follicular plugging, genetics, Propionibacterium acnes, diet, medications, innate immunity, and alterations in follicular keratinization and differentiation2. Dr. Rekha Sheth MD, DVD Dermatologist Vice President The PCOS Society (India) ovaries, adrenal glands, and peripheral conversion. Ovarian-derived androgens include androstenedione and testosterone, whereas adrenal glands produce dehydroepiandrosterone (DHEA), DHEA-S, androstenedione, and testosterone. Peripheral conversion of androstenedione and DHEA also generates testosterone in women. Androgen-stimulated sebum production contributes to the pathophysiology of acne in women3. In skin, androgen receptors are located in sebaceous glands and in the outer root sheath of the hair follicle6. Androgens in the sebaceous glands are metabolized through a multi-step process from DHEA to 5-alphadihydrotestosterone, stimulating sebocyte proliferation and activity7. Sebum production is also regulated by other hormones, including estrogens, growth hormone, insulin, insulin-like growth factor-1, glucocorticoids, adrenocorticotropic hormone, and melanocortins5. Treatment of acne In the treatment of adult female patients with acne, it is important to treat the cause of acne; an endocrinal evaluation can be helpful. A systematic treatment algorithm for acne should be utilized8,9. The role of androgens in adult women with acne has been well supported in the literature3, and four clinical observations highlight this important role. First, androgen-insensitive individuals do not produce sebum and do not develop acne. Second, conditions of hyperandrogenism, such as polycystic ovary syndrome (PCOS), are associated with acne that is highly responsive to hormonal therapies 4. Third, even in women with normal androgen levels, hormonalbased therapies such as oral contraceptives and antiandrogen medications are effective treatments for acne. Fourth, rising levels of dehydroepiandrosterone sulfate (DHEA-S) are associated with the onset of acne in pre-menarcheal girls, and higher levels in pre-menarche may predict the development of more clinically severe acne in puberty. Elevated DHEA- S also correlates with clinical acne in a subset of patients with PCOS5. Androgens in women derive from three sources: the 8 Women over the age of 25 years have higher rates of treatment failure; 82% fail multiple courses of systemic antibiotics, and 32% relapse after isotretinoin9. Recurrence shortly after treatment with isotretinoin should trigger suspicion for an underlying hormonal disorder. A thorough review of systems for an underlying endocrine disorder should be performed prior to initiating isotretinoin10. Isotretinoin Isotretinoin remains a highly viable and important non- hormonal treatment option for acne in adult women8. In this patient population, there are special considerations of teratogenicity, and individuals over 35 years old may have increased risk of adverse skeletal side effects. Low-dose isotretinoin (10-20 mg/day) can be used to minimize side effects associated with systemic retinoid therapy, and this is an effective treatment of choice in this population9. Hormones Hormonal therapies, such as oral contraceptive pills (OCPs) and anti-androgen therapy, also provide an important and effective opportunity to increase treatment options for acne. As many adult women present with comedonal disease, hormonal therapies can be utilized across the entire clinical spectrum of acne, including mild and/or comedonal only disease 11 . Evidence-based recommendations supporting an algorithm for use of hormonal therapies in acne are currently lacking. An important goal of hormonal treatment is to reduce sebum production. The mainstay of hormonal acne therapy in the USA includes OCPs and spironolactone, other treatment options include flutamide and cyproterone4. Hormonal therapy provides an effective adjunct to the current acne treatments or may serve as primary therapy. Patients should be educated that this strategy will require time, up to several months, to see results, and may require long-term systemic treatment and ongoing monitoring for side effects. Hormonal therapy is safe and effective in postmenarcheal females over the age of 14 years, even in those with normal androgen levels. Spironolactone Spironolactone is a highly effective treatment for acne in adult women and may surpass the efficacy of OCPs. A potassium-sparing diuretic, spironolactone at low doses (25 mg /day) blocks aldosterone and at higher doses (50-100 mg / day) blocks androgens at the receptor level. Drospirenone is a synthetic progestin that is an analog to spironolactone. In commonly-available OCP preparations, the 3 mg drospirenone is estimated to have anti-androgenic activity equivalent to 25 mg of spironolactone. Spironolactone is not FDA approved for the indication of acne, but spironolactone alone or combined with an OCPs at a dose of 50-200 mg/day is effective in 33-85% reduction in acne lesion counts and also improves seborrhea. Studies with lower dose spironolactone (50-100 mg/day) demonstrate 33% improvement, suggesting a dosage effect. Studies with a higher dose of 100 mg plus drospirenone demonstrated an 85% improvement in acne, suggesting a highly effective combination treatment2,12,13 . Spironolactone is a safe and well-tolerated medication, yet patients should be counseled on potential side effects14. Side effects include breast tenderness (17%), menstrual irregularities (22%), headache (13%), fatigue (15%), blood pressure reduction (with mean decrease of 5 mmHg systolic, 2.6 mmHg diastolic blood pressure), and a minimal rise in serum potassium levels in 13% with no cardiovascular or renal sequelae. The investigators recommended checking potassium levels at baseline and at 4 weeks in certain patient populations, like patients over the age of 45 years, those with cardiac or renal disease, or those on concomitant drospirenone 15. Importantly, spironolactone is a potential teratogen associated with hypospadias and feminization of male fetuses and is not recommended in pregnancy or in women contemplating pregnancy1,15. Flutamide Flutamide is a non steroidal androgen-receptor blocker used in prostate cancer and is effective in the treatment of hirsutism and acne in women11,1. Typical doses are 250- 500 mg/day. Due to its risk of hepatotoxicity, it is rarely used in the management of acne. Other side effects include gastrointestinal upset, hot flashes, and decreased libido 2. Cyproterone acetate (CPA) CPA is a 17-hydroxyprogesterone derivative with potent androgen blockade. CPA is available in two forms: in combination with OCPs or in a non-OCP form that can be used in combination with OCP or spironolactone. As a non-OCP medication, CPA is given on days 1-10 of the menstrual cycle (day 1 marking the first day of menstruation)2. Conclusion Acne is common in adults and especially in women. Acne in adult women has significant psychosocial co morbidity and may be challenging to treat. It may also be a sign of an underlying systemic disorder such as PCOS. Dermatologists likely play a critical role in the diagnosis of PCOS, as acne is a common cutaneous presenting sign. It is important to look for and ask about potential symptoms and signs of hyperandrogenism and to exclude an underlying hormonal disorder by complete history and physical examination. Isotretinoin remains a highly-viable treatment option. Hormonal therapies are also safe and effective, even when androgen levels are normal, and they provide an important opportunity to better treat this patient population. Hormonal therapies such as spironolactone and flutamide are effective even when other standard therapies for acne have failed, including antibiotics and isotretinoin. A strong therapeutic alliance with the patient is vital in this patient population, to attempt different combinations of therapies and to identify the best personalized treatment for acne. References 1. Kamangar F, Shinkai K. Acne in the adult female patient: a practical approach. Int J Dermatol. 2012 Oct;51(10):1162-74. 2. Zaenglein AL, Pathy AL, Schlosser BJ, Alikhan A, Baldwin HE, Berson DS, Bowe WP, Graber EM, Harper JC, Kang S, Keri JE, Leyden JJ,Reynolds RV, Silverberg NB, Stein Gold LF, Tollefson MM, Weiss JS, Dolan NC, Sagan AA, Stern M, Boyer KM, Bhushan R. Guidelines of care for the management of acne vulgaris.J Am Acad Dermatol. 2016 May;74(5):945-973. 3. Harper JC. Evaluating hyperandrogenism: a challenge in acne management. J Drugs Dermatol 2008; 7: 527-530. 4. Lolis MS, Bowe WP, Shalita AR. Acne and systemic disease. Med Clin North Am 2009; 93: 1161-1181. 5. Chen MJ, Chen CD, Yang JH, et al. High serum dehydroepiandrosterone sulfate is associated with phenotypic acne and a reduced risk of abdominal obesity in women with polycystic ovary syndrome. Human Reprod 2011; 26: 227-234. 6. Imperato-McGinley J, Gautier T, Cai LQ, et al. The androgen control of sebum production. Studies of subjects with dihydrotestosterone deficiency and complete androgen insensitivity. J Clin Endocrinol Metab 1993; 76: 524-528. Improve Outcomes in Acne group. J Am Acad Dermatol 2009; 60(5 Suppl): S1-S50. 9. Gollnick H, Cunliffe W, Berson D, et al. Management of acne: a report from a Global Alliance to Improve Outcomes in Acne. J Am Acad Dermatol 2003; 49(1 Suppl.): S1-S37. 10. Lowenstein EJ. Diagnosis and management of the dermatologic manifestations of the polycystic ovary syndrome. Dermatol Ther 2006; 19: 210-223. 11. George R, Clarke S, Thiboutot D. Hormonal therapy for acne. Semin Cutan Med Surg 2008; 27: 188-196. 12. Brown J, Farquhar C, Lee O, et al. Spironolactone versus placebo or in combination with steroids for hirsutism and/or acne. Cochrane Database Syst Rev 2009 13. Shaw JC. Low-dose adjunctive spironolactone in the treatment of acne in women: a retrospective analysis of 85 consecutively treated patients. J Am Acad Dermatol 2000; 43: 498-502. 7. George R, Clarke S, Thiboutot D. Hormonal therapy for acne. Semin Cutan Med Surg 2008; 27: 188-196. 14. Friedman AJ. Spironolactone for Adult Female Acne.Cutis. 2015 Oct;96(4):216-7. 8. Thiboutot D, Gollnick H, Bettoli V, et al. New insights into the management of acne: an update from the Global Alliance to 15. Haider A, Shaw JC. Treatment of acne vulgaris. JAMA ?2004; 292: 726-735. 9 Systematic Reviews in PCOS – Abstracts Abstract 1 Abstract 2 Abstract 3 Does Metformin help in assisted reproduction in PCOS patients? Letrozole Vs. Clomiphene citrate for ovulation induction in PCOS – Which is better? In vitro maturation (IVM) in PCOS & non-PCOS patients – Is it comparable? Nine randomized controlled trials, with 816 PCOS women were included in this systematic review, A systematic review & meta analysis was done on In vitro maturation (IVM) was evaluated in sub fertile where metformin was compared with placebo in women undergoing IVF/ICSI. the results of randomized controlled trials (RCTs) which compared letrozole and clomiphene citrate PCOS & non-PCOS women undergoing IVF. The clinical pregnancy rates in metformin group compared to the placebo group were 32-49% and (CC) for ovarian stimulation in women with Polycystic Ovary Syndrome (PCOS). patients undergoing IVM were included in the metaanalysis. A higher birth rate was observed among 31%, respectively. Seven RCTs with 1833 patients (906 in the letrozole group & 927 in the CC group) and 4999 ovulation the PCOS patients who underwent IVM compared to non-PCPS controls. Clinical pregnancy and induction cycles were included in the review. Live birth & pregnancy rates were statistically higher in implantation rates were also higher , whereas cancellation rates lower among PCOS vs. non-PCOS the letrozole group, with no differences in the multiple gestations and miscarriage rates among the patients. two groups. Ref: Letrozole versus clomiphene citrate in polycystic as far as maturation and miscarriage rates were concerned. and decreases risk of ovarian hyperstimulation. ovary syndrome: systematic review and metaanalysisRoque M, Tostes AC, Valle M, Sampaio M, Ref: Metformin treatment before and during IVF or Ref: In Vitro Maturation in Women with vs. without Polycystic Ovarian Syndrome: A Systematic Review Geber S. and Meta-Analysis. Gynecol Endocrinol. 2015 Dec; 31(12):917-21. Siristatidis C1, Sergentanis TN2, Vogiatzi P1, The risk of OHSS in metformin and placebo groups, respectively, was 6-15% and 27%. However, there was no conclusive evidence that metformin improved live birth rates in women with PCOS undergoing IVF/ICSI treatment. Metformin treatment during or before IVF/ICSI in women with PCOS increases clinical pregnancy rates ICSI in women with polycystic ovary syndrome. Tso LO, Costello MF, Albuquerque LE, Andriolo RB, Eleven studies with 268 PCOS & 440 non-PCOS However, there was no difference in the two groups Kanavidis P2, Chrelias C3, Papantoniou N3, Psaltopoulou T2 Macedo CR. Cochrane Database Syst Rev. 2014 Nov 18;11: PLoS One. 2015 Aug 4;10(8):e0134696. CD006105 PCOS Quiz 1. What percentage of PCOS patients has elevated prolactin levels? 4. Which of the following adipocytokines is not involved in pathogenesis of PCOS? a. <5% a. TNF-ALHPA b. 5-10% b. Retinol binding protein-4 c. 15% c. Monocyte chemoattractant protein-1 d. 25% d. None 2. Which among the following statements is false? 5. Leptin intake is associated with which of thefollowing options a. Androgen levels are elevated in obese as well as non obese PCOS patients a. Decreased hypothalamic Neuropeptide Y b. Hyperandrogenemism is amplified by increasing obesity c. Increase in thermogenesis c. Hyperandrogenism is amplified by increasing insulin resistance d. Hyperandrogenemia occurs as a result of decreased Cytochrome P450 alpha enzyme activity 3. Which among the following statements is false? a. Gonatropins stimulate adrenal androgen production directly b. Prolactin can stimulate DHEA-S production c. DHEA-S has low androgenic potential d. DHEA-S is co-secreted with cortisol from adrenals b. Increased GnRH activity d. All of the above 6. Which of the following does not contribute to anovulation in POCS patients? a. Increased insulin levels b. Deranged early follicular development c. Hyperresponsiveness of granulose cells to FSG in terms of estradiol production d. None of the above 7. The risk of developing moderate to severe OHSS in PCOS women undergoing gonadotropin stimulation is a. 5-8% b. 8-12% 10 c. 10-18% d. 15-21% 8. The unfavourable reproductive outcomes in PCOS patients are related to all of these except a. High BMI b. Increased waist to hip ratio c. Insulin resistance d. None of the above 9. Using the NCEP criteria, what is the prevalence of Metabolic Syndrome in PCOS patients? a. <10% b. 20% c. 30% d. 40% 10. What percentage of PCOS patients have insulin resistance using the HOMA-IR index? a. 20% b. 30-45% c. 50-55% d. 65-80% Cussions et al published a study in 2009 that examined the effects of omega-3 fatty acids on liver fat in PCOS women. Twenty five PCOS women were randomized to receive 4 gm per day of Omega-3 fatty acids or placebo for 8 weeks. They concluded 21. Artini PG, Di Berardino OM, Papini F, Genazzani AD, Simi G, Ruggiero M, Cela V.Endocrine and clinical effects of myo-inositol administration in polycystic ovary syndrome.A randomized study.GynecolEndocrinol. 2013 Apr;29(4):375-9. doi: 10.3109/09513590.2012.743020. Epub 2013 Jan 22. 2. Brazaan JC, Vale W, Burgus N, Lang N, Buteler M &Gullemin R. Hypothalamic polypeptide that inhibits the secretion of immunoreactive pituitary growth hormone. Science 1973 179 77-79. 22. Galazis N, Galazi M, AtiomoW.GynecolEndocrinol.D-Chiro-inositol and its significance in polycystic ovary syndrome: a systematic review.2011 Apr; 27(4):256-62. Epub 2010 Dec 10. 3. Hsu WH, Xiang HD, Rajan AS, Kunze DL & Boyd AE .Somatostatin inhibits insulin secretion by a G-protein-mediated decrease in Ca2+ entry through voltage-dependent Ca2+ channels in the beta-cell. Journal of Biological Chemistry 1991 266 837-843. 23. Oner G, MuderrisII.Eur J ObstetGynecolReprod Biol.Clinical, endocrine and metabolic effects of metformin vs N-acetyl-cysteine in women with polycystic ovary syndrome.2011 Nov;159(1):12731. 4. Prevelic GM, Wurzburger MI, Balin-Peric L &Nesic JS. Inhibitory effect of sandostatin on secretion of luteinizing hormone and ovarian steroids in polycystic ovary syndrome. Lancet 1990 336 900-903. 24. Rizk AY, Bedaiwy MA, Al-Inany HG.N-acetyl-cysteine is a novel adjuvant to clomiphene citrate in clomiphene citrate-resistant patients with polycystic ovary syndrome.FertilSteril. 2005 Feb;83(2):367-70. 5. Prelevic GM, Wurzburger MI, Balint-Peric L, Hardiman P, Okolo S, Maletic D & Ginsburg J. Effects of the somatostatin analogue, octreotide, in polycystic ovary syndrome. Metabolism 1992 41 7679. 25. Nasr A.Effect of N-acetyl-cysteine after ovarian drilling in clomiphene citrate-resistant PCOS women: a pilot study.Reprod Biomed Online. 2010 Mar;20(3):403-9. 6. Prelevic GM, Ginsburg J, Maletic D, Hardiman P, Okolo S, Balint-Peric L, Thomas M &Orskov H. The effects of the somatostatin analogue octreotide on ovulatory performance in women with polycystic ovaries. Human Reproduction 1995 10 28-32. 7. Morris RS, Carmina E, Vijod MA, Stanczyk FZ & Lobo RA. Alterations in the sensitivity of serum insulin-like growth factor 1 and insulin-like growth factor binding protein-3 to octreotide in polycystic ovary syndrome. Fertility and Sterility 1995 63 742-746. 8. Fulghesu AM, Lanzone A, Andreani CL, Pierro E, Caruso A & Mancuso S. Effectiveness of a somatostatin analogue in lowering luteinizing hormone and insulin stimulated secretion in hyperinsulinemic women with polycystic ovary disease. Fertility and Sterility 1995 64 703-708. 9. Morris RS, Karande VC, Dudkiewicz A, Morris JL &Gleicher N. Octreotide is not useful for clomiphene citrate resistance in patients with polycystic ovary syndrome but may reduce the likelihood of ovarian hyperstimulation syndrome. Fertility and Sterility 1999 71 452-456. 10. Lidor A, Soriano D, Seidman DS, Dor J, Mashiach S &Rabinovici J. Combined somatostatin analog and follicle-stimulating hormone for women with polycystic ovary syndrome resistant to conventional treatment. Gynecological Endocrinology 1998 12 97-101. 11. Ciotta L, De Leo V, Galvani F, La Marca A &Cianci A. Endocrine and metabolic effects of octreotide, a somatostatin analogue, in lean PCOS patients with either hyperinsulinemia or normoinsulinemia. Human Reproduction 1999 14 2951-2958. 12. Wenzl R, Lehner R, Schurz B, Karas H & Huber JC. Successful ovulation induction by sandostatin-therapy of polycystic ovarian disease.ActaObstetriciaetGynecologicaScandinavica 1996 75 298299. 13. Prelevic GM, Wurzburger MI, Balint-Peric L, Hardiman P, Okolo S, Maletic D & Ginsburg J. Effects of the somatostatin analogue, octreotide, in polycystic ovary syndrome. Metabolism 1992 41 7679. 14. Gambineri A, Patton L, De Iasio R, Cantelli B, Cognini GE, Filicori M, Barreca A, Diamanti-Kandarakis E, Pagotto U &Pasquali R. Efficacy of octreotide-LAR in dieting women with abdominal obesity and polycystic ovary syndrome. Journal of Clinical Endocrinology and Metabolism 2005 90 3854-3862. 15. Gillis JC, Noble S & Goa KL. Octreotide long-acting release (LAR).A review of its pharmacological properties and therapeutic use in the management of acromegaly. Drugs 1997 53 681-699. 16. Bertoli A, Magnaterra R, Borboni P, Marini MA, Barini A, Fusco A &Bollea MR. Dose-dependent effect of octreotide on insulin secretion after OGTT in obesity. Hormone Research 1996 49 17-21. 17. Strass MC, Seelig AS, Weiss JM, Diedrich K &Ortmenn O. Expression of somatostatin and its receptors in human ovary 19th Annual Meeting of the ESHRE 2003. Madrid, Spain, 2003. 18. Colazingari S, Treglia M, Najjar R, Bevilacqua A.The combined therapy myo-inositol plus D-chiro-inositol, rather than D-chiro-inositol, is able to improve IVF outcomes: results from a randomized controlled trial.Arch Gynecol Obstet. 2013 May 25. 19. Minozzi M, Nordio M, Pajalich R.The Combined therapy myo-inositol plus D-Chiro-inositol, in a physiological ratio, reduces the cardiovascular risk by improving the lipid profile in PCOS patients.Eur Rev Med Pharmacol Sci. 2013 Feb;17(4):537-40. 20. Colazingari S, Treglia M, Najjar R, Bevilacqua A.The combined therapy myo-inositol plus D-chiro-inositol, rather than D-chiro-inositol, is able to improve IVF outcomes: results from a randomized controlled trial.Arch Gynecol Obstet. 2013 May 25. 26. Rymarz A, Durlik M, Rydzewski A.Intravenous administration of Nacetylcysteine reduces plasma total homocysteine levels in renal transplant recipients.Transplant. 2009 Oct-Dec;14(4):5-9. 27. Thomson RL, Spedding S, Buckley JD.Vitamin D in the aetiology and management of polycystic ovary syndrome.ClinEndocrinol (Oxf). 2012 Sep;77(3):343-50. 28. Pal L, Berry A, Coraluzzi L, Kustan E, Danton C, Shaw J, Taylor H.Therapeutic implications of vitamin D and calcium in overweight women with polycystic ovary syndrome.GynecolEndocrinol. 2012 Dec;28(12):965-8. 29. Wehr E, Pieber TR, Obermayer-Pietsch B.Effect of vitamin D3 treatment on glucose metabolism and menstrual frequency in polycystic ovary syndrome women: a pilot study.J Endocrinol Invest. 2011 Nov;34(10):757-63. 30. Kauffman RP, Tullar PE, Nipp RD, Castracane VD.Serum magnesium concentrations and metabolic variables in polycystic ovary syndrome.ActaObstetGynecol Scand. 2011 May;90(5):452-8. 31. Sharifi F, Mazloomi S, Hajihosseini R, Mazloomzadeh S.Serum magnesium concentrations in polycystic ovary syndrome and its association with insulin resistance.GynecolEndocrinol. 2012 Jan;28(1):7-11. 32. Chakraborty P, Ghosh S, Goswami SK, Kabir SN, Chakravarty B, Jana K.Altered trace mineral milieu might play an aetiological role in the pathogenesis of polycystic ovary syndrome.Biol Trace Elem Res. 2013 Apr;152(1):9-15. 33. Evans JL, Heymann CJ, Goldfine ID, Gavin LA. Pharmacokinetics, tolerability, and fructosamine-lowering effect of a novel, controlledrelease formulation of alpha-lipoic acid.EndocrPract. 2002;8(1):2935. 34. Masharani U, Gjerde C, Evans JL, Youngren JF, Goldfine ID.Effects of controlled-release alpha lipoic acid in lean, nondiabetic patients with polycystic ovary syndrome.J Diabetes Sci Technol. 2010 Mar 1;4(2):359-64. 35. Cerda C, Pérez-Ayuso RM, Riquelme A, Soza A, Villaseca P, SirPetermann T, Espinoza M, Pizarro M, Solis N, Miquel JF, Arrese M. 2007 Nonalcoholic fatty liver disease in women with polycystic ovary syndrome.J Hepatol 47:412-417 CrossRefMedline. 36. Gambarin-Gelwan M, Kinkhabwala SV, Schiano TD, Bodian C, Yeh HC, Futterweit W. 2007 Prevalence of nonalcoholic fatty liver disease in women with polycystic ovary syndrome.ClinGastroenterolHepatol 5:496-501 CrossRefMedline. 37. Alwayn IP, Andersson C, Zauscher B, Gura K, Nosé V, Puder M. 2005 Omega-3 fatty acids improve hepatic steatosis in a murine model: potential implications for the marginal steatotic liver donor.Transplantation 79:606-608 CrossRefMedline. 38. Cussons AJ, Watts GF, Mori TA, Stuckey BG.Omega-3 fatty acid supplementation decreases liver fat content in polycystic ovary syndrome: a randomized controlled trial employing proton magnetic resonance spectroscopy.J ClinEndocrinolMetab. 2009 Oct;94(10):3842-8. doi: 10.1210/jc.2009-0870. 39. Mohammadi E, Rafraf M, Farzadi L, Asghari-Jafarabadi M, Sabour S.Effects of omega-3 fatty acids supplementation on serum adiponectin levels and some metabolic risk factors in women with polycystic ovary syndrome.Asia Pac J ClinNutr. 2012;21(4):511-8. Answers for PCOS QUIZ Omega-3 Fatty Acids A link between PCOS and non-alcoholic fatty liver disease (NAFLD) has been demonstrated for few years now. Prevalence of NAFLD in women with PCOS may be as high as 40-55%35, 36. NAFLD is characterized by increased hepatic storage of triglycerides and carries risk of cirrhosis. Very few published studies have tested various treatment options for NAFLD in association with PCOS. Animal studies of marine derived omega-3 fatty acids have demonstrated beneficial effects in NAFLD37. 1. Chiodera P, Volpi R, d'Amato L, Fatone M, Cigarini C, Fava A, Caiazza A, Rossi G &Coiro V. Inhibition by somatostatin of LH-RH-induced LH release in normal menstruating women. Gynecologic and Obstetric Investigation 1986 22 17-21. 9. D 10. D Lipoic Acid Alpha lipoic acid is a potent antioxidant. We know that oxidative stress is a likely mechanism leading to insulin resistance in PCOS women. Controlledrelease alpha lipoic acid (CRLA) has been reported to improve glucose control in Type 2 Diabetic patients33. Masharane et al have reported the effects of CRLA on the features of PCOS women. Six lean, non diabetic PCOS women were given CRLA 600 mg twice daily for 16 weeks. Insulin sensitivity was measured by euglycemic, hyperinsulenemic clamp. Plasma lipids and serum oxidative markers were measured. Results showed a significant improvement in insulin sensitivity and a lowering of triglyceride levels. This was, however, not associated with increase in plasma antioxidant capacity34. They concluded that CRLA has positive effects on PCOS phenotype. This agent needs further studies to substantiate its likely benefits. References 7. C 8. D Magnesium There are some reports linking hypomagnesaemia with PCOS. Whether serum magnesium concentrations co-relate with insulin resistance, hypertension, dyslipidemias of PCOS women is currently unknown. Kauffmann et al, in 100 PCOS women, could not find any co-relation between PCOS and non PCOS women, in their magnesium levels 30. Sharifi et al 31 too, could not find any evidence to show that magnesium deficiency is associated with insulin resistance of PCOS. However, a very recent study reported in 2013 by Chakraborty et al studied 132 PCOS women for multiple trace elements including copper, magnesium, zinc, manganese, chromium and calcium. They divided PCOS women into insulin resistant and non-insulin resistant. They found highly significant correlation between low serum calcium and magnesium levels with insulin resistance in PCOS women32. Mohammads et al, in a double blind randomised controlled trial conducted on 64 PCOS patients, concluded that Omega-3 fatty acids had some beneficial effects on serum adiponectin levels, insulin resistance and lipid profile in PCOS patients and may contribute to the improvement of metabolic complications in these women39. 5. D 6. D Their results showed improved glucose metabolism and menstrual frequency in these women, but no changes in androgens29 Thus, Vitamin-D deficiency may play a role in exacerbating PCOS and there may be a role for vitamin-D supplementation in the management of this syndrome, but current evidence is limited. Additional randomized controlled trials are needed to confirm place of vitamin-D in management of PCOS27 that Omega-3 fatty acid supplementation had a beneficial effect on liver fat content and other cardiovascular risk factors in women with PCOS, including those with hepatic steatosis38. 3. A 4. D Current Controversies & Consensus for Adjuvants in PCOS 1. D 2. D Continued from page 04 www.pcosindia.org | www.pcosindia.com 11