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Managing the complications of polycystic ovarian syndrome Draion M. Burch, DO Paige E. Paladino, DO P olycystic ovarian syndrome (PCOS) is the most common endocrine abnormality of reproductive-aged women.1 This chronic condition affects 5 million to 6 million females in the United States.2 In addition, an estimated 50% to 75% of cases remain undiagnosed.3 April 2011 DOs Against DIABETES AOA Health Watch 19 PCOS is classified by the presence of two of the following three criteria: (a) oligo- and/or anovulation; (b) clinical and/or biochemical signs of hyperandrogenism; and (c) polycystic ovaries, all in the absence of other known etiologies.4 Women with PCOS may seek care from physicians in various medical specialties, including endocrinology, internal medicine, obstetrics and gynecology, dermatology and family medicine. Therefore, physicians in these specialties must understand management of the short- and long-term complications associated with PCOS. Short-term complications Following are short-term complications related to PCOS, as well as treatment options. 䡲 Menstrual irregularities The prevalence of menstrual dysfunction in women with PCOS is 14.6% to 22.8%, and irregularities range from amenorrhea to menorrhagia with a classic peripubertal onset.5,6 Recommendations: A modest weight reduction of 5% can return menses to normal.7 Combination oral contraceptives (COCs) or progestins are also effective at regulating the menstrual cycle in these patients. Metformin has been shown to have positive effects on ovulatory dysfunction and hyperandrogenism, ultimately restoring normal menstruation.8,9 added if acceptable results are not achieved, but these medications must be used in conjunction with COCs due to known risk of congenital anomalies. Eflornithine, a topical medication, has been shown to be effective in hirsute women, and waxing, shaving, depilatories, electrolysis and laser treatments are alternative options for hirsutism.10-12 Topical retinoids and antimicrobials or oral antibiotics can be effective in the treatment of acne.13 Limited data support the use of topical minoxidil in the treatment of alopecia.14 Hyperandrogenism has also been shown to improve with dietary modification.15 䡲 Hyperandrogenism Cutaneous hyperandrogenism 䡲 Infertility manifests as hirsutism, acne and Infertility due to anovulation affects androgenic alopecia. Its prevalence 75% of women with PCOS.16 in the PCOS population in the form of acne is 15% to 25%; hirsutism, Recommendations: Lifestyle 65% to 75%; and alopecia, 5% to 50%.5 modifications, including weight reduction, decreasing alcohol Recommendations: COCs are consumption, smoking cessation beneficial for all forms of cutaneous and limiting caffeine intake, are hyperandrogenism; however, the beneficial.17 Weight loss induces selection of a low-androgenic ovulation in overweight patients. progestin component is essential. Clomiphene citrate (CC) is Anti-androgens, such as spironolactone, a first-line pharmacologic treatment flutamide or finasteride can then be 20 AOA Health Watch in anovulatory women with PCOS. Other agents used in ovulation induction include metformin and thiazolidinediones. Referral to a reproductive endocrinologist is appropriate if CC fails to achieve pregnancy. Treatment with exogenous gonadotropins or laparoscopic ovarian surgery such as ovarian diathermy is second-line intervention. The ovarian wedge resection has been abandoned, secondary to increased adhesion formation. The recommended third-line intervention is in vitro fertilization.18 䡲 Obesity Obesity in the PCOS patient tends to be central (android) or visceral in its distribution.19 The prevalence of obesity is 40% to 60% in this population.20 This epidemic exacerbates insulin resistance, ovulatory and menstrual dysfunction and pregnancy outcome. Obesity is associated with increased prevalence of metabolic syndrome, glucose intolerance, cardiovascular risk factors and sleep apnea.21 DOs Against DIABETES April 2011 Recommendations: Lifestyle higher concentrations of smallerand higher-density LDL particles. modification is crucial. Modest amounts of weight loss have been Recommendations: Lifestyle shown to restore spontaneous modification with diet, exercise ovulation and menstruation and to and weight loss is essential. improve insulin sensitivity.20 No HMG-CoA, reductase inhibitors particular type of dietary modification (statins) have been shown to has been shown to be superior.22 effectively treat dyslipidemia Anti-obesity medications, such as and decrease levels of circulating orlistat, sibutramine and rimonabant, androgens. Other treatments include and surgical weight loss have been nicotinic acid and fibrates.31 found to be effective and even more sustainable in the long term for 䡲 Obstructive sleep apnea (OSA) weight loss.23,24 Metformin has also Patients with PCOS have a higher appeared to have some benefit.8 risk for obstructive sleep apnea, even when compared with obese non䡲 Insulin resistance PCOS control subjects.32 Insulin and hyperinsulinemia resistance seems to be a better Insulin resistance and compensatory predictor of sleep-disordered hyperinsulinemia affect 40% to 70% breathing. Glucose tolerance is of women with PCOS independent directly related to the severity of of obesity.5,25 The strongest predictors sleep apnea in these patients.33 of insulin resistance in a patient with PCOS are body mass index, Recommendations: Weight loss, hyperandrogenemia, and hirsutism.26 avoidance of alcohol, sleep position Insulin resistance is also associated changes, avoidance of medications with obstructive sleep apnea, that inhibit the central nervous nonalcoholic steatohepatitis (or, nonalcoholic fatty liver disease) and metabolic abnormalities such as metabolic syndrome, dyslipidemia and type 2 diabetes mellitus (T2DM), which are all more prevalent in these patients.5 Hyperinsulinemia also exacerbates cutaneous hyperandrogenism. system and positive airway pressure have been shown to be effective.34 䡲 Pregnancy loss Pregnant women with PCOS have a 30% to 50% increased risk of early spontaneous abortion.35 Recommendations: Weight reduction and medications such as metformin have been shown to reduce first trimester spontaneous abortion (SAB) rates.35 The optimum time to discontinue metformin has yet to be elucidated.36 䡲 Pregnancy complications Women with PCOS also have an increased risk of preterm delivery, hypertensive disorders, gestational diabetes and perinatal mortality.37 Maternal and neonatal risk are increased by iatrogenic multiple gestation from infertility treatment.18 Recommendations: Metformin continued during pregnancy decreases rates of gestational diabetes.38 Recommendations: Weight reduction and medications such as metformin and thiazolidinediones have all been shown to decrease insulin resistance.27-29 䡲 Dyslipidemia Lipid abnormalities, including elevated low-density lipoprotein cholesterol levels, triglyceride levels, total cholesterol to high-density lipoprotein cholesterol ratios, and decreased high-density lipoprotein cholesterol levels are found in women with PCOS.5 The prevalence of abnormal lipid levels, according to National Cholesterol Education Program criteria, approaches 70% in these patients.30 PCOS patients have April 2011 DOs Against DIABETES AOA Health Watch 21 Long-term complications Following are long-term complications related to PCOS, as well as treatment options. 䡲 Endometrial hyperplasia and carcinoma The chronic unopposed estrogen exposure in PCOS increases the risk of endometrial hyperplasia and endometrial carcinoma.39 An increased incidence of endometrial hyperplasia and atypia in the obese PCOS patient has been observed.40 Increased progression to carcinoma, however, has not been supported by epidemiologic evidence.39 PCOS patients have other risk factors for endometrial cancer including chronic hyperinsulinemia, increased concentrations of serum insulin-like growth factor, hyperandrogenemia and obesity.41 Recommendations: To prevent endometrial hyperplasia, the use of COCs or the use of intermittent progestins is warranted. For women with oligomenorrhea or amenorrhea, menstruation is induced by the administration of medroxyprogesterone acetate prior to initiation of COCs. Progestins can be given every one month to three months to induce a withdrawal bleed. Endometrial biopsy should be performed for all women older than 35 years with abnormal bleeding and women younger than 35 years with risk factors for endometrial hyperplasia. PCOS patients have other risk factors for endometrial cancer including chronic hyperinsulinemia, increased concentrations of serum insulin-like growth factor, hyperandrogenemia and obesity.41 䡲 Metabolic syndrome: Metabolic syndrome is associated with an increased risk of cardiovascular disease (CVD) and T2DM.43 Metabolic syndrome occurs in up to 43.6% of women with PCOS.42 Specifically for the PCOS patient, the presence of three of the following provides the diagnosis of metabolic syndrome: — abdominal obesity (waist circumference, ⬎35 inches) — triglycerides, ⬎150 mg/dL — high-density lipoprotein cholesterol, ⬎50 mg/dL — blood pressure, ⬎130 systolic and/or ⬎85 diastolic mm Hg — fasting glucose level, 110 mg/dL to 126 mg/dL, and/or two-hour glucose tolerance test result, 140 mg/dL to 199 mg/dL Recommendations: Treatment starts with lifestyle modification such as diet and exercise to reduce weight. Prevention of T2DM is achieved by administration of oral hypoglycemic metformin and thiazolidinediones. Use of lipid-lowering and antihypertensive therapies is effective in reducing cardiovascular risk.44 䡲 T2DM/Impaired glucose intolerance Fifty percent to 75% of women with PCOS have T2DM or prediabetes.45 The conversion rate from impaired glucose tolerance to frank diabetes is fivefold to tenfold higher in women with PCOS.45 Recommendations: Women should be screened with a fasting glucose test followed by a two-hour glucose test after ingesting a 75-gram glucose load.46 Management involving lifestyle modification, including diet, 22 AOA Health Watch exercise and weight reduction, and an oral hypoglycemic and insulin should be initiated. Lifestyle modification has been shown to be the superior treatment for improving insulin sensitivity, reducing weight, decreasing the incidence of T2DM and metabolic syndrome and improving risk factors for CVD.47 䡲 Cardiovascular disease Insulin-resistant states are associated with a greater susceptibility to coronary artery disease.25 Women with PCOS have increased CVD risk factors such as obesity, metabolic syndrome, hypertension, T2DM and dyslipidemia.45 These women exhibit greater endothelial dysfunction, arterial stiffness in the internal and external carotid arteries, presence of carotid and aortic plaque, increased thickness of intima media layers of the carotid artery and coronary artery and cerebrovascular artery calcification.48-50 Increased early left ventricular diastolic dysfunction, lower ejection fraction and a 7.1-times-higher risk than a non-PCOS patient for developing a myocardial infarction.50 Death from CVD is more common in women with PCOS.48 These risk factors could be the result of inflammation because C-reactive protein levels are elevated in PCOS patients.45 Recommendations: Women with PCOS should be screened for cardiovascular risk by determination of body mass index, fasting lipid and lipoprotein levels, and metabolic syndrome risk factors. Management focuses on modifying the CVD risk factors.51 䡲 Nonalcoholic steatohepatitis (NASH) The prevalence of nonalcoholic steatohepatitis is increased in the PCOS patient and is associated with obesity, T2DM, and hyperlipidemia.52 Insulin resistance may be the key mechanism leading to hepatic steatosis. DOs Against DIABETES April 2011 Recommendations: There is no proven effective therapy for nonalcoholic steatohepatitis, although modification of risk factors is recommended.53 䡲 Psychological disorders The prevalence of depression in PCOS patients is reported to be as high as 40%.44 Depression has been associated with insulin resistance, impaired glucose intolerance and obesity. Patients with PCOS may have low self-esteem and poor selfimage.53 They can suffer from social withdrawal, eating disorders, and anxiety and may attempt suicide. Recommendations: Treatment should include behavioral and psychological interventions adjunctive to standard medical care.45 Final notes PCOS is a complex medical condition that requires a multidisciplinary team approach for optimal treatment. It is important to understand that PCOS is a syndrome, not a disease, reflecting multiple potential etiologies with variable clinical expression of these and other features in adolescents and adults with this syndrome. PCOS treatments must be directed at addressing the immediate goals of patients and preventing short- and long-term complications. By addressing these complications and making lifestyle changes that are supported by appropriate pharmacologic interventions with continuous surveillance, patients’ quality of life can be improved. References 1. Carmina E, Lobo RA. Polycystic ovary syndrome (PCOS): arguably the most common endocrinopathy is associated with significant morbidity in women. J Clin Endocrinol Metab. 1999;84(6):1897-1899. 2. U.S. Department of Health and Human Services. The National Women’s Health Information Center. Office of Women’s Health Web site: Polycystic Ovary Syndrome (PCOS). http://www. womenshealth.gov/faq/polycystic-ovarysyndrome.cfm#b. Accessed January 25, 2011. 3. Futterweit W. Polycystic ovary syndrome: a common reproductive and metabolic disorder necessitating early recognition and treatment. Prim Care. 2007;34(4):761-789. April 2011 DOs Against DIABETES 4. Rotterdam ESHRE/ASRM-Sponsored PCOS Consensus Workshop Group. Revised 2003 consensus on diagnostic criteria and long-term health risks related to polycystic ovary syndrome. Fertil Steril. 2004;81(1):19-25. syndrome. Hum Reprod. 2008;23(3):462-477. Erratum in: Hum Reprod. 2008;23(6):1474. 19. Nishizawa H, Shimomura I, Kishida K, et al. Androgens decrease plasma adiponectin, and insulin-sensitizing adipocyte-derived protein. Diabetes. 2002;51(9):2734-2741. 5. Azziz R, Carmina E, Dewailly D, et al; Task Force on the Phenotype of the Polycystic Ovary Syndrome of The Androgen Excess and PCOS Society. The Androgen Excess and PCOS Society criteria for the polycystic ovary syndrome: the complete task force report. Fertil Steril. 2009;91(2):456-488. 20. Moran LJ, Pasquali R, Teede HJ, Hoeger KM, Norman RJ. Treatment of obesity in polycystic ovary syndrome: a position statement of the Androgen Excess and Polycystic Ovary Syndrome Society. Fertil Steril. 2009;92(6):1966-1982. 6. Stankiewicz M, Norman R. Diagnosis and management of polycystic ovary syndrome: a practical guide. Drugs. 2006;66(7):903-912. 21. Bohler H, Mokshagundam S, Winters SJ. Adipose tissue and reproduction in women. Fertil Steril. 2010;94(3):795-825. 7. Crosignani PG, Colombo M, Vegetti W, Somigliana E, Gessati A, Ragni G. Overweight and obese anovulatory patients with polycystic ovaries: parallel improvements in anthropometric indices, ovarian physiology and fertility rate induced by diet. Hum Reprod. 2003;18(9):1928-1932. 22. Krauss RM, Eckel RH, Howard B, et al. AHA Dietary Guidelines: revision 2000— a statement for healthcare professionals from the Nutrition Committee of the American Heart Association. Circulation. 2000;102(18):2284-2299. 8. Haas DA, Carr BR, Attia GR. Effects of metformin on body mass index, menstrual cyclicity, and ovulation induction in women with polycystic ovary syndrome. Fertil Steril. 2003;79(3):469-481. 9. Kolodziejczyk B, Duleba AJ, Spaczynski RZ, Pawelczyk L. Metformin therapy decreases hyperandrogenism and hyperinsulinemia in women with polycystic ovary syndrome. Fertil Steril. 2000;73(6):1149-1154. 10. Moghetti P, Tosi F, Tosti A, et al. Comparison of spironolactone, flutamide and finasteride efficacy in the treatment of hirsutism: a randomized, double-blind, placebo-controlled trial. J Clin Endocrinol Metab. 2000;85(1):89-94. 11. Azziz R. The evaluation and management of hirsutism. Obstet Gynecol. 2003;101(5 pt 1):995-1007. 12. Harwood K, Vuguin P, DiMartino-Nardi J. Current approaches to the diagnosis and treatment of polycystic ovarian syndrome in youth. Horm Res. 2007;68(5):209-217. 13. Haider A, Shaw JC. Treatment of acne vulgaris. JAMA. 2004;292(6):726-735. 14. Lucky AW, Piacquadio DJ, Ditre CM, et al. A randomized, placebo-controlled trial of 5% and 2% topical minoxidil solutions in the treatment of female pattern hair loss. J Am Acad Dermatol. 2004;50(4):541-553. 15. Van Dam EW, Roelfsema F, Veldjuis JD, et al. Retention of estradiol negative feedback relationship to LH predicts ovulation in response to caloric restriction and weight loss in obese patients with polycystic ovary syndrome. Am J Physiol Endocrinol Metab. 2004;286(4):E615-E620. 16. Patel SM, Nestler JE. Fertility in polycystic ovary syndrome. Endocrinol Metab Clin North Am. 2006;35(1):137-155. 17. Hassan MA, Killick SR. Negative lifestyle is associated with a significant reduction in fecundity. Fertil Steril. 2004;81(2):384-392. 18. Thessaloniki ESHRE/ASRM-Sponsored PCOS Consensus Workshop Group. Consensus on infertility treatment related to polycystic ovary 23. Bray GA. Medical therapy for obesity—current status and future hopes. Med Clin North Am. 2007;91(6):1225-1253. 24. Buchwald H, Avidor Y, Braunwald E, et al. Bariatric surgery: a systematic review and meta-analysis. JAMA. 2004;292(14):1724-1737. Erratum in: JAMA. 2005;293(14):1728. 25. Goodarzi MO, Korenman SG. The importance of insulin resistance in polycystic ovary syndrome. Fertil Steril. 2003;80(2):255-258. 26. Svendsen PF, Madsbad S, Nilas L. The insulin-resistant phenotype of polycystic ovary syndrome. Fertil Steril. 2010;94(3):1052-1058. 27. Norman RJ, Davies MJ, Lord J, Moran LJ. The role of lifestyle modification in polycystic ovary syndrome. Trends Endocrinol Metab. 2002;13(6):251-257. 28. Moghetti P, Castello R, Negri C, et al. Metformin effects on clinical features, endocrine and metabolic profiles, and insulin sensitivity in polycystic ovary syndrome: a randomized, double-blind, placebo controlled 6-month trial, followed by open, long-term clinical evaluation. J Clin Endocrinol Metab. 2000;85(1):139-146. 29. Ortega-Gonzalez C, Luna S, Hernandez L, et al. Responses of serum androgen and insulin resistance to metformin and pioglitazone in obese, insulin-resistant women with polycystic ovary syndrome. J Clin Endocrinol Metab. 2005;90(3):1360-1365. 30. Legro RS, Kunselman AR, Dunaif A. Prevalence and predictors of dyslipidemia in women with polycystic ovary syndrome. Am J Med. 2001;111(8):607-613. 31. Rizzo M, Berneis K, Carmina E, Rini GB. How should we manage atherogenic dyslipidemia in women with polycystic ovary syndrome? Am J Obstet Gynecol. 2008;198(1):28.e1-28.e5. 32. Vgontzas AN, Legro RS, Bixler EO, Grayev A, Kales A, Chrousos GP. Polycystic ovary syndrome is associated with obstructive sleep apnea and daytime sleepiness: role of insulin resistance. J Clin Endocrinol Metab. 2001;86(2):517-520. AOA Health Watch 23 33. Tasali E, Van Cauter E, Ehrmann DA. Relationships between sleep disordered breathing and glucose metabolism in polycystic ovary syndrome. J Clin Endocrinol Metab. 2006;91(1):36-42. 34. Epstein LJ, Kristo D, Strollo PJ, et al. Adult Obstructive Sleep Apnea Task Force of the American Academy of Sleep Medicine. Clinical guideline for the evaluation, management, and long-term care of obstructive sleep apnea in adults. J Clin Sleep Med. 2009;5(3):263-276. 35. Glueck CJ, Wang P, Goldenberg N, Sieve-Smith L. Pregnancy outcomes among women with polycystic ovary syndrome treated with metformin. Hum Reprod. 2002;17(11):2858-2864. 36. Thatcher SS, Jackson EM. Pregnancy outcome in infertile patients with polycystic ovary syndrome who were treated with metformin. Fertil Steril. 2006;85(4):1002-1009. 37. Boomsma CM, Eijkemans MJC, Hughes EG, Visser GH, Fauser BC, Macklon NS. A metaanalysis of pregnancy outcomes in women with polycystic ovary syndrome. Hum Reprod Update. 2006;12(6):673-683. 38. Glueck CJ, Wang P, Kobayashi S, Phillips H, Sieve-Smith L. Metformin therapy throughout pregnancy reduces the development of gestational diabetes in women with polycystic ovary syndrome. Fertil Steril. 2002;77(3):520-525. 39. Hardiman P, Pillay OC, Atiomo W. Polycystic ovary syndrome and endometrial carcinoma. Lancet. 2003;361(9371):1810-1812. 40. Cheung AP. Ultrasound and menstrual history in predicting endometrial hyperplasia in polycystic ovary syndrome. Obstet Gynecol. 2001;98(2):325-331. 41. Giudice LC. Endometrium in PCOS: Implantation and predisposition to endocrine CA. Best Pract Res Clin Endocrinol Metab. 2006;20(2):235-244. 44. Glueck CJ, Papanna R, Wang P, Goldenberg N, Sieve-Smith L. Incidence and treatment of metabolic syndrome in newly referred women with confirmed polycystic ovarian syndrome. Metabolism. 2003;52(7):908-915. 45. Farrell K, Antoni MH. Insulin resistance, obesity, inflammation, and depression in polycystic ovary syndrome: biobehavioral mechanisms and interventions. Fertil Steril. 2010;94(5):1565-1574. 46. Ovalle F, Azziz R. Insulin resistance, polycystic ovary syndrome, and type 2 diabetes mellitus. Fertil Steril. 2002;77(6):1095-1105. 47. American Diabetes Association. Standards of medical care in diabetes—2010. Diabetes Care. 2010;33(suppl 1):S11-S61. For more information You can find out more about PCOS by contacting womenshealth.gov at (800) 994-9662 or the following organizations: Women’s Health Research, National Institute of Child Health and Human Development, NIH, HHS Telephone: (800) 370-2943 http://www.nichd.nih.gov/ womenshealth American Association of Clinical Endocrinologists 48. Moran LJ, Misso ML, Wild RA, Norman RJ. Impaired glucose tolerance, type 2 diabetes and metabolic syndrome in polycystic ovary syndrome: a systematic review and meta-analysis. Hum Reprod Update. 2010;16(4):347-363. Telephone: (904) 353-7878 http://www.aace.com 49. Dokras A, Bochner M, Hollinrake E, Markham S, Vanvoorhis B, Jagasia DH. Screening women with polycystic ovary syndrome for metabolic syndrome. Obstet Gynecol. 2005;106(1):131-137. Telephone: (202) 638-5577 http://www.acog.org 50. Rizzo M, Berneis K, Spinas G, Rini GB, Carmina E. Long-term consequences of polycystic ovary syndrome on cardiovascular risk. Fertil Steril. 2009;91(suppl 4):1563-1567. Telephone: (205) 978-5000 http://www.asrm.org 51. Sharma ST, Nestler JE. Prevention of diabetes and cardiovascular disease in women with PCOS: treatment with insulin sensitizers. Best Pract Res Clin Endocrinol Metab. 2006;20(2): 245-260. 52. Cerda C, Perez-Ayuso RM, Riquelme A, et al. Nonalcoholic fatty liver disease in women with polycystic ovary syndrome. J Hepatol. 2007;47:412-417. 42. Grundy SM, Cleeman JI, Daniels SR, et al. Diagnosis and management of the metabolic syndrome: an American Heart Association/ National Heart, Lung, and Blood Institute Scientific Statement. Circulation. 2005;112(17):2735-2752. 53. Schwimmer JB, Khorram O, Chiu V, Schwimmer WB. Abnormal aminotransferase activity in women with polycystic ovary syndrome. Fertil Steril. 2005;83(2):494-497. 43. Apridonidze T, Essah PA, Iuorno MJ, Nestler JE. Prevalence and characteristics of the metabolic syndrome in women with polycystic ovary syndrome. J Clin Endocrinol Metab. 2005;90(4):1929-1935. 54. Hollinrake E, Abreu A, Maifeld M, Van Voorhis BJ, Dokras A. Increased risk of depressive disorders in women with polycystic ovary syndrome. Fertil Steril. 2007;87(6):1369-1376. HW American College of Obstetricians and Gynecologists American Society for Reproductive Medicine Center for Applied Reproductive Science Telephone: (423) 461-8880 http://www.ivf-et.com InterNational Council on Infertility Information Dissemination, Inc. Telephone: (703) 379-9178 http://www.inciid.org Polycystic Ovarian Syndrome Association, Inc. http://www.pcosupport.org The Hormone Foundation Telephone: (800) 467-6663 http://www.hormone.org Draion M. Burch, DO, an obstetrics and gynecology resident from Detroit, serves as the intern and resident representative to the American Osteopathic Association Board of Trustees. Dr. Burch also serves as an intern/resident trustee to the Michigan Osteopathic Association Board of Trustees. He also serves as the chief resident of the obstetrics and gynecology residency program for the Statewide Campus System Michigan State University College of Osteopathic Medicine/St. John Providence Health System Osteopathic Division Macomb-Oakland Hospital, Macomb Center, in Warren, Michigan. Dr. Burch received the 2009 St. John Osteopathic Division OBGYN Resident of the Year award and has been very active at state and national levels. He can be reached at [email protected]. Paige Paladino, DO, is a first year resident in obstetrics and gynecology at St. John Macomb-Oakland Hospital, Macomb Center in Warren, Michigan. She graduated from Kansas City University of Medicine and Biosciences, College of Osteopathic Medicine in 2010. Dr. Paladino can be reached at [email protected]. 24 AOA Health Watch DOs Against DIABETES April 2011