Araştırma Makalesi
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Polikistik Over Sendromlu Adölesanlarda Serum Ürokortin 2, Ürokortin 3 ve Antimüllerian Hormon Düzeyleri

Yıl 2018, Cilt: 3 Sayı: 2, 21 - 26, 31.05.2018

Öz



Amaç: Polikistik over sendromu (PKOS) kronik anovulasyon ve hiperandrojenizm ile karakterize, üreme çağındaki kadınların %5-10’unu etkileyen yaygın bir endokrin bozukluktur. PKOS’lu adölesanlarda serum ürokortin 2 ve ürokortin 3 ve Antimüllerian Hormon (AMH) düzeylerinin araştırılması ve sağlıklı kontroller ile karşılaştırılması amaçlanmıştır. Gereç ve Yöntem: Çalışmaya Rotterdam kriterlerine göre PKOS tanısı alan (ortalama yaş: 16.1±0.98 yıl) 37 adölesan ve 39 sağlıklı (ortalama yaş: 16.1±1.08) kontrol olmak üzere 76 adölesan alındı. Tüm hastaların antropometrik ölçümleri ve pubertal gelişim evreleri kaydedildi. Modifiye Ferriman- Gallwey skorlama sistemine göre hirsutizm skorlaması yapıldı. Homa-IR >4 değeri insülin direnci olarak kabul edildi. Biyoelektriksel impedans analizi ile olguların vücut yağ-kas oranı değerlendirildi. Açlık serum glukoz, insülin, lipit, Follikül Stimüle Edici Hormon, Lüteinleştiren Hormon, Seks Hormonu Bağlayıcı Globulin, Serbest Testosteron, Total Testosteron düzeyleri ölçüldü. USG ile PKOS tanısı alan olguların over morfolojileri değerlendirildi. Bulgular: Her iki grup arasında yaş ortalaması açısından fark saptanmadı (p>.05). PKOS’lu grupta VKİ SDS, boy SDS ve bel çevresi SDS kontrol grubundan daha yüksek bulundu (p<.05). Obezite, akne, alopesi, akantozis, stria, oligo-amonere ve hirsutizm skoru PKOS grubunda istatiksel olarak anlamlı yüksek saptandı (p<.01). AMH ve ürokortin 2-3 düzeyleri açısından iki grup arasında farklılık yoktu (p>.05). Hirsutizm şiddeti ile AMH, ürokortin 2 ve 3 düzeyleri arasında ilişki saptanmadı (p>.05). AMH, ürokortin 2 ve ürokortin 3 arasında anlamlı pozitif korelasyon tespit edilirken, LH, FSH, serbest testosteron, total testosteron ve SHBG düzeyleri ile AMH, ürokortin 2 ve ürokortin 3 düzeyleri arasında korelasyon gösterilemedi. Sonuç: Bu çalışmada ürokortin 2 ve ürokortin 3 ve AMH düzeyleri ile PKOS arasında ilişki saptanamamıştır. Bu konuda daha ileri çalışmalara ihtiyaç vardır.


Objective: Polycystic ovary syndrome (PCOS) is a frequent endocrine disorder characterized by chronic anovulation and hyperandrogenism, affecting 5 to 10 percent of women in reproductive age. It was aimed in this study to examine serum urocortin 2, urocortin 3 and AMH levels in adolescents with PCOS and to compare the results with those of healthy adolescents. Material and Methods: 37 adolescent girls (16.1±0.98 years) with PCOS diagnosed according to Rotterdam criteria and 39 healthy adolescent girls (16.1±1.08 years) were recruited to the study. All patients’ anthropometric measurements and pubertal development stages were recorded. Hirsutism was scored according to Ferriman-Gallwey scoring system. Insulin resistance was diagnosed when HOMA-IR was >4. Bioelectrical impedance analysis was used to measure body fat percentage and fat free mass. Levels of fasting glucose, insulin, lipids, follicle stimulating hormone, luteinizing hormone, sex hormone binding globulin, free and total testosterone, urocortin 2 and 3, and AMH were measured. Suprapubic pelvic USG was also performed in the PCOS group. Findings: The mean age of the two groups was similar (p>.05). In the PCOS group, body mass index SDS, height SDS and waist circumference SDS was significantly higher than the control group (p<.05). Obesity, acne, alopecia, acanthosis, stria, oligomenorrhea and hirsutism score were significantly higher in the PCOS group (p<.01). AMH, urocortin 2 and urocortin 3 levels showed no significant difference between the two groups (p>.05). There was no significant correlation between hirsutism score and AMH, urocortin 2 and urocortin 3 levels (p>.05). There was a significant positive correlation between AMH, urocortin 2 and urocortin 3, but no correlation was found between LH, FSH, free testosteron, total testosterone, SHBG levels and AMH, urocortin 2 and urocortin 3. Conclusion: This study did not find any relationship between urocortin 2, urocortin 3 and AMH levels and PCOS. Further studies are needed to search about this topic.

Kaynakça

  • 1. Stein IF, Leventhal ML. Amenorrhea associated with bilateral polycystic ovaries. Am J Obstet Gynecol 1935; 29: 181-191. 2. Piouka A et al.:Anti-Mu¨llerian hormone levels reflect severity of PCOS but are negatively influenced by obesity: relationship with increased luteinizing hormone levels. Am J Physi ol Endocrinol Metab 296: E238, 2009. 3. Hassan A, Gordon CM. Polycystic ovary syndrome update in adolescence. Curr Opin Pediatr. 2007; 19: 389-397. 4. Azziz R, Carmina E, Dewailly D, Diamanti-Kandarakis E, Escobar-Morreale HF, Futterweit W, Janssen OE, Legro RS, Norman RJ, Taylor AE, Witchel SF. Positions statement: criteria for defining polycystic ovary syndrome as a predominantly hyperandrogenic syndrome: an Androgen Excess Society guideline. J Clin Endocrinol Metab. 2006; 91: 4237-4245. 5. Rotterdam ESHRE/ASRM-Sponsored PCOS consensus workshop group. Revised 2003 consensus on diagnostic criteria and longterm health risks related to polycystic ovary syndrome (PCOS). Hum Reprod 2004;19(1): 41-47. 6. Bundak R, Furman A, Gunoz H, Darendeliler F, Bas F,Neyzi O. Body mass index references for Turkish children. Acta pediatri 2006;95(2):194-198. 7. Hatipoglu N, Ozturk A, Mazicioglu MM, Kurtoglu S, Seyhan S, Lokoglu F. Waist circumference percentiles for 7 to 17 years old Turkish children and adolescents. Eur J Pediatr 2008;167(4):383-389 8. Ten S, Maclaren N. Insulin Resistance Syndrome in children. J Clin Endocrinol Metab 2004; 89: 2526-2539 9. Ehrmann DA, Sturis J, Byrne MM, Karrison T, Rosenfield RL, Polonsky KS. Insulin secretory defects in polycystic ovary syndrome. Relationship to insulin sensitivity and family history of non-insulin-dependent diabetes mellitus. J Clin Invest 1995; 96: 520–527. 10. Kurtoglu S, Hatipoglu N, Mazıcığğlu M, Kendirci M, Keskin M, Kondolot M. Insulin Resistance in Obese Children and Adolescents: Homa-IR Cut-Off Levels in the Prepubertal and Pubertal Periods. J Clin Res Ped Endo 2010;100-106. 11. Farquhar CM, Birdsall M, Manning P, et al. The prevalence of polycystic ovaries on ultrasound scanning in a population of randomly selected women. Australian and NewZealand Obstetrics and Gynaecology 1994;34:67-72. 12. Boomsma CM, Fauser BC, Macklon NS. Pregnancy complications in women with polycystic ovary syndrome.Semin Reprod Med. 2008; 26: 72-84. Review. 13. Nair MK, Pappachan P, Balakrishnan S, Leena ML, George B, Russell PS. Menstrual irregularity and poly cystic ovarian syndrome among adolescent girls--a 2 year follow-up study. Indian J Pediatr. 2012; 79: 69-73. 14. Yetim A, Yetim Ç, Baş F, Erol OB, Çığ G, Uçar A, Darendeliler F. Anti-Müllerian hormone and inhibin-A levels may be used as surrogates of polycystic ovary syndrome in adolescents, but not inhibin-B or insulin-like peptide-3:Preliminary results. J Clin Endocrinol Metab 2016; 10: 3253-3255. 15. Broekmans FJ, Knauff EAH, Valkenburg O, Laven JS, Eijkemans MJ, Fauser BCJM. PCOS according to the Rotterdam consensus criteria: change in prevalence among WHO-II anovulation and association with metabolic factors. BJOG 2006;113:1210-1217. 16. Moran LJ, Pasquali R, Teede HJ, et al. Treatment of obesity in polycystic ovary syndrome: a position statement of the androgen excess and polycystic ovary syndrome society. Fertil Steril 2009; 92: 1966-1982. 17. Hızlı D, Kosger H, Hacıvelioglu S, Kosus N, Kosus A, Kamalak Z, Akcal B. The Effect of Body Mass Index on Acne, Hirsutism and Menstrual Irregularity Symptoms in Turkish Adolescent Girls Gazi Medical Journal. 2013;24: 67-69. 18. Eilertsen TB, Vanky E, Carlsen SM. Anti-Mullerian hormone in the diagnosis of polycystic ovary syndrome: can morphologic description be replaced? Hum Reprod 2012;27(8):2494-2502. 19. Goldzieher JW. Polycystic ovarian disease. Fertility Sterility 1981;35:371-394. 20. Pfeifer SM, Kives S. Polycystic ovary syndrome in the adolescent. Obstet Gynecol Clin North Am 2009; 36: 129–152. 21. Cela E, Robertson C, Rush K, Kousta E, White DM, Wilson H, Lyons G, Kingsley P, McCarthy MI, Franks S. Eur. J. Endocrinol, 2003 11; 149(5): 439-442. 22. Hassan A, Gordon CM. Polycystic ovary syndrome update in adolescence. Curr Opin Pediatr. 2007; 19: 389-397. 23. Coviello AD, Legro RS, Dunaif A. Adolescent girls with polycystic ovary syndrome have an increased risk of the metabolic syndrome associated with increasing androgen levels in-dependent of obesity and insulin resistance. J Clin Endocrinol Metab 2006; 91: 492–497. 24. Alemzadeh R, Kichler J, Calhoun M. Spectrum of metabolic dysfunction in relationship with hyperandrogenemia in obese adolescent girls with polycystic ovary syndrome. Eur J Endocrinol 2010; 162: 1093–1099. 25. Hooff MH, Voorhorst FJ, Kaptein MB, et al. Polycystic ovaries in adolescents and the relationship with menstrual cycle patterns, luteinizing hormone, androgens, and insulin. Fertil Steril 2000; 74: 49–58. 26. Çalışkan E, Kılıç T, Bodur H, Zeteroğlu Ş. The frequency of metabolic syndrome in women with polycystic ovaries at reproductive ages and comparison of different metabolic syndrome diagnostic criteri J Turk Ger Gynecol Assoc. 2007;8:402-407. 27. Furuzetti F, Perini D, Lazzarini V, et al. Adolescent girls with polycystic ovaary syndrome showing different phenotypes have a different metabolic profile associated with increasing androgen levels. Fertil Steril 2009; 92: 626-634. 28. Sawathiparnich P, Weerakulwattana L, Santiprabhob J, Likit-maskul S. Obese adolescent girls with polycystic ovary syndrome (PCOS) have more severe insulin resistance measured by HOMA-IR score than obese girls without PCOS. J Med Assoc Thai 2005; 88: 33–37. 29. Hart R. Polycystic ovarian syndrome-prognosis and treatment outcomes. Curr Opin Obstet Gynecol. 2007; 19: 529-535. 30. Dunaif A, Wu X, Lee A, Diamanti-Kandarakis E. Defects in insulin receptorsignaling in vivo in the polycystic ovary syndrome (PCOS). Am J Physiol Endocrinol Metab 2001; 281: E392–E399. 31. Topçu H.0, Topçu S, Oskovi A, Güzel A. Comparison oft he clinical and laboratory outcomes in adolescent and adults with polycystic ovary syndrome. The Journal of Gynecology-Obstetrics and Neonatoloogy 2014;11: 82-84. 32. Hızlı D, Kosger H, Hacıvelioglu S, Kosus N, Kosus A, Kamalak Z, Akcal B. The Effect of Body Mass Index on Acne, Hirsutism and Menstrual Irregularity Symptoms in Turkish Adolescent Girls Gazi Medical Journal. 2013;24: 67-69. 33. Cengiz H, Ekin M, Dagdeviren H, Yıldız S, Kaya C, Kanawati A. Comparison of serum anti-müllerian hormone levels in normal weight and overweight-obese adolescent patients with polycystic ovary syndrome. Eur. J. Obstet Gynecol Reprod Biol. 2014;180: 46-50. 34. Villarroel C, Lopez P, Merino PM, Iniguez G, Sir-Peterman T. Hirsutism and oligomenorrhea are appropriate screening screening criteria for polycystic ovary syndrome in adolescents. Gynecol Endocrinol 2015;31: 625-629. 35. Sopher AB, Grigoriev G, Laura D, Cameo T, Lerner JP, Chang RJ, Mcmahon DJ. Anti-Müllerian hormone may be a useful adjunct in the diagnosis of polycystic ovary syndrome in nonobese adolescents. J Pediatr Endocrinol Metab. 2014;27: 1175-1179. 36. Increased circulating urocortin-3 levels is associated with polycystic ovary syndrome. Muzaffer Temur, Özgür Yilmaz, Saliha Aksun, Pelin Özün Özbay, Mehmet Calan, Tuncay Küme, Murat Karakulak Hüseyin Anıl Korkmaz Gynecol Endocrinol. 2016 Mar;32(3):218-222.
Yıl 2018, Cilt: 3 Sayı: 2, 21 - 26, 31.05.2018

Öz

Kaynakça

  • 1. Stein IF, Leventhal ML. Amenorrhea associated with bilateral polycystic ovaries. Am J Obstet Gynecol 1935; 29: 181-191. 2. Piouka A et al.:Anti-Mu¨llerian hormone levels reflect severity of PCOS but are negatively influenced by obesity: relationship with increased luteinizing hormone levels. Am J Physi ol Endocrinol Metab 296: E238, 2009. 3. Hassan A, Gordon CM. Polycystic ovary syndrome update in adolescence. Curr Opin Pediatr. 2007; 19: 389-397. 4. Azziz R, Carmina E, Dewailly D, Diamanti-Kandarakis E, Escobar-Morreale HF, Futterweit W, Janssen OE, Legro RS, Norman RJ, Taylor AE, Witchel SF. Positions statement: criteria for defining polycystic ovary syndrome as a predominantly hyperandrogenic syndrome: an Androgen Excess Society guideline. J Clin Endocrinol Metab. 2006; 91: 4237-4245. 5. Rotterdam ESHRE/ASRM-Sponsored PCOS consensus workshop group. Revised 2003 consensus on diagnostic criteria and longterm health risks related to polycystic ovary syndrome (PCOS). Hum Reprod 2004;19(1): 41-47. 6. Bundak R, Furman A, Gunoz H, Darendeliler F, Bas F,Neyzi O. Body mass index references for Turkish children. Acta pediatri 2006;95(2):194-198. 7. Hatipoglu N, Ozturk A, Mazicioglu MM, Kurtoglu S, Seyhan S, Lokoglu F. Waist circumference percentiles for 7 to 17 years old Turkish children and adolescents. Eur J Pediatr 2008;167(4):383-389 8. Ten S, Maclaren N. Insulin Resistance Syndrome in children. J Clin Endocrinol Metab 2004; 89: 2526-2539 9. Ehrmann DA, Sturis J, Byrne MM, Karrison T, Rosenfield RL, Polonsky KS. Insulin secretory defects in polycystic ovary syndrome. Relationship to insulin sensitivity and family history of non-insulin-dependent diabetes mellitus. J Clin Invest 1995; 96: 520–527. 10. Kurtoglu S, Hatipoglu N, Mazıcığğlu M, Kendirci M, Keskin M, Kondolot M. Insulin Resistance in Obese Children and Adolescents: Homa-IR Cut-Off Levels in the Prepubertal and Pubertal Periods. J Clin Res Ped Endo 2010;100-106. 11. Farquhar CM, Birdsall M, Manning P, et al. The prevalence of polycystic ovaries on ultrasound scanning in a population of randomly selected women. Australian and NewZealand Obstetrics and Gynaecology 1994;34:67-72. 12. Boomsma CM, Fauser BC, Macklon NS. Pregnancy complications in women with polycystic ovary syndrome.Semin Reprod Med. 2008; 26: 72-84. Review. 13. Nair MK, Pappachan P, Balakrishnan S, Leena ML, George B, Russell PS. Menstrual irregularity and poly cystic ovarian syndrome among adolescent girls--a 2 year follow-up study. Indian J Pediatr. 2012; 79: 69-73. 14. Yetim A, Yetim Ç, Baş F, Erol OB, Çığ G, Uçar A, Darendeliler F. Anti-Müllerian hormone and inhibin-A levels may be used as surrogates of polycystic ovary syndrome in adolescents, but not inhibin-B or insulin-like peptide-3:Preliminary results. J Clin Endocrinol Metab 2016; 10: 3253-3255. 15. Broekmans FJ, Knauff EAH, Valkenburg O, Laven JS, Eijkemans MJ, Fauser BCJM. PCOS according to the Rotterdam consensus criteria: change in prevalence among WHO-II anovulation and association with metabolic factors. BJOG 2006;113:1210-1217. 16. Moran LJ, Pasquali R, Teede HJ, et al. Treatment of obesity in polycystic ovary syndrome: a position statement of the androgen excess and polycystic ovary syndrome society. Fertil Steril 2009; 92: 1966-1982. 17. Hızlı D, Kosger H, Hacıvelioglu S, Kosus N, Kosus A, Kamalak Z, Akcal B. The Effect of Body Mass Index on Acne, Hirsutism and Menstrual Irregularity Symptoms in Turkish Adolescent Girls Gazi Medical Journal. 2013;24: 67-69. 18. Eilertsen TB, Vanky E, Carlsen SM. Anti-Mullerian hormone in the diagnosis of polycystic ovary syndrome: can morphologic description be replaced? Hum Reprod 2012;27(8):2494-2502. 19. Goldzieher JW. Polycystic ovarian disease. Fertility Sterility 1981;35:371-394. 20. Pfeifer SM, Kives S. Polycystic ovary syndrome in the adolescent. Obstet Gynecol Clin North Am 2009; 36: 129–152. 21. Cela E, Robertson C, Rush K, Kousta E, White DM, Wilson H, Lyons G, Kingsley P, McCarthy MI, Franks S. Eur. J. Endocrinol, 2003 11; 149(5): 439-442. 22. Hassan A, Gordon CM. Polycystic ovary syndrome update in adolescence. Curr Opin Pediatr. 2007; 19: 389-397. 23. Coviello AD, Legro RS, Dunaif A. Adolescent girls with polycystic ovary syndrome have an increased risk of the metabolic syndrome associated with increasing androgen levels in-dependent of obesity and insulin resistance. J Clin Endocrinol Metab 2006; 91: 492–497. 24. Alemzadeh R, Kichler J, Calhoun M. Spectrum of metabolic dysfunction in relationship with hyperandrogenemia in obese adolescent girls with polycystic ovary syndrome. Eur J Endocrinol 2010; 162: 1093–1099. 25. Hooff MH, Voorhorst FJ, Kaptein MB, et al. Polycystic ovaries in adolescents and the relationship with menstrual cycle patterns, luteinizing hormone, androgens, and insulin. Fertil Steril 2000; 74: 49–58. 26. Çalışkan E, Kılıç T, Bodur H, Zeteroğlu Ş. The frequency of metabolic syndrome in women with polycystic ovaries at reproductive ages and comparison of different metabolic syndrome diagnostic criteri J Turk Ger Gynecol Assoc. 2007;8:402-407. 27. Furuzetti F, Perini D, Lazzarini V, et al. Adolescent girls with polycystic ovaary syndrome showing different phenotypes have a different metabolic profile associated with increasing androgen levels. Fertil Steril 2009; 92: 626-634. 28. Sawathiparnich P, Weerakulwattana L, Santiprabhob J, Likit-maskul S. Obese adolescent girls with polycystic ovary syndrome (PCOS) have more severe insulin resistance measured by HOMA-IR score than obese girls without PCOS. J Med Assoc Thai 2005; 88: 33–37. 29. Hart R. Polycystic ovarian syndrome-prognosis and treatment outcomes. Curr Opin Obstet Gynecol. 2007; 19: 529-535. 30. Dunaif A, Wu X, Lee A, Diamanti-Kandarakis E. Defects in insulin receptorsignaling in vivo in the polycystic ovary syndrome (PCOS). Am J Physiol Endocrinol Metab 2001; 281: E392–E399. 31. Topçu H.0, Topçu S, Oskovi A, Güzel A. Comparison oft he clinical and laboratory outcomes in adolescent and adults with polycystic ovary syndrome. The Journal of Gynecology-Obstetrics and Neonatoloogy 2014;11: 82-84. 32. Hızlı D, Kosger H, Hacıvelioglu S, Kosus N, Kosus A, Kamalak Z, Akcal B. The Effect of Body Mass Index on Acne, Hirsutism and Menstrual Irregularity Symptoms in Turkish Adolescent Girls Gazi Medical Journal. 2013;24: 67-69. 33. Cengiz H, Ekin M, Dagdeviren H, Yıldız S, Kaya C, Kanawati A. Comparison of serum anti-müllerian hormone levels in normal weight and overweight-obese adolescent patients with polycystic ovary syndrome. Eur. J. Obstet Gynecol Reprod Biol. 2014;180: 46-50. 34. Villarroel C, Lopez P, Merino PM, Iniguez G, Sir-Peterman T. Hirsutism and oligomenorrhea are appropriate screening screening criteria for polycystic ovary syndrome in adolescents. Gynecol Endocrinol 2015;31: 625-629. 35. Sopher AB, Grigoriev G, Laura D, Cameo T, Lerner JP, Chang RJ, Mcmahon DJ. Anti-Müllerian hormone may be a useful adjunct in the diagnosis of polycystic ovary syndrome in nonobese adolescents. J Pediatr Endocrinol Metab. 2014;27: 1175-1179. 36. Increased circulating urocortin-3 levels is associated with polycystic ovary syndrome. Muzaffer Temur, Özgür Yilmaz, Saliha Aksun, Pelin Özün Özbay, Mehmet Calan, Tuncay Küme, Murat Karakulak Hüseyin Anıl Korkmaz Gynecol Endocrinol. 2016 Mar;32(3):218-222.
Toplam 1 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Bölüm Araştırma Makaleleri
Yazarlar

Selin Öztürk Bu kişi benim

Bumin Nuri Dündar

Cemil Koçyiğit Bu kişi benim

Gönül Çatlı Bu kişi benim

Yayımlanma Tarihi 31 Mayıs 2018
Gönderilme Tarihi 2 Mayıs 2018
Yayımlandığı Sayı Yıl 2018 Cilt: 3 Sayı: 2

Kaynak Göster

APA Öztürk, S., Dündar, B. N., Koçyiğit, C., Çatlı, G. (2018). Polikistik Over Sendromlu Adölesanlarda Serum Ürokortin 2, Ürokortin 3 ve Antimüllerian Hormon Düzeyleri. İzmir Katip Çelebi Üniversitesi Sağlık Bilimleri Fakültesi Dergisi, 3(2), 21-26.
AMA Öztürk S, Dündar BN, Koçyiğit C, Çatlı G. Polikistik Over Sendromlu Adölesanlarda Serum Ürokortin 2, Ürokortin 3 ve Antimüllerian Hormon Düzeyleri. İKÇÜSBFD. Mayıs 2018;3(2):21-26.
Chicago Öztürk, Selin, Bumin Nuri Dündar, Cemil Koçyiğit, ve Gönül Çatlı. “Polikistik Over Sendromlu Adölesanlarda Serum Ürokortin 2, Ürokortin 3 Ve Antimüllerian Hormon Düzeyleri”. İzmir Katip Çelebi Üniversitesi Sağlık Bilimleri Fakültesi Dergisi 3, sy. 2 (Mayıs 2018): 21-26.
EndNote Öztürk S, Dündar BN, Koçyiğit C, Çatlı G (01 Mayıs 2018) Polikistik Over Sendromlu Adölesanlarda Serum Ürokortin 2, Ürokortin 3 ve Antimüllerian Hormon Düzeyleri. İzmir Katip Çelebi Üniversitesi Sağlık Bilimleri Fakültesi Dergisi 3 2 21–26.
IEEE S. Öztürk, B. N. Dündar, C. Koçyiğit, ve G. Çatlı, “Polikistik Over Sendromlu Adölesanlarda Serum Ürokortin 2, Ürokortin 3 ve Antimüllerian Hormon Düzeyleri”, İKÇÜSBFD, c. 3, sy. 2, ss. 21–26, 2018.
ISNAD Öztürk, Selin vd. “Polikistik Over Sendromlu Adölesanlarda Serum Ürokortin 2, Ürokortin 3 Ve Antimüllerian Hormon Düzeyleri”. İzmir Katip Çelebi Üniversitesi Sağlık Bilimleri Fakültesi Dergisi 3/2 (Mayıs 2018), 21-26.
JAMA Öztürk S, Dündar BN, Koçyiğit C, Çatlı G. Polikistik Over Sendromlu Adölesanlarda Serum Ürokortin 2, Ürokortin 3 ve Antimüllerian Hormon Düzeyleri. İKÇÜSBFD. 2018;3:21–26.
MLA Öztürk, Selin vd. “Polikistik Over Sendromlu Adölesanlarda Serum Ürokortin 2, Ürokortin 3 Ve Antimüllerian Hormon Düzeyleri”. İzmir Katip Çelebi Üniversitesi Sağlık Bilimleri Fakültesi Dergisi, c. 3, sy. 2, 2018, ss. 21-26.
Vancouver Öztürk S, Dündar BN, Koçyiğit C, Çatlı G. Polikistik Over Sendromlu Adölesanlarda Serum Ürokortin 2, Ürokortin 3 ve Antimüllerian Hormon Düzeyleri. İKÇÜSBFD. 2018;3(2):21-6.