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Abstract Number: 2514

Subclinical Reduced Ovarian Reserve in Adult Polymiositis Patients

Fernando Henrique Carlos de Souza1, Clovis A Silva2, Lucas Yugo Shiguehara Yamakami3, Vilma S. T. Viana4, Eloisa Bonfá5 and Samuel Katsuyuki Shinjo1, 1Rheumatology Division, Rheumatology Division, Faculdade de Medicina da USP, São Paulo, Brazil, 2Pediatric Rheumatology, Faculdade de Medicina da Universidade de São Paulo, Sao Paulo, Brazil, 3Gynecology Department, Faculdade de Medicina da Universidade de São Paulo, Sao Paulo, Brazil, 4Rheumatology Division, University of Sao Paulo, Sao Paulo, Brazil, 5Clínica Médica, Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP (HC-FMUSP), Sao Paulo, Brazil

Meeting: 2015 ACR/ARHP Annual Meeting

Date of first publication: September 29, 2015

Keywords: Idiopathic Inflammatory Myopathies (IIM), ovarian and polymyositis

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Session Information

Date: Tuesday, November 10, 2015

Title: Reproductive Issues in Rheumatic Disorders: Basic and Clinical Aspects Poster Session

Session Type: ACR Poster Session C

Session Time: 9:00AM-11:00AM

Background/Purpose: Polymyositis (PM) affects female gender during reproductive age. Ovarian reserve and future fertility are relevant, however there is no study performing a complete assessment of ovarian function in these patients.

Methods: From March 2011 to May 2014, 32 female PM patients (Bohan and Peter criteria, 1975), with age 18-40 years old, followed at the Outpatient Myopathy Clinic, Rheumatology Division of our tertiary center were screened. Twenty-four patients were excluded due to unwillingness to participate(n=8), hormonal contraceptive use(n=6), other autoimmune diseases(n=5), neoplasia(n=2), gynaecological surgery(n=2) and current pregnancy(n=1). Thus, a total of eight PM patients and 16 healthy volunteer age-matched women were enrolled in the study. All PM patients and healthy controls were evaluated at early follicular phase of menstrual cycle. Follicle stimulating hormone (FSH), estradiol, inhibin B and anti-Müllerian hormone (AMH) serum levels (ELISA) were determined. Transvaginal ultrasound was performed in all PM patients and controls by a blind sonographer using a 6.5 MHz endovaginal transducer. Ovarian volumes and antral follicle count (AFC) were also assessed.

Results: PM patients and controls had comparable mean age (31.4±6.5 vs. 30.7±6.2 years, P=0.946), ethnicity and socioeconomic class (P>0.05). PM mean age of onset was 27.3±6.5 years and disease duration of 6.5±4.1 years. Menstrual cycles were alike in both groups with a similar frequency of age at menarche, gynecological age, duration and length of menstrual cycle (P>0.05). The median serum level of AMH was significantly lower in PM compared to controls [0.7(0.3-3.4) vs. 3.1(1.4-4.0), P=0.021] and AMH levels ≤1ng/mL (50%vs. 6.3%, P=0.024) and very low AFC (37.5% vs. 6.3%, P=0.037) were more frequently observed in PM. The other ovarian reserve parameters (ovarian volume, FSH, inhibin B and estradiol levels) were similar in both groups (P>0.05). With regard to drugs, 6/8 (75%) were exposed to potentially gonodotoxic agents, one (12.5%) was treated with intravenous cyclophosphamide with a cumulative dose of 15g and five (62.5%) were treated with high cumulative methotrexate dose (>5g/m2).  Of these six exposed patients, 4 (67%) had low AMH levels and 3 (50%) had concomitant very low AFC.

Conclusion: The present study was the first to identify a subclinical ovarian dysfunction in PM patients during reproductive ages possible associated with a gonadotoxic effect of immunosuppressive drugs on ovarian follicular pool.


Disclosure: F. H. C. de Souza, None; C. A. Silva, None, 2; L. Y. S. Yamakami, None; V. S. T. Viana, None; E. Bonfá, None; S. K. Shinjo, None.

To cite this abstract in AMA style:

de Souza FHC, Silva CA, Yamakami LYS, Viana VST, Bonfá E, Shinjo SK. Subclinical Reduced Ovarian Reserve in Adult Polymiositis Patients [abstract]. Arthritis Rheumatol. 2015; 67 (suppl 10). https://acrabstracts.org/abstract/subclinical-reduced-ovarian-reserve-in-adult-polymiositis-patients/. Accessed .
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