Anti-Müllerian Hormone Serum Levels as Biomarker of Ovarian Reserve in Adult Women with Juvenile Idiopathic Arthritis Treated with csDMARDs and/or bDMARDs: A Pilot Study

<b>Background/Objectives:</b> Juvenile idiopathic arthritis (JIA) is a chronic childhood disease that often persists into the reproductive years. JIA may impact long-term fertility due to the prolonged exposure to immunosuppressive therapies. <b>Methods:</b> A total of 35 adu...

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Main Authors: Clara Di Mario, Maria Rita Gigante, Angelina Barini, Luca Petricca, Antonella Barini, Antonio Bianchi, Stefano Alivernini, Barbara Tolusso, Elisa Gremese
Format: Article
Language:English
Published: MDPI AG 2024-10-01
Series:BioChem
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Online Access:https://www.mdpi.com/2673-6411/4/4/16
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Summary:<b>Background/Objectives:</b> Juvenile idiopathic arthritis (JIA) is a chronic childhood disease that often persists into the reproductive years. JIA may impact long-term fertility due to the prolonged exposure to immunosuppressive therapies. <b>Methods:</b> A total of 35 adult JIA female patients of childbearing age and 20 age-matched healthy controls were studied to test their anti-Müllerian hormone (AMH) serum levels as a biomarker of ovarian reserve. Demographic characteristics, disease duration, previous and current treatments, disease activity (DAS44), and a health assessment questionnaire (HAQ) were recorded. <b>Results:</b> JIA patients had a mean age of 22.3 ± 2.9 years, a disease duration of 12.3 ± 6.1 years, and a DAS44 of 1.24 ± 0.61. No differences were found in AMH serum levels between JIA and controls (5.78 ± 2.37 ng/mL vs. 6.60 ± 2.68 ng/mL, respectively; <i>p</i> = 0.17). Among the patients, 22 (62.9%) were receiving a stable dose of methotrexate (MTX) and 19 (54.3%) a dose of TNFα inhibitors. No difference in AMH serum levels was observed between JIA patients who were or were not exposed to MTX (<i>p</i> = 0.29) or to TNFα inhibitors (<i>p</i> = 0.50). <b>Conclusions:</b> Ovarian reserve as assessed by AMH serum levels appears to be comparable between those with JIA and age-matched controls and does not appear to be influenced by disease characteristics or prior/concomitant exposure to immunosuppressive drugs.
ISSN:2673-6411