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Pubertal disorders in juvenile idiopathic arthritis: a systemic review

  • Soumaya Boussaid ORCID logo EMAIL logo , Sonia Rekik , Hanene Lassoued Ferjani , Maissa Abbes , Safa Rahmouni , Khaoula Zouaoui , Rim Dhahri , Wafa Hamdi and Hela Sahli
Published/Copyright: March 28, 2025

Abstract

Introduction

Juvenile idiopathic arthritis (JIA) is a chronic inflammatory disease beginning before 16 years. Inflammatory cytokine, medication, and genetic factors may lead to puberty disorders in children with JIA. The main objectives of this systematic review were to elucidate the impact of JIA on puberty and identify the influential factors that disrupt puberty.

Content

A systematic literature review was performed on pubertal disorders from Medline, Google Scholar, and Scopus databases. This systematic review followed the preferred reporting items for systematic review guidelines. The initial search yielded 4,011 articles: identified by Google Scholar (3,880), PubMed (99), and Scopus (940). Finally, 11 articles were retained.

Summary and Outlook

The age of menarche onset, Tanner stage, and pubertal signs were later compared with controls. The mean age of menarche onset ranged from 12.0 ± 0.3 to 13.39 ± 0.93 years for the JIA girls. This delay was more reported in the polyarticular and oligoarticular subtypes. Menstrual irregularities, metrorrhagia with irregular cycles, primary oligomenorrhea, and secondary amenorrhea were also reported. Factors found to influence delayed menarche and puberty were steroid use, JIA subtype, disease duration, and age at onset. Any studies have focused on the effect of puberty on JIA outcomes. Overall, our review revealed that pubertal disorders are frequent in JIA patients with polyarticular and systemic subtypes. However, some influencing factors remain editable if well-assessed and controlled.


Corresponding author: Soumaya Boussaid, Associate Professor, Rheumatology Department, Rabta Hospital, 1007 Tunis, Tunisia; and Faculty of Medicine of Tunis, University Tunis El Manar, Tunis, Tunisia, E-mail:

  1. Research ethics: Not applicable.

  2. Informed consent: Not applicable.

  3. Author contributions: The authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  4. Use of Large Language Models, AI and Machine Learning Tools: Artificial Intelligence was utilized to enhance the English and properly structure the references.

  5. Conflict of interest: The authors state no conflict of interest.

  6. Research funding: None declared.

  7. Data availability: Not applicable.

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Received: 2024-08-25
Accepted: 2025-03-05
Published Online: 2025-03-28
Published in Print: 2025-06-26

© 2025 Walter de Gruyter GmbH, Berlin/Boston

Articles in the same Issue

  1. Frontmatter
  2. Reviews
  3. Pubertal disorders in juvenile idiopathic arthritis: a systemic review
  4. Hormonal therapy for impaired growth due to pediatric-onset inflammatory bowel disease: a systematic review and meta-analysis with trial sequential analysis
  5. Mini Review
  6. Neonatal hypoglycaemia in the offsprings of parents with maturity-onset diabetes of the young (MODY)
  7. Original Articles
  8. Cord blood metabolomic profiling in high risk newborns born to diabetic, obese, and overweight mothers: preliminary report
  9. Impact of Covid-19 on children and adolescents with type 1 diabetes: lifestyle, telecommunication service, and quality of life
  10. The diagnostic utility of bioelectrical impedance analysis in distinguishing precocious puberty from premature thelarche
  11. Infant gonadotropins predict spontaneous puberty in girls with Turner syndrome
  12. Bioinformatics analysis explores key pathways and hub genes in central precocious puberty
  13. Impact of growth hormone therapy on bone and body composition in prepubertal children with idiopathic short stature
  14. Presence of hyperandrogenemia in cases evaluated due to menstrual irregularity, the effect of clinical and/or biochemical hyperandrogenemia on polycystic ovary syndrome
  15. Cardiac function in children with congenital adrenal hyperplasia
  16. Short Communication
  17. Clinical and genetic insights into congenital lipoid adrenal hyperplasia: a case series from a tertiary care center in North India
  18. Case Reports
  19. Two families, two pathways: a case series of 46, XY DSD with 17α-hydroxylase deficiency and isolated 17,20-lyase deficiency due to novel CYB5A variant
  20. Coexistence of SRY, DHX37 and POR gene variants in a patient with 46,XY disorder of sex development
  21. Diabetes, macrocytosis, and skin changes in large-scale mtDNA deletion
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