Comorbidities of antiphospholipid syndrome and systemic lupus erythematosus in children

Ummusen Kaya Akca1, Nuray Aktay Ayaz2

  • 1Division of Pediatric Rheumatology, Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Turkey.

Insights

Antiphospholipid syndrome (APS) and systemic lupus erythematosus (SLE) patients face increased risks of infections, cardiovascular issues, and malignancies. Awareness of these comorbidities is crucial for managing disease progression and improving patient outcomes.

Area of Science:

  • Autoimmune diseases
  • Rheumatology
  • Internal Medicine

Background:

  • Antiphospholipid syndrome (APS) and systemic lupus erythematosus (SLE) are autoimmune conditions impacting multiple organ systems.
  • Improved survival in APS and SLE necessitates a focus on associated comorbidities.
  • Comorbidities significantly influence disease course and patient prognosis.

Purpose of the Study:

  • To review comorbidities in APS and SLE that negatively affect disease progression.
  • To highlight the impact of comorbidities on patient outcomes.
  • To inform clinicians about potential complications in APS and SLE management.

Main Methods:

  • Literature review focusing on comorbidities in APS and SLE.
  • Analysis of studies examining disease-related complications.
  • Synthesis of findings on common and significant comorbidities.

Main Results:

  • Infections are the most frequent comorbidity in pediatric APS and SLE, linked to immunosuppression and immune dysregulation.
  • Cardiovascular and cerebrovascular diseases are significant causes of mortality and morbidity.
  • Increased risks include malignancies, ophthalmologic, neurologic, renal, and musculoskeletal conditions (e.g., vitamin D deficiency, low bone density, avascular necrosis).

Conclusions:

  • Clinicians must be vigilant for comorbidities during the follow-up of APS and SLE patients.
  • Understanding and managing comorbidities is essential for optimizing patient care.
  • Further research is needed to fully elucidate the spectrum of comorbidities in APS and SLE.
Abstract

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