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Published on: November 1, 2015
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.
Purpose Of Review:
Antiphospholipid syndrome (APS) and systemic lupus erythematosus (SLE) are autoimmune diseases that can affect multiple organ systems. Increased awareness and new treatment strategies ultimately improved the survival of patients, and disease-related comorbidities became more important. The purpose of this review is to focus on comorbidities in these diseases that had a negative influence on the course of the disease.
Recent Findings:
There are limited numbers of studies regarding to comorbidities associated with these diseases during childhood. Infections were found to be the most common comorbidity as a result of immunosuppressive agents and dysregulations of the immune system. Other common comorbidities after infections are cardiovascular and cerebrovascular diseases as important causes of mortality and morbidity. In addition, the risk of malignancies, ophthalmologic manifestations, neurologic and renal diseases, musculoskeletal diseases such as vitamin D deficiency, low bone mineral density, and the risk of avascular necrosis were increased in both patient groups. For clinicians, it is important to be aware of the comorbidities that may develop during follow-up of APS and SLE patients. Further studies will shed more light on the comorbidities of these diseases.
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