[Hyperhomocysteinemia in children and adolescents with systemic lupus erythematosus: evolutive evaluation]

Maria Teresa R A Terreri1, Roseli Oselka Saccardo Sarni, Rogério do Prado

  • 1Disciplina de Alergia, Imunologia Clínica e Reumatologia, Departamento de Pediatria, Universidade Federal de São Paulo, São Paulo, SP, Brazil. teterreri@terra.com.br

Insights

Elevated homocysteine persists in over a quarter of juvenile systemic lupus erythematosus (SLE) patients, indicating a potential cardiovascular disease risk. Further research into therapeutic strategies and nutritional education is recommended for these patients.

Area of Science:

  • Pediatric Rheumatology
  • Cardiovascular Disease Pathogenesis
  • Metabolic Disorders

Context:

  • Juvenile systemic lupus erythematosus (SLE) is associated with an increased risk of cardiovascular disease.
  • Hyperhomocysteinemia is a known risk factor for cardiovascular disease and has been implicated in SLE pathogenesis.
  • Longitudinal data on homocysteine levels in juvenile SLE patients are limited.

Purpose:

  • To investigate the presence and persistence of hyperhomocysteinemia in patients with juvenile SLE.
  • To assess the association of elevated homocysteine with clinical factors including renal involvement, disease activity, and nutritional status.
  • To compare homocysteine levels in juvenile SLE patients with healthy controls.

Summary:

  • This study followed 18 juvenile SLE patients, measuring plasma homocysteine levels twice over a median of 1.5 years.
  • Five patients (27.8%) consistently showed elevated homocysteine levels.
  • No significant association was found between elevated homocysteine and renal involvement, disease activity, or nutritional status in this cohort.

Impact:

  • Highlights the persistence of hyperhomocysteinemia in a significant subset of juvenile SLE patients.
  • Underscores the need for evaluating interventions to mitigate cardiovascular disease risk in this population.
  • Suggests the importance of nutritional education and therapeutic strategies targeting homocysteine levels in juvenile SLE management.
Abstract

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