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Managing hypertriglyceridemia in children with systemic lupus erythematosus: Two sides of the same coin
Biswanath Basu1, Binu George Babu1, Suman Bhattacharyya1
1Division of Pediatric Nephrology, Department of Pediatrics, NRS Medical College & Hospital, Kolkata, India.
Insights
Extreme hypertriglyceridemia in children with systemic lupus erythematosus (SLE) can be caused by steroid treatment or anti-lipoprotein-lipase (LPL) autoantibodies. Individualized management based on the cause is crucial for effective treatment.
Area of Science:
- Pediatrics
- Rheumatology
- Endocrinology
Background:
- Hypertriglyceridemia is a frequent comorbidity in pediatric patients diagnosed with systemic lupus erythematosus (SLE).
- Understanding the specific etiologies of severe hypertriglyceridemia in this population is essential for effective management.
- This study investigates two pediatric cases of SLE presenting with extreme hypertriglyceridemia.
Observation:
- The first patient developed severe hypertriglyceridemia after one week of oral prednisolone, with no detectable anti-lipoprotein-lipase (LPL) autoantibodies.
- The second patient presented with extreme hypertriglyceridemia and tested positive for anti-LPL autoantibodies.
- Both patients were managed with immunosuppressants and lipid-lowering agents, with individualized therapeutic adjustments.
Findings:
- Extreme hypertriglyceridemia in pediatric SLE can be induced by corticosteroid therapy.
- The presence of anti-LPL autoantibodies represents another significant cause of severe hypertriglyceridemia in these patients.
- Treatment outcomes varied, with the first patient improving after switching from prednisolone to mycophenolate mofetil (MMF), and the second patient responding to plasmapheresis and increased immunosuppression.
Implications:
- These findings highlight the need for careful monitoring of lipid profiles in children with SLE, particularly during corticosteroid treatment.
- Differentiating between steroid-induced hypertriglyceridemia and autoimmune-related hypertriglyceridemia is critical for tailoring treatment strategies.
- Individualized management approaches, considering the specific etiology, are paramount for optimizing outcomes in pediatric SLE patients with hypertriglyceridemia.
Abstract:
Hypertriglyceridemia is common in children with systemic lupus erythematosus (SLE). A retrospective analysis of the baseline clinical-pathological presentation and treatment outcome (status of lipid profiles) was performed in two children with SLE, who presented with extreme hypertriglyceridemia over a follow-up period of four weeks. The children were treated with prednisolone, mycophenolate mofetil (MMF), hydroxychloroquine and hypolipidemic agents, depending on their disease status. On serial follow-up, the first child showed a significantly raised serum triglyceride level after receiving one week of oral prednisolone therapy. Anti-lipoprotein-lipase (LPL) autoantibody was absent. Lipid profile levels of this child gradually improved after replacing oral prednisolone with another immunosuppressant, namely MMF. The second child presented with extreme hypertriglyceridemia with positive anti-LPL autoantibody. She responded to plasmapheresis followed by increasing the dose of immunosuppressant. So, extreme hypertriglyceridemia in children with SLE may be steroid induced or due to presence of anti-LPL auto antibody. Management should be individualized depending on the etiology.
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