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Atorvastatin safety in Kawasaki disease patients with coronary artery aneurysms
Elizabeth Niedra1, Nita Chahal, Cedric Manlhiot
1Labatt Family Heart Centre, The Hospital for Sick Children, University of Toronto, 555 University Avenue, Toronto, ON, M5G 1X8, Canada.
Insights
Atorvastatin is safe for treating coronary artery aneurysms in children with Kawasaki disease, with good compliance and minimal side effects. Long-term monitoring is recommended for safety and efficacy in this young population.
Area of Science:
- Cardiology
- Pediatrics
- Pharmacology
Background:
- Kawasaki disease (KD) can lead to coronary artery aneurysms (CAAs) in children.
- Statins, like atorvastatin, are HMG-CoA reductase inhibitors that may reduce inflammation and promote vascular remodeling.
- Limited data exist on the safety and efficacy of statins in young children with KD-associated CAAs.
Purpose of the Study:
- To evaluate the safety and tolerability of atorvastatin in young children with CAAs following KD.
- To assess the impact of atorvastatin on lipid profiles and anthropometric measurements in this patient group.
Main Methods:
- A cohort of twenty pediatric patients with CAAs post-KD were treated with atorvastatin (5/10 mg daily) for a median of 2.5 years.
- Lipid profiles (total cholesterol, LDL, HDL, triglycerides), liver enzymes, creatine phosphokinase, and anthropometric data (weight, height, BMI) were monitored.
- Patient compliance and adverse events were recorded.
Main Results:
- Atorvastatin significantly reduced total cholesterol (-14%) and LDL cholesterol (-20%) (p<0.05).
- Excellent treatment compliance was observed, with only one patient reporting minor joint pain.
- Transient mild elevations in liver enzymes occurred in 35% of patients; no severe increases or significant impact on growth parameters were noted.
Conclusions:
- Atorvastatin is a safe and well-tolerated treatment option for young children with KD-complicated CAAs.
- The medication effectively improves lipid profiles without adversely affecting growth.
- Close monitoring is advised for young children undergoing atorvastatin therapy for KD-related CAAs.
Abstract:
Statins (HMG-CoA reductase inhibitors) may decrease inflammation in postacute Kawasaki disease (KD) complicated by coronary artery aneurysm (CAA) and promote vascular remodeling. There are limited data on their safety in young children. Twenty patients with CAAs after KD (median CAA z-score = +25) were treated with 5/10 mg atorvastatin daily for a median of 2.5 years (range 0.5-6.8) starting at a median of 2.3 years (range 0.3-8.9) after acute KD (median age 9.3 years [range 0.7-14.3]). Compliance with treatment was excellent: only one patient reported minor side effects (joint pain, no change in medication). Average total cholesterol before atorvastatin was 3.73 ± 0.84 mmol/L and after atorvastatin was 3.21 ± 0.46 mmol/L (relative decrease -14 %, p = 0.02); low-density lipoprotein cholesterol was 1.99 ± 0.76 mmol/L before and only 1.49 ± 0.27 mmol/L after (relative decrease -20 %, p = 0.04); high-density lipoprotein was 1.39 ± 0.36 mmol/L before and 1.30 ± 0.27 mmol/L after (relative decrease -4 %, p = 0.35); and triglycerides were 0.71 ± 0.28 mmol/L before and 0.71 ± 0.18 mmol/L after (relative decrease -5 %, p = 0.38). Nine of 20 patients (45 %) experienced at least 1 episode of hypocholesterolemia (total cholesterol <3.1 mmol/L), and 2 patients required atorvastatin dose lowering. Transient mild increase of liver enzymes (aspartate aminotransferase/alanine aminotransferase 45-60 U/L) were seen in 7 of 20 (35 %) patients with no patients experiencing more severe increases. Only one patient experienced increased creatine phosphokinase levels (>500 U/L). Serial measurements of age- and sex-specific percentiles of weight (estimated change: 1.4 [2.7] % per year, p = 0.60), height (estimated change: -3.2 [3.2] % per year, p = 0.32), and body mass index (estimated change: 1.0 [2.9] % per year, p = 0.73) showed no association between anthropomorphic growth and atorvastatin treatment. Atorvastatin use in very young children with KD is safe but should be closely monitored.
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