A 58-year-old man with chronic renal failure developed severe muscle pain and tenderness I week after starting bezafibrate 400 mg daily. Serum creatine kinase was 32,280 U/l. Muscle biopsy revealed scattered necrotic fibers and mild type 2b atrophy. Muscle total and free carnitine were at the upper limits of the normal range. Biochemical investigations of muscle homogenate showed normal carnitine pelmityl transferase (CPT) as well as normal individual glycolytic and mitochondrial enzyme activities. Withdrawal of the drug was followed by rapid clinical improvement. Our study casts doubt on the hypothesis that bezafibrate is able to affect muscle metabolic pathways. It is likely that the drug acts on cholesterol constituents of the muscle membrane. producing discontinuities of the sarcolemma and initiating cell necrosis.
Bezafibrate-induced myopathy: no evidence for defects in muscle metabolism.
VITA, Giuseppe;TOSCANO, Antonio;GAGLIARDI, Maria;MESSINA, Corrado
1993-01-01
Abstract
A 58-year-old man with chronic renal failure developed severe muscle pain and tenderness I week after starting bezafibrate 400 mg daily. Serum creatine kinase was 32,280 U/l. Muscle biopsy revealed scattered necrotic fibers and mild type 2b atrophy. Muscle total and free carnitine were at the upper limits of the normal range. Biochemical investigations of muscle homogenate showed normal carnitine pelmityl transferase (CPT) as well as normal individual glycolytic and mitochondrial enzyme activities. Withdrawal of the drug was followed by rapid clinical improvement. Our study casts doubt on the hypothesis that bezafibrate is able to affect muscle metabolic pathways. It is likely that the drug acts on cholesterol constituents of the muscle membrane. producing discontinuities of the sarcolemma and initiating cell necrosis.Pubblicazioni consigliate
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