A new diagnostic test for VLCAD deficiency using immunohistochemistry

Y. Ohashi, Y. Hasegawa, K. Murayama, M. Ogawa, T. Hasegawa, M. Kawai, N. Sakata, K. Yoshida, H. Yarita, K. Imai, I. Kumagai, K. Murakami, H. Hasegawa, S. Noguchi, I. Nonaka, S. Yamaguchi, Ichizo Nishino

Research output: Contribution to journalArticlepeer-review

40 Citations (Scopus)


Background: Muscle pathology is often unhelpful in elucidating the specific underlying abnormality in patients with metabolic myopathy with rhabdomyolysis, including very-long chain acyl-CoA dehydrogenase (VLCAD) deficiency. Biochemical analyses require large amounts of biopsy samples for each enzyme assay. Objective: To develop a more efficient diagnostic method for VLCAD deficiency. Methods: The authors performed immunohistochemical analysis using an antibody to VLCAD on muscles from 344 patients (226 men and 118 women) without a specific diagnosis who had at least one of the following symptoms: myoglobinuria, high CK level, muscle pain, muscle stiffness, sudden infant death syndrome, and Reye-like syndrome. Results: Immunoreactivity to VLCAD was absent or markedly reduced in 13 patients. Biochemical analyses confirmed that all these patients had low enzymatic activity and reduced amount of protein. They all had the myopathic phenotype. The authors identified homozygous or compound heterozygous mutations in all of them. All recombinant proteins had reduced enzymatic activity except for 128G>A (G43D) and 796C>G (P266A) mutants, indicating that they are neutral polymorphisms. Conclusions: The new screening method for the detection of VLCAD deficiency using an immunohistochemical technique identified 13 new Japanese patients with VLCAD deficiency.

Original languageEnglish
Pages (from-to)2209-2213
Number of pages5
Issue number12
Publication statusPublished - 2004 Jun 22

ASJC Scopus subject areas

  • Clinical Neurology


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