A Korean Female Patient with Thiamine-responsive Pyruvate Dehydrogenase Complex Deficiency Due to a Novel Point Mutation (Y161C)in the PDHA1 Gene.
10.3346/jkms.2006.21.5.800
- Author:
Eun Ha LEE
1
;
Mi Sun AHN
;
Jin Soon HWANG
;
Kyung Hwa RYU
;
Sun Jun KIM
;
Sung Hwan KIM
Author Information
1. Department of Pediatrics and Research Laboratory for Human Mitochondrial Disorders, Ajou University School of Medicine, Suwon, Korea. pedkim@ajou.ac.kr
- Publication Type:Case Reports ; Research Support, Non-U.S. Gov't
- Keywords:
Pyruvate Dehydrogenase Complex Deficiency Disease;
Pyruvate Dehydrogenase (Lipoamide);
E1alpha Subunit;
Thiamine Pyrophosphate
- MeSH:
Thiamine Pyrophosphate/metabolism;
Thiamine/*therapeutic use;
Pyruvate Dehydrogenase Complex Deficiency Disease/drug therapy/*genetics;
Pyruvate Dehydrogenase (Lipoamide)/*genetics;
*Point Mutation;
Infant, Newborn;
Humans;
Female;
Cells, Cultured
- From:Journal of Korean Medical Science
2006;21(5):800-804
- CountryRepublic of Korea
- Language:English
-
Abstract:
Pyruvate dehydrogenase complex (PDHC) deficiency is mostly due to mutations in the X-linked E1alpha subunit gene (PDHA1). Some of the patients with PDHC deficiency showed clinical improvements with thiamine treatment. We report the results of biochemical and molecular analysis in a female patient with lactic acidemia. The PDHC activity was assayed at different concentrations of thiamine pyrophosphate (TPP). The PDHC activity showed null activity at low TPP concentration (1 x 10(-3) mM), but significantly increased at a high TPP concentration (1 mM). Sequencing analysis of PDHA1 gene of the patient revealed a substitution of cysteine for tyrosine at position 161 (Y161C). Thiamine treatment resulted in reduction of the patient's serum lactate concentration and dramatic clinical improvement. Biochemical, molecular, and clinical data suggest that this patient has a thiamine-responsive PDHC deficiency due to a novel mutation, Y161C. Therefore, to detect the thiamine responsiveness it is necessary to measure activities of PDHC not only at high but also at low concentration of TPP.
