Comparison of maltose and acarbose as inhibitors of maltase-glucoamylase activity in assaying acid alpha-glucosidase activity in dried blood spots for the diagnosis of infantile Pompe disease.
Published
Journal Article
PURPOSE: The study's purpose was to compare acarbose and maltose as inhibitors of maltase-glucoamylase activity for determining acid alpha-glucosidase activity in dried blood spot specimens for early identification of patients with infantile Pompe disease, a severe form of acid alpha-glucosidase deficiency. METHODS: Acid alpha-glucosidase activities in dried blood spot extracts were determined fluorometrically using the artificial substrate 4-methylumbelliferyl-alpha-D-pyranoside. Acarbose or maltose was used to inhibit maltase-glucoamylase, an enzyme present in polymorphonuclear neutrophils that contributes to the total alpha-glucosidase activity at acidic pH. RESULTS: Complete discrimination between patients with proven infantile Pompe disease (n = 20), obligate heterozygotes (n = 16), and controls (n = 150) was achieved using 8 micromol/L acarbose as the inhibitor. Higher acarbose concentration (80 micromol/L) did not improve the assay. By using 4 mM maltose as the inhibitor, heterozygotes and patients were not completely separated. The results using acarbose compared well with those using the skin fibroblast assay in the same group of patients with proven infantile Pompe disease. CONCLUSION: Acid alpha-glucosidase activity measurements in dried blood spot extracts can reliably detect infantile Pompe disease in patients. The convenience of collecting and shipping dried blood specimens plus rapid turnaround time makes this assay an attractive alternative to established methods.
Full Text
Duke Authors
- Bali, Deeksha Sarihyan
- Chen, Yuan-Tsong
- Kishnani, Priya Sunil
- Millington, David Stuart
- Young, Sarah Phyllis
Cited Authors
- Zhang, H; Kallwass, H; Young, SP; Carr, C; Dai, J; Kishnani, PS; Millington, DS; Keutzer, J; Chen, Y-T; Bali, D
Published Date
- May 2006
Published In
Volume / Issue
- 8 / 5
Start / End Page
- 302 - 306
PubMed ID
- 16702880
Pubmed Central ID
- 16702880
International Standard Serial Number (ISSN)
- 1098-3600
Digital Object Identifier (DOI)
- 10.1097/01.gim.0000217781.66786.9b
Language
- eng
Conference Location
- United States