Article ID Journal Published Year Pages File Type
1214807 Journal of Chromatography B 2009 5 Pages PDF
Abstract

BackgroundSjögren-Larsson syndrome is a metabolic disorder characterized by accumulation of long-chain fatty alcohols in plasma of patients due to mutations in the ALDH3A2 gene, that codes for a microsomal fatty aldehyde dehydrogenase (FALDH). Recent studies have demonstrated that FALDH is involved in the last step of the conversion of 22-hydroxy-C22:0 into the dicarboxylic acid of C22:0 (C22:0-DCA).MethodsFALDH activity was determined by incubating fibroblast homogenates with ω-hydroxy-C22:0 in the presence of NAD+. Electrospray ionization mass spectrometry (ESI-MS) was used to quantify the amounts of C22:0-DCA produced.ResultsAll SLS patients were deficient in C22:0-DCA productions with activities ranging from 3.2–26.3% of mean control.ConclusionsThe new assay described in this paper has substantial advantages over previous assays, and allows for the easy, reliable and rapid diagnosis of SLS.

Related Topics
Physical Sciences and Engineering Chemistry Analytical Chemistry
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