Evaluation of Metabolic Defects in Fatty Acid Oxidation Using Peripheral Blood Mononuclear Cells Loaded with Deuterium-Labeled Fatty Acids. (7th February 2019)

• Record Type: Journal Article
• Authors: Yuasa, Miori; Hata, Ikue; Sugihara, Keiichi; Isozaki, Yuko; Ohshima, Yusei; Hara, Keiichi; Tajima, Go; Shigematsu, Yosuke
• Other Names: Chace Donald H. Academic Editor.
• Is Part Of: Disease markers. Volume 2019(2019)
• Publication Date: 2019-02-07
• Subjects: Diagnosis -- Periodicals; Biochemical markers -- Periodicals; Pathology -- Periodicals; 616
• DOI: 10.1155/2019/2984747
• Languages: English
• ISSNs: 0278-0240

Abstract

Abstract : Because tandem mass spectrometry- (MS/MS-) based newborn screening identifies many suspicious cases of fatty acid oxidation and carnitine cycle disorders, a simple, noninvasive test is required to confirm the diagnosis. We have developed a novel method to evaluate the metabolic defects in peripheral blood mononuclear cells loaded with deuterium-labeled fatty acids directly using the ratios of acylcarnitines determined by flow injection MS/MS. We have identified diagnostic indices for the disorders as follows: decreased ratios of d27 -C14-acylcarnitine/d31 -C16-acylcarnitine and d23 -C12-acylcarnitine/d31 -C16-acylcarnitine for carnitine palmitoyltransferase-II (CPT-II) deficiency, decreased ratios of d23 -C12-acylcarnitine/d27 -C14-acylcarnitine for very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency, and increased ratios of d29 -C16-OH-acylcarnitine/d31 -C16-acylcarnitine for trifunctional protein (TFP) deficiency, together with increased ratios of d7 -C4-acylcarnitine/d31 -C16-acylcarnitine for carnitine palmitoyltransferase-I deficiency. The decreased ratios of d1 -acetylcarnitine/d31 -C16-acylcarnitine could be indicative of β -oxidation ability in patients with CPT-II, VLCAD, and TFP deficiencies. Overall, our data showed that the present method was valuable for establishing a rapid diagnosis of fatty acid oxidation disorders and carnitine cycle disorders and for complementing gene analysis because our diagnostic indices may overcome the weaknesses of conventional enzyme activity measurements using fibroblasts or mononuclear cells with assumedly uncertain viability.