دورية أكاديمية
Diagnosis of atypical myopathy based on organic acid and acylcarnitine profiles and evolution of biomarkers in surviving horses
العنوان: | Diagnosis of atypical myopathy based on organic acid and acylcarnitine profiles and evolution of biomarkers in surviving horses |
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المؤلفون: | Déborah Mathis, Jörn Oliver Sass, Claudia Graubner, Angelika Schoster |
المصدر: | Molecular Genetics and Metabolism Reports, Vol 29, Iss , Pp 100827- (2021) |
بيانات النشر: | Elsevier, 2021. |
سنة النشر: | 2021 |
المجموعة: | LCC:Medicine (General) LCC:Biology (General) |
مصطلحات موضوعية: | Acquired multiple acyl-CoA dehydrogenase deficiency, Seasonal pasture myopathy, Hypoglycin A, Medicine (General), R5-920, Biology (General), QH301-705.5 |
الوصف: | Background: Atypical myopathy (AM), an acquired multiple acyl-CoA dehydrogenase deficiency (MADD) in horses, induce changes in mitochondrial metabolism. Only few veterinary laboratories offer diagnostic testing for this disease. Inborn and acquired MADD exist in humans, therefore determination of organic acids (OA) in urine and acylcarnitines (AC) in blood by assays available in medical laboratories can serve as AM diagnostics. The evolution of OA and AC profiles in surviving horses is unreported. Methods: AC profiles using electrospray ionization tandem mass spectrometry (ESI-MS/MS) and OA in urine using gas chromatography mass spectrometry (GC–MS) were determined in dried blot spots (DBS, n = 7) and urine samples (n = 5) of horses with AM (n = 7) at disease presentation and in longitudinal samples from 3/4 survivors and compared to DBS (n = 16) and urine samples (n = 7) from control horses using the Wilcoxon test. Results: All short- (C2-C5) and medium-chain (C6-C12) AC in blood differed significantly (p |
نوع الوثيقة: | article |
وصف الملف: | electronic resource |
اللغة: | English |
تدمد: | 2214-4269 |
Relation: | http://www.sciencedirect.com/science/article/pii/S2214426921001221; https://doaj.org/toc/2214-4269 |
DOI: | 10.1016/j.ymgmr.2021.100827 |
URL الوصول: | https://doaj.org/article/94ed41f643b04f99b3a8537fa780aea2 |
رقم الأكسشن: | edsdoj.94ed41f643b04f99b3a8537fa780aea2 |
قاعدة البيانات: | Directory of Open Access Journals |
تدمد: | 22144269 |
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DOI: | 10.1016/j.ymgmr.2021.100827 |