Plasma fibroblast growth factor-21 levels in patients with inborn errors of metabolism
Fibroblast growth factor-21 (FGF21) levels are elevated in patients with primary mitochondrial disorders but have not been studied in patients with inborn errors of metabolism (IEM) known to have secondary mitochondrial dysfunction. We measured plasma FGF21 by ELISA in patients with and without IEM....
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Series: | Molecular Genetics and Metabolism Reports |
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doaj-9d209d9c70ae4a5189cf1377e3b362732020-11-24T22:39:23ZengElsevierMolecular Genetics and Metabolism Reports2214-42692017-12-0113C525410.1016/j.ymgmr.2017.04.001Plasma fibroblast growth factor-21 levels in patients with inborn errors of metabolismBrian Kirmse0Juan Cabrerra-Luque1Omar Ayyub2Kristina Cusmano3Kimberly Chapman4Marshall Summar5University of Mississippi Medical Center, Department of Pediatrics, Jackson, MS, United StatesChildren's National Health System, Division of Genetics & Metabolism, Washington, DC, United StatesChildren's National Health System, Division of Genetics & Metabolism, Washington, DC, United StatesChildren's National Health System, Division of Genetics & Metabolism, Washington, DC, United StatesChildren's National Health System, Division of Genetics & Metabolism, Washington, DC, United StatesChildren's National Health System, Division of Genetics & Metabolism, Washington, DC, United StatesFibroblast growth factor-21 (FGF21) levels are elevated in patients with primary mitochondrial disorders but have not been studied in patients with inborn errors of metabolism (IEM) known to have secondary mitochondrial dysfunction. We measured plasma FGF21 by ELISA in patients with and without IEM. FGF21 levels were higher in patients with IEM compared to without IEM (370 pg/dL vs. 0–65 pg/dL). Further study of FGF21 as a biomarker in IEM is warranted.http://www.sciencedirect.com/science/article/pii/S2214426917300253 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Brian Kirmse Juan Cabrerra-Luque Omar Ayyub Kristina Cusmano Kimberly Chapman Marshall Summar |
spellingShingle |
Brian Kirmse Juan Cabrerra-Luque Omar Ayyub Kristina Cusmano Kimberly Chapman Marshall Summar Plasma fibroblast growth factor-21 levels in patients with inborn errors of metabolism Molecular Genetics and Metabolism Reports |
author_facet |
Brian Kirmse Juan Cabrerra-Luque Omar Ayyub Kristina Cusmano Kimberly Chapman Marshall Summar |
author_sort |
Brian Kirmse |
title |
Plasma fibroblast growth factor-21 levels in patients with inborn errors of metabolism |
title_short |
Plasma fibroblast growth factor-21 levels in patients with inborn errors of metabolism |
title_full |
Plasma fibroblast growth factor-21 levels in patients with inborn errors of metabolism |
title_fullStr |
Plasma fibroblast growth factor-21 levels in patients with inborn errors of metabolism |
title_full_unstemmed |
Plasma fibroblast growth factor-21 levels in patients with inborn errors of metabolism |
title_sort |
plasma fibroblast growth factor-21 levels in patients with inborn errors of metabolism |
publisher |
Elsevier |
series |
Molecular Genetics and Metabolism Reports |
issn |
2214-4269 |
publishDate |
2017-12-01 |
description |
Fibroblast growth factor-21 (FGF21) levels are elevated in patients with primary mitochondrial disorders but have not been studied in patients with inborn errors of metabolism (IEM) known to have secondary mitochondrial dysfunction. We measured plasma FGF21 by ELISA in patients with and without IEM. FGF21 levels were higher in patients with IEM compared to without IEM (370 pg/dL vs. 0–65 pg/dL). Further study of FGF21 as a biomarker in IEM is warranted. |
url |
http://www.sciencedirect.com/science/article/pii/S2214426917300253 |
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1725709271116546048 |