Lipid changes in the metabolome of a single case study with maple syrup urine disease (MSUD) after five days of improved diet adherence of controlled branched-chain amino acids (BCAA).
| dc.contributor.author | Douglas, Teresa D | |
| dc.contributor.author | Newby, L Kristin | |
| dc.contributor.author | Eckstrand, Julie | |
| dc.contributor.author | Wixted, Douglas | |
| dc.contributor.author | Singh, Rani H | |
| dc.date.accessioned | 2022-12-07T20:03:21Z | |
| dc.date.available | 2022-12-07T20:03:21Z | |
| dc.date.issued | 2020-12 | |
| dc.date.updated | 2022-12-07T20:03:18Z | |
| dc.description.abstract | BackgroundDistinguishing systemic metabolic disruptions in maple syrup urine disease (MSUD) beyond amino acid pathways is under-investigated, yet important to understanding disease pathology and treatment options.MethodsAn adolescent female (15 years) with MSUD without liver transplant, attended 2 study visits, 5 days apart. Medical diet adherence was determined based on her 3-day diet records and plasma branched-chain amino acid (BCAA) concentrations at both study visits. Plasma from a single age- and sex-matched control (MURDOCK Study, Duke University) and the case patient were analyzed with UPLC/MS/MS for intensity (m/z), annotated, and normalized against a median of 1 (Metabolon, Morrisville NC). Differences between case/control and 5-day comparisons were defined as ≥ ǀ 0.5 ǀ.Results434 lipid metabolites were identified across samples; 90 (20.7%) were higher and 120 (27.6%) lower in the MSUD case at baseline compared with control. By study visit 2, plasma BCAA had declined, while 48 (53%) of elevated lipids and 14 (11.7%) of lower lipid values had moved to within ǀ 0.5 ǀ of control. Most shifts towards control by day 5 were seen in long-chain fatty acid intermediates (42%) and acylcarnitines (32%). Although androgenic (28%) and bile acid (23%) metabolites increased towards control, neither reached control level by day 5.DiscussionThis comparative metabolomics study in a single MSUD case and healthy control suggests intrinsic differences in MSUD lipid metabolism potentially influenced by therapeutic diet. Findings suggest influences on hormone regulation, fatty acid oxidation, and bile acid synthesis, but further studies are needed to confirm an association between MSUD and lipid dysregulation.SynopsisWithin 5 days of improved dietary adherence, a single MSUD case experienced substantial changes in lipid markers potentially related to changes in plasma branched-chain amino acids. | |
| dc.identifier | S2214-4269(20)30097-5 | |
| dc.identifier.issn | 2214-4269 | |
| dc.identifier.issn | 2214-4269 | |
| dc.identifier.uri | ||
| dc.language | eng | |
| dc.publisher | Elsevier BV | |
| dc.relation.ispartof | Molecular genetics and metabolism reports | |
| dc.relation.isversionof | 10.1016/j.ymgmr.2020.100651 | |
| dc.subject | Alloisoleucine | |
| dc.subject | BCKDH | |
| dc.subject | Branched-chain amino acids | |
| dc.subject | Branched-chain ketoacid dehydrogenase deficiency | |
| dc.subject | Isoleucine | |
| dc.subject | Leucine | |
| dc.subject | Lipids | |
| dc.subject | MSUD | |
| dc.subject | Maple syrup urine disease | |
| dc.subject | Metabolomics | |
| dc.subject | Mitochondria | |
| dc.subject | Peroxisomes | |
| dc.subject | Valine | |
| dc.title | Lipid changes in the metabolome of a single case study with maple syrup urine disease (MSUD) after five days of improved diet adherence of controlled branched-chain amino acids (BCAA). | |
| dc.type | Journal article | |
| duke.contributor.orcid | Newby, L Kristin|0000-0002-6394-8187 | |
| duke.contributor.orcid | Wixted, Douglas|0000-0002-6128-7813 | |
| pubs.begin-page | 100651 | |
| pubs.organisational-group | Duke | |
| pubs.organisational-group | School of Medicine | |
| pubs.organisational-group | Staff | |
| pubs.organisational-group | Clinical Science Departments | |
| pubs.organisational-group | Institutes and Centers | |
| pubs.organisational-group | Medicine | |
| pubs.organisational-group | Medicine, Cardiology | |
| pubs.organisational-group | Duke Clinical Research Institute | |
| pubs.organisational-group | Duke Clinical & Translational Science Institute | |
| pubs.publication-status | Published | |
| pubs.volume | 25 |
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