Metabolomic Associations with Serum Bone Turnover Markers.
Adult
Bile Acids and Salts
/ metabolism
Biomarkers
/ blood
Bone Remodeling
/ physiology
Collagen Type I
/ blood
Female
Gastrointestinal Microbiome
/ physiology
Humans
Male
Metabolome
Micronutrients
/ metabolism
Nutritional Physiological Phenomena
/ physiology
Osteoblasts
Osteoclasts
Osteogenesis
/ physiology
Peptide Fragments
/ blood
Peptides
/ blood
Procollagen
/ blood
Vitamins
/ metabolism
bone
metabolism
microbiome
nutrition
osteoblast
osteoclast
Journal
Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595
Informations de publication
Date de publication:
16 Oct 2020
16 Oct 2020
Historique:
received:
21
09
2020
revised:
13
10
2020
accepted:
14
10
2020
entrez:
21
10
2020
pubmed:
22
10
2020
medline:
20
4
2021
Statut:
epublish
Résumé
Bone is a dynamic tissue that is in a constant state of remodeling. Bone turnover markers (BTMs), procollagen type I N-terminal propeptide (P1NP) and C-terminal telopeptides of type I collagen (CTX), provide sensitive measures of bone formation and resorption, respectively. This study used ultra-high-resolution metabolomics (HRM) to determine plasma metabolic pathways and targeted metabolites related to the markers of bone resorption and formation in adults. This cross-sectional clinical study included 34 adults (19 females, mean 27.8 years), without reported illnesses, recruited from a US metropolitan area. Serum BTM levels were quantified by an ELISA. Plasma HRM utilized dual-column liquid chromatography and mass spectrometry to identify metabolites and metabolic pathways associated with BTMs. Metabolites significantly associated with P1NP (
Identifiants
pubmed: 33081124
pii: nu12103161
doi: 10.3390/nu12103161
pmc: PMC7602719
pii:
doi:
Substances chimiques
Bile Acids and Salts
0
Biomarkers
0
Collagen Type I
0
Micronutrients
0
Peptide Fragments
0
Peptides
0
Procollagen
0
Vitamins
0
collagen type I trimeric cross-linked peptide
0
procollagen Type I N-terminal peptide
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : NIH HHS
ID : P30 ES019776
Pays : United States
Organisme : NIH HHS
ID : R01 AR068157
Pays : United States
Organisme : NIH HHS
ID : K24 DK096574
Pays : United States
Organisme : NIH HHS
ID : R01 DK108842
Pays : United States
Organisme : Office of Academic Affiliations, Department of Veterans Affairs
ID : 5I01BX000105
Organisme : NIEHS NIH HHS
ID : P30 ES019776
Pays : United States
Organisme : NIH HHS
ID : R21 AG065977
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM008602
Pays : United States
Organisme : NIH HHS
ID : U54 AG062334
Pays : United States
Organisme : NIH HHS
ID : UL1 TR002378
Pays : United States
Organisme : NIH HHS
ID : R01 AR070091
Pays : United States
Organisme : NIH HHS
ID : R03 AG066559
Pays : United States
Organisme : NIH HHS
ID : R01 DK112946
Pays : United States
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