Biomarkers of PTA
dc.contributor.author | Golightly, YM | |
dc.contributor.author | Adams, SB | |
dc.contributor.author | Kraus, VB | |
dc.date.accessioned | 2015-11-10T22:18:41Z | |
dc.date.issued | 2015-01-01 | |
dc.description.abstract | © Springer Science+Business Media New York 2015.Prognostic biomarkers may indicate the likelihood of disease development and speed of progression or may serve as predictive indicators of responsiveness to treatment. Joint injuries, particularly severe injuries, may result in post-traumatic osteoarthritis (PTOA), and pre- and post-injury prognostic biomarkers are needed to enhance primary and secondary prevention approaches for PTOA. Several macromolecules from joint structures found in serum, urine, and synovial fluid are promising biochemical markers for monitoring joint metabolism and health before and after joint injury. The use of metabolic profiling (analysis of small molecules) as a predictive tool for osteoarthritis (OA) has increased in the past decade. Although there is some question as to whether PTOA and idiopathic OA are comparable conditions, there is some evidence to suggest that components of their pathogenesis are similar. Potentially, biomarkers important to the high-risk PTOA profile translate to idiopathic OA. Further work is needed to confirm the utility of macromolecules and metabolites as biomarkers for PTOA, particularly focusing on those strongly correlated to clinical efficacy measures important to the patient (e.g., symptoms, physical function, and quality of life) and the causal pathway of PTOA. | |
dc.identifier.isbn | 9781489976062 | |
dc.identifier.uri | ||
dc.publisher | Springer US | |
dc.relation.ispartof | Post-Traumatic Arthritis: Pathogenesis, Diagnosis and Management | |
dc.relation.isversionof | 10.1007/978-1-4899-7606-2_25 | |
dc.title | Biomarkers of PTA | |
dc.type | Book section | |
duke.contributor.orcid | Adams, SB|0000-0003-1020-1167 | |
duke.contributor.orcid | Kraus, VB|0000-0001-8173-8258 | |
pubs.begin-page | 317 | |
pubs.end-page | 330 | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Duke | |
pubs.organisational-group | Duke Molecular Physiology Institute | |
pubs.organisational-group | Institutes and Centers | |
pubs.organisational-group | Medicine | |
pubs.organisational-group | Medicine, Rheumatology and Immunology | |
pubs.organisational-group | Orthopaedics | |
pubs.organisational-group | Pathology | |
pubs.organisational-group | School of Medicine | |
pubs.publication-status | Published |
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