Protein biomarker indicators of neurological injury and/or disease and methods of use thereof
AssigneeBrainbox Solutions, Inc.
InventorsDonna J. EDMONDS, Timothy E. VAN METER, Nazanin MIRSHAHI, James SNIDER
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AssigneeBrainbox Solutions, Inc.
InventorsDonna J. EDMONDS, Timothy E. VAN METER, Nazanin MIRSHAHI, James SNIDER
Estimating the term…
Methods, compositions and kits useful in the detection, assessment, diagnosis, prognosis and/or treatment of neurological injury or disease or brain injury, such as traumatic brain injury (TBS), are provided in which certain newly discovered protein biomarkers are detected in a biological sample of a subject undergoing testing or evaluation. The methods allow for detection of changes in levels, amounts, or concentrations of the protein biomarkers in a subject compared with those of controls. Detection of the protein biomarkers, and/or levels thereof, provides an indication of biological and biochemical events, e.g., at a cellular level, which are occurring in the subject who is undergoing testing or analysis for the neurological injury or brain injury.
1-48. (canceled)
A method of diagnosing and treating a neurological or brain injury in a subject that has, or is suspected of having, a neurological or brain injury, the method comprising:
A method of treating post-traumatic brain injury (“TBI”) seizures, post-TBI depression, post-TBI anxiety, post-TBI post-traumatic stress disorder (PTSD), post-TBI sleep disorder, post-TBI headache, post-TBI chronic pain, post-TBI oculomotor deficits, post-TBI attention and cognitive defects, and/or post-TBI balance and gait problems in a subject, the method comprising:
A composition comprising a solid substrate and a plurality of binding agents immobilized on the substrate, and the binding agents specifically bind to a plurality of protein biomarkers comprising soluble Suppression of Tumorigenicity 2 protein (sST2), Glial Fibrillary Acidic Protein (GFAP) and Neurogranin (NRGN)), and optionally bind to one or more additional protein biomarkers selected from Aldolase C (ALDOC), Brain Derived Neurotrophic Factor (BDNF), Calcitonin Gene Related Peptide (CGRP), Endothelin 1 (ET1), Eotaxin (CCL11), Fatty Acid Binding Protein 7 (FABP7), Growth Associated Protein 43 (GAP-43), Intercellular Adhesion Molecule 5 (ICAM-5), Interleukin 6 (IL-6), Interleukin 8 (IL-8), Interleukin 10 (IL-10), Metallothionein 3 (MT3), Neurofilament heavy chain (NF-H), Neurofilament light chain (NF-L), Neurofilament medium chain (NF-M), Neuron Specific Enolase (ENO2/NSE), Oligodendrocyte Myelin Glycoprotein (OMG), Reticulon (RTN1), Synuclein alpha (SNCA), Synuclein beta (SNCB), Tau microtubule binding protein (TAU/MAPT), and Vascular Endothelial Growth Factor (VEGF-A, B, C, or D homo- or heterodimers).
Dependencies are inferred from the claim text.