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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004429naa a2200469 4500
001oai:lup.lub.lu.se:79ef5c8a-b0e1-4d71-ba6d-27cc3e00a042
003SwePub
008210716s2021 | |||||||||||000 ||eng|
024a https://lup.lub.lu.se/record/79ef5c8a-b0e1-4d71-ba6d-27cc3e00a0422 URI
024a https://doi.org/10.1089/neu.2020.73172 DOI
040 a (SwePub)lu
041 a engb eng
042 9 SwePub
072 7a art2 swepub-publicationtype
072 7a ref2 swepub-contenttype
100a Karlsson, Michaelu Lund University,Lunds universitet,Mitokondriell Medicin,Forskargrupper vid Lunds universitet,Mitochondrial Medicine,Lund University Research Groups,Copenhagen University Hospital,Cochin Hospital4 aut0 (Swepub:lu)med-mck
2451 0a Evaluation of Diffusion Tensor Imaging and Fluid Based Biomarkers in a Large Animal Trial of Cyclosporine in Focal Traumatic Brain Injury
264 1b Mary Ann Liebert Inc,c 2021
300 a 9 s.
520 a All phase III trials evaluating medical treatments for traumatic brain injury (TBI), performed to date, have failed. To facilitate future success there is a need for novel outcome metrics that can bridge pre-clinical studies to clinical proof of concept trials. Our objective was to assess diffusion tensor imaging (DTI) and biofluid-based biomarkers as efficacy outcome metrics in a large animal study evaluating the efficacy of cyclosporine in TBI. This work builds on our previously published study that demonstrated a reduced volume of injury by 35% with cyclosporine treatment based on magnetic resonance imaging (MRI) results. A focal contusion injury was induced in piglets using a controlled cortical impact (CCI) device. Cyclosporine in a novel Cremophor/Kolliphor EL-free lipid emulsion, NeuroSTAT, was administered by continuous intravenous infusion for 5 days. The animals underwent DTI on day 5. Glial fibrillary acidic protein (GFAP), as a measure of astroglia injury, and neurofilament light (NF-L), as a measure of axonal injury, were measured in blood on days 1, 2, and 5, and in cerebrospinal fluid (CSF) on day 5 post-injury. Normalized fractional anisotropy (FA) was significantly (p = 0.027) higher in in the treatment group, indicating preserved tissue integrity with treatment. For the biomarkers, we observed a statistical trend of a decreased level of NF-L in CSF (p = 0.051), in the treatment group relative to placebo, indicating less axonal injury. Our findings suggest that DTI, and possibly CSF NF-L, may be feasible as translational end-points assessing neuroprotective drugs in TBI.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Neurologi0 (SwePub)302072 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Neurology0 (SwePub)302072 hsv//eng
653 a biomarkers
653 a cyclosporine
653 a diffusion tensor imaging
653 a traumatic brain injury
700a Yang, Zhihuiu Florida Museum Natural History4 aut
700a Chawla, Sanjeevu Cochin Hospital4 aut
700a Delso, Nileu Cochin Hospital4 aut
700a Pukenas, Bryanu Cochin Hospital4 aut
700a Elmér, Eskilu Lund University,Lunds universitet,Mitokondriell Medicin,Forskargrupper vid Lunds universitet,Mitochondrial Medicine,Lund University Research Groups,Abliva AB4 aut0 (Swepub:lu)expb-eel
700a Hugerth, Matildau Abliva AB4 aut
700a Margulies, Susan S.u Georgia Institute of Technology4 aut
700a Ehinger, Johannesu Lund University,Lunds universitet,Mitokondriell Medicin,Forskargrupper vid Lunds universitet,Mitochondrial Medicine,Lund University Research Groups4 aut0 (Swepub:lu)med-jeg
700a Hansson, Magnus J.u Lund University,Lunds universitet,Mitokondriell Medicin,Forskargrupper vid Lunds universitet,Mitochondrial Medicine,Lund University Research Groups,Abliva AB4 aut0 (Swepub:lu)expb-mha
700a Wang, Kevin K.W.u Florida Museum Natural History4 aut
700a Kilbaugh, Todd J.u Cochin Hospital4 aut
710a Mitokondriell Medicinb Forskargrupper vid Lunds universitet4 org
773t Journal of Neurotraumad : Mary Ann Liebert Incg 38:13, s. 1870-1878q 38:13<1870-1878x 0897-7151x 1557-9042
856u http://dx.doi.org/10.1089/neu.2020.7317y FULLTEXT
8564 8u https://lup.lub.lu.se/record/79ef5c8a-b0e1-4d71-ba6d-27cc3e00a042
8564 8u https://doi.org/10.1089/neu.2020.7317

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