Sökning: WFRF:(Hamilton Alan) > (2020-2024) > Plasma biomarkers o...
Fältnamn | Indikatorer | Metadata |
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000 | 03709naa a2200469 4500 | |
001 | oai:gup.ub.gu.se/334958 | |
003 | SwePub | |
008 | 240528s2023 | |||||||||||000 ||eng| | |
024 | 7 | a https://gup.ub.gu.se/publication/3349582 URI |
024 | 7 | a https://doi.org/10.1017/S00332917230019522 DOI |
040 | a (SwePub)gu | |
041 | a eng | |
042 | 9 SwePub | |
072 | 7 | a ref2 swepub-contenttype |
072 | 7 | a art2 swepub-publicationtype |
100 | 1 | a Hamilton, Calum Alexander4 aut |
245 | 1 0 | a Plasma biomarkers of neurodegeneration in mild cognitive impairment with Lewy bodies |
264 | 1 | c 2023 |
520 | a Background. Blood biomarkers of Alzheimer's disease (AD) may allow for the early detection of AD pathology in mild cognitive impairment (MCI) due to AD (MCI-AD) and as a co-pathology in MCI with Lewy bodies (MCI-LB). However not all cases of MCI-LB will feature AD pathology. Disease-general biomarkers of neurodegeneration, such as glial fibrillary acidic protein (GFAP) or neurofilament light (NfL), may therefore provide a useful supplement to AD biomarkers. We aimed to compare the relative utility of plasma A beta 42/40, p-tau181, GFAP and NfL in differentiating MCI-AD and MCI-LB from cognitively healthy older adults, and from one another.Methods. Plasma samples were analysed for 172 participants (31 healthy controls, 48 MCI-AD, 28 possible MCI-LB and 65 probable MCI-LB) at baseline, and a subset (n = 55) who provided repeated samples after >= 1 year. Samples were analysed with a Simoa 4-plex assay for A beta 42, A beta 40, GFAP and NfL, and incorporated previously-collected p-tau181 from this same cohort.Results. Probable MCI-LB had elevated GFAP (p < 0.001) and NfL (p = 0.012) relative to controls, but not significantly lower A beta 42/40 (p = 0.06). GFAP and p-tau181 were higher in MCI-AD than MCI-LB. GFAP discriminated all MCI subgroups, from controls (AUC of 0.75), but no plasma-based marker effectively differentiated MCI-AD from MCI-LB. NfL correlated with disease severity and increased with MCI progression over time (p = 0.011).Conclusion. Markers of AD and astrocytosis/neurodegeneration are elevated in MCI-LB. GFAP offered similar utility to p-tau181 in distinguishing MCI overall, and its subgroups, from healthy controls. | |
650 | 7 | a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Neurovetenskaper0 (SwePub)301052 hsv//swe |
650 | 7 | a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Neurosciences0 (SwePub)301052 hsv//eng |
653 | a Alzheimer's disease | |
653 | a dementia with Lewy bodies | |
653 | a mild cognitive impairment | |
653 | a neurodegeneration | |
653 | a plasma biomarkers | |
700 | 1 | a O'Brien, John4 aut |
700 | 1 | a Heslegrave, Amanda4 aut |
700 | 1 | a Laban, Rhiannon4 aut |
700 | 1 | a Donaghy, Paul4 aut |
700 | 1 | a Durcan, Rory4 aut |
700 | 1 | a Lawley, Sarah4 aut |
700 | 1 | a Barnett, Nicola4 aut |
700 | 1 | a Roberts, Gemma4 aut |
700 | 1 | a Firbank, Michael4 aut |
700 | 1 | a Taylor, John-Paul4 aut |
700 | 1 | a Zetterberg, Henrik,d 1973u Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi,Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry4 aut0 (Swepub:gu)xzethe |
700 | 1 | a Thomas, Alan4 aut |
710 | 2 | a Göteborgs universitetb Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi4 org |
773 | 0 | t PSYCHOLOGICAL MEDICINEg 53:16, s. 7865-7873q 53:16<7865-7873x 0033-2917x 1469-8978 |
856 | 4 8 | u https://gup.ub.gu.se/publication/334958 |
856 | 4 8 | u https://doi.org/10.1017/S0033291723001952 |
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