Plasma proteome profiling identifies changes associated to AD but not to FTD

Autor: Mofrad, R.B., Campo, M. del, Peeters, C.F.W., Meeter, L.H.H., Seelaar, H., Koel-Simmelink, M., Ramakers, I.H.G.B., Middelkoop, H.A.M., Deyn, P.P. de, Claassen, J.A.H.R., Swieten, J.C. van, Bridel, C., Hoozemans, J.J.M., Scheltens, P., Flier, W.M. van der, Pijnenburg, Y.A.L., Teunissen, C.E.
Přispěvatelé: Molecular Neuroscience and Ageing Research (MOLAR), Psychology 2, RS: MHeNs - R1 - Cognitive Neuropsychiatry and Clinical Neuroscience, Psychiatrie & Neuropsychologie, Neurology, Clinical chemistry, Epidemiology and Data Science, Human genetics, Pathology, Amsterdam Neuroscience - Neurodegeneration, Amsterdam Neuroscience - Neuroinfection & -inflammation, APH - Personalized Medicine, APH - Methodology
Jazyk: angličtina
Rok vydání: 2022
Předmět:
Zdroj: Mofrad, R B, Del Campo, M, Peeters, C F W, Meeter, L H H, Seelaar, H, Koel-Simmelink, M, Ramakers, I H G B, Middelkoop, H A M, De Deyn, P P, Claassen, J A H R, van Swieten, J C, Bridel, C, Hoozemans, J J M, Scheltens, P, van der Flier, W M, Pijnenburg, Y A L & Teunissen, C E 2022, ' Plasma proteome profiling identifies changes associated to AD but not to FTD ', Acta neuropathologica communications, vol. 10, no. 1, 148, pp. 148 . https://doi.org/10.1186/s40478-022-01458-w
Acta neuropathologica communications, 10(1):148. BioMed Central Ltd.
Acta Neuropathologica Communications, 10
Acta Neuropathologica Communications 10 (2022) 1
Acta neuropathologica communications, 10(1):148. BioMed Central Ltd
Acta Neuropathologica Communications, 10(1)
Acta Neuropathologica Communications, 10, 1
Acta neuropathologica communications, 10(1):148. BioMed Central
Acta neuropathologica communications
Acta Neuropathologica Communications, 10(1). BMC
ISSN: 2051-5960
DOI: 10.1186/s40478-022-01458-w
Popis: Background Frontotemporal dementia (FTD) is caused by frontotemporal lobar degeneration (FTLD), characterized mainly by inclusions of Tau (FTLD-Tau) or TAR DNA binding43 (FTLD-TDP) proteins. Plasma biomarkers are strongly needed for specific diagnosis and potential treatment monitoring of FTD. We aimed to identify specific FTD plasma biomarker profiles discriminating FTD from AD and controls, and between FTD pathological subtypes. In addition, we compared plasma results with results in post-mortem frontal cortex of FTD cases to understand the underlying process. Methods Plasma proteins (n = 1303) from pathologically and/or genetically confirmed FTD patients (n = 56; FTLD-Tau n = 16; age = 58.2 ± 6.2; 44% female, FTLD-TDP n = 40; age = 59.8 ± 7.9; 45% female), AD patients (n = 57; age = 65.5 ± 8.0; 39% female), and non-demented controls (n = 148; 61.3 ± 7.9; 41% female) were measured using an aptamer-based proteomic technology (SomaScan). In addition, exploratory analysis in post-mortem frontal brain cortex of FTD (n = 10; FTLD-Tau n = 5; age = 56.2 ± 6.9, 60% female, and FTLD-TDP n = 5; age = 64.0 ± 7.7, 60% female) and non-demented controls (n = 4; age = 61.3 ± 8.1; 75% female) were also performed. Differentially regulated plasma and tissue proteins were identified by global testing adjusting for demographic variables and multiple testing. Logistic lasso regression was used to identify plasma protein panels discriminating FTD from non-demented controls and AD, or FTLD-Tau from FTLD-TDP. Performance of the discriminatory plasma protein panels was based on predictions obtained from bootstrapping with 1000 resampled analysis. Results Overall plasma protein expression profiles differed between FTD, AD and controls (6 proteins; p = 0.005), but none of the plasma proteins was specifically associated to FTD. The overall tissue protein expression profile differed between FTD and controls (7-proteins; p = 0.003). There was no difference in overall plasma or tissue expression profile between FTD subtypes. Regression analysis revealed a panel of 12-plasma proteins discriminating FTD from AD with high accuracy (AUC: 0.99). No plasma protein panels discriminating FTD from controls or FTD pathological subtypes were identified. Conclusions We identified a promising plasma protein panel as a minimally-invasive tool to aid in the differential diagnosis of FTD from AD, which was primarily associated to AD pathophysiology. The lack of plasma profiles specifically associated to FTD or its pathological subtypes might be explained by FTD heterogeneity, calling for FTD studies using large and well-characterize cohorts.
Databáze: OpenAIRE
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