Modelling the cascade of biomarker changes in GRN-related frontotemporal dementia

• Published in: Journal of neurology, neurosurgery and psychiatry Vol. 92; no. 5; pp. 494 - 501
• Main Authors: Panman, Jessica L, Venkatraghavan, Vikram, van der Ende, Emma L, Jiskoot, Lize C, Poos, Jackie M, Dopper, Elise G P, Meeter, Lieke H H, Rombouts, Serge A R B, Vernooij, Meike W, Kievit, Anneke J A, Premi, Enrico, Cosseddu, Maura, Bonomi, Elisa, Olives, Jaume, Rohrer, Jonathan D, Borroni, Barbara, Bron, Esther E, Van Swieten, John C, Papma, Janne M, Klein, Stefan, Anderl-Straub, Sarah, Andersson, Christin, Antonell, Anna, Arighi, Andrea, Balasa, Mircea, Barandiaran, Myriam, Bargalló, Nuria, Bartha, Robart, Bender, Benjamin, Bras, Jose, Bruffaerts, Rose, Cash, David, Castelo-Branco, Miguel, Convery, Rhian, Cope, Thomas, Danek, Adrian, Arriba, María de, Mendonça, Alexandre de, Fede, Giuseppe Di, Díaz, Zigor, Duro, Diana, Fenoglio, Chiara, Ferreira, Catarina B, Finger, Elizabeth, Gabilondo, Alazne, Galimberti, Daniela, Gasparotti, Roberto, Gauthier, Serge, Gazzina, Stefano, Graff, Caroline, Indakoetxea, Begoña, Jelic, Vesna, Karnath, Hans-Otto, Keren, Ron, Laforce, Robert, Leitão, Maria João, Levin, Johannes, Lladó, Albert, Loosli, Sandra, Masellis, Mario, Mead, Simon, Miltenberger, Gabriel, Minkelenm, Rick van, Mitchell, Sara, Moore, Katrina, Moreno, Fermin, Nicholas, Jennifer, Öijerstedt, Linn, Peakman, Georgia, Pijnenburg, Yolande, Polito, Cristina, Rademakers, Rosa, Redaelli, Veronica, Rittman, Tim, Rosa-Neto, Pedro, Rossi, Giacomina, Rosser, Martin, Rowe, James, Santana, Isabel, Santiago, Beatriz, Scarpini, Elio, Shoesmith, Christen, Synofzik, Matthis, Tábuas-Pereira, Miguel, Tagliavini, Fabrizio, Tartaglia, Carmela, Tainta, Mikel, Taipa, Ricardo, Tang-Wai, David, Thomas, David L, Tiraboschi, Pietro, Todd, Emily, Vandenberghe, Rik, Vandenbulcke, Mathieu, Veldsman, Michele, Verdelho, Ana, Villanua, Jorge, WilkeIone, Carlo, Elisabeth, Woollacott, Henrik, Wlasich
• Format: Journal Article
• Language: English
• Published: England BMJ Publishing Group Ltd 01.05.2021; BMJ Publishing Group LTD; BMJ Publishing Group
• Series: Original research
• Subjects: Age; Aged; Anisotropy; Biomarkers; Brain - diagnostic imaging; Cognition & reasoning; Cognition - physiology; Dementia; Disease Progression; Estimates; Female; Frontotemporal Dementia - blood; Frontotemporal Dementia - diagnostic imaging; Frontotemporal Dementia - genetics; Gray Matter - diagnostic imaging; Humans; Language; Magnetic Resonance Imaging; Male; Medical imaging; Medicin och hälsovetenskap; Middle Aged; Mutation; Neurodegeneration; Neurofilament Proteins - blood; Neuropsychological Tests; Phenotype; Progranulins - genetics; White Matter - diagnostic imaging; Netherlands
• ISSN: 0022-3050; 1468-330X; 1468-330X
• DOI: 10.1136/jnnp-2020-323541

ObjectiveProgranulin-related frontotemporal dementia (FTD-GRN) is a fast progressive disease. Modelling the cascade of multimodal biomarker changes aids in understanding the aetiology of this disease and enables monitoring of individual mutation carriers. In this cross-sectional study, we estimated the temporal cascade of biomarker changes for FTD-GRN, in a data-driven way.MethodsWe included 56 presymptomatic and 35 symptomatic GRN mutation carriers, and 35 healthy non-carriers. Selected biomarkers were neurofilament light chain (NfL), grey matter volume, white matter microstructure and cognitive domains. We used discriminative event-based modelling to infer the cascade of biomarker changes in FTD-GRN and estimated individual disease severity through cross-validation. We derived the biomarker cascades in non-fluent variant primary progressive aphasia (nfvPPA) and behavioural variant FTD (bvFTD) to understand the differences between these phenotypes.ResultsLanguage functioning and NfL were the earliest abnormal biomarkers in FTD-GRN. White matter tracts were affected before grey matter volume, and the left hemisphere degenerated before the right. Based on individual disease severities, presymptomatic carriers could be delineated from symptomatic carriers with a sensitivity of 100% and specificity of 96.1%. The estimated disease severity strongly correlated with functional severity in nfvPPA, but not in bvFTD. In addition, the biomarker cascade in bvFTD showed more uncertainty than nfvPPA.ConclusionDegeneration of axons and language deficits are indicated to be the earliest biomarkers in FTD-GRN, with bvFTD being more heterogeneous in disease progression than nfvPPA. Our data-driven model could help identify presymptomatic GRN mutation carriers at risk of conversion to the clinical stage.