Relationship between CSF tau biomarkers and structural brain MRI measures in frontotemporal lobar degeneration

被引:2
|
作者
Fenu, Giuseppe [1 ]
Oppo, Valentina [1 ]
Serra, Giulia [1 ]
Lorefice, Lorena [2 ]
Di Sfefano, Francesca [1 ]
Deagostini, Dario [1 ]
Mancosu, Cristina [2 ]
Fadda, Elisabetta [2 ]
Melis, Cristina [2 ]
Siotto, Paolo [3 ]
Cocco, Eleonora [2 ]
Melis, Maurizio [1 ]
Cossu, Giovanni [1 ]
机构
[1] ARNAS Brotzu, Dept Neurosci, Cagliari, Italy
[2] Univ Cagliari, Multiple Sclerosis Ctr, Cagliari, Italy
[3] ARNAS Brotzu, Radiol Unit, Cagliari, Italy
关键词
Frontotemporal lobar degeneration; Cerebrospinal fluid; Biomarkers; Brain volume; Tau; MRI; BEHAVIORAL VARIANT; DEMENTIA; DIAGNOSIS; ACCURATE; CRITERIA; DISEASE; ATROPHY;
D O I
10.1016/j.jns.2022.120415
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Recently in the field neurodegenerative diseases increasing attention has been pointed to CSF bio-markers and their integration with neuroimaging (1). Frontotemporal lobar degeneration (FTLD) refers to a heterogeneous group of clinical syndromes with different underlying proteinopathies including tau pathology. CSF biomarkers have been proposed as diagnostic and prognostic factors. Aim of our study was to evaluate the relationship between CSF tau biomarkers and structural MRI brain measures in FTLD. Methods: We included early FTLD patient. All included patients underwent lumbar puncture to evaluate amyloid, total-tau (t-tau), phospho-tau 181 (p-tau); p-tau/t-tau ratio was also calculated; brain MRI was performed to estimate whole brain volume, volume of principal deep grey matter structures and regional cortical thickness. Results: Demographic characteristics of the 28 included patients were as follows: female/male: 9/19; mean +/- SD age: 68.1 +/- 7.8 years. The p-tau/t-tau ratio was significantly correlated with whole brain volume (r = 0.69; p: 0.001), left putamen volume (r = 0.55 p: 0.009), left pallidum volume (r = 0.41; p: 0.01), right accumbens area (r = 0.47; p: 0.02). P-tau/t tau ratio showed also a significant correlation with cortical thickness of left temporal lobe (r = 0.74; p: 0.001) and right lateral orbital frontal cortex (r = 0.45; p: 0.03). Linear regression showed a significant relationship between p-tau/t-tau ratio and left temporal pole (p = 0.01; r(2): 0.60) and brain volume (p:0.002; r(2): 0.56) after controlling for age and gender. Conclusions: Our data suggest that CSF biomarkers, especially p-tau/t-tau ratio, could play a role as prognostic factor in FTLD. Further longitudinal investigations are needed to confirm these findings.
引用
收藏
页数:5
相关论文
共 50 条
  • [31] Biomarkers to Identify the Pathological Basis for Frontotemporal Lobar Degeneration
    Grossman, Murray
    JOURNAL OF MOLECULAR NEUROSCIENCE, 2011, 45 (03) : 366 - 371
  • [32] Biomarkers to Identify the Pathological Basis for Frontotemporal Lobar Degeneration
    Murray Grossman
    Journal of Molecular Neuroscience, 2011, 45 : 366 - 371
  • [33] Hippocampal sclerosis in tau-negative frontotemporal lobar degeneration
    Josephs, Keith A.
    Dickson, Dennis W.
    NEUROBIOLOGY OF AGING, 2007, 28 (11) : 1718 - 1722
  • [34] Review: Neuropathology of non-tau frontotemporal lobar degeneration
    Neumann, M.
    Mackenzie, I. R. A.
    NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 2019, 45 (01) : 19 - 40
  • [35] Diagnostic value of CSF biomarker profile in frontotemporal lobar degeneration
    Kapaki, Elisabeth
    Paraskevas, George P.
    Papageorgiou, Sokratis G.
    Bonakis, Anastasios
    Kalfakis, Nikolaos
    Zalonis, Ioannis
    Vassilopoulos, Demetris
    ALZHEIMER DISEASE & ASSOCIATED DISORDERS, 2008, 22 (01): : 47 - 53
  • [36] The relationship between microtubule associated protein-tau (MAPT) haplotype and predicted pathology in frontotemporal lobar degeneration (FTLD)
    Racine, Caroline
    Karydas, Anna
    Wittenberg, Dana
    Kramer, Joel
    Boxer, Adam
    Bonasera, Stephen J.
    Miller, Bruce
    NEUROLOGY, 2008, 70 (11) : A241 - A241
  • [37] Tau and Aβ42 protein in CSF of patients with frontotemporal degeneration
    Riemenschneider, M
    Wagenpfeil, S
    Diehl, J
    Lautenschlager, N
    Theml, T
    Heldmann, B
    Drzezga, A
    Jahn, T
    Förstl, H
    Kurz, A
    NEUROLOGY, 2002, 58 (11) : 1622 - 1628
  • [38] Tau and Aβ42 protein in CSF of patients with frontotemporal degeneration
    Pijnenburg, YAL
    Schoonenboom, NSNM
    Scheltens, P
    NEUROLOGY, 2003, 60 (02) : 353 - 353
  • [39] MRI Signatures of Brain Macrostructural Atrophy and Microstructural Degradation in Frontotemporal Lobar Degeneration Subtypes
    Zhang, Yu
    Tartaglia, Maria Carmela
    Schuff, Norbert
    Chiang, Gloria C.
    Ching, Christopher
    Rosen, Howard J.
    Gorno-Tempini, Maria Luisa
    Miller, Bruce L.
    Weiner, Michael W.
    JOURNAL OF ALZHEIMERS DISEASE, 2013, 33 (02) : 431 - 444
  • [40] Imaging Biomarkers for Neurodegeneration in Presymptomatic Familial Frontotemporal Lobar Degeneration
    Chen, Qin
    Kantarci, Kejal
    FRONTIERS IN NEUROLOGY, 2020, 11