4.7 Article

Cortical microstructure in the amyotrophic lateral sclerosis-frontotemporal dementia continuum

Journal

NEUROLOGY
Volume 95, Issue 18, Pages E2565-E2576

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0000000000010727

Keywords

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Funding

  1. Fondo de Investigaciones Sanitario, Instituto de Salud Carlos III [PI14/01126, PI17/01019, PI13/01532, PI16/01825, INT19/00016, PI18/00435, PI15/01618, PI14/1561, PI18/00326, PI17/01896]
  2. CIBERNED program (Program 1, Alzheimer Disease) - Fondo Europeo de Desarrollo Regional, Union Europea, Una manera de hacer Europa
  3. CIBERNED program (SIGNAL study) - Fondo Europeo de Desarrollo Regional, Union Europea, Una manera de hacer Europa
  4. NIH (National Institute on Agiging) [1R01AG056850-01A1, R21AG056974, R01AG061566]
  5. Departament de Salut de la Generalitat de Catalunya, Pla Estrategic de Recerca i Innovacio en Salut [SLT002/16/00408]
  6. Fundacio La Marato de TV3 [20141210, 044412, 201437.10]
  7. Agency for Management of University and Research Grant [2017 SGR 547]
  8. Rio Hortega grant from Accion Estrategica en Salud 2013-2016 [CM17/00074]
  9. European Social Fund
  10. Global Brain Health Institute (Atlantic Fellow for Equity in Brain Health)
  11. Association for Frontotemporal Degeneration (Clinical Research Postdoctoral Fellowship, AFTD 2019-2021)
  12. Generalitat de Catalunya [SLT006/17/00119, SLT006/17/125]
  13. Fundacio Bancaria La Caixa
  14. Fundacion Espanola para el Fomento de la Investigacion de la Esclerosis Lateral Amiotrofica FUNDELA

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Objective To characterize the cortical macrostructure and microstructure of behavioral and cognitive changes along the amyotrophic lateral sclerosis (ALS)-frontotemporal dementia (FTD) continuum. Methods We prospectively recruited 88 participants with a 3T MRI structural and diffusion-weighted imaging sequences: 31 with ALS, 20 with the behavioral variant of FTD (bvFTD), and 37 cognitively normal controls. Participants with ALS underwent a comprehensive cognitive and behavioral assessment and were dichotomized into ALS without cognitive or behavioral impairment (ALSno-cbi; n = 12) and ALS with cognitive or behavioral impairment (ALScbi; n = 19). We computed cortical thickness and cortical mean diffusivity using a surface-based approach and explored the cortical correlates of cognitive impairment with the Edinburgh Cognitive and Behavioral ALS Screen. Results The ALSno-cbi and ALScbi groups showed different patterns of reduced cortical thickness and increased cortical mean diffusivity. In the ALSno-cbi group, cortical thinning was restricted mainly to the dorsal motor cortex. In contrast, in the ALScbi group, cortical thinning was observed primarily on frontoinsular and temporal regions bilaterally. There were progressive cortical mean diffusivity changes along the ALSno-cbi, ALScbi, and bvFTD clinical continuum. Participants with ALS with either cognitive or behavioral impairment showed increased cortical mean diffusivity in the prefrontal cortex in the absence of cortical thickness. Conclusions Cortical mean diffusivity might be a useful biomarker for the study of extramotor cortical neurodegeneration in the ALS-FTD clinical spectrum. Classification of evidence This study provides Class III evidence that the cortical microstructure correlates with cognitive impairment in the ALS-FTD continuum.

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