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Association of Physical Activity With Neurofilament Light Chain Trajectories in Autosomal Dominant Frontotemporal Lobar Degeneration Variant Carriers.
Casaletto, Kaitlin B; Kornack, John; Paolillo, Emily W; Rojas, Julio C; VandeBunte, Anna; Staffaroni, Adam S; Lee, Shannon; Heuer, Hilary; Forsberg, Leah; Ramos, Eliana M; Miller, Bruce L; Kramer, Joel H; Yaffe, Kristine; Petrucelli, Leonard; Boxer, Adam; Boeve, Brad; Gendron, Tania F; Rosen, Howard.
Afiliação
  • Casaletto KB; Memory and Aging Center, Department of Neurology, University of California, San Francisco.
  • Kornack J; Memory and Aging Center, Department of Neurology, University of California, San Francisco.
  • Paolillo EW; Memory and Aging Center, Department of Neurology, University of California, San Francisco.
  • Rojas JC; Memory and Aging Center, Department of Neurology, University of California, San Francisco.
  • VandeBunte A; Memory and Aging Center, Department of Neurology, University of California, San Francisco.
  • Staffaroni AS; Memory and Aging Center, Department of Neurology, University of California, San Francisco.
  • Lee S; Memory and Aging Center, Department of Neurology, University of California, San Francisco.
  • Heuer H; Memory and Aging Center, Department of Neurology, University of California, San Francisco.
  • Forsberg L; Department of Neurology, Mayo Clinic, Rochester, Minnesota.
  • Ramos EM; Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles.
  • Miller BL; Memory and Aging Center, Department of Neurology, University of California, San Francisco.
  • Kramer JH; Memory and Aging Center, Department of Neurology, University of California, San Francisco.
  • Yaffe K; Memory and Aging Center, Department of Neurology, University of California, San Francisco.
  • Petrucelli L; Department of Neuroscience, Mayo Clinic, Jacksonville, Florida.
  • Boxer A; Mayo Clinic Graduate School of Biomedical Sciences, Mayo Clinic, Jacksonville, Florida.
  • Boeve B; Memory and Aging Center, Department of Neurology, University of California, San Francisco.
  • Gendron TF; Department of Neurology, Mayo Clinic, Rochester, Minnesota.
  • Rosen H; Department of Neuroscience, Mayo Clinic, Jacksonville, Florida.
JAMA Neurol ; 80(1): 82-90, 2023 01 01.
Article em En | MEDLINE | ID: mdl-36374516
ABSTRACT
Importance Physical activity is associated with cognitive health, even in autosomal dominant forms of dementia. Higher physical activity is associated with slowed cognitive and functional declines over time in adults carrying autosomal dominant variants for frontotemporal lobar degeneration (FTLD), but whether axonal degeneration is a potential neuroprotective target of physical activity in individuals with FTLD is unknown.

Objective:

To examine the association between physical activity and longitudinal neurofilament light chain (NfL) trajectories in individuals with autosomal dominant forms of FTLD. Design, Setting, and

Participants:

This cohort study included individuals from the ALLFTD Consortium, which recruited patients from sites in the US and Canada. Symptomatic and asymptomatic adults with pathogenic variants in one of 3 common genes associated with FTLD (GRN, C9orf72, or MAPT) who reported baseline physical activity levels and completed annual blood draws were assessed annually for up to 4 years. Genotype, clinical measures, and blood draws were collected between December 2014 and June 2019; data were analyzed from August 2021 to January 2022. Associations between reported baseline physical activity and longitudinal plasma NfL changes were assessed using generalized linear mixed-effects models adjusting for baseline age, sex, education, functional severity, and motor symptoms. Exposures Baseline physical activity levels reported via the Physical Activity Scale for the Elderly. To estimate effect sizes, marginal means were calculated at 3 levels of physical activity 1 SD above the mean represented high physical activity, 0 SD represented average physical activity, and 1 SD below the mean represented low physical activity. Main Outcomes and

Measures:

Annual plasma NfL concentrations were measured with single-molecule array technology.

Results:

Of 160 included FTLD variant carriers, 84 (52.5%) were female, and the mean (SD) age was 50.7 (14.7) years. A total of 51 (31.8%) were symptomatic, and 77 carried the C9orf72 variant; 39, GRN variant; and 44, MAPT variant. Higher baseline physical activity was associated with slower NfL trajectories over time. On average, NfL increased 45.8% (95% CI, 22.5 to 73.7) over 4 years in variant carriers. Variant carriers with high physical activity demonstrated 14.0% (95% CI, -22.7 to -4.3) slower NfL increases compared with those with average physical activity and 30% (95% CI, -52.2 to -8.8) slower NfL increases compared with those with low physical activity. Within genotype, C9orf72 and MAPT carriers with high physical activity evidenced 18% to 21% (95% CI, -43.4 to -7.2) attenuation in NfL, while the association between physical activity and NfL trajectory was not statistically significant in GRN carriers. Activities associated with higher cardiorespiratory and cognitive demands (sports, housework, and yardwork) were most strongly correlated with slower NfL trajectories (vs walking and strength training). Conclusions and Relevance In this study, higher reported physical activity was associated with slower progression of an axonal degeneration marker in individuals with autosomal dominant FTLD. Physical activity may serve as a primary prevention target in FTLD.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Degeneração Lobar Frontotemporal / Demência Frontotemporal Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Degeneração Lobar Frontotemporal / Demência Frontotemporal Idioma: En Ano de publicação: 2023 Tipo de documento: Article