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Progression to corticobasal syndrome: a longitudinal study of patients with nonfluent primary progressive aphasia and primary progressive apraxia of speech.
Garcia-Guaqueta, Danna P; Botha, Hugo; Utianski, Rene L; Duffy, Joseph R; Clark, Heather M; Goodrich, Austin W; Pham, Nha Trang Thu; Machulda, Mary M; Baker, Matt; Rademakers, Rosa; Whitwell, Jennifer L; Josephs, Keith A.
Affiliation
  • Garcia-Guaqueta DP; Department of Neurology, Behavioral Neurology & Movement Disorders, Mayo Clinic, College of Medicine and Science, Rochester, MN, 55905, USA.
  • Botha H; Department of Neurology, Behavioral Neurology & Movement Disorders, Mayo Clinic, College of Medicine and Science, Rochester, MN, 55905, USA.
  • Utianski RL; Department of Neurology, Behavioral Neurology & Movement Disorders, Mayo Clinic, College of Medicine and Science, Rochester, MN, 55905, USA.
  • Duffy JR; Department of Neurology, Behavioral Neurology & Movement Disorders, Mayo Clinic, College of Medicine and Science, Rochester, MN, 55905, USA.
  • Clark HM; Department of Neurology, Behavioral Neurology & Movement Disorders, Mayo Clinic, College of Medicine and Science, Rochester, MN, 55905, USA.
  • Goodrich AW; Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, 55905, USA.
  • Pham NTT; Department of Radiology, Mayo Clinic, Rochester, MN, 55905, USA.
  • Machulda MM; Department of Psychiatry and Psychology, Mayo Clinic, Rochester, MN, 55905, USA.
  • Baker M; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
  • Rademakers R; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
  • Whitwell JL; VIB Center for Molecular Neurology, University of Antwerp, Antwerp, Belgium.
  • Josephs KA; Department of Radiology, Mayo Clinic, Rochester, MN, 55905, USA.
J Neurol ; 271(7): 4168-4179, 2024 Jul.
Article in En | MEDLINE | ID: mdl-38583104
ABSTRACT
BACKGROUND AND

OBJECTIVES:

Nonfluent variant primary progressive aphasia (nfvPPA) and primary progressive apraxia of speech (PPAOS) can be precursors to corticobasal syndrome (CBS). Details on their progression remain unclear. We aimed to examine the clinical and neuroimaging evolution of nfvPPA and PPAOS into CBS.

METHODS:

We conducted a retrospective longitudinal study in 140 nfvPPA or PPAOS patients and applied the consensus criteria for possible and probable CBS for every visit, evaluating limb rigidity, akinesia, limb dystonia, myoclonus, ideomotor apraxia, alien limb phenomenon, and nonverbal oral apraxia (NVOA). Given the association of NVOA with AOS, we also modified the CBS criteria by excluding NVOA and assigned every patient to either a progressors or non-progressors group. We evaluated the frequency of every CBS feature by year from disease onset, and assessed gray and white matter volume loss using SPM12.

RESULTS:

Asymmetric akinesia, NVOA, and limb apraxia were the most common CBS features that developed; while limb dystonia, myoclonus, and alien limb were rare. Eighty-two patients progressed to possible CBS; only four to probable CBS. nfvPPA and PPAOS had a similar proportion of progressors, although nfvPPA progressed to CBS earlier (p-value = 0.046), driven by an early appearance of limb apraxia (p-value = 0.0041). The non-progressors and progressors both showed premotor/motor cortex involvement at baseline, with spread into prefrontal cortex over time.

DISCUSSION:

An important proportion of patients with nfvPPA and PPAOS progress to possible CBS, while they rarely develop features of probable CBS even after long follow-up.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Apraxias / Disease Progression / Primary Progressive Nonfluent Aphasia Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: J Neurol Year: 2024 Document type: Article Affiliation country: United States Country of publication: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Apraxias / Disease Progression / Primary Progressive Nonfluent Aphasia Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: J Neurol Year: 2024 Document type: Article Affiliation country: United States Country of publication: Germany