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Comorbid neuropathology and atypical presentation of Alzheimer's disease.
Pina-Escudero, Stefanie D; La Joie, Renaud; Spina, Salvatore; Hwang, Ji-Hye; Miller, Zachary A; Huang, Eric J; Grant, Harli; Mundada, Nidhi S; Boxer, Adam L; Gorno-Tempini, Maria Luisa; Rosen, Howard J; Kramer, Joel H; Miller, Bruce L; Seeley, William W; Rabinovici, Gil D; Grinberg, Lea Tenenholz.
Afiliação
  • Pina-Escudero SD; Global Brain Health Institute University of California San Francisco California USA.
  • La Joie R; Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California San Francisco California USA.
  • Spina S; Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California San Francisco California USA.
  • Hwang JH; Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California San Francisco California USA.
  • Miller ZA; Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California San Francisco California USA.
  • Huang EJ; Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California San Francisco California USA.
  • Grant H; Department of Pathology University of California San Francisco California USA.
  • Mundada NS; Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California San Francisco California USA.
  • Boxer AL; Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California San Francisco California USA.
  • Gorno-Tempini ML; Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California San Francisco California USA.
  • Rosen HJ; Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California San Francisco California USA.
  • Kramer JH; Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California San Francisco California USA.
  • Miller BL; Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California San Francisco California USA.
  • Seeley WW; Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California San Francisco California USA.
  • Rabinovici GD; Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California San Francisco California USA.
  • Grinberg LT; Department of Pathology University of California San Francisco California USA.
Alzheimers Dement (Amst) ; 16(3): e12602, 2024.
Article em En | MEDLINE | ID: mdl-39040464
ABSTRACT

INTRODUCTION:

Alzheimer's disease (AD) neuropathological changes present with amnestic and nonamnestic (atypical) syndromes. The contribution of comorbid neuropathology as a substratum of atypical expression of AD remains under investigated.

METHODS:

We examined whether atypical AD exhibited increased comorbid neuropathology compared to typical AD and if such neuropathologies contributed to the accelerated clinical decline in atypical AD.

RESULTS:

We examined 60 atypical and 101 typical AD clinicopathological cases. The number of comorbid pathologies was similar between the groups (p = 0.09). Argyrophilic grain disease was associated with atypical presentation (p = 0.008) after accounting for sex, age of onset, and disease duration. Vascular brain injury was more common in typical AD (p = 0.022). Atypical cases had a steeper Mini-Mental Status Examination (MMSE) decline over time (p = 0.033).

DISCUSSION:

Comorbid neuropathological changes are unlikely to contribute to atypical AD presentation and the steeper cognitive decline seen in this cohort. Highlights Autopsy cohort of 60 atypical and 101 typical AD; does comorbid pathology explain atypical presentation?Atypical versus Typical AD No significant differences in comorbid neuropathologies were found (p = 0.09).Argyrophilic Grain Disease Association significantly correlates with atypical AD presentations, suggesting a unique neuropathological pattern (p = 0.008).Vascular Brain Injury Prevalence Vascular brain injury is more common in typical AD than in atypical AD (p = 0.022).Cognitive Decline in Atypical AD Atypical AD patients experience a steeper cognitive decline measured by MMSE than those with typical AD despite lacking more comorbid neuropathology, highlighting the severity of atypical AD pathogenesis (p = 0.033).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Alzheimers Dement (Amst) Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Alzheimers Dement (Amst) Ano de publicação: 2024 Tipo de documento: Article