Visuoperception test predicts pathologic diagnosis of Alzheimer disease in corticobasal syndrome

Clara D Boyd1, Michael Tierney2, Eric M Wassermann2

  • 1From the Department of Neurology (C.D.B., E.H.), Columbia University Medical Center, New York, NY; Behavioral Neurology Unit (M.T., E.M.W.), National Institute of Neurological Disorders and Stroke, Bethesda, MD; Department of Pathology and Laboratory Medicine (S.S., A.L.O., B.G.), Indiana University School of Medicine, Indianapolis; and Department of Physical Medicine and Rehabilitation (J.G.), Northwestern University Feinberg School of Medicine, Chicago IL. cdboyd@fastmail.us.

Neurology
|July 4, 2014
PubMed

Insights

Specific Visual Object and Space Perception Battery (VOSP) subtests can help differentiate Alzheimer disease (AD) from other pathologies in corticobasal syndrome (CBS). This aids in diagnosing underlying AD in CBS patients.

Area of Science:

  • Neuroscience
  • Neurology
  • Pathology

Background:

  • Corticobasal syndrome (CBS) presents with diverse underlying pathologies, complicating diagnosis.
  • Distinguishing Alzheimer disease (AD) from non-AD pathologies in CBS is crucial for appropriate patient management.
  • The Visual Object and Space Perception Battery (VOSP) assesses visuospatial abilities, potentially offering diagnostic clues.

Purpose of the Study:

  • To evaluate the efficacy of the VOSP in differentiating AD from non-AD pathologies within the CBS cohort.
  • To identify specific VOSP subtests that serve as reliable indicators of underlying AD in CBS patients.

Main Methods:

  • A clinicopathologic study involving 36 autopsied patients with CBS.
  • Patients were categorized into CBS with AD pathology (CBS-AD, n=10) and CBS without AD pathology (CBS-nonAD, n=26).
  • Performance on VOSP subtests was analyzed, along with sensitivity and specificity calculations.

Main Results:

  • Patients with CBS-AD exhibited earlier onset and lower memory scores compared to CBS-nonAD.
  • Failure on VOSP subtests including Incomplete Letters, Position Discrimination, Number Location, and Cube Analysis was significantly associated with CBS-AD.
  • Cube Analysis demonstrated the highest accuracy (AUC 0.91) in distinguishing CBS-AD from CBS-nonAD.

Conclusions:

  • Specific VOSP subtest failures are linked to a higher likelihood of underlying AD in patients with CBS.
  • Findings suggest a potential preferential involvement of the dorsal visual stream in CBS-AD.
  • The VOSP, particularly Cube Analysis, shows promise as a diagnostic tool for identifying AD pathology in CBS.
Abstract

Related Concept Videos

Alzheimer Disease ll: Pathophysiology01:23

Alzheimer Disease ll: Pathophysiology

Alzheimer disease involves structural changes in the brain that begin long before symptoms appear. The most distinctive features are extracellular neuritic plaques and intracellular neurofibrillary tangles.Neuritic plaques form in the cerebral cortex and around blood vessels. These plaques contain a dense core of beta-amyloid (Aβ)—a toxic protein fragment that clumps outside neurons. The core is surrounded by damaged neuronal extensions, as well as reactive astrocytes and...
32
Visual Agnosia01:12

Visual Agnosia

Visual agnosia is a condition characterized by the inability to recognize visually presented objects despite having normal vision. For instance, a person with visual agnosia can describe the shape and color of an object but cannot identify or name it. This impairment does not affect their visual field, acuity, color vision, brightness discrimination, language, or memory. An example of this condition in a social setting is someone at a dinner party asking for "that silver thing with a round...
2.0K
Alzheimer's Disease: Overview01:26

Alzheimer's Disease: Overview

Alzheimer's Disease (AD) is a continually advancing neurodegenerative disorder, distinguished by escalating memory loss, cognitive dysfunction, and dementia. The disease unfolds in three stages: preclinical, mild cognitive impairment (MCI), and dementia. Its onset is insidious, and the progression gradual, with the cause not well explained by other disorders.
The clinical diagnosis of AD hinges on the presence of memory and other cognitive impairments. Biomarkers, such as changes in Aβ...
1.7K
Prosopagnosia01:24

Prosopagnosia

Prosopagnosia, also known as face blindness, is the inability to recognize faces. In severe cases, individuals with prosopagnosia may not recognize close family members, including parents and spouses, by their faces. For instance, someone with prosopagnosia might walk past their child in a crowd, only realizing their mistake upon noticing their child's distinctive backpack or favorite jacket. Prosopagnosia specifically impairs facial recognition, while the recognition of other objects or...
1.2K
Alzheimer Disease l: Introduction01:29

Alzheimer Disease l: Introduction

Alzheimer disease is a chronic, progressive, and irreversible neurodegenerative disorder and the most common cause of dementia in older adults. It leads to gradual neuronal loss, causing cognitive decline, behavioral changes, and loss of functional independence.Risk Factors and EtiologyThe disease is multifactorial. Age is the strongest risk factor, with prevalence doubling every 5 years after age 65. Genetic factors include mutations in genes such as APP, PSEN1, and PSEN2, which are associated...
20
Association Areas of the Cortex01:21

Association Areas of the Cortex

Association areas are regions of the cerebral cortex that do not have a specific sensory or motor function. Instead, they integrate and interpret information from various sources to enable higher cognitive processes such as memory, learning, and decision-making. Some key association areas include the following:
Prefrontal Association Area: This area is located in the frontal lobe and is involved in planning, decision-making, and moderating social behavior. It connects with primary motor areas,...
10.2K