AI Article Synopsis

  • Remote screening for cognitive impairment related to Alzheimer's disease (AD) is increasingly important due to an aging population and new treatments.
  • Two tests, the Telephone Interview for Cognitive Status (TICS) and the telephone adaptation of the Montreal Cognitive Assessment (T-MoCA), were validated for their effectiveness in remote cognitive evaluation among participants with varying degrees of cognitive health.
  • Both TICS and T-MoCA showed strong correlations with each other and effectively detected cognitive impairment, while also correlating negatively with specific AD biomarkers in cerebrospinal fluid.

Article Abstract

Introduction: Remote screening for cognitive impairment associated with Alzheimer's disease (AD) has grown in importance with the expected rise in prevalence of AD in an aging population and with new potential treatment options.

Methods: The Telephone Interview for Cognitive Status (TICS) and new telephone adaptation of the Montreal Cognitive Assessment (T-MoCA) were administered to participants independently classified through in-person clinical evaluation as cognitively normal (CN; n = 167), mild cognitive impairment (MCI; n = 25), or dementia (n = 23). Cerebrospinal fluid AD biomarkers were measured (n = 79).

Results: TICS and T-MoCA were highly correlated (r = 0.787; P < 0.001): groups differed on both (CN
Discussion: TICS and T-MoCA are effective for remotely detecting cognitive impairment associated with AD in older adults. Strong correlation between tests provides construct validity for the newer T-MoCA.

Highlights: Construct validity for the telephone adaptation of the Montreal Cognitive Assessment (T-MoCA) was newly established against the Telephone Interview for Cognitive Status (TICS). TICS and T-MoCA effectively detected cognitive impairment with remote administration. Both tests negatively correlated with a composite cerebrospinal fluid Alzheimer's disease (AD) biomarker (tau/amyloid beta 1-42).

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509307PMC
http://dx.doi.org/10.1002/alz.13039DOI Listing

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