There is a major unmet need for timely, non-invasive, and low-burden evaluation of patients presenting with mild cognitive impairment (MCI) and dementia. MCI impacts 12-18% of people in the United States over age 60 years (Alzheimer's Association. Mild Cognitive Impairment (MCI) available at https://www.alz.org/alzheimers-dementia/what-is-dementia/related\_conditions/mild-cognitive-impairment. Accessed August 16, 2022). MCI does not substantially interfere with daily activities, although complex functional tasks may be performed less efficiently (Knopman DS, Petersen RC. Mild cognitive impairment and mild dementia: a clinical perspective. Mayo Clin Proc. 2014;89(10):1452-1459. doi:10.1016/j.mayocp.2014.06.019). Approximately 30% of MCI patients have Alzheimer's disease (AD) as a cause of their symptoms (Lopez,OL, Kuller LH, Becker JT, et al. Incidence of dementia in mild cognitive impairment in the cardiovascular health study cognition study. Arch Neurol. 2007;64(3):416-420.doi:10.1001/archneur.64.3.416)). In contrast, dementia is defined by chronic, acquired loss of two or more cognitive abilities caused by brain disease or injury, often associated with significant interference with the ability to function at work or at usual activities. (Knopman DS, Petersen RC. Mild cognitive impairment and mild dementia: a clinical perspective. Mayo Clin Proc. 2014;89(10):1452-1459. doi:10.1016/j.mayocp.2014.06.019). Approximately 60-80% of dementia patients have AD as a cause of their symptoms (Alzheimer's Association. Mild Cognitive Impairment (MCI) available at https://www.alz.org/alzheimers-dementia/what-is-dementia/related\_conditions/mild-cognitive-impairment. Accessed August 16, 2022).
The Quality Improvement PrecivityAD2(TM) Clinician Survey and Clinical Utility Study (QUIP II) represents a large-scale initiative for the PrecivityAD2 blood test for use by neurologists, geriatricians, and geropsychiatrists (memory care specialists) who see patients aged 55 years and older with signs or symptoms of MCI or dementia. C₂N Diagnostics, LLC is a CLIA-certified, CAP-accredited diagnostic testing laboratory based in St. Louis, MO. Its new test, the PrecivityAD2 blood test, measures plasma amyloid beta (Aβ) peptides 42 and 40 (Aβ42/40) Ratio and phosphorylated tau (p-tau) compared to non-phosphorylated tau (np-tau) at amino acid 217 of the tau peptide (p-tau217/np-tau217) ratio to determine whether a patient with signs or symptoms of cognitive impairment is likely to have brain amyloid plaques, a pathological hallmark of AD.
Study Type
OBSERVATIONAL
Enrollment
400
The PrecivityAD2 blood test measures plasma amyloid beta (Aβ) peptides 42 and 40 (Aβ42/40) Ratio and phosphorylated tau (p-tau) compared to non-phosphorylated tau (np-tau) at amino acid 217 of the tau peptide (p-tau217/np-tau217) ratio to determine whether a patient with signs or symptoms of cognitive impairment is likely to have brain amyloid plaques, a pathological hallmark of AD.
UCSF Memory and Aging Center
San Francisco, California, United States
Pacific Brain Health Center
Santa Monica, California, United States
Advocate Memory Center
Park Ridge, Illinois, United States
Josephson Wallack Munshower Neurology, P.C.
Indianapolis, Indiana, United States
Tulane Doctors Neurosurgery Clinic
New Orleans, Louisiana, United States
Memorial Healthcare Institute for Neuroscience
Owosso, Michigan, United States
Sharlin Health and Neurology
Ozark, Missouri, United States
C2N Diagnostics
St Louis, Missouri, United States
Palmetto Primary Care Physicians
Summerville, South Carolina, United States
Change in planned clinical management (Cohort A and B)
The association of the test result on medical decision making
Time frame: Day 20
Change in planned clinical management (Cohort B)
Evaluate the planned versus subsequent planned change in clinical management as a result of receiving the test result
Time frame: Day 0 vs Day 20
Difference between the actual age and symptomatology versus intended use criteria (Cohort A and B)
Evaluate the intended use criteria
Time frame: Day 90
Relationship between the test result and actual clinical management (Cohort B)
Association of the test result on subsequent conducted changes in clinical management and test results when evaluating individuals with MCI or dementia in an ambulatory setting
Time frame: Day 90
Change in planned clinical management compared to conducted clinical management (Cohort B only)
The evaluation of planned versus conducted change in management as a result of receiving the test result
Time frame: Day 20 vs Day 90
Change in probability of AD (Cohort A and B)
Evaluate the probability of an AD Dx pre and post receipt of the test result
Time frame: Day 0 vs Day 20
Change in anti-AD medication use (Cohort A and B)
Evaluate anti-AD medication use pre- and post-receipt of the test result
Time frame: Day 0 vs Day 20
Change in diagnosis (Cohort B)
Evaluate any changes in diagnoses as a result of receiving the AD test result
Time frame: Day 0 vs Day 90
Relationship between the test result and planned testing (Cohort B)
Evaluate the association between subsequent test ordering pre and post testing
Time frame: Day 0 vs Day 20 vs Day 90
Correlations between the net promoter score and ease of use by APS2 result (Cohort B)
Focus group questions around net promoter score and ease of use, strengths, and limitations of testing
Time frame: Day 90
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