The executive prominent / memory prominent spectrum in Alzheimer’s disease is highly heritable

Abstract Late-onset Alzheimer’s disease (LOAD) can present heterogeneously, with several subtypes recognized, including dysexecutive AD. One way to identify people with dysexecutive AD is to consider the difference between memory and executive functioning, which we refer to as the executive prominen...

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Veröffentlicht in:Neurobiology of aging 2016-05, Vol.41, p.115-121
Hauptverfasser: Mez, Jesse, MD MS, Mukherjee, Shubhabrata, PhD, Thornton, Timothy, PhD, Fardo, David W., PhD, Trittschuh, Emily, PhD, Sutti, Sheila, MS, Sherva, Richard, PhD, Kauwe, John S., PhD, Naj, Adam C., PhD, Beecham, Gary W., PhD, Gross, Alden, PhD, Saykin, Andrew J., PsyD, Green, Robert C., MD MPH, Crane, Paul K., MD MPH
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Sprache:eng
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Zusammenfassung:Abstract Late-onset Alzheimer’s disease (LOAD) can present heterogeneously, with several subtypes recognized, including dysexecutive AD. One way to identify people with dysexecutive AD is to consider the difference between memory and executive functioning, which we refer to as the executive prominent / memory prominent spectrum. We aimed to determine if this spectrum was heritable. We used neuropsychological and genetic data from people with mild LOAD (Clinical Dementia Rating 0.5 or 1.0) from the National Alzheimer’s Coordinating Center (NACC) and the Alzheimer’s Disease Neuroimaging Initiative (ADNI). We co-calibrated the neuropsychological data to obtain executive functioning and memory scores, and used their difference as a continuous phenotype to calculate its heritability overall and by chromosome. Narrow-sense heritability of the difference between memory and executive functioning scores was 0.68 (SE 0.12). Single nucleotide polymorphisms on chromosomes 1, 2, 4, 11, 12, and 18 explained the largest fraction of phenotypic variance, with signals from each chromosome accounting for 5-7%. The chromosomal pattern of heritability differed substantially from that of LOAD itself.
ISSN:0197-4580
1558-1497
DOI:10.1016/j.neurobiolaging.2016.02.015