TY - JOUR
T1 - Cognitive domains that predict time to diagnosis in prodromal Huntington disease
AU - The PREDICT-HD Investigators of the Huntington Study Group
AU - Harrington, Deborah L.
AU - Smith, Megan M.
AU - Zhang, Ying
AU - Carlozzi, Noelle E.
AU - Paulsen, Jane S.
AU - Wassink, Thomas
AU - Cross, Stephen
AU - Kimble, Mycah
AU - Ryan, Patricia
AU - Wood, Jessica
AU - Epping, Eric A.
AU - Beglinger, Leigh J.
AU - Chiu, Edmond
AU - Yastrubetskaya, Olga
AU - Preston, Joy
AU - Goh, Anita
AU - Fonseka, Chathushka
AU - Antonopoulos, Stephanie
AU - Loi, Samantha
AU - Chua, Phyllis
AU - Komiti, Angela
AU - Raymond, Lynn
AU - Dar Santos, Rachelle
AU - Carter, Kimberley
AU - Decolongon, Joji
AU - Rosenblatt, Adam
AU - Ross, Christopher A.
AU - Shpritz, Barnett
AU - Yoritomo, Nadine
AU - Welsh, Claire
AU - Mallonee, William M.
AU - Suter, Greg
AU - Addison, Judy
AU - Samii, Ali
AU - Macaraeg, Alma
AU - Jones, Randi
AU - Wood-Siverio, Cathy
AU - Factor, Stewart A.
AU - Testa, Claudia
AU - Barker, Roger A.
AU - Mason, Sarah
AU - Goodman, Anna
AU - Dipietro, Anna
AU - McCusker, Elizabeth
AU - Griffith, Jane
AU - Loy, Clement
AU - Gunn, David
AU - Perlmutter, Joel
AU - Mazzoni, Pietro
AU - Hershey, Tamara
PY - 2012/6/1
Y1 - 2012/6/1
N2 - Background: Prodromal Huntington's disease (prHD) is associated with a myriad of cognitive changes but the domains that best predict time to clinical diagnosis have not been studied. This is a notable gap because some domains may be more sensitive to cognitive decline, which would inform clinical trials. Objectives: The present study sought to characterise cognitive domains underlying a large test battery and for the first time, evaluate their ability to predict time to diagnosis. Methods: Participants included gene negative and gene positive prHD participants who were enrolled in the PREDICT-HD study. The CAG - age product (CAP) score was the measure of an individual's genetic signature. A factor analysis of 18 tests was performed to identify sets of measures or latent factors that elucidated core constructs of tests. Factor scores were then fit to a survival model to evaluate their ability to predict time to diagnosis. Results: Six factors were identified: (1) speed/inhibition, (2) verbal working memory, (3) motor planning/speed, (4) attention - information integration, (5) sensory - perceptual processing and (6) verbal learning/memory. Factor scores were sensitive to worsening of cognitive functioning in prHD, typically more so than performances on individual tests comprising the factors. Only the motor planning/speed and sensory - perceptual processing factors predicted time to diagnosis, after controlling for CAP scores and motor symptoms. Conclusions: The results suggest that motor planning/speed and sensory - perceptual processing are important markers of disease prognosis. The findings also have implications for using composite indices of cognition in preventive Huntington's disease trials where they may be more sensitive than individual tests.
AB - Background: Prodromal Huntington's disease (prHD) is associated with a myriad of cognitive changes but the domains that best predict time to clinical diagnosis have not been studied. This is a notable gap because some domains may be more sensitive to cognitive decline, which would inform clinical trials. Objectives: The present study sought to characterise cognitive domains underlying a large test battery and for the first time, evaluate their ability to predict time to diagnosis. Methods: Participants included gene negative and gene positive prHD participants who were enrolled in the PREDICT-HD study. The CAG - age product (CAP) score was the measure of an individual's genetic signature. A factor analysis of 18 tests was performed to identify sets of measures or latent factors that elucidated core constructs of tests. Factor scores were then fit to a survival model to evaluate their ability to predict time to diagnosis. Results: Six factors were identified: (1) speed/inhibition, (2) verbal working memory, (3) motor planning/speed, (4) attention - information integration, (5) sensory - perceptual processing and (6) verbal learning/memory. Factor scores were sensitive to worsening of cognitive functioning in prHD, typically more so than performances on individual tests comprising the factors. Only the motor planning/speed and sensory - perceptual processing factors predicted time to diagnosis, after controlling for CAP scores and motor symptoms. Conclusions: The results suggest that motor planning/speed and sensory - perceptual processing are important markers of disease prognosis. The findings also have implications for using composite indices of cognition in preventive Huntington's disease trials where they may be more sensitive than individual tests.
UR - http://www.scopus.com/inward/record.url?scp=84862829257&partnerID=8YFLogxK
U2 - 10.1136/jnnp-2011-301732
DO - 10.1136/jnnp-2011-301732
M3 - Article
C2 - 22451099
AN - SCOPUS:84862829257
SN - 0022-3050
VL - 83
SP - 612
EP - 619
JO - Journal of Neurology, Neurosurgery and Psychiatry
JF - Journal of Neurology, Neurosurgery and Psychiatry
IS - 6
ER -