4.0 Article

Using the LASSI-L to Detect Robust Interference Effects in Premanifest Huntington Disease

Journal

COGNITIVE AND BEHAVIORAL NEUROLOGY
Volume 36, Issue 2, Pages 100-107

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/WNN.0000000000000329

Keywords

semantic interference; cognitive; Huntington disease; executive function; premanifest HD

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The LASSI-L is a sensitive instrument for detecting early cognitive decline in individuals with preHD and outperforms commonly used neuropsychological tests.
Background:Diagnosis of manifest Huntington disease (HD) is based primarily on motor symptoms, but premanifest HD (preHD) is often associated with subtle cognitive decline. The Loewenstein-Acevedo Scales for Semantic Interference and Learning (LASSI-L) is a validated verbal learning test that can be used to detect early cognitive decline. Objective:To determine the utility of the LASSI-L for detecting early cognitive decline in individuals with preHD and to compare the results of the LASSI-L with those of commonly used neuropsychological tests in HD. Method:We administered the LASSI-L to 13 individuals with preHD and 13 healthy controls matched for age, sex, and education as part of a longitudinal study of disease progression. For comparison purposes, we administered the Mini-Mental State Examination; Stroop Color and Word Test; Symbol Digit Modalities Test; Trail-Making Test, Parts A and B; and category fluency (animals) task. Results:Five of the seven sections on the LASSI-L captured group differences: Proactive Semantic Interference (PSI; P < 0.001), Failure to Recover From PSI (P = 0.038), Retroactive Semantic Interference (RSI; P = 0.013), Delayed Recall (P < 0.001), and B1 Cued Recall Intrusions (P = 0.036). Using a false discovery rate of <0.05, PSI, RSI, and Delayed Recall remained significant. Conclusion:The LASSI-L is a sensitive instrument for detecting early interference effects in individuals with preHD that outperforms commonly used neuropsychological tests. The LASSI-L could be a useful addition to clinical and research protocols involving individuals with preHD.

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