好色先生

好色先生

Explore the latest content from across our publications

Log In

Forgot Password?
Create New Account

Loading... please wait

Abstract Details

Exploring Cognitive Decline vs Motor Decline in ALS Patients
Aging, Dementia, and Behavioral Neurology
Behavioral and Cognitive Neurology Posters (7:00 AM-5:00 PM)
008
We explored the relationship between cognitive, behavioral and motor symptoms in ALS patients presenting to LSUHSC ALS Clinic.
Cognitive impairment in Amyotrophic Lateral Sclerosis [ALS] is described as ALS patients with fronto-temporal dys-executive syndrome, including apathy and anosognosia.  Cognitively impaired ALS patients, especially those with behavioral dysfunction, have poorer quality of life and faster disease progression.
A retrospective chart review was conducted of all patients seen in LSU-Health ALS Clinic from March, 2014 through December, 2015 and thirty-five patients (20 M/15 F, ages 43-85 y) were identified. Demographic information, neurological history, current medical status, scores on the ALS Cognitive Behavioral test, and scores on the ALS Functional Rating Scales were recorded and explored using bivariate correlations.

Neither the ALS Cognitive Score (Pearson=0.075; p=0.673; N=34) nor the ALS Behavioral Score (Pearson=0.271; p=0.127; N=33) was associated with the ALS Functional Rating Scale-Revised Score. Region of onset did not correlate with any variable.  ALS Cognitive Score was positively correlated with the number of months post diagnosis (Pearson=0.415; p=0.015; N=34) and the number of months post symptom onset (Pearson=0.475; p=0.005; N=33).

Our retrospective study using the ALS Cognitive-Behavioral Screen found that cognitive changes in ALS patients do not correlate to motor decline or laterality of onset (bulbar/limb-onset). Our study results support certain prior studies that used frontal-lobe cognitive/behavior assessment batteries and showed similar results. Our study results contradict prior studies that used MoCA-screening and demonstrated cognitive decline correlates with motor decline and poorer performance in bulbar-onset ALS. Our study also shows positive correlation between ALS Cognitive Score and months post-diagnosis/post symptom-onset which is consistent with previous studies suggesting that patients with intact cognition live longer.

With equivocal evidence regarding a cognitive-motor relationship in ALS, it is important to assess cognitive and motor symptoms independently and not assume physical disability equals cognitive disability. 

Authors/Disclosures
Aditi V. Varma-Doyle, MD (Brigham and Women's Hospital, Mass General Brigham)
PRESENTER
Dr. Varma-Doyle has nothing to disclose.
Nicole Villemarette-Pittman, PhD (LSUHSC-NONeurology) The institution of Dr. Villemarette-Pittman has received personal compensation in the range of $100,000-$499,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for Elsevier. The institution of Dr. Villemarette-Pittman has received research support from Acadia Pharma.
No disclosure on file
Amparo Gutierrez, MD, FAAN (Orlando Health) Dr. Gutierrez has nothing to disclose.