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Abstract Details

Fat mass loss correlates with survival in amyotrophic lateral sclerosis patients: prospective cohort study
Neuromuscular and Clinical Neurophysiology (EMG)
P4 - Poster Session 4 (5:30 PM-6:30 PM)
12-013
To assess the utility of Dual-energy x-ray absorptiometry (DXA) in amyotrophic lateral sclerosis (ALS) patients. 

Weight loss is one of the strongest predictors of shorter survival in ALS. High calorie diet increases fat mass, and might have survival benefit. Longitudinal study following changes in fat mass is lacking.

This is a preliminary analysis of patients enrolled in the prospective ALS Smad biomarker study. In this study, patients with probable or definite ALS are recruited for 1-year study period during which DXA scan and other measures are obtained at 0, 6 and 12 months. Detailed demographic information, disease-related history, and monthly ALSFRS-R scores are obtained. Patients who had more than 2 DXA scans were included in this analysis.

A total of 6 ALS patients had 14 DXA scans. Mean age was 57 at enrollment and 5 (83%) were males. The rate of decline in the ALSFRS-R score from disease onset to the second DXA scan was used to group patients. Three patients with fast progression (decline rate of ALSFRS-R score by >1 point/month) died with a mean survival from symptom onset of 21 months (Fast group). All patients used positive pressure ventilation and two had gastrostomy. The other 3 patients had slow progression (decline rate <1 point /month) and survived with a mean disease duration time of 36 months (Slow group). Compared to the Slow group, the Fast group had more weight loss (12.5kg vs 1.2kg, p=0.053), lean mass loss (4.6kg vs 0.7kg, p=0.2) and fat mass loss (7.9kg vs -1.8 kg, p=0.03). One patient in the Fast group had 9.8 kg (42%) fat mass loss while lean mass increased by 0.7kg.

Fat mass change in addition to weight change might serve as a biomarker for disease progression. Additional patient data are being acquired to further evaluate this possibility.

Authors/Disclosures
Ikjae Lee, MD (Columbia University)
PRESENTER
Dr. Lee has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Regeneron. The institution of Dr. Lee has received research support from NIH. The institution of Dr. Lee has received research support from Spastic Paraplegia Foundation.
Mohamed Kazamel, MD (UAB) Dr. Kazamel has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Alnylam Pharamceuticals. Dr. Kazamel has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Akcea Therapeutics.
Peter H. King, MD The institution of Dr. King has received research support from Department of Veterans Affairs. The institution of Dr. King has received research support from NIH.