The role of hyperlipidemia and lipid lowering therapy (LLT) in Amyotrophic Lateral Sclerosis (ALS) pathophysiology and its impact on disease progression and survival is unclear. The investigators analyzed the correlation between lipid levels with disease progression and survival in ALS patients and the association of LLT with these outcomes.
Study Type
OBSERVATIONAL
Enrollment
267
the Methodist Neurological Institute
Houston, Texas, United States
survial(tracheostomy free,<23 hours on NIPPV, from enrollment)
Death was confirmed from Social Security Death Index or newspaper obituaries. Tracheostomy- ventilation was also considered as an end of the life time point.
Time frame: 3years
ALSFRS(measure of disability)
DeltaFS = (48-ALSFRS at first evaluation )/duration from onset to diagnosis (month) changeFS=(ALSFRS at six months-ALSFRS at first evaluation)/6
Time frame: at first evaluation(time 0-T0) to six months (T6)
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