To date there is no satisfactory serum or cerebrospinal fluid (CSF) metabol
ic marker with which to identify patients with ALS, The goal of finding a s
uitable marker will be more feasible following the identification of define
d subgroups of patients with ALS. Some aspects of neurotransmitter chemistr
y in CSF seem worthy of further investigation, in particular, clarification
of whether there is a significant elevation of CSF glutamate in a subgroup
of patients and whether there are robust alterations in the noradrenaline
transmitter system. It seems unlikely, in the face of present evidence, tha
t the presence of aberrant exitatory amino acid transporter I transcripts i
n CSF will prove to be a useful marker of ALS. Increased levels of 3-nitrot
yrosine and neurofilament light in CSF, while not entirely disease-specific
for ALS, may nevertheless prove useful confirmatory markers of the disease
and its progression.