To compare brain metabolite levels in patients with primary progressive (PP
) and relapsing remitting (RR) MS and controls. Hypotheses: (1) creatine (C
r), a putative marker of gliosis, is elevated and N-acetylospartate (NAA),
a putative marker of axonal density and functional integrity, is reduced in
PPMS lesions and normal appearing white matter (NAWM) compared to control
white matter; (2) The pattern of metobolite change in PPMS is different tha
n in RRMS. Methods: MRI and proton magnetic resonance spectroscopic imaging
(H-1 MRSI) were collected from 15 PPMS patients, 13 RRMS patients, and 20
controls. Results: Cr was increased in PPMS NAWM compared to controls (P=0.
035), and compared to RRMS NAWM (P=0.038). Cr was increased in focal MRI le
sions from PPMS compared to lesions from RRMS (P=0.044) and compared to con
trol white matter (P=0.041). NAA was similarly reduced in PPMS and RRMS NAW
M compared to control. NAA was similarly reduced in PPMS and RRMS lesions,
compared to control white matter. Conclusions: Creatine is higher in PPMS t
han RRMS NAWM and focal lesions. This observation is consistent with the no
tion that progressive disability in PPMS reflects increased gliosis and axo
nal loss whereas disability in RRMS reflects the cumulative effects of acut
e inflammatory lesions and axonal loss.