VARIATION OF THE MAGNETIC-RELAXATION RATE-1-T1 OF WATER PROTONS WITH MAGNETIC-FIELD STRENGTH (NMRD PROFILE) OF UNTREATED, NON-CALCIFIED, HUMAN ASTROCYTOMAS - CORRELATION WITH HISTOLOGY AND SOLIDS CONTENT
M. Spiller et al., VARIATION OF THE MAGNETIC-RELAXATION RATE-1-T1 OF WATER PROTONS WITH MAGNETIC-FIELD STRENGTH (NMRD PROFILE) OF UNTREATED, NON-CALCIFIED, HUMAN ASTROCYTOMAS - CORRELATION WITH HISTOLOGY AND SOLIDS CONTENT, Journal of neuro-oncology, 21(2), 1994, pp. 113-125
The magnetic relaxation rate 1/T1 of tissue water protons was measured
over a wide range of magnetic field strengths (NMRD profile) for 92 f
resh surgical specimens of astrocytomas to search for correlations of
1/T1 with tumor histology, as determined by light microscopy, and to a
ssess the diagnostic potential of NMRD profiles for grading astrocytom
as. A third goal was to elucidate the molecular determinants of lin. E
ach specimen was histologically graded and inspected for evidence of m
ineral deposits (Ca, Fe); its dry weight was determined and expressed
in % of original wet weight. To minimize variability not directly rela
ted to tumor grade, this initial report is limited to NMRD profiles of
47 non-calcified, non-mehorrhagic, untreated astrocytomas. For these,
the mean value of 1/T1 at very low magnetic field sterilants was foun
d to increase with increasing grade of malignancy; no clear correlatio
n could be demonstrated at high fields where most imaging is done. The
spread of 1/T1 for different grades of malignancy is large, however,
and the overlap significant, even at the lowest field, so that astrocy
tomas can not be graded by NMRD profiles alone. Average 1/T1 and avera
ge dry weight increase with grade of malignancy; but the variability o
f lin among specimens of the same dry weight is large, indicating that
at least one other cellular parameter, not variable in normal tissue,
influences 1/T1 strongly. We hypothesize that this parameter reflects
changes at the molecular level in size distribution, mobility, or int
ermolecular interaction of cytoplasmic proteins. Which specific change
s are induced by malignant transformation in astrocytomas remains to b
e investigated.