TY - JOUR
T1 - Cortical demyelination and diffuse white matter injury in multiple sclerosis
AU - Kutzelnigg, Alexandra
AU - Lucchinetti, Claudia F.
AU - Stadelmann, Christine
AU - Brück, Wolfgang
AU - Rauschka, Helmut
AU - Bergmann, Markus
AU - Schmidbauer, Manfred
AU - Parisi, Joseph E.
AU - Lassmann, Hans
N1 - Funding Information:
The authors thank Marianne Leiszer and Ulrike Köck for their expert technical assistance. This study was supported by the Fonds zur Förderung der wissenschaftlichen Forschung, Austria (grant P 16848-B02), by a research prize from the Roman, Marga und Marielle Sobek Stiftung, and by the US National Multiple Sclerosis Society (grant RG 3051-A-1). W.B. and C.S. are supported by the Gemeinnützige Hertie-Stiftung. C.S. is furthermore supported by the medical faculty of the University of Göttingen (junior research group).
PY - 2005/11
Y1 - 2005/11
N2 - Focal demyelinated plaques in white matter, which are the hallmark of multiple sclerosis pathology, only partially explain the patient's clinical deficits. We thus analysed global brain pathology in multiple sclerosis, focusing on the normal-appearing white matter (NAWM) and the cortex. Autopsy tissue from 52 multiple sclerosis patients (acute, relapsing-remitting, primary and secondary progressive multiple sclerosis) and from 30 controls was analysed using quantitative morphological techniques. New and active focal inflammatory demyelinating lesions in the white matter were mainly present in patients with acute and relapsing multiple sclerosis, while diffuse injury of the NAWM and cortical demyelination were characteristic hallmarks of primary and secondary progressive multiple sclerosis. Cortical demyelination and injury of the NAWM, reflected by diffuse axonal injury with profound microglia activation, occurred on the background of a global inflammatory response in the whole brain and meninges. There was only a marginal correlation between focal lesion load in the white matter and diffuse white matter injury, or cortical pathology, respectively. Our data suggest that multiple sclerosis starts as a focal inflammatory disease of the CNS, which gives rise to circumscribed demyelinated plaques in the white matter. With chronicity, diffuse inflammation accumulates throughout the whole brain, and is associated with slowly progressive axonal injury in the NAWM and cortical demyelination.
AB - Focal demyelinated plaques in white matter, which are the hallmark of multiple sclerosis pathology, only partially explain the patient's clinical deficits. We thus analysed global brain pathology in multiple sclerosis, focusing on the normal-appearing white matter (NAWM) and the cortex. Autopsy tissue from 52 multiple sclerosis patients (acute, relapsing-remitting, primary and secondary progressive multiple sclerosis) and from 30 controls was analysed using quantitative morphological techniques. New and active focal inflammatory demyelinating lesions in the white matter were mainly present in patients with acute and relapsing multiple sclerosis, while diffuse injury of the NAWM and cortical demyelination were characteristic hallmarks of primary and secondary progressive multiple sclerosis. Cortical demyelination and injury of the NAWM, reflected by diffuse axonal injury with profound microglia activation, occurred on the background of a global inflammatory response in the whole brain and meninges. There was only a marginal correlation between focal lesion load in the white matter and diffuse white matter injury, or cortical pathology, respectively. Our data suggest that multiple sclerosis starts as a focal inflammatory disease of the CNS, which gives rise to circumscribed demyelinated plaques in the white matter. With chronicity, diffuse inflammation accumulates throughout the whole brain, and is associated with slowly progressive axonal injury in the NAWM and cortical demyelination.
KW - Cortical demyelination
KW - Multiple sclerosis
KW - Normal-appearing white matter
KW - PPMS
KW - SPMS
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U2 - 10.1093/brain/awh641
DO - 10.1093/brain/awh641
M3 - Article
C2 - 16230320
AN - SCOPUS:27644552194
SN - 0006-8950
VL - 128
SP - 2705
EP - 2712
JO - Brain
JF - Brain
IS - 11
ER -