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August 13, 2013; 81 (7) Article

Contribution of cortical lesion subtypes at 7T MRI to physical and cognitive performance in MS

A. Scott Nielsen, Revere P. Kinkel, Nancy Madigan, Emanuele Tinelli, Thomas Benner, Caterina Mainero
First published July 17, 2013, DOI: https://doi.org/10.1212/WNL.0b013e3182a08ce8
A. Scott Nielsen
From Virginia Mason Medical Center (A.S.N.), Seattle; University of Washington (A.S.N.), Seattle, WA; Beth Israel Deaconess Medical Center (R.P.K., N.M.), Boston; Harvard Medical School (R.P.K., N.M., C.M.), Boston, MA; Department of Neurology and Psychiatry (E.T.), University of Rome La Sapienza, Italy; and Athinoula A. Martinos Center for Biomedical Imaging (T.B., C.M.), Massachusetts General Hospital, Boston, MA.
MD, MMSc
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Revere P. Kinkel
From Virginia Mason Medical Center (A.S.N.), Seattle; University of Washington (A.S.N.), Seattle, WA; Beth Israel Deaconess Medical Center (R.P.K., N.M.), Boston; Harvard Medical School (R.P.K., N.M., C.M.), Boston, MA; Department of Neurology and Psychiatry (E.T.), University of Rome La Sapienza, Italy; and Athinoula A. Martinos Center for Biomedical Imaging (T.B., C.M.), Massachusetts General Hospital, Boston, MA.
MD
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Nancy Madigan
From Virginia Mason Medical Center (A.S.N.), Seattle; University of Washington (A.S.N.), Seattle, WA; Beth Israel Deaconess Medical Center (R.P.K., N.M.), Boston; Harvard Medical School (R.P.K., N.M., C.M.), Boston, MA; Department of Neurology and Psychiatry (E.T.), University of Rome La Sapienza, Italy; and Athinoula A. Martinos Center for Biomedical Imaging (T.B., C.M.), Massachusetts General Hospital, Boston, MA.
PhD
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Emanuele Tinelli
From Virginia Mason Medical Center (A.S.N.), Seattle; University of Washington (A.S.N.), Seattle, WA; Beth Israel Deaconess Medical Center (R.P.K., N.M.), Boston; Harvard Medical School (R.P.K., N.M., C.M.), Boston, MA; Department of Neurology and Psychiatry (E.T.), University of Rome La Sapienza, Italy; and Athinoula A. Martinos Center for Biomedical Imaging (T.B., C.M.), Massachusetts General Hospital, Boston, MA.
MD
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Thomas Benner
From Virginia Mason Medical Center (A.S.N.), Seattle; University of Washington (A.S.N.), Seattle, WA; Beth Israel Deaconess Medical Center (R.P.K., N.M.), Boston; Harvard Medical School (R.P.K., N.M., C.M.), Boston, MA; Department of Neurology and Psychiatry (E.T.), University of Rome La Sapienza, Italy; and Athinoula A. Martinos Center for Biomedical Imaging (T.B., C.M.), Massachusetts General Hospital, Boston, MA.
PhD
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Caterina Mainero
From Virginia Mason Medical Center (A.S.N.), Seattle; University of Washington (A.S.N.), Seattle, WA; Beth Israel Deaconess Medical Center (R.P.K., N.M.), Boston; Harvard Medical School (R.P.K., N.M., C.M.), Boston, MA; Department of Neurology and Psychiatry (E.T.), University of Rome La Sapienza, Italy; and Athinoula A. Martinos Center for Biomedical Imaging (T.B., C.M.), Massachusetts General Hospital, Boston, MA.
MD, PhD
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Full PDF
Citation
Contribution of cortical lesion subtypes at 7T MRI to physical and cognitive performance in MS
A. Scott Nielsen, Revere P. Kinkel, Nancy Madigan, Emanuele Tinelli, Thomas Benner, Caterina Mainero
Neurology Aug 2013, 81 (7) 641-649; DOI: 10.1212/WNL.0b013e3182a08ce8

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Abstract

Objectives: Evaluate cross-sectionally the contribution of focal cortical lesion (CL) subtypes at ultra-high-field MRI and traditional MRI metrics of brain damage to neurologic disability and cognitive performance in a heterogeneous multiple sclerosis (MS) cohort.

Methods: Thirty-four patients with early or established disease including clinically isolated syndrome, relapsing-remitting MS, and secondary progressive MS were scanned on a human 7-tesla (7T) (Siemens) scanner to acquire fast low-angle shot (FLASH) T2*-weighted images for characterization of white matter and deep gray matter lesion volume, and CL types. Patients also underwent anatomical 3T MRI for cortical thickness estimation, and neuropsychological testing within 1 week of the 7T scan. Twenty-seven patient scans were acceptable for further analysis. Neurologic disability was measured using the Expanded Disability Status Scale.

Results: Type III-IV CLs had the strongest relationship to physical disability (ρ = 0.670, p < 0.0001). White matter lesion volume and type I CLs are each significantly associated with 6 of 11 neuropsychological test variables. Type III-IV CLs significantly correlate with 4 of 11 neuropsychological test variables whereas type II CLs, deep gray matter lesion volume, and cortical thickness metrics are less frequently associated with cognitive performance.

Conclusions: Leukocortical (type I) and subpial (III-IV) CLs identified on 7T FLASH-T2* sequences are potential cortical biomarkers of cognitive and neurologic status in MS.

GLOSSARY

ANT=
Animal Naming Test;
BDI=
Beck Depression Inventory, 2nd edition;
BVMTR=
Brief Visual Memory Test–Revised;
CL=
cortical lesion;
CLR=
cortical lesion ratio;
COWAT=
Controlled Oral Word Association Test;
CT=
cortical thickness;
CVLT2=
California Verbal Learning Test, 2nd edition;
DGMLV=
deep gray matter lesion volume;
DIR=
double inversion recovery;
EDSS=
Expanded Disability Status Scale;
FLASH=
fast low-angle shot;
GM=
gray matter;
JLOT=
Judgment of Line Orientation Test;
MEMPR=
magnetization-prepared rapid acquisition with multiple gradient echoes;
MS=
multiple sclerosis;
NPT=
neuropsychological test;
SDMT=
Symbol Digit Modalities Test;
SPMS=
secondary progressive multiple sclerosis;
WCST=
Wisconsin Card Sorting Test–64 card deck;
WM=
white matter;
WMLV=
white matter lesion volume;
WTAR=
Wechsler Test of Adult Reading

Footnotes

  • Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Supplemental data at www.neurology.org

  • Received October 3, 2012.
  • Accepted in final form April 29, 2013.
  • © 2013 American Academy of Neurology
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