Pittsburgh compound-B PET white matter imaging and cognitive function in late multiple sclerosis

Author:

Zeydan Burcu1,Lowe Val J2,Schwarz Christopher G2,Przybelski Scott A3,Tosakulwong Nirubol3,Zuk Samantha M2,Senjem Matthew L4,Gunter Jeffrey L5,Roberts Rosebud O6,Mielke Michelle M6,Benarroch Eduardo E7,Rodriguez Moses7,Machulda Mary M8,Lesnick Timothy G3,Knopman David S7,Petersen Ronald C7,Jack Clifford R2,Kantarci Kejal2,Kantarci Orhun H7

Affiliation:

1. Department of Neurology, Mayo Clinic College of Medicine, Mayo Clinic and Foundation, Rochester, MN, USA/Department of Radiology, Mayo Clinic College of Medicine, Mayo Clinic and Foundation, Rochester, MN, USA

2. Department of Radiology, Mayo Clinic College of Medicine, Mayo Clinic and Foundation, Rochester, MN, USA

3. Department of Health Sciences Research, Mayo Clinic College of Medicine, Mayo Clinic and Foundation, Rochester, MN, USA

4. Department of Radiology, Mayo Clinic College of Medicine, Mayo Clinic and Foundation, Rochester, MN, USA/Department of Information Technology, Mayo Clinic College of Medicine, Mayo Clinic and Foundation, Rochester, MN, USA

5. Department of Information Technology, Mayo Clinic College of Medicine, Mayo Clinic and Foundation, Rochester, MN, USA

6. Department of Neurology, Mayo Clinic College of Medicine, Mayo Clinic and Foundation, Rochester, MN, USA/Department of Health Sciences Research, Mayo Clinic College of Medicine, Mayo Clinic and Foundation, Rochester, MN, USA

7. Department of Neurology, Mayo Clinic College of Medicine, Mayo Clinic and Foundation, Rochester, MN, USA

8. Department of Psychiatry and Psychology, Mayo Clinic College of Medicine, Mayo Clinic and Foundation, Rochester, MN, USA

Abstract

Background: There is growing interest in white matter (WM) imaging with positron emission tomography (PET). Objectives: We studied the association of cognitive function in late multiple sclerosis (MS) with cortical and WM Pittsburgh compound-B PET (PiB-PET) binding. Methods: In the population-based Mayo Clinic Study of Aging, 24 of 4869 participants had MS (12 underwent PiB-PET). Controls were age and sex matched (5:1). We used automated or semi-automated processing for quantitative image analyses and conditional logistic regression for group differences. Results: MS patients had lower memory ( p = 0.03) and language ( p = 0.02) performance; smaller thalamic volumes ( p = 0.003); and thinner temporal ( p = 0.001) and frontal ( p = 0.045) cortices on magnetic resonance imaging (MRI) than controls. There was no difference in global cortical PiB standardized uptake value ratios between MS and controls ( p = 0.35). PiB uptake was lower in areas of WM hyperintensities compared to normal-appearing white matter (NAWM) in MS ( p = 0.0002). Reduced PiB uptake in both the areas of WM hyperintensities ( r = 0.65; p = 0.02) and NAWM ( r = 0.69; p = 0.01) was associated with decreased visuospatial performance in MS. Conclusion: PiB uptake in the cortex in late MS is not different from normal age-matched controls. PiB uptake in the WM in late MS may be a marker of the large network structures’ integrity such as those involved in visuospatial performance.

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology

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