Serial PIB and MRI in normal, mild cognitive impairment and Alzheimer's disease: implications for sequence of pathological events in Alzheimer's disease

The purpose of this study was to use serial imaging to gain insight into the sequence of pathologic events in Alzheimer's disease, and the clinical features associated with this sequence. We measured change in amyloid deposition over time using serial 11C Pittsburgh compound B (PIB) positron em...

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Veröffentlicht in:Brain (London, England : 1878) England : 1878), 2009-05, Vol.132 (5), p.1355-1365
Hauptverfasser: Jack, Clifford R., Lowe, Val J., Weigand, Stephen D., Wiste, Heather J., Senjem, Matthew L., Knopman, David S., Shiung, Maria M., Gunter, Jeffrey L., Boeve, Bradley F., Kemp, Bradley J., Weiner, Michael, Petersen, Ronald C.
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Sprache:eng
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Zusammenfassung:The purpose of this study was to use serial imaging to gain insight into the sequence of pathologic events in Alzheimer's disease, and the clinical features associated with this sequence. We measured change in amyloid deposition over time using serial 11C Pittsburgh compound B (PIB) positron emission tomography and progression of neurodegeneration using serial structural magnetic resonance imaging. We studied 21 healthy cognitively normal subjects, 32 with amnestic mild cognitive impairment and 8 with Alzheimer's disease. Subjects were drawn from two sources—ongoing longitudinal registries at Mayo Clinic, and the Alzheimer's disease Neuroimaging Initiative (ADNI). All subjects underwent clinical assessments, MRI and PIB studies at two time points, approximately one year apart. PIB retention was quantified in global cortical to cerebellar ratio units and brain atrophy in units of cm3 by measuring ventricular expansion. The annual change in global PIB retention did not differ by clinical group (P = 0.90), and although small (median 0.042 ratio units/year overall) was greater than zero among all subjects (P 
ISSN:0006-8950
1460-2156
DOI:10.1093/brain/awp062