TY - JOUR
T1 - Characterizing regional correlation, laterality and symmetry of amyloid deposition in mild cognitive impairment and Alzheimer's disease with Pittsburgh Compound B
AU - Raji, Cyrus A.
AU - Becker, James T.
AU - Tsopelas, Nicholas D.
AU - Price, Julie C.
AU - Mathis, Chester A.
AU - Saxton, Judith A.
AU - Lopresti, Brian J.
AU - Hoge, Jessica A.
AU - Ziolko, Scott K.
AU - DeKosky, Steven T.
AU - Klunk, William E.
N1 - Funding Information:
Supported by The National Institutes of Health: R01 AG018402, P50 AG005133, K02 AG001039, R01 AG020226, R01 MH070729, K01MH001976, R37 AG025516, P01 AG025204, The Alzheimer's Association: TLL-01-3381, The U.S. Department of Energy DE-FD02-03 ER63590.
PY - 2008/7/30
Y1 - 2008/7/30
N2 - We evaluated the region-to-region correlation, laterality and asymmetry of amyloid deposition in subjects with mild cognitive impairment (MCI) or Alzheimer's disease (AD) using the amyloid tracer, Pittsburgh Compound B (PiB). Seventeen subjects, including 7 with MCI (MMSE 26.7 ± 2.4) and 10 with AD (MMSE of 24.8 ± 2.7) underwent PiB imaging. Measures of laterality (i.e., group-wise predilection for right or left) and asymmetry (i.e., group-wise predilection for unequal PiB retention between the two hemispheres) were calculated for 17 Regions of Interest (ROIs). Regional correlations were calculated along with within-group and between-groups statistical analyses of laterality and asymmetry metrics. The median correlation between PiB retention across all pairs of ROIs was 0.65, with highest correlations found in areas of highest PiB retention (r = 0.74). Overall, PiB retention was symmetric bilaterally, but there was PiB laterality in MCI in dorsal frontal cortex [(t(6) = 3.05, p = 0.02, L > R] and sensory-motor area [t(6) = 3.10, p = 0.02, L > R] and in AD in the occipital pole (t(9) = -2.63, p = 0.03, R > L). The most significant asymmetries in PiB retention were found in sub-cortical white matter (t(6) = 3.99, p = 0.01) and middle precuneus [(t(6) = 3.57, p = 0.01] in MCI, and in lateral temporal cortex (t(9) = 3.02, p = 0.01) and anterior ventral striatum [t(9) = 2.37, p = 0.04] in AD. No group differences (AD versus MCI) were detected in laterality [F (1, 15) = 0.15, p = 0.7] or asymmetry [F (1, 15) = 0.7, p = 0.42].
AB - We evaluated the region-to-region correlation, laterality and asymmetry of amyloid deposition in subjects with mild cognitive impairment (MCI) or Alzheimer's disease (AD) using the amyloid tracer, Pittsburgh Compound B (PiB). Seventeen subjects, including 7 with MCI (MMSE 26.7 ± 2.4) and 10 with AD (MMSE of 24.8 ± 2.7) underwent PiB imaging. Measures of laterality (i.e., group-wise predilection for right or left) and asymmetry (i.e., group-wise predilection for unequal PiB retention between the two hemispheres) were calculated for 17 Regions of Interest (ROIs). Regional correlations were calculated along with within-group and between-groups statistical analyses of laterality and asymmetry metrics. The median correlation between PiB retention across all pairs of ROIs was 0.65, with highest correlations found in areas of highest PiB retention (r = 0.74). Overall, PiB retention was symmetric bilaterally, but there was PiB laterality in MCI in dorsal frontal cortex [(t(6) = 3.05, p = 0.02, L > R] and sensory-motor area [t(6) = 3.10, p = 0.02, L > R] and in AD in the occipital pole (t(9) = -2.63, p = 0.03, R > L). The most significant asymmetries in PiB retention were found in sub-cortical white matter (t(6) = 3.99, p = 0.01) and middle precuneus [(t(6) = 3.57, p = 0.01] in MCI, and in lateral temporal cortex (t(9) = 3.02, p = 0.01) and anterior ventral striatum [t(9) = 2.37, p = 0.04] in AD. No group differences (AD versus MCI) were detected in laterality [F (1, 15) = 0.15, p = 0.7] or asymmetry [F (1, 15) = 0.7, p = 0.42].
KW - Alzheimer's disease
KW - Amyloid
KW - PiB
UR - http://www.scopus.com/inward/record.url?scp=46249096584&partnerID=8YFLogxK
U2 - 10.1016/j.jneumeth.2008.05.005
DO - 10.1016/j.jneumeth.2008.05.005
M3 - Article
C2 - 18582948
AN - SCOPUS:46249096584
SN - 0165-0270
VL - 172
SP - 277
EP - 282
JO - Journal of Neuroscience Methods
JF - Journal of Neuroscience Methods
IS - 2
ER -