Abstract

AbstractBackgroundWhole‐brain volume loss using T1‐weighted imaging is an established measurement of neurodegeneration. The Boundary Shift Integral (BSI) produces reliable metrics of longitudinal volume loss, used in research studies and clinical trials. With the increased acquisition of volumetric T2‐FLAIR imaging in studies, there is opportunity to produce atrophy metrics using a composite atrophy measure (T1‐weighted and T2‐FLAIR) that is more precise than either modality alone.MethodData from Alzheimer’s Disease Neuroimaging Initiative (ADNI3) were used. Volumetric T1 and T2‐FLAIR weighted imaging were obtained (n = 269), for baseline and follow‐up; Table 1. T1‐weighted images were bias corrected and underwent Geodesic Information Flow (GIF), producing probabilistic brain masks. Masks were resampled to T2‐FLAIR space. The BSI was performed on serial T1‐weighted (gBSI), and T2‐FLAIR (fBSI) separately. We tested differences by diagnosis (control (CN), mild cognitive impairment (MCI) and Alzheimer’s disease (AD)) between indirect volume change, gBSI, fBSI, and composite BSI, using linear regression and effect size. We further compared metric differences within diagnosis, using pairwise correlation, paired samples t‐test, and Pitman’s test of variance.ResultDemographic information is reported in Table 1. fBSI showed good Pearson’s correlation (r) with both gBSI (CN 0.7, p < 0.001; MCI 0.8, p < 0.001; AD 0.9, p < 0.001), and indirect change (CN 0.6, p < 0.001; MCI 0.6, < 0.001; AD 0.7, < 0.001). The composite BSI further showed good correlation with indirect change (CN 0.8, p < 0.001; MCI 0.8, p < 0.001; AD 0.8, 0.004). Mean values by diagnosis are shown in figure 1, along with paired samples t and variance tests. Pairwise comparisons reported in table 2, highlight good diagnostic group separation in all BSI metrics, with overall strong effect sizes for fBSI, composite BSI, and gBSI respectively.ConclusionCalculating atrophy using T2‐weighted imaging is possible using fBSI. This can be used in a composite atrophy measure using fBSI and gBSI. Both fBSI and composite BSI perform well with group separation, and with good correlations with classical atrophy metrics. Future work will explore the influence of White Matter Hyperintensities on BSI.

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