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. 2015 Feb 11;35(6):1005–1014. doi: 10.1038/jcbfm.2015.12

Table 1. Diffusion tensor and magnetization transfer MRI biomarker values in long-term hypoperfused (N=20) and sham (N=11) mice.

Region of interest Biomarker Sham Hypoperfused Statistics % Change
Corpus callosum FA 0.45±0.01 0.41±0.01 F(1,25)=13.9, P=0.001 −8.33
  MTR 29.7±0.68 29.2±0.38 F(1,25)=0.45, P=0.508 −1.65
  MD 6.58±0.14 6.91±0.12 F(1,25)=3.00, P=0.096 +4.88
           
Internal capsule FA 0.50±0.01 0.37±0.02 F(1,25)=21.9, P=0.000 −33.0
  MTR 30.2±1.00 30.0±0.42 F(1,25)=0.36, P=0.792 −0.82
  MD 7.15±0.29 7.23±0.25 F(1,25)=0.00, P=0.956 +1.23
           
Fimbria FA 0.56±0.02 0.42±0.03 F(1,25)=10.5, P=0.004 −35.5
  MTR 29.1±0.64 24.7±1.40 F(1,25)=14.4, P=0.001 −17.9
  MD 9.14±0.22 10.6±0.02 F(1,25)=2.39, P=0.136 +4.00
           
Subcortex FA 0.26±0.01 0.28±0.01 F(1,25)=8.34, P=0.008 +7.14
  MTR 27.2±0.61 27.9±0.39 F(1,25)=1.04, P=0.317 +2.26
  MD 7.23±0.12 7.30±0.09 F(1,25)=0.03, P=0.866 −0.95

Abbreviations: FA, fractional anisotropy; MD, mean diffusivity; MRI, magnetic resonance imaging; MTR, magnetization transfer ratio.

Cerebral hypoperfusion (6 months) results in significant reductions in FA in the corpus callosum, internal capsule, and fimbria, along with a significant atypical increase in the subcortex, suggesting underlying axonal disruption. MTR (%) is significantly reduced in the fimbria only, whereas MD ( × 10−4 mm2/s) is not significantly altered in any of the regions studied.