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. Author manuscript; available in PMC: 2018 Jun 4.
Published in final edited form as: Stroke. 2017 Aug 30;48(10):2799–2804. doi: 10.1161/STROKEAHA.117.018101

Table 2.

Relationship between extent of fibrinogen immunolabelling and risk (Odds Ratio, OR) of clinical dementia.

OR 95% CI (OR) p-value
MRI-defined WMH
MRI normal 0.74 (0.58; 0.94) 0.013
MRI NAWM 0.96 (0.56; 1.65) 0.887
MRI WMH 1.27 (0.92; 1.75) 0.139
Histopathology-defined white matter lesions
Histology non-lesion 0.83 (0.70; 0.98) 0.032
Histological lesion 2.26 (1.25; 4.08) 0.007
Combined MRI and histopathology
MRI normal, histology non-lesion 0.72 (0.56; 0.93) 0.010
MRI NAWM, histology non-lesion 0.77 (0.42; 1.40) 0.391
MRI WMH, histology non-lesion 1.00 (0.72; 1.38) 0.988
MRI WMH, histological lesion 1.82 (0.81; 4.09) 0.146

To test BBB dysfunction as a risk factor for dementia we conducted weighted logistic regression analysis, with clinical dementia status (dementia, without dementia) as dependent variable and fibrinogen area fraction as independent variable. P<0.05 considered significant. Abbreviations: WMH: white matter hyperintensity. NAWM: normal appearing white matter.