Probing Evidence of Cerebral White Matter Microstructural Disruptions in Ischemic Heart Disease Before and Following Cardiac Rehabilitation: A Diffusion Tensor MR Imaging Study

Author:

Poirier Stefan E.12ORCID,Suskin Neville G.3,Khaw Alexander V.4,Thiessen Jonathan D.125,Shoemaker Joel K.6,Anazodo Udunna C.12478ORCID

Affiliation:

1. Lawson Imaging Lawson Health Research Institute London Ontario Canada

2. Department of Medical Biophysics, Schulich School of Medicine and Dentistry Western University London Ontario Canada

3. Division of Cardiology, Schulich School of Medicine and Dentistry Western University London Ontario Canada

4. Department of Clinical Neurological Sciences, Schulich School of Medicine and Dentistry Western University London Ontario Canada

5. Department of Medical Imaging, Schulich School of Medicine and Dentistry Western University London Ontario Canada

6. School of Kinesiology Western University London Ontario Canada

7. Research Centre for Studies in Aging McGill University Montréal Québec Canada

8. Department of Neurology and Neurosurgery McGill University Montréal Québec Canada

Abstract

BackgroundIschemic heart disease (IHD) is linked to brain white matter (WM) breakdown but how age or disease effects WM integrity, and whether it is reversible using cardiac rehabilitation (CR), remains unclear.PurposeTo assess the effects of brain aging, cardiovascular disease, and CR on WM microstructure in brains of IHD patients following a cardiac event.Study TypeRetrospective.PopulationThirty‐five IHD patients (9 females; mean age = 59 ± 8 years), 21 age‐matched healthy controls (10 females; mean age = 59 ± 8 years), and 25 younger controls (14 females; mean age = 26 ± 4 years).Field Strength/Sequence3 T diffusion‐weighted imaging with single‐shot echo planar imaging acquired at 3 months and 9 months post‐cardiac event.AssessmentTract‐based spatial statistics (TBSS) and tractometry were used to compare fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (AD), and radial diffusivity (RD) in cerebral WM between: 1) older and younger controls to distinguish age‐related from disease‐related WM changes; 2) IHD patients at baseline (pre‐CR) and age‐matched controls to investigate if cardiovascular disease exacerbates age‐related WM changes; and 3) IHD patients pre‐CR and post‐CR to investigate the neuroplastic effect of CR on WM microstructure.Statistical TestsTwo‐sample unpaired t‐test (age: older vs. younger controls; IHD: IHD pre‐CR vs. age‐matched controls). One‐sample paired t‐test (CR: IHD pre‐ vs. post‐CR). Statistical threshold: P < 0.05 (FWE‐corrected).ResultsTBSS and tractometry revealed widespread WM changes in older controls compared to younger controls while WM clusters of decreased FA in the fornix and increased MD in body of corpus callosum were observed in IHD patients pre‐CR compared to age‐matched controls. Robust WM improvements (increased FA, increased AD) were observed in IHD patients post‐CR.Data ConclusionIn IHD, both brain aging and cardiovascular disease may contribute to WM disruptions. IHD‐related WM disruptions may be favorably modified by CR.Level of Evidence3Technical EfficacyStage 2

Funder

Canadian Institutes of Health Research

Heart and Stroke Foundation of Canada

Publisher

Wiley

Subject

Radiology, Nuclear Medicine and imaging

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