scholarly journals White matter hyperintensities and normal-appearing white matter integrity in the aging brain

2015 ◽  
Vol 36 (2) ◽  
pp. 909-918 ◽  
Author(s):  
Susana Muñoz Maniega ◽  
Maria C. Valdés Hernández ◽  
Jonathan D. Clayden ◽  
Natalie A. Royle ◽  
Catherine Murray ◽  
...  
2010 ◽  
Vol 53 (5) ◽  
pp. 373-381 ◽  
Author(s):  
Liya Wang ◽  
Felicia C. Goldstein ◽  
Allan I. Levey ◽  
James J. Lah ◽  
Carolyn C. Meltzer ◽  
...  

2006 ◽  
Vol 14 (7S_Part_12) ◽  
pp. P655-P655
Author(s):  
Burcu Zeydan ◽  
Christopher G. Schwarz ◽  
Val J. Lowe ◽  
Robert I. Reid ◽  
Scott A. Przybelski ◽  
...  

2020 ◽  
Vol 16 (S4) ◽  
Author(s):  
Alexis Moscoso ◽  
A.J. Whitman ◽  
Suzanne L. Baker ◽  
Renaud La Joie ◽  
Tharick A. Pascoal ◽  
...  

2018 ◽  
Author(s):  
Susana Muñoz Maniega ◽  
Rozanna Meijboom ◽  
Francesca M. Chappell ◽  
Maria C. Valdés Hernández ◽  
John M. Starr ◽  
...  

AbstractBrain white matter hyperintensities (WMH), common in older adults, may contribute to cortical disconnection and cognitive dysfunction. The presence of WMH within white matter (WM) tracts indicates underlying microstructural WM changes that may also affect the normal-appearing WM (NAWM) of a tract. We performed an exploratory study using diffusion magnetic resonance imaging of 52 healthy participants from the Lothian Birth Cohort 1936 (age 72.2 ± 0.7 years) selected to include a range of WMH burden, to quantify microstructural changes of tracts intersecting WMH. We reconstructed tracts using automated tractography and identified intersections with WMH. Tissue volumes and water diffusion tensor parameters (mean diffusivity (MD) and fractional anisotropy (FA)) were established for tract-WMH and tract-NAWM. MD and FA were also measured for tract-NAWM at 2 mm incremental distances from the tract-WMH edge, and from the edge of nearby, non-intersecting, WMH. We observed microstructural changes in tract-WMH suggestive of tissue damage. Tract-NAWM also showed a spatial gradient of FA and MD abnormalities, which diminished with distance from the tract-WMH. Nearby WMH lesions, not directly crossed by the tract, also affected tract microstructure with a similar pattern. Additionally, both FA and MD changes in tract-NAWM were predicted by FA and MD changes respectively in tract-WMH. FA was also predicted by tract-WMH overlap volume, whereas MD was better predicted by whole-brain WMH load. These results suggest that tract-NAWM microstructure is affected by the pathological process underlying WMH, when WMH are either within or near to the tract. The changes in NAWM tract tissue may indicate future lesion progression and may play an important role in cognitive ageing.


2016 ◽  
Vol 37 (2) ◽  
pp. 644-656 ◽  
Author(s):  
Susana Muñoz Maniega ◽  
Francesca M Chappell ◽  
Maria C Valdés Hernández ◽  
Paul A Armitage ◽  
Stephen D Makin ◽  
...  

White matter hyperintensities accumulate with age and occur in patients with stroke, but their pathogenesis is poorly understood. We measured multiple magnetic resonance imaging biomarkers of tissue integrity in normal-appearing white matter and white matter hyperintensities in patients with mild stroke, to improve understanding of white matter hyperintensities origins. We classified white matter into white matter hyperintensities and normal-appearing white matter and measured fractional anisotropy, mean diffusivity, water content (T1-relaxation time) and blood–brain barrier leakage (signal enhancement slope from dynamic contrast-enhanced magnetic resonance imaging). We studied the effects of age, white matter hyperintensities burden (Fazekas score) and vascular risk factors on each biomarker, in normal-appearing white matter and white matter hyperintensities, and performed receiver-operator characteristic curve analysis. Amongst 204 patients (34.3–90.9 years), all biomarkers differed between normal-appearing white matter and white matter hyperintensities ( P < 0.001). In normal-appearing white matter and white matter hyperintensities, mean diffusivity and T1 increased with age ( P < 0.001), all biomarkers varied with white matter hyperintensities burden ( P < 0.001; P = 0.02 signal enhancement slope), but only signal enhancement slope increased with hypertension ( P = 0.028). Fractional anisotropy showed complex age-white matter hyperintensities-tissue interactions; enhancement slope showed white matter hyperintensities-tissue interactions. Mean diffusivity distinguished white matter hyperintensities from normal-appearing white matter best at all ages. Blood–brain barrier leakage increases with hypertension and white matter hyperintensities burden at all ages in normal-appearing white matter and white matter hyperintensities, whereas water mobility and content increase as tissue damage accrues, suggesting that blood–brain barrier leakage mediates small vessel disease-related brain damage.


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