| Literature DB >> 28756941 |
Walter Swardfager1, Di Yu2, Gustavo Scola3, Hugo Cogo-Moreira4, Parco Chan5, Yi Zou6, Nathan Herrmann7, Krista L Lanctôt8, Joel Ramirez9, Fuqiang Gao9, Mario Masellis10, Richard H Swartz10, Demetrios J Sahlas11, Pak Cheung Chan12, Carmen Ojeda-Lopez13, Angela Milan-Tomas13, Jacqueline A Pettersen14, Ana C Andreazza15, Sandra E Black16.
Abstract
Subcortical white matter hyperintensities (WMH), presumed to indicate small vessel ischemic vascular disease, are found commonly in elderly individuals with and without Alzheimer's disease (AD). Oxidative stress may instigate or accelerate the development of vascular disease, and oxidative stress markers are elevated in AD. Here, we assess independent relationships between three serum lipid peroxidation markers (lipid hydroperoxides [LPH], 8-isoprostane, and 4-hydroxynonenal) and the presence of extensive subcortical WMH and/or AD. Patients were recruited from memory and stroke prevention clinics into four groups: minimal WMH, extensive WMH, AD with minimal WMH, and AD with extensive WMH. Extensive WMH, but not AD, was associated with higher serum concentrations of 8-isoprostane and LPH. Peripheral LPH concentrations mediated the effect of hypertension on deep, but not periventricular, WMH volumes. 4-hydroxynonenal was associated with hyperlipidemia and cerebral microbleeds, but not with extensive WMH or AD. We conclude that lipid peroxidation mediates hypertensive injury to the deep subcortical white matter and that peripheral blood lipid peroxidation markers indicate subcortical small vessel disease regardless of an AD diagnosis.Entities:
Keywords: Cerebrovascular disease; Oxidative stress; Small vessel disease; White matter hyperintensities
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Year: 2017 PMID: 28756941 DOI: 10.1016/j.neurobiolaging.2017.06.029
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673