کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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6034892 | 1188759 | 2011 | 13 صفحه PDF | دانلود رایگان |

We examined how wide ranges in levels of risk factors for cerebrovascular disease are associated with thickness of the human cerebral cortex in 115 individuals ages 43-83 with no cerebrovascular or neurologic history. Cerebrovascular risk factors included blood pressure, cholesterol, body mass index, creatinine, and diabetes-related factors. Variables were submitted into a principal components analysis that confirmed four orthogonal factors (blood pressure, cholesterol, cholesterol/metabolic and glucose). T1-weighted MRI was used to create models of the cortex for calculation of regional cortical thickness. Increasing blood pressure factor scores were associated with numerous regions of reduced thickness. Increasing glucose scores were modestly associated with areas of regionally decreased thickness. Increasing cholesterol scores, in contrast, were associated with thicker cortex across the whole brain. All findings were primarily independent of age. These results provide evidence that normal and moderately abnormal levels of parameters used to assess cerebrovascular health may impact brain structure, even in the absence of cerebrovascular disease. Our data have important implications for the clinical management of vascular health, as well as for what is currently conceptualized as “normal aging” as they suggest that subclinical levels of risk may impact cortical gray matter before a disease process is evident.
Research Highlights⺠Higher blood pressure scores are associated with areas of lower cortical thickness. ⺠Higher cholesterol scores are associated with higher thickness across the entire cortex. ⺠Higher glucose scores are associated with modest areas of lower thickness. ⺠Normal and moderately elevated levels of cerebrovascular risk may impact brain structure. ⺠Cerebrovascular risk factors may partly explain age-related changes in brain structure.
Journal: NeuroImage - Volume 54, Issue 4, 14 February 2011, Pages 2659-2671