4.3 Article

C-reactive protein, but not homocysteine, is related to cognitive dysfunction in older adults with cardiovascular disease

Journal

JOURNAL OF CLINICAL NEUROSCIENCE
Volume 13, Issue 5, Pages 540-546

Publisher

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.jocn.2005.08.010

Keywords

homocysteine; C-reactive protein; cognition

Funding

  1. NHLBI NIH HHS [F32 HL074568, F32-HL74568] Funding Source: Medline
  2. NIA NIH HHS [F32 AG022773-01, P30 AG013846-06, P30 AG013846, R01-AG017975, F32 AG022773, R01 AG017975, F32-AG022773] Funding Source: Medline
  3. NIMH NIH HHS [K23 MH065857, K23-MH065857] Funding Source: Medline
  4. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [F32HL074568] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE OF MENTAL HEALTH [K23MH065857] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE ON AGING [P30AG013846, R01AG017975, F32AG022773] Funding Source: NIH RePORTER

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Cardiovascular disease (CVD) is a risk factor for cognitive impairment and dementia. Recent studies implicate homocysteine (HCY) and C-reactive protein (CRP) in this increased risk, as both are associated with cognitive dysfunction in demented and non-demented patients. However, it remains unclear whether they confer added risk in older adults with CVD. A total of 126 older CVD patients underwent blood and neuropsychological evaluation as part of a prospective examination of the neurocognitive consequences of CVD. A subset of these participants (n = 37) also underwent neuroimaging to quantify the degree of white matter disease. After adjusting for demographic and medical factors, no significant relationship emerged between HCY and cognitive performance. In contrast, CRP showed significant independent relationships to test performance, including global cognitive performance, attention/psychomotor function, executive function, memory, and visuospatial abilities. Neither HCY nor CRP was related to extent of white matter disease or whole brain volume on magnetic resonance imaging. Further study is needed to identify mechanisms by which inflammatory processes impact on cognitive function and to determine whether reducing circulating levels of inflammatory markers results in improved cognition. (C) 2006 Elsevier Ltd. All rights reserved.

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