4.4 Article

Increased pulse wave velocity is related to impaired working memory and executive function in older adults with metabolic syndrome

期刊

GEROSCIENCE
卷 44, 期 6, 页码 2831-2844

出版社

SPRINGER
DOI: 10.1007/s11357-022-00640-1

关键词

Metabolic syndrome; Vascular cognitive impairment; Arterial stiffness; Brain aging; Neuropsychological tests

资金

  1. National Institutes of Health [UL1 TR002014]
  2. American Heart Association
  3. National Institute on Aging [RF1AG072295, R01AG055395, R01AG068295, R01AG070915, K01AG073614]
  4. National Institute of Neurological Disorders and Stroke [R01NS100782]
  5. National Cancer Institute [R01CA255840]
  6. Cellular and Molecular GeroScience CoBRE [P20GM125528]
  7. National Center for Advancing Translational Sciences

向作者/读者索取更多资源

Age-related vascular alterations contribute to the development of vascular cognitive impairment (VCI). Metabolic syndrome (MetS) exacerbates cognitive impairment, and arterial stiffening moderates the association between cognitive dysfunction and MetS in older adults.
Age-related vascular alterations promote the pathogenesis of vascular cognitive impairment (VCI). Cardiovascular risk factors that accelerate vascular aging exacerbate VCI. Metabolic syndrome (MetS) constitutes a cluster of critical cardiovascular risk factors (abdominal obesity, hypertension, elevated triglycerides, elevated fasting glucose, reduced HDL cholesterol), which affects nearly 37% of the adult US population. The present study was designed to test the hypotheses that MetS exacerbates cognitive impairment and that arterial stiffening moderates the association between cognitive dysfunction and MetS in older adults. MetS was defined by the NCEP ATP III guidelines. Cognitive function (digit span and trail-making tests) and brachial-ankle pulse wave velocity (baPWV; a non-invasive clinical measurement of arterial stiffness) were assessed in older adults with MetS and age- and sex-matched controls. Multiple linear regression models were applied to test for the main effects of MetS, baPWV, and their interaction on cognitive performance. Fifty-three participants with MetS (age: 68 +/- 8 years) and 39 age-matched individuals without MetS (age: 66 +/- 9 years) were enrolled into the study. In adjusted multivariable regression analyses of the digit span backward length score, both MetS (ss = 1.97, p = 0.048) and MetS by baPWV interaction (ss = - 0.001, p = 0.026) were significant predictors. In participants with MetS, higher baPWV was associated with poorer performance on digit span backward length score, a test of working memory (R = - 0.44, p = 0.0012), but there was no association in those without MetS (R = 0.035, p = 0.83). MetS was negatively associated with performance on the digit span backward length score, baPWV was negatively associated with multiple neuropsychological outcomes, and baPWV moderated the association between digit span backward length score and MetS, as individuals with both MetS and higher baPWV had the most impaired cognitive function. Our findings add to the growing body of evidence that individuals with MetS and higher baPWV may be prone to VCI.

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