4.7 Article

Biomarkers of microvascular endothelial dysfunction predict incident dementia: a population-based prospective study

期刊

JOURNAL OF INTERNAL MEDICINE
卷 282, 期 1, 页码 94-101

出版社

WILEY
DOI: 10.1111/joim.12621

关键词

adrenomedullin; atrial natriuretic peptide; biomarkers; dementia; endothelial dysfunction; endothelin

资金

  1. Swedish Medical Research Council
  2. Swedish Heart and Lung Foundation
  3. Medical Faculty of Lund University
  4. Malmo University Hospital
  5. Albert Pahlsson Research Foundation
  6. Crafoord Foundation
  7. Ernhold Lundstroms Research Foundation
  8. Region Skane
  9. Hulda and Conrad Mossfelt Foundation
  10. King Gustaf V and Queen Victoria Foundation
  11. Wallenberg Foundation
  12. Lennart Hanssons Memorial Fund
  13. Skane University Hospital (SUS) Foundations and Donations
  14. European Research Council
  15. Swedish Brain Foundation
  16. Swedish Alzheimer foundation
  17. Marianne och Marcus Wallenberg foundation

向作者/读者索取更多资源

Background. Cerebral endothelial dysfunction occurs in a spectrum of neurodegenerative diseases. Whether biomarkers of microvascular endothelial dysfunction can predict dementia is largely unknown. We explored the longitudinal association of midregional pro-atrial natriuretic peptide (MR-proANP), C-terminal endothelin-1 (CT-proET-1) and midregional proadrenomedullin (MR-proADM) with dementia and subtypes amongst community-dwelling older adults. Methods. A population-based cohort of 5347 individuals (men, 70%; age, 69 +/- 6 years) without prevalent dementia provided plasma for determination of MR-proANP, CT-proET-1 and MR-proADM. Three-hundred-and-seventy-three patients (7%) were diagnosed with dementia (120 Alzheimer's disease, 83 vascular, 102 mixed, and 68 other aetiology) over a period of 4.6 +/- 1.3 years. Relations between baseline biomarker plasma concentrations and incident dementia were assessed using multivariable Cox regression analysis. Results. Higher levels of MR-proANP were significantly associated with increased risk of all-cause and vascular dementia (hazard ratio [HR] per 1 SD: 1.20, 95% confidence interval [CI], 1.07-1.36; P = 0.002, and 1.52; 1.21-1.89; P < 0.001, respectively). Risk of all-cause dementia increased across the quartiles of MR-proANP (p for linear trend = 0.004; Q4, 145-1681 pmol L-1 vs. Q1, 22-77 pmol L-1 : HR: 1.83; 95% CI: 1.23-2.71) and was most pronounced for vascular type (p for linear trend = 0.005: HR: 2.71; 95% CI: 1.14-6.46). Moreover, the two highest quartiles of CT-proET-1 predicted vascular dementia with a cut-off value at 68 pmol L-1 (Q3-Q4, 68-432 pmol L-1 vs. Q1-Q2,4-68 pmol L-1; HR: 1.94; 95% CI: 1.12-3.36). Elevated levels of MR-proADM indicated no increased risk of developing dementia after adjustment for traditional risk factors. Conclusions. Elevated plasma concentration of MR-proANP is an independent predictor of all-cause and vascular dementia. Pronounced increase in CT-proET-1 indicates higher risk of vascular dementia.

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