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Apolipoprotein A-I and Paraoxonase-1 Are Potential Blood Biomarkers for Ischemic Stroke Diagnosis.

Publication ,  Journal Article
Walsh, KB; Hart, K; Roll, S; Sperling, M; Unruh, D; Davidson, WS; Lindsell, CJ; Adeoye, O
Published in: J Stroke Cerebrovasc Dis
June 2016

BACKGROUND: Blood biomarkers for ischemic and hemorrhagic stroke diagnosis remain elusive. Recent investigations suggested that apolipoprotein (Apo), matrix metalloproteinase (MMP), and paraoxonase-1 may be associated with stroke. We hypothesized that Apo A-I, Apo C-I, Apo C-III, MMP-3, MMP-9, and paraoxonase-1 are differentially expressed in ischemic stroke, hemorrhagic stroke, and controls. METHODS: In a single-center prospective observational study, consecutive stroke cases were enrolled if blood samples were obtainable within 12 hours of symptom onset. Age- (±5 years), race-, and sex-matched controls were recruited. Multiplex assays were used to measure protein levels. The Wilcoxon signed-rank test and the Mann-Whitney U-test were used to compare biomarker values between ischemic stroke patients and controls, hemorrhagic stroke patients and controls, and ischemic and hemorrhagic stroke patients. The 95% confidence intervals (CIs) for the difference of 2 medians were calculated. RESULTS: Fourteen ischemic stroke case-control pairs and 23 intracerebral hemorrhage (ICH) case-control pairs were enrolled. Median Apo A-I levels were lower in ischemic stroke cases versus controls (140 mg/dL versus 175 mg/dL, difference of 35 mg/dL, 95% CI -54 to -16) and in ischemic stroke versus ICH cases (140 mg/dL versus 180 mg/dL, difference of 40 mg/dL, 95% CI -57 to -23). Median paraoxonase-1 was lower in ischemic stroke cases than in both ICH cases and matched controls. Median Apo C-I was slightly lower in ischemic stroke cases than in ICH cases. There were no differences between groups for MMP-3, MMP-9, and Apo C-III. CONCLUSION: Apo A-I and paraoxonase-1 levels may be clinically useful for ischemic stroke diagnosis and for differentiating between ischemic and hemorrhagic strokes.

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Published In

J Stroke Cerebrovasc Dis

DOI

EISSN

1532-8511

Publication Date

June 2016

Volume

25

Issue

6

Start / End Page

1360 / 1365

Location

United States

Related Subject Headings

  • Stroke
  • Prospective Studies
  • Predictive Value of Tests
  • Ohio
  • Neurology & Neurosurgery
  • Middle Aged
  • Male
  • Humans
  • Female
  • Diagnosis, Differential
 

Citation

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MLA
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Walsh, K. B., Hart, K., Roll, S., Sperling, M., Unruh, D., Davidson, W. S., … Adeoye, O. (2016). Apolipoprotein A-I and Paraoxonase-1 Are Potential Blood Biomarkers for Ischemic Stroke Diagnosis. J Stroke Cerebrovasc Dis, 25(6), 1360–1365. https://doi.org/10.1016/j.jstrokecerebrovasdis.2016.02.027
Walsh, Kyle B., Kimberly Hart, Susan Roll, Matthew Sperling, Dusten Unruh, W Sean Davidson, Christopher J. Lindsell, and Opeolu Adeoye. “Apolipoprotein A-I and Paraoxonase-1 Are Potential Blood Biomarkers for Ischemic Stroke Diagnosis.J Stroke Cerebrovasc Dis 25, no. 6 (June 2016): 1360–65. https://doi.org/10.1016/j.jstrokecerebrovasdis.2016.02.027.
Walsh KB, Hart K, Roll S, Sperling M, Unruh D, Davidson WS, et al. Apolipoprotein A-I and Paraoxonase-1 Are Potential Blood Biomarkers for Ischemic Stroke Diagnosis. J Stroke Cerebrovasc Dis. 2016 Jun;25(6):1360–5.
Walsh, Kyle B., et al. “Apolipoprotein A-I and Paraoxonase-1 Are Potential Blood Biomarkers for Ischemic Stroke Diagnosis.J Stroke Cerebrovasc Dis, vol. 25, no. 6, June 2016, pp. 1360–65. Pubmed, doi:10.1016/j.jstrokecerebrovasdis.2016.02.027.
Walsh KB, Hart K, Roll S, Sperling M, Unruh D, Davidson WS, Lindsell CJ, Adeoye O. Apolipoprotein A-I and Paraoxonase-1 Are Potential Blood Biomarkers for Ischemic Stroke Diagnosis. J Stroke Cerebrovasc Dis. 2016 Jun;25(6):1360–1365.
Journal cover image

Published In

J Stroke Cerebrovasc Dis

DOI

EISSN

1532-8511

Publication Date

June 2016

Volume

25

Issue

6

Start / End Page

1360 / 1365

Location

United States

Related Subject Headings

  • Stroke
  • Prospective Studies
  • Predictive Value of Tests
  • Ohio
  • Neurology & Neurosurgery
  • Middle Aged
  • Male
  • Humans
  • Female
  • Diagnosis, Differential