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February 27, 2018; 90 (9) Article

The value of plasma fibrillin-1 level in patients with spontaneous cerebral artery dissection

Zhu Zhu, Weijun Tang, Liang Ge, Xiang Han, Qiang Dong
First published January 31, 2018, DOI: https://doi.org/10.1212/WNL.0000000000005027
Zhu Zhu
From the Department of Neurology (Z.Z., X.H., Q.D.), Huashan Hospital, State Key Laboratory of Medical Neurobiology, Fudan University; and Department of Radiology (W.T., L.G.), Huashan Hospital, Fudan University, Shanghai, China.
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Weijun Tang
From the Department of Neurology (Z.Z., X.H., Q.D.), Huashan Hospital, State Key Laboratory of Medical Neurobiology, Fudan University; and Department of Radiology (W.T., L.G.), Huashan Hospital, Fudan University, Shanghai, China.
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Liang Ge
From the Department of Neurology (Z.Z., X.H., Q.D.), Huashan Hospital, State Key Laboratory of Medical Neurobiology, Fudan University; and Department of Radiology (W.T., L.G.), Huashan Hospital, Fudan University, Shanghai, China.
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Xiang Han
From the Department of Neurology (Z.Z., X.H., Q.D.), Huashan Hospital, State Key Laboratory of Medical Neurobiology, Fudan University; and Department of Radiology (W.T., L.G.), Huashan Hospital, Fudan University, Shanghai, China.
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Qiang Dong
From the Department of Neurology (Z.Z., X.H., Q.D.), Huashan Hospital, State Key Laboratory of Medical Neurobiology, Fudan University; and Department of Radiology (W.T., L.G.), Huashan Hospital, Fudan University, Shanghai, China.
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Citation
The value of plasma fibrillin-1 level in patients with spontaneous cerebral artery dissection
Zhu Zhu, Weijun Tang, Liang Ge, Xiang Han, Qiang Dong
Neurology Feb 2018, 90 (9) e732-e737; DOI: 10.1212/WNL.0000000000005027

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Abstract

Objective To explore the value of plasma fibrillin-1 levels in patients with spontaneous cerebral artery dissection (sCeAD).

Methods A single-center prospective cohort of 99 consecutive patients with sCeAD between February 2013 and December 2015 were age and sex matched with 115 patients with non-sCeAD ischemic stroke and 20 healthy participants undergoing routine physical examination. The plasma fibrillin-1 level was measured with ELISA and compared among the 3 groups. The associations of fibrillin-1 with site, acuity, and severity of dissection, as well as clinical and radiographic prognosis of patients, were analyzed.

Results One hundred nine plasma samples from 99 patients with sCeAD, 115 from disease control patients, and 20 from healthy participants were collected. The plasma fibrillin-1 level of the dissection group (mean 85.56 ng/mL [95% confidence interval 81.53–89.59]) was higher than that of non-sCeAD ischemic stroke group (77.13 ng/mL [73.64–80.63], p = 0.015) or healthy controls (73.04 ng/mL [65.94–80.13], p = 0.029). Such differences were most prominent in the acute stage (97.64 ng/mL [91.64–103.64], 74.39 ng/mL [68.95–79.84], and 73.04 ng/mL [65.95–80.13], respectively). A cutoff value of 88.455 ng/mL was determined to differentiate acute dissection from nondissection stroke with a sensitivity of 0.778 and a specificity of 0.800. Higher fibrillin-1 level was detected in patients with more severe dissection radiographically (p < 0.001), while patients with lower fibrillin-1 concentration at baseline achieved better morphologic recovery on follow-up imaging tests (p = 0.003).

Conclusion Plasma fibrillin-1 is a promising biomarker for aiding the diagnosis of acute sCeAD and may have potential value in lesion severity grading and radiographic prognosis prediction.

Classification of evidence This study provides Class III evidence that patients with sCeAD have significantly higher levels of plasma fibrillin-1 than patients with ischemic stroke attributable to a cause other than sCeAD.

Glossary

CI=
confidence interval;
NIHSS=
NIH Stroke Scale;
sCeAD=
spontaneous cerebral artery dissection

Footnotes

  • Go to Neurology.org/N for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Class of Evidence: NPub.org/coe

  • Editorial, page 399

  • Received June 20, 2017.
  • Accepted in final form October 22, 2017.
  • © 2018 American Academy of Neurology
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