Von Willebrand Factor Antigen Levels Predict Poor Outcomes in Patients With Stroke and Cancer: Findings From the Multicenter, Prospective, Observational SCAN Study

Author:

Kawano Tomohiro1ORCID,Gon Yasufumi1ORCID,Sakaguchi Manabu12ORCID,Yamagami Hiroshi3ORCID,Abe Soichiro4,Hashimoto Hiroyuki5ORCID,Ohara Nobuyuki6ORCID,Takahashi Daisuke7ORCID,Abe Yuko8ORCID,Takahashi Tsutomu9ORCID,Okazaki Shuhei1ORCID,Todo Kenichi1ORCID,Mochizuki Hideki1ORCID,Sasaki Tsutomu110ORCID,

Affiliation:

1. Department of Neurology Osaka University Graduate School of Medicine Osaka Japan

2. Department of Neurology Osaka General Medical Center Osaka Japan

3. Department of Neurology National Hospital Organization Osaka National Hospital Osaka Japan

4. Department of Neurology National Cerebral and Cardiovascular Center Osaka Japan

5. Department of Neurology Osaka Rosai Hospital Osaka Japan

6. Department of Neurology Kobe City Medical Center General Hospital Kobe Hyogo Japan

7. Department of Neurology National Hospital Organization Osaka Minami Medical Center Osaka Japan

8. Department of Neurology Yodogawa Christian Hospital Osaka Japan

9. Department of Neurology Hoshigaoka Medical Center Osaka Japan

10. StemRIM Institute of Regeneration‐Inducing Medicine Osaka University Osaka Japan

Abstract

Background Patients with acute ischemic stroke and active cancer have more severe neurological symptoms, elevated risks of stroke recurrence, and death compared with the general population. We examined whether von Willebrand factor (vWF) antigen levels at stroke onset were associated with the poor outcomes of patients with stroke and cancer. Methods and Results Using data from 90 patients with acute ischemic stroke and active cancer who were registered in the SCAN (Ischemic Stroke in Patients With Cancer and Neoplasia) study, a prospective multicenter, observational study in Japan, we divided patients into 2 groups according to their median vWF antigen levels (high, n=46; or low, n=44). The high‐vWF group had a significantly higher initial National Institutes of Health Stroke Scale score (median, 7 [interquartile range, 3–11.25] versus 3 [interquartile range, 1–8.5]; P <0.05) and a significantly higher incidence of cryptogenic stroke (32 [70%] versus 16 [36%]; P <0.01) and venous thromboembolism (7 [15%] versus 0 [0%]; P <0.01), as well as multiple lesions (28 [62%] versus 12 [27%]; P <0.001), than the low‐vWF group. We observed no significant difference in the rate of stroke recurrence within 1 year between the groups. However, increased vWF levels were an independent predictor of death within 1 year of stroke onset, after adjusting for potential confounders (odds ratio, 6.77 [95% CI, 1.49–30.78]; P <0.05). Conclusions Elevated vWF antigen levels were associated with adverse outcomes in patients with cancer‐associated stroke and may represent a useful biomarker to guide future therapeutic interventions.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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