Association of red blood cells, D-dimer, and 13-(S)-HODE with cancer-related ischemic stroke: a case-control study

Lingyun Xie1, Kun Hao2, Jian Shen1

  • 1Department of Cardiology, The First Affiliated Hospital of Chongqing Medical University No. 1 Youyi Road, Yuzhong District, Chongqing 400016, China.

PubMed

Insights

Cancer-related ischemic stroke (CRIS) is associated with decreased red blood cells (RBCs), elevated D-dimer, and reduced 13-(S)-hydroxyoctadecadienoic acid [13-(S)-HODE]. A combined model of these markers shows potential for distinguishing CRIS from non-cancer ischemic stroke.

Area of Science:

  • Neurology
  • Oncology
  • Biochemistry

Background:

  • Cancer-related ischemic stroke (CRIS) presents unique clinical challenges.
  • Identifying reliable biomarkers for CRIS is crucial for early diagnosis and management.
  • Previous research has not fully elucidated the specific laboratory indicators associated with CRIS.

Purpose of the Study:

  • To investigate the clinical characteristics of CRIS.
  • To identify potential laboratory indicators for distinguishing CRIS from non-cancer ischemic stroke (NC-IS).
  • To evaluate the diagnostic performance of identified indicators and a combined model.

Main Methods:

  • Retrospective enrollment of acute ischemic stroke (AIS) patients into CRIS (n=41) and NC-IS (n=213) groups.
  • Propensity score matching (1:1) to balance baseline characteristics.
  • Measurement of serum 13-(S)-hydroxyoctadecadienoic acid [13-(S)-HODE] and nine routine laboratory indicators.
  • Univariate and multivariate logistic regression, ROC curve analysis, and comparison with cancer patients without stroke (CNSP) and healthy controls (NC).

Main Results:

  • Decreased red blood cells (RBCs), elevated D-dimer, and decreased 13-(S)-HODE were identified as independent risk factors for CRIS.
  • The combined model incorporating these three indicators achieved an AUC of 0.819 for distinguishing CRIS.
  • CRIS patients exhibited significantly higher D-dimer compared to CNSP and NC groups, and lower RBC and creatinine compared to NCs.

Conclusions:

  • Decreased RBCs, elevated D-dimer, and decreased 13-(S)-HODE are significantly associated with CRIS.
  • A combined model using these biomarkers demonstrates potential utility in differentiating CRIS from NC-IS.
  • Further research may validate these findings for clinical application in stroke diagnosis.