4.6 Article

Pulmonary Tuberculosis-Related Ischemic Stroke: A Retrospective Case Control Study

Journal

JOURNAL OF INFLAMMATION RESEARCH
Volume 15, Issue -, Pages 4239-4249

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/JIR.S368183

Keywords

pulmonary tuberculosis; ischemic stroke; tuberculosis-related ischemic stroke; independent risk factor; pathogenesis

Categories

Funding

  1. Foundation of National Key R&D Program of China [2018YFC 1311300]
  2. Guangxi Medical and Health and Appropriate Technology Development and Promotion Application Project [S2021101, S2020013]

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This study explores the clinical features and underlying pathogenesis of pulmonary tuberculosis-related ischemic stroke (TBRIS) in patients with active pulmonary tuberculosis. The study finds that most TBRIS patients experienced ischemic stroke events within 3 months after tuberculosis diagnosis. The study also identifies several independent risk factors for TBRIS and establishes an index that helps clinicians identify high-risk TBRIS patients among pulmonary tuberculosis patients.
Objective: There have been only a few studies of ischemic stroke in patients with pulmonary tuberculosis (pTB). This study aimed to explore the clinical features and the underlying pathogenesis of pulmonary tuberculosis-related ischemic stroke (TBRIS). Methods: Active pulmonary tuberculosis patients with acute ischemic stroke (without conventional vascular risk factors) were recruited as the TBRIS group. Patients who solely had active pulmonary tuberculosis were recruited as the control group (pTB group). Clinical data were collected, and multiple logistic regression analysis was applied to analyze the independent risk factors for TBRIS. Results: A total of 179 TBRIS patients and 179 pTB patients were enrolled. Most (56.42%) of the TBRIS patients experienced the ischemic stroke events within 3 months after the diagnosis of tuberculosis. The multiple logistic regression analysis revealed that an increased mean platelet volume; elevated plasma D-dimer, C-reactive protein, and serum ferritin levels; and an increased monocyte percentage were independent risk factors for TBRIS. The AUC of the identification model was 0.778, with a sensitivity of 70.30% and a specificity of 78.90%. Conclusion: The findings in the present study suggested that most of the TBRIS patients experienced ischemic stroke within 3 months after the diagnosis of tuberculosis. And the more intensive immune response to the tuberculosis infection in the TBRIS group contributed to the initiation of platelet activation and to the development of a hypercoagulable state, which were attributed to the pathogenesis of TBRIS. Index of TBRIS equaling to 0.3234 facilitates clinicians to identify the pTB patients who were at higher risk for TBRIS, and allow physicians to take further effective measures to prevent ischemic stroke in patients with pTB. However, our findings will need to be confirmed by further studies.

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