4.7 Article

Enlarged perivascular spaces and small diffusion-weighted lesions in intracerebral hemorrhage

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NEUROLOGY
卷 85, 期 23, 页码 2045-2052

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LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0000000000002169

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资金

  1. Sichuan University Academic Research Fellowship
  2. National Natural Science Foundation of China [81371283]
  3. National Key Technology R&D Program for the 12th Five-year Plan of Peoples Republic of China [2011BAI08B05]
  4. NIH/NINDS [U01 NS074425]

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Objective: To examine the association between enlarged perivascular spaces (EPVS) and the prevalence and extent of small acute diffusion-weighted imaging (DWI) lesions (SA-DWIL) in patients with spontaneous supratentorial intracerebral hemorrhage (ICH). Methods: We conducted a retrospective review of a consecutive cohort of 201 patients with spontaneous supratentorial ICH who had brain MRI with DWI within 1 month of ICH onset. We compared the clinical and imaging characteristics, including EPVS, of patients with and without SA-DWIL. We used univariate and multivariate logistic regression analyses to determine the variables associated with SA-DWIL. Results: Small acute DWI lesions were detected in 27.9% (n = 56) of patients. Intraventricular and subarachnoid extension of ICH (p <= 0.001), high centrum semiovale (CSO)-EPVS (p < 0.001), high basal ganglia-EPVS (p = 0.007), overall extent of white matter hyperintensity (p = 0.018), initial ICH volume (p = 0.001), and mean change in mean arterial blood pressure (delta MAP = MAP at admission - the lowest MAP before MRI scan) (p = 0.027) were associated with SA-DWIL on univariate analyses. On multivariate logistic regression analyses, larger ICH volume (odds ratio [OR] 1.03; 95% confidence interval [CI] 1.01-1.06; p = 0.006) and high CSO-EPVS (OR 12.56; 95% CI 4.40-35.85; p < 0.001) were independently associated with the presence of SA-DWIL. Conclusions: In our cohort, high EPVS, in particular CSO-EPVS, and larger hematoma volume emerged as independent predictors for SA-DWIL after ICH. Our findings might provide a new explanation for the pathophysiologic mechanisms predisposing to SA-DWIL after ICH.

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