Influence of fluid-attenuated inversion-recovery on stroke apparent diffusion coefficient measurements and its

Jian-Ming Ni1, Monique A Mogensen, Zeng-Ai Chen

  • 1Medical Imaging Department, Wuxi Second Hospital Affiliated Nanjing Medical University, 68 Zhong Shan Road, Wuxi, Jiangsu Province 214002, China.

Abstract

Insights

Fluid-attenuated inversion-recovery diffusion-weighted MRI (FLAIR DWI) offers more accurate apparent diffusion coefficient (ADC) measurements in chronic ischemic stroke by reducing cerebrospinal fluid effects. This technique may aid in determining lesion age.

Area of Science:

  • Neuroimaging
  • Radiology
  • Medical Physics

Background:

  • Diffusion-weighted MRI (DWI) is crucial for evaluating ischemic stroke.
  • Cerebrospinal fluid (CSF) partial volume effects can impact apparent diffusion coefficient (ADC) measurements.
  • Fluid-attenuated inversion-recovery (FLAIR) sequences may mitigate CSF partial volume effects in DWI.

Purpose of the Study:

  • To quantitatively compare FLAIR DWI and conventional DWI in ischemic stroke.
  • To assess the impact of FLAIR on ADC measurements across different stroke ages.
  • To evaluate the potential advantages of FLAIR DWI in stroke assessment.

Main Methods:

  • Analysis of 139 DWI studies in ischemic stroke patients (hyperacute to chronic).
  • Measurement of ADC values in lesions and contralateral normal tissue.
  • Comparison of ADC values between FLAIR DWI and conventional DWI sequences.

Main Results:

  • No significant difference in ADC measurements for lesions <14 days old (p>0.05).
  • Significantly decreased ADC values on FLAIR DWI for lesions aged 15-30 days and >31 days (p<0.01).
  • Significantly decreased contralateral ADC values on FLAIR DWI compared to conventional DWI (p<0.01).

Conclusions:

  • FLAIR DWI does not significantly affect ADC in early ischemic stroke (<14 days).
  • FLAIR DWI provides more accurate relative ADC measurements by reducing CSF partial volume effects.
  • FLAIR DWI may assist in determining the age of ischemic lesions.