Automated diffusion‐weighted image analysis along the perivascular space index reveals glymphatic dysfunction in association with brain parenchymal lesions

Author:

Li Wen‐Xin1ORCID,Liu Zi‐Yue1,Zhai Fei‐Fei1,Han Fei1,Li Ming‐Li2,Zhou Li‐Xin1,Ni Jun1,Yao Ming1,Zhang Shu‐Yang3,Cui Li‐Ying1,Jin Zheng‐Yu2,Zhu Yi‐Cheng1ORCID

Affiliation:

1. Department of Neurology State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College Beijing China

2. Department of Radiology State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College Beijing China

3. Department of Cardiology State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College Beijing China

Abstract

AbstractBrain glymphatic dysfunction is critical in neurodegenerative processes. While animal studies have provided substantial insights, understandings in humans remains limited. Recent attention has focused on the non‐invasive evaluation of brain glymphatic function. However, its association with brain parenchymal lesions in large‐scale population remains under‐investigated. In this cross‐sectional analysis of 1030 participants (57.14 ± 9.34 years, 37.18% males) from the Shunyi cohort, we developed an automated pipeline to calculate diffusion‐weighted image analysis along the perivascular space (ALPS), with a lower ALPS value indicating worse glymphatic function. The automated ALPS showed high consistency with the manual calculation of this index (ICC = 0.81, 95% CI: 0.662–0.898). We found that those with older age and male sex had lower automated ALPS values (β = −0.051, SE = 0.004, p < .001, per 10 years, and β = −0.036, SE = 0.008, p < .001, respectively). White matter hyperintensity (β = −2.458, SE = 0.175, p < .001) and presence of lacunes (OR = 0.004, 95% CI < 0.002–0.016, p < .001) were significantly correlated with decreased ALPS. The brain parenchymal and hippocampal fractions were significantly associated with decreased ALPS (β = 0.067, SE = 0.007, p < .001 and β = 0.040, SE = 0.014, p = .006, respectively) independent of white matter hyperintensity. Our research implies that the automated ALPS index is potentially a valuable imaging marker for the glymphatic system, deepening our understanding of glymphatic dysfunction.

Publisher

Wiley

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