White Matter Lesions May Aid in Differentiating Idiopathic Normal Pressure Hydrocephalus and Alzheimer's Disease

• Published in: Journal of Alzheimer's disease Vol. 85; no. 2; p. 851
• Main Authors: Kuroda, Takeshi, Honma, Motoyasu, Mori, Yukiko, Futamura, Akinori, Sugimoto, Azusa, Kasai, Hideyo, Yano, Satoshi, Hieda, Sotaro, Kasuga, Kensaku, Ikeuchi, Takeshi, Ono, Kenjiro
• Format: Journal Article
• Language: English
• Published: Netherlands 01.01.2022
• Subjects: Aged; Aged, 80 and over; Alzheimer Disease - cerebrospinal fluid; Alzheimer Disease - pathology; Amyloid beta-Peptides - cerebrospinal fluid; Biomarkers - cerebrospinal fluid; Diagnosis, Differential; Female; Humans; Hydrocephalus, Normal Pressure - cerebrospinal fluid; Hydrocephalus, Normal Pressure - pathology; Male; Middle Aged; Peptide Fragments - cerebrospinal fluid; tau Proteins - cerebrospinal fluid; White Matter - pathology; white matter; amyloid; hydrocephalus; Alzheimer disease; glymphatic system; cerebrospinal fluid
• DOI: 10.3233/JAD-215187

Idiopathic normal pressure hydrocephalus (iNPH) is often misdiagnosed as Alzheimer's disease (AD) due to overlapping pathophysiology and similar imaging characteristics, including ventricular enlargement and increased white matter lesions (WMLs). To compare the extent and distribution of WMLs directly between iNPH and AD and examine the association with underlying pathophysiology. Twelve patients with iNPH (mean age: 78.08 years; 5 females), 20 with AD (mean age: 75.40 years; 13 females), and 10 normal cognition (NC) participants (mean age: 76.60 years; 7 females) were recruited. The extent and distribution of WMLs and the lateral ventricular volume (LV-V) were evaluated on MRI using voxel-based morphometry analysis. Concentrations of cerebrospinal fluid biomarkers, such as amyloid-β protein (Aβ)42, Aβ40, Aβ38, and tau species, were also measured. Risk factors for small vessel disease (SVD) were assessed by blood examination and medical records. The periventricular WML volume (PWML-V) and deep WML volume (DWML-V) were significantly larger in iNPH than in AD and NC. The DWML-V was dominant in iNPH, while the PWML-V was dominant in AD and NC. GM-V was significantly smaller in AD than in iNPH and NC. The LV-V positively correlated with WML-V in all participants. There was a significant negative correlation between LV-V and Aβ38 in iNPH. Furthermore, there was no significant difference in SVD risk factors between the groups. The differences in the extent and distribution of WMLs between iNPH and AD, especially predominance of DWML-V over PWML-V in iNPH, may reflect decreased fluid and Aβ clearance.