Assessing of the glymphatic system using DTI‐ALPS MRI in patients with neurodegenerative diseases

Abstract Background Dysfunction of the glymphatic system (GS), a recently discovered brain by‐product elimination system, is considered to be one of the pathophysiological mechanisms for common neurodegenerative diseases such as Alzheimer's disease (AD), dementia with Lewy bodies (DLB) and Parkinson's disease (PD). In 2017 a new way to assess the GS was proposed – a diffusion tensor images analysis along perivascular spaces (DTI‐ALPS). In our work we evaluated the DTI‐ALPS index in groups of patients with AD, DLB, PD and in a comparison group of patients with normal pressure hydrocephalus (NPH). Methods We examined 32 patients diagnosed with AD [69.5±8.0 years], 15 patients with DLB [71.1±8.0 years], 31 patients with PD without dementia [64.0±6.9 years], 11 patients NPH [68.5±9.8 years] and 27 healthy controls [63.2±7.0 years]. In four patient groups cognitive impairment was rated with Montreal Cognitive Assessment scale (MоCA). The diffusion images were acquired on a SIEMENS Prisma scanner using a 2D EPI diffusion sequence. TE=82 ms, TR=5600 ms. The b‐values were 1000 and 2500 s/mm². The number of diffusion sampling directions were 64 and 64, respectively. The slice thickness was 2 mm. Post‐processing steps were performed using DSI studio software. Next, we identified ROIs corresponding to projection and associative fibers with further extraction of tensor values in the directions Dxx, Dyy, Dzz, which were entered into a table to calculate the DTI‐ALPS index using formula ALPS‐index=mean(Dxx proj +Dxx associ )/mean(Dyy proj +Dzz associ ) for further statistical processing. Results Patients with AD, DLB and NPH had a significantly lower values of DTI‐ALPS index on both sides compared to healthy volunteers (p<0.001). The differences between PD and healthy controls turned out to be statistically insignificant. In addition, analysis of all the patients revealed a significant direct correlation between the MoCA score and DTI‐ALPS values on both sides (p L =0.002; p R =0.035). Conclusion The obtained results showed that the glymphatic dysfunction assessed by DTI‐ALPS index could be considered as a possible participant in the pathogenesis of AD and DLB as well as in NPH reflecting cognitive decline. Whereas the glymphatic dysfunction in PD was not confirmed.

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Journal
Alzheimer s & Dementia
Published
2024-12-01
DOI
https://doi.org/10.1002/alz.086358
Primary Topic
Cerebrospinal fluid and hydrocephalus
Type
article
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article

Assessing of the glymphatic system using DTI‐ALPS MRI in patients with neurodegenerative diseases

М. В. Кротенкова, Р. Н. Коновалов, Alina Liaskovik, E. Yu. Fedotova et al.
Alzheimer s & Dementia
Cerebrospinal fluid and hydrocephalus
article

Assessing of the glymphatic system using DTI‐ALPS MRI in patients with neurodegenerative diseases

М. В. Кротенкова, Р. Н. Коновалов, Alina Liaskovik, E. Yu. Fedotova, L. A. Brsikyan, Yu. A. Shpilyukova, Kseniya Nevzorova
article en

Abstract

Abstract Background Dysfunction of the glymphatic system (GS), a recently discovered brain by‐product elimination system, is considered to be one of the pathophysiological mechanisms for common neurodegenerative diseases such as Alzheimer's disease (AD), dementia with Lewy bodies (DLB) and Parkinson's disease (PD). In 2017 a new way to assess the GS was proposed – a diffusion tensor images analysis along perivascular spaces (DTI‐ALPS). In our work we evaluated the DTI‐ALPS index in groups of patients with AD, DLB, PD and in a comparison group of patients with normal pressure hydrocephalus (NPH). Methods We examined 32 patients diagnosed with AD [69.5±8.0 years], 15 patients with DLB [71.1±8.0 years], 31 patients with PD without dementia [64.0±6.9 years], 11 patients NPH [68.5±9.8 years] and 27 healthy controls [63.2±7.0 years]. In four patient groups cognitive impairment was rated with Montreal Cognitive Assessment scale (MоCA). The diffusion images were acquired on a SIEMENS Prisma scanner using a 2D EPI diffusion sequence. TE=82 ms, TR=5600 ms. The b‐values were 1000 and 2500 s/mm². The number of diffusion sampling directions were 64 and 64, respectively. The slice thickness was 2 mm. Post‐processing steps were performed using DSI studio software. Next, we identified ROIs corresponding to projection and associative fibers with further extraction of tensor values in the directions Dxx, Dyy, Dzz, which were entered into a table to calculate the DTI‐ALPS index using formula ALPS‐index=mean(Dxx proj +Dxx associ )/mean(Dyy proj +Dzz associ ) for further statistical processing. Results Patients with AD, DLB and NPH had a significantly lower values of DTI‐ALPS index on both sides compared to healthy volunteers (p<0.001). The differences between PD and healthy controls turned out to be statistically insignificant. In addition, analysis of all the patients revealed a significant direct correlation between the MoCA score and DTI‐ALPS values on both sides (p L =0.002; p R =0.035). Conclusion The obtained results showed that the glymphatic dysfunction assessed by DTI‐ALPS index could be considered as a possible participant in the pathogenesis of AD and DLB as well as in NPH reflecting cognitive decline. Whereas the glymphatic dysfunction in PD was not confirmed.

Alzheimer s & DementiaVol. 20(S2)
Research Center of Neurology (RU)
Openalex Percentile: Top 73%
Cerebrospinal fluid and hydrocephalus
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