Evidence map›Paper›PMID 42455155›Full record

ArticleClinical neuroradiology2026

Evaluation of Glymphatic System Activity in Pediatric Wilson Disease Patients Using Diffusion Tensor Imaging Along the Perivascular Space.

Sevgi Demiröz Taşolar, Hüseyin Ayvaz, Emre Gök, Hilal Er Ulubaba, Nurullah Dağ, Şükrü Güngör, Hakan Taşolar, Fatma İlknur Varol

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Article in Clinical neuroradiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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8 authors.

Sevgi Demiröz TaşolarDepartments of Radiology, Inonu University, Malatya, Turkey. drsevgidemiroz@gmail.com.ORCID https://orcid.org/0000-0002-9836-6814
Hüseyin AyvazDepartments of Radiology, Inonu University, Malatya, Turkey.
Emre GökDepartment of Pediatric Gastroenterology, Inonu University, Malatya, Turkey.
Hilal Er UlubabaDepartments of Radiology, Inonu University, Malatya, Turkey.
Nurullah DağDepartments of Radiology, Inonu University, Malatya, Turkey.
Şükrü GüngörDepartment of Pediatric Gastroenterology, Inonu University, Malatya, Turkey.
Hakan TaşolarDepartment of Cardiology, Inonu University, Malatya, Turkey.
Fatma İlknur VarolDepartment of Pediatric Gastroenterology, Inonu University, Malatya, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeWilson disease is an autosomal recessive disorder of copper metabolism that results in toxic copper accumulation in the liver and brain, thereby causing neurological injury. Previous reports have described astrocyte dysfunction, oxidative stress, glial pathology, and impaired aquaporin-4-mediated water transport in Wilson disease, suggesting a potential disruption of glymphatic fluid dynamics. However, glymphatic function has not been quantitatively assessed in this population using diffusion tensor imaging analysis along the perivascular space (DTI-ALPS).

methodsThis retrospective single-center study aimed to quantify glymphatic system function in pediatric patients with Wilson disease using the DTI-ALPS index. Brain MRI/DTI data (30 directions, b = 1000 s/mm

resultsRight-, left-, and mean ALPS indices were significantly lower in patients with Wilson's disease than in controls, with this group effect persisting after demographic adjustment (F = 13.90, p < 0.001; adjusted means: controls 1.51, WD 1.34, NWD 1.38). ALPS indices did not differ between the WD and NWD subgroups despite higher liver severity scores in the latter. ALPS values did not correlate with liver severity scores, urinary copper, ceruloplasmin or sex.

conclusionThese findings suggest that the DTI-ALPS index may reflect glymphatic system-related processes, as well as disease-related microstructural and perivascular alterations, in pediatric Wilson disease. The DTI-ALPS index may provide complementary, non-invasive imaging information regarding early perivascular microstructural alterations. Prospective multicenter longitudinal studies are warranted to clarify the temporal relationships among ALPS index changes, neurological progression, and treatment response.

Indexed as

Diffusion tensor imagingDTI-ALPSGlymphatic systemNeurological impactsPerivascular spacesWilson disease

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.