Association of spinal cord structure with cognition in hereditary spastic paraplegia type 5

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Authors: Xuanyu Chen, Kunxin Lin, Liangliang Qiu, Ruying Yuan, Yusen Qiu, Jin Bi, Zhixian Ye, Wanjin Chen, N. Wang, Ying Fu
Cited by: 0
References: 37

Abstract

Background and objectives Cognitive deficits often accompany brain structural changes, but the association between spinal cord atrophy and cognitive function remains unclear. Spastic paraplegia type 5 (SPG5) is a subtype of hereditary spastic paraplegias (HSPs), caused by mutations in cholesterol metabolism genes, with radiological features of spinal cord atrophy. Our study aims to explore cognitive impairment in SPG5 and its relation to spinal cord structure. Methods We conducted a prospective cross-sectional study with 30 HSPs patients and 47 healthy controls (HC), performing brain and spinal cord MRI and neuropsychological assessments. We investigated correlations between cognitive performance and MRI measurements. Results Compared to HC, SPG5 patients exhibited significant impairments in the Benton Judgment of Line Orientation Test ( p = 0.033), Controlled Oral Word Association Test ( p = 0.028), and Symbol Digit Modalities Test ( p = 0.023). SPG5 patients also demonstrated significant reductions in spinal cord and thoracic cord cross-sectional area (CSA), anterior-posterior (AP) diameter, and right-left (RL) total (All p < 0.01). Specifically, the thoracic cord RL total was positively correlated with scores on the Brief Visuospatial Memory Test - Revisited delayed recall (BVMT-R DR) and Montreal Cognitive Assessment (MoCA). The spinal cord RL total explained 81% of the variance in BVMT-R DR ( p = 0.015) and 74% of the variance in MoCA ( p = 0.027). Discussion SPG5 patients demonstrate deficits in visuospatial perception, executive function, and information processing speed. Thoracic spinal cord RL total was positively associated with visual memory and global cognition.

Fields of Study & Subjects

Hereditary Neurological Disorders Botulinum Toxin and Related Neurological Disorders Genomics and Rare Diseases

Publication details

Journal / source
Frontiers in Neurology
Volume
16
Pages
1639011–1639011
Publication date
2 January 2026
Language
EN