Evidence map›Paper›PMID 41032233›Full record

SynthesisNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2025

The cognitive profile of hereditary spastic paraplegia: a systematic review of the literature.

Alessia Quinzi, Elettra Capogna, Lucia Guidi, Giovanni Rizzo, David Neil Manners, Rocco Liguori, Raffaele Lodi, Caterina Tonon, Magali Jane Rochat

Abstract readSystematic Review
PubMed Publisher
In one paragraph

Synthesis in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Alessia QuinziFunctional and Molecular Neuroimaging Unit, IRCCS Istituto Delle Scienze Neurologiche Di Bologna, Bologna, Italy.
Elettra CapognaFunctional and Molecular Neuroimaging Unit, IRCCS Istituto Delle Scienze Neurologiche Di Bologna, Bologna, Italy.
Lucia GuidiFunctional and Molecular Neuroimaging Unit, IRCCS Istituto Delle Scienze Neurologiche Di Bologna, Bologna, Italy.
Giovanni RizzoUOC Neurological Clinic, IRCCS Istituto Delle Scienze Neurologiche Di Bologna, Bologna, Italy.
David Neil MannersFunctional and Molecular Neuroimaging Unit, IRCCS Istituto Delle Scienze Neurologiche Di Bologna, Bologna, Italy.
Rocco LiguoriDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
Raffaele LodiDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy. raffaele.lodi@unibo.it.ORCID http://orcid.org/0000-0003-3878-304X
Caterina TononFunctional and Molecular Neuroimaging Unit, IRCCS Istituto Delle Scienze Neurologiche Di Bologna, Bologna, Italy.
Magali Jane RochatFunctional and Molecular Neuroimaging Unit, IRCCS Istituto Delle Scienze Neurologiche Di Bologna, Bologna, Italy.

Funding

Ministero della Salute Bando Ricerca Corrente 2023-2024
6 · The paper itself

Abstract

backgroundHereditary Spastic Paraplegia (HSP) is a heterogeneous group of genetic diseases characterized by involvement of the corticospinal bundle. In addition to motor manifestations, the phenotypic spectrum of HSP can also include cognitive disorders. Our aim was to examine the cognitive profile of patients with HSP and investigate potential subtype-phenotype associations on the basis of a systematic review of the literature.

methodsFollowing PRISMA criteria, Pubmed, Cochrane Libraries, APA PsycInfo, Scopus, and Web of Science were searched for studies performing a comprehensive neuropsychological assessment in patients with pure or complex HSP and different Spastic Paraplegia Genes (SPG).

resultsA total of 343 articles were selected, among which 38 met the eligibility criteria for inclusion. The occurrence and the degree of cognitive impairment varied significantly, depending on the specific clinical and genetic HSP subtype. Global cognitive functioning was more severely compromised in complex forms of HSP (such as SPG11), whereas pure forms (such as SPG4) may show more subtle cognitive impairment. Overall, executive functions appeared to be the most affected cognitive domain in both conditions. DISCUSSION: Given the high prevalence of cognitive impairment in HSP patients, it is desirable to incorporate a standardized neuropsychological assessment into routine clinical practice. Therefore, we propose a potential neuropsychological assessment protocol to address the cognitive deficits most frequently observed in this clinical population and provide a framework for future research.

Indexed as

Cognition DisordersCognitive DysfunctionSpastic Paraplegia, HereditaryHumansNeuropsychological TestsCognitive disorderGenotypeHereditary spastic paraplegia (HSP)Neuropsychological assessmentPhenotype

Identifiers

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Registered trials

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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.