Evidence map›Paper›PMID 39978794›Full record

ArticleClinical genetics2025

Expanding the Phenotypic Spectrum of SPG7 Rare Damaging Variants: Insights From a Hungarian Cohort.

Idris Janos Jimoh, Peter Balicza, Tamas Szlepak, Dora Csaban, Aniko Gal, Adrienn Geresi, Zoltan Grosz, Agnes Palasti, Judit Boczan, Peter Klivenyi and 1 more

Abstract read
In one paragraph

Article in Clinical genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 3-Methyl Glutaconic Aciduria and Elevated Plasma Growth Differentiation Factor 15 Level in an Adult with MonoallelicActa myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology · 2025
    Article
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

11 authors.

Idris Janos JimohInstitute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary.
Peter BaliczaInstitute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary.
Tamas SzlepakInstitute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary.
Dora CsabanInstitute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary.
Aniko GalInstitute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary.
Adrienn GeresiInstitute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary.
Zoltan GroszInstitute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary.
Agnes PalastiInstitute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary.
Judit BoczanDepartment of Neurology, University of Debrecen, Debrecen, Hungary.
Peter KlivenyiDepartment of Neurology, University of Szeged, Szeged, Hungary.
Maria Judit MolnarInstitute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary.

Funding

TKP2021-EGA-25, TKP2021-NVA-15, and OTKA 139010 from the National Research, Development and Innovation Office, and the Eötvös Loránd Research Network, Multiomics Neurodegeneration Research Group
6 · The paper itself

Abstract

Mitochondria-associated paraplegin dysfunction is primarily linked to spastic paraplegia; however, genetic alterations in SPG7 have been associated with a broader spectrum of clinical symptoms. To identify disease-causing variants in the SPG7 gene, 437 patients with spastic ataxia, mitochondrial dysfunction-associated symptoms, or motoneuron lesions detected by EMG have been tested. We aimed to assess the clinical spectrum and determine the frequency of damaging variants within patient groups, particularly those less studied. Using ACMG criteria, we identified 10 pathogenic or likely pathogenic variants, 5 variants of uncertain significance with predicted damaging effects, and a probable risk factor variant in 58 patients. We identified 25 biallelic and 33 monoallelic cases. The most common variant was p. Leu78Ter (N = 23), followed by p. Ala510Val (N = 21). The point prevalence of SPG7-associated conditions in Hungary in 2024 is 0.46 per 100 000. In addition to well-characterized cohorts, SPG7 alterations were frequently identified in cohorts with multisystemic mitochondrial disease and lower motoneuron lesions. Multiple mtDNA deletions and histological abnormalities were consistently observed across all groups. In monoallelic cases, no evidence of a digenic effect involving AFG3L2 was found. Both autosomal dominant and recessive inheritance patterns were documented, with monoallelic cases typically presenting with a milder phenotype.

Indexed as

Genetic Predisposition to DiseaseMetalloendopeptidasesParaplegiaSpastic Paraplegia, HereditarySpinocerebellar AtaxiasAdolescentAdultAllelesATPases Associated with Diverse Cellular ActivitiesChildCohort StudiesDNA, MitochondrialFemaleGenetic Association StudiesHumansHungaryATPases Associated with Diverse Cellular ActivitiesDNA, MitochondrialMetalloendopeptidasesSPG7 protein, humancarrier risksepidemiologyinheritancemitochondrial diseaseparapleginphenotypic spectraSPG7

Identifiers

PMID39978794
PMCPMC12215234

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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.