Evidence map›Paper›PMID 42493651›Full record

ArticleJournal of neurology2026

Longitudinal spinal cord MRI in adult 5q-SMA: biomarker and pathophysiological insights.

Felipe Franco da Graça, Thiago Junqueira Ribeiro de Rezende, Cristina Iwabe, Carelis González-Salazar, Rodrigo de Holanda Mendonça, Edmar Zanoteli, Marcondes Cavalcante França-Jr

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Article in Journal of neurology, 2026. 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
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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

7 authors.

Felipe Franco da GraçaDepartment of Neurology, Faculdade de Ciências Médicas, Universidade Estadual de Campinas (UNICAMP), Sao Paulo, Brazil.
Thiago Junqueira Ribeiro de RezendeDepartment of Neurology, Faculdade de Ciências Médicas, Universidade Estadual de Campinas (UNICAMP), Sao Paulo, Brazil.
Cristina IwabeDepartment of Neurology, Faculdade de Ciências Médicas, Universidade Estadual de Campinas (UNICAMP), Sao Paulo, Brazil.
Carelis González-SalazarDepartment of Neurology, Faculdade de Ciências Médicas, Universidade Estadual de Campinas (UNICAMP), Sao Paulo, Brazil.
Rodrigo de Holanda MendonçaDepartment of Neurology, Faculdade de Medicina, Universidade de São Paulo (FMUSP), São Paulo, Brazil.
Edmar ZanoteliDepartment of Neurology, Faculdade de Medicina, Universidade de São Paulo (FMUSP), São Paulo, Brazil.
Marcondes Cavalcante França-JrDepartment of Neurology, Faculdade de Ciências Médicas, Universidade Estadual de Campinas (UNICAMP), Sao Paulo, Brazil. mcfjr@unicamp.br.ORCID http://orcid.org/0000-0003-0898-2419

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo 2013/07559-3
6 · The paper itself

Abstract

backgroundSpinal muscular atrophy (SMA) is a progressive neuromuscular disease caused by biallelic SMN1 mutations and widespread lower motor neuron degeneration. Objective biomarkers to monitor progression and treatment response are critically needed. Spinal cord (SC) MRI, including diffusion tensor imaging (DTI), is a promising non-invasive approach, but data in adults remain scarce.

methodsWe conducted an exploratory longitudinal study in 26 adults with 5q-SMA (type 2: n = 4; type 3: n = 22; median age 29.5 years) and 27 controls undergoing 3 T cervical SC MRI. Gray matter (GM) and total cross-sectional area (CSA) and DTI metrics (FA, MD, AD, RD) were extracted from three white matter tracts. Patients underwent motor (MFM-32, HFMSE, RULM), neurophysiological (CMAP, MUNIX) and fatigue assessments. 22 patients completed 12-14-month follow-up.

resultsTotal SC CSA was reduced across C2-C6 (Cohen d up to 1.02) but showed limited functional correlations. GM CSA was reduced in SMA versus controls (11.90 ± 2.56 vs. 13.92 ± 1.72 mm

conclusionsSelective GM CSA yields robust functional correlations, supporting its role as a candidate imaging biomarker and outperforming total CSA. DTI abnormalities in sensory tracts extend the known pathological scope of adult SMA beyond motor neurons. Longer follow-up is warranted to detect disease progression.

Indexed as

Magnetic Resonance ImagingMuscular Atrophy, SpinalSpinal CordAdultBiomarkersDiffusion Tensor ImagingFemaleGray MatterHumansLongitudinal StudiesMaleWhite MatterYoung AdultBiomarkersAdult SMABiomarkerDiffusion tensor imagingGray matterMRISpinal cordSpinal muscular atrophy

Identifiers

PMID42493651
PMCPMC13395906

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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.