Evidence map›Paper›PMID 40577678›Full record

ArticleNeurology2025

Spinal Muscular Atrophy Functional Composite Score Revised (SMA-FCR) in Untreated and Nusinersen-Treated Patient Cohorts.

Amy Pasternak, Michael P McDermott, Jacqueline Montes, Allan M Glanzman, Giorgia Coratti, Sally Dunaway Young, Trinh Tina Duong, William B Martens, John W Day, Zarazuela Zolkipli-Cunningham and 8 more

Abstract read
In one paragraph

Article in Neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Observational
  3. Article
  4. 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

18 authors.

Amy PasternakDepartment of Physical and Occupational Therapy Services, Boston Children's Hospital, MA.
Michael P McDermottDepartment of Biostatistics and Compulational Biology, University of Rochester, NY.ORCID 0000-0001-7443-9145
Jacqueline MontesDepartment of Rehabilitation and Regenerative Medicine, Columbia University Irving Medical Center, New York, NY.ORCID 0000-0002-7357-0819
Allan M GlanzmanDepartment of Physical Therapy, Children's Hospital of Philadelphia, PA.ORCID 0000-0002-7145-2608
Giorgia CorattiCentro Clinico Nemo, U.O.C. Neuropsichiatria Infantile Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.ORCID 0000-0001-6666-5628
Sally Dunaway YoungDepartments of Neurology and Clinical Neurosciences, Stanford University, Palo Alto, CA.ORCID 0000-0001-9322-0608
Trinh Tina DuongDepartments of Neurology and Clinical Neurosciences, Stanford University, Palo Alto, CA.ORCID 0000-0003-3177-4722
William B MartensDepartment of Neurology, University of Rochester, NY.ORCID 0009-0006-6261-3701
John W DayDepartments of Neurology and Clinical Neurosciences, Stanford University, Palo Alto, CA.ORCID 0000-0002-0086-9529
Zarazuela Zolkipli-CunninghamDivision of Human Genetics, Children's Hospital of Philadelphia, University of Philadelphia, PA.ORCID 0000-0002-0743-8879
Valeria Ada SansoneThe NEMO Center in Milan, Neurorehabilitation Unit, University of Milan, ASST Niguarda Hospital, Italy.ORCID 0000-0002-1354-3800
Adele D'AmicoUnit of Neuromuscular and Neurodegenerative Disorders, IRCCS Bambino Gesu Children's Hospital, Rome, Italy.ORCID 0000-0003-2438-2624
Sonia MessinaDepartment of Clinical and Experimental Medicine and Centro Clinico Nemo Sud, University of Messina, Italy.ORCID 0000-0001-7994-3391
Claudio BrunoCenter of Experimental and Translational Myology, IRCCS Isituto Giannina Gaslini, Genoa, Italy.ORCID 0000-0002-3426-2901
Eugenio MercuriCentro Clinico Nemo, U.O.C. Neuropsichiatria Infantile Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.ORCID 0000-0002-9851-5365
Darryl C De VivoDepartment of Neurology, Columbia University Irving Medical Center, New York, NY; and.
Basil T DarrasDepartment of Neurology, Boston Children's Hospital, Harvard Medical School, MA.ORCID 0000-0002-1536-8145
as the Pediatric Neuromuscular Clinical Research (PNCR) Network and the International SMA Consortium (iSMAc)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesThe Spinal Muscular Atrophy Functional Composite (SMA-FC) combines scores from the Hammersmith Functional Motor Scale Expanded (HFMSE), Upper Limb Module (ULM), and Six-Minute Walk Test (6MWT) into a single score and removes the floor and ceiling effects of the HFMSE. Our objective was to evaluate a revised version of the SMA-FC (SMA-FCR) by including the Revised ULM (RULM) in untreated and nusinersen-treated SMA.

methodsWe included participants with HFMSE, RULM, and 6MWT data at the same visit. The SMA-FCR represented the average of the 3 test scores, each expressed as the percentage of the maximum possible score (HFMSE and RULM) or the percent of predicted normative performance (6MWT). Mean annual rates of change were calculated in participants who had SMA-FCR data at 2 or more visits while untreated and/or while treated.

resultsThere were 580 participants (49.6% female) with a mean (SD) age of 19.2 (15.5) years (range 1.3-70.6 years). The median (interquartile range) SMA-FCR scores were 3.6 (0.0-8.1) for nonsitters, 22.3 (16.3-31.2) for sitters, and 75.1 (63.7-86.6) for walkers. The SMA-FCR score reduced the ceiling effect seen with the RULM in walkers and the floor effect seen with the HFMSE in nonsitters. The mean annual rate of change in the SMA-FCR was -0.62 (95% CI -1.15 to -0.08, DISCUSSION: The SMA-FCR broadens the spectrum of abilities captured in SMA. Analyses of the treated-untreated differences in mean annual rate of change suggest that the SMA-FCR may be more sensitive to change than the HFMSE. The use of the SMA-FCR in clinical trials might allow for study designs with broader eligibility criteria including weaker individuals who score minimally on the HFMSE and stronger individuals who score maximally on the RULM.

Indexed as

Muscular Atrophy, SpinalOligonucleotidesAdolescentAdultAgedChildChild, PreschoolCohort StudiesFemaleHumansInfantMaleMiddle AgedSeverity of Illness IndexWalk TestYoung AdultnusinersenOligonucleotides

Identifiers

PMID40577678
PMCPMC12205743

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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.