Evidence map›Paper›PMID 31882526›Full record

ArticleNeurology2020

Serum creatinine is a biomarker of progressive denervation in spinal muscular atrophy.

Christiano R R Alves, Ren Zhang, Alec J Johnstone, Reid Garner, Pann H Nwe, Jennifer J Siranosian, Kathryn J Swoboda

Open access · greenAbstract read
In one paragraph

Article in Neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 4% of its field
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

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 80 citations in OpenAlex.

  1. Pooled it
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  4. Longitudinal multi-omics profiling of spinal muscular atrophy.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
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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 at 1 institution in 2 countries.

Christiano R R AlvesDepartment of Neurology, Center for Genomic Medicine, Massachusetts General Hospital, Boston.ORCID 0000-0002-2646-9689
Ren ZhangDepartment of Neurology, Center for Genomic Medicine, Massachusetts General Hospital, Boston.
Alec J JohnstoneDepartment of Neurology, Center for Genomic Medicine, Massachusetts General Hospital, Boston.
Reid GarnerDepartment of Neurology, Center for Genomic Medicine, Massachusetts General Hospital, Boston.
Pann H NweDepartment of Neurology, Center for Genomic Medicine, Massachusetts General Hospital, Boston.
Jennifer J SiranosianDepartment of Neurology, Center for Genomic Medicine, Massachusetts General Hospital, Boston.
Kathryn J SwobodaDepartment of Neurology, Center for Genomic Medicine, Massachusetts General Hospital, Boston. kswoboda@mgh.harvard.edu.
Massachusetts General Hospital · US

Funding

Therapeutic Opportunities in Spinal Muscular AtrophyR01HD054599 · NICHD · UNIVERSITY OF UTAH · PI SWOBODA, KATHRYN J. · 2007 to 2011
$1.5M
NICHD NIH HHS R01 HD054599
6 · The paper itself

Abstract

objectiveIdentifying simple biomarkers that can predict or track disease progression in patients with spinal muscular atrophy (SMA) remains an unmet clinical need. To test the hypothesis that serum creatinine (Crn) could be a prognostic biomarker for monitoring progression of denervation in patients with SMA, we determined whether serum Crn concentration correlates with disease severity in patients with SMA.

methodsWe examined a cohort of 238 patients with SMA with 1,130 Crn observations between 2000 and 2016. Analyses were corrected for age, and 156 patients with SMA had dual-energy x-ray absorptiometry data available for correction for lean mass. We investigated the relationship between Crn and SMA type, survival motor neuron 2 (

resultsPatients with SMA type 3 had 2.2-fold (95% confidence interval [CI] 1.93-2.49;

conclusionsThese findings indicate that decreased Crn levels reflect disease severity, suggesting that Crn is a candidate biomarker for SMA progression. We conclude that Crn measurements should be included in the routine analysis of all patients with SMA. In future studies, it will be important to determine whether Crn levels respond to molecular and gene therapies.

Indexed as

Action PotentialsBiomarkersCell CountChildCreatinineDisease ProgressionDNA Copy Number VariationsFemaleHumansInfantMaleMotor NeuronsMuscle, SkeletalMuscular Atrophy, SpinalNerve DegenerationPredictive Value of TestsBiomarkersCreatinineSurvival of Motor Neuron 2 Protein

Identifiers

PMID31882526
PMCPMC7238944
OpenAlexW2997839939

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.