Evidence map›Paper›PMID 37345346›Full record

ArticleMuscle & nerve2023

Sensitivity and specificity of the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised to detect dysarthria in individuals with amyotrophic lateral sclerosis.

Cara Donohue, Jennifer L Chapin, Amber Anderson, Lauren DiBiase, Lauren Tabor Gray, James P Wymer, Emily K Plowman

Open access · hybridAbstract read
In one paragraph

Article in Muscle & nerve, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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 4 institutions in 1 country.

Cara DonohueAerodigestive Research Core Laboratory, University of Florida, Gainesville, Florida, USA.ORCID 0000-0002-5546-6081
Jennifer L ChapinAerodigestive Research Core Laboratory, University of Florida, Gainesville, Florida, USA.
Amber AndersonAerodigestive Research Core Laboratory, University of Florida, Gainesville, Florida, USA.
Lauren DiBiaseAerodigestive Research Core Laboratory, University of Florida, Gainesville, Florida, USA.
Lauren Tabor GrayAerodigestive Research Core Laboratory, University of Florida, Gainesville, Florida, USA.
James P WymerDepartment of Neurology, University of Florida, Gainesville, Florida, USA.
Emily K PlowmanAerodigestive Research Core Laboratory, University of Florida, Gainesville, Florida, USA.ORCID 0000-0002-0198-4297
University of Florida Health · USNova Southeastern University · USUniversity of Florida · USVanderbilt University · US

Funding

Landis Outstanding Mentor Award SupplementR01NS100859 · NINDS · UNIVERSITY OF FLORIDA · PI PLOWMAN, EMILY KATE · 2017 to 2021
$2.0M
NINDS NIH HHS R01 NS100859
6 · The paper itself

Abstract

INTRODUCTION/

aimsGiven the widespread use of the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised (ALSFRS-R) to measure disease progression in ALS and recent reports demonstrating its poor sensitivity, we aimed to determine the sensitivity and specificity of the ALSFRS-R bulbar subscale and speech item to detect validated clinical ratings of dysarthria in individuals with ALS.

methodsPaired ALSFRS-R and validated Speech Intelligibility Test (SIT) data from individuals with ALS were analyzed. Trained raters completed duplicate, independent, and blinded ratings of audio recordings to obtain speech intelligibility (%) and speaking rate (words per minute, WPM). Binary dysarthria profiles were derived (dysarthria ≤96% intelligible and/or <150 WPM). Data were obtained using the Kruskal-Wallis test, receiver-operating characteristic (ROC) curve, area under the curve (AUC), sensitivity and specificity percentages, and positive/negative predictive values (PPV/NPV).

resultsA total of 250 paired SIT and ALSFRS-R data points were analyzed. Dysarthria was confirmed in 72.4% (n = 181). Dysarthric speakers demonstrated lower ALSFRS-R bulbar subscale (8.9 vs. 11.2) and speech item (2.7 vs. 3.7) scores (P < .0001). The ALSFRS-R bulbar subscale score had an AUC of 0.81 (95% confidence interval [CI] 0.75 to 0.86). A subscale score of ≤11 yielded a sensitivity of 86%, specificity of 57%, PPV of 84%, and NPV of 60% to correctly identify dysarthria status. The ALSFRS-R speech item score demonstrated an AUC of 0.81 to detect dysarthria (95% CI 0.76 to 0.85), with sensitivity of 79%, specificity of 75%, PPV of 89%, and NPV of 58% for a speech item cutpoint of ≤3. DISCUSSION: The ALSFRS-R bulbar and speech item subscale scores may be useful, inexpensive, and quick tools for monitoring dysarthria status in ALS.

Indexed as

Amyotrophic Lateral SclerosisDysarthriaHumansROC CurveSensitivity and SpecificitySeverity of Illness Indexamyotrophic lateral sclerosisdysarthrianeurogenerative diseasescreeningspeech

Identifiers

PMID37345346
PMCPMC10529444
OpenAlexW4381598583

What OpenQuestion holds

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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.