Evidence map›Paper›PMID 33956876›Full record

ArticlePloS one2021

Fat mass loss correlates with faster disease progression in amyotrophic lateral sclerosis patients: Exploring the utility of dual-energy x-ray absorptiometry in a prospective study.

Ikjae Lee, Mohamed Kazamel, Tarrant McPherson, Jeremy McAdam, Marcas Bamman, Amy Amara, Daniel L Smith, Peter H King

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

23 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Potential Roles of Neuroimaging in Motor Neuron Disease.Current neurology and neuroscience reports · 2026
    Review
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  4. Changes in body composition in genetic C9orf72 carriers: The role of the hypothalamus and thalamus.Alzheimer's & dementia : the journal of the Alzheimer's Association · 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

8 authors at 1 institution in 1 country.

Ikjae LeeDepartment of Neurology, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.ORCID 0000-0003-0537-9622
Mohamed KazamelDepartment of Neurology, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Tarrant McPhersonDepartment of Biostatistics, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Jeremy McAdamDepartment of Cell, Developmental, & Integrative Biology, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Marcas BammanDepartment of Cell, Developmental, & Integrative Biology, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Amy AmaraDepartment of Neurology, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Daniel L SmithDepartment of Nutrition Sciences, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Peter H KingDepartment of Neurology, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
University of Alabama at Birmingham · US

Funding

Why is the prevalence of obesity so high in U.S. Southern States? Regional predictors of BMI and obesity treatment response.P30DK056336 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BARBARA A GOWER · 2000 to 2026
$31.9M
Smad Signaling in Skeletal Muscle as a Biomarker of Disease Progression in ALSR01NS092651 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KING, PETER H · 2016 to 2020
$1.6M
FGF23: a novel biomarker in ALS and moreR21NS111275 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KING, PETER H · 2019 to 2019
$422k
RNA-Targeted Dysregulation of Survival Factors in ALS: HuR to the RescueI01BX001148 · VA · BIRMINGHAM VA MEDICAL CENTER · PI KING, PETER H · 2012 to 2015
–
Role of Microglial Hur in promoting neuroinflammation and ALS disease progressionI01BX004419 · VA · BIRMINGHAM VA MEDICAL CENTER · PI KING, PETER H · 2019 to 2022
–
BLRD VA I01 BX001148BLRD VA I01 BX004419NIDDK NIH HHS P30 DK056336NINDS NIH HHS R01 NS092651NINDS NIH HHS R21 NS111275
6 · The paper itself

Abstract

BACKGROUND/

objectiveWeight loss is a predictor of shorter survival in amyotrophic lateral sclerosis (ALS). We performed serial measures of body composition using Dual-energy X-ray Absorptiometry (DEXA) in ALS patients to explore its utility as a biomarker of disease progression.

methodsDEXA data were obtained from participants with ALS (enrollment, at 6- and 12- months follow ups) and Parkinson's disease (enrollment and at 4-month follow up) as a comparator group. Body mass index, total lean mass index, appendicular lean mass index, total fat mass index, and percentage body fat at enrollment were compared between the ALS and PD cohorts and age-matched normative data obtained from the National Health and Nutrition Examination Survey database. Estimated monthly changes of body composition measures in the ALS cohort were compared to those of the PD cohort and were correlated with disease progression measured by the Revised Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS-R).

resultsThe ALS cohort (N = 20) had lower baseline total and appendicular lean mass indices compared to the PD cohort (N = 20) and general population. Loss in total and appendicular lean masses were found to be significantly associated with follow-up time. Low baseline percentage body fat (r = 0.72, p = 0.04), loss of percentage body fat (r = 0.81, p = 0.01), and total fat mass index (r = 0.73, p = 0.04) during follow up correlated significantly with monthly decline of ALSFRS-R scores in ALS cohort who had 2 or more follow-ups (N = 8).

conclusionMeasurement of body composition with DEXA might serve as a biomarker for rapid disease progression in ALS.

Indexed as

Absorptiometry, PhotonAdipose TissueAmyotrophic Lateral SclerosisBiomarkersBody Mass IndexDisease ProgressionFemaleHumansMaleMiddle AgedProspective StudiesBiomarkers

Identifiers

PMID33956876
PMCPMC8101939
OpenAlexW3157428027

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.