Evidence map›Paper›PMID 41889160›Full record

ArticleJournal of cachexia, sarcopenia and muscle2026

Validity of Bioelectrical Impedance Analysis for the Assessment of Body Composition in Patients With Systemic Sclerosis.

Lucas Denardi Dória, Rafaela Cavalheiro do Espírito Santo, Vanessa Hax, André Luiz Mallmann, Leonardo Peterson Dos Santos, Stephanie Pilotti, Daniel Nóbrega de Moraes, Bruno Eduardo Lara Da Silva, Vinícius Hammel Lovison, Ronaldo Legati Junior and 6 more

Abstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

16 authors.

Lucas Denardi DóriaDivision of Rheumatology, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Rio Grande do Sul, Brazil.ORCID https://orcid.org/0000-0002-9595-5875
Rafaela Cavalheiro do Espírito SantoFaculty of Health Sciences, Klaipeda University, Klaipėda, Lithuania.
Vanessa HaxDivision of Rheumatology, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Rio Grande do Sul, Brazil.
André Luiz MallmannDivision of Rheumatology, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Rio Grande do Sul, Brazil.
Leonardo Peterson Dos SantosDivision of Rheumatology, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Rio Grande do Sul, Brazil.
Stephanie PilottiDivision of Rheumatology, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Rio Grande do Sul, Brazil.
Daniel Nóbrega de MoraesDivision of Rheumatology, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Rio Grande do Sul, Brazil.
Bruno Eduardo Lara Da SilvaDivision of Rheumatology, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Rio Grande do Sul, Brazil.
Vinícius Hammel LovisonDivision of Rheumatology, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Rio Grande do Sul, Brazil.
Ronaldo Legati JuniorDivision of Rheumatology, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Rio Grande do Sul, Brazil.
Poliana Espíndola CorreiaDivision of Endocrinology, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Rio Grande do Sul, Brazil.
Tayane Muniz FigheraDivision of Endocrinology, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Rio Grande do Sul, Brazil.
Fernando GerchmanDivision of Endocrinology, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Rio Grande do Sul, Brazil.
Poli Mara SpritzerDivision of Endocrinology, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Rio Grande do Sul, Brazil.
Ricardo Machado XavierDivision of Rheumatology, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Rio Grande do Sul, Brazil.
Rafael Mendonça da Silva ChakrDivision of Rheumatology, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Rio Grande do Sul, Brazil.

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brazil (CAPES)Hospital de Clínicas de Porto Alegre (HCPA; https://ror.org/010we4y38), Research Incentive Fund (FIPE)Rheumatology Society of Rio Grande do Sul (SRRS) - Research Support Fund (FAPE)
6 · The paper itself

Abstract

backgroundSystemic sclerosis (SSc) is an autoimmune disease characterized by vasculopathy and progressive fibrosis. Reduced muscle mass is common and contributes to myopenia, sarcopenia and adverse clinical outcomes. Dual-energy X-ray absorptiometry (DXA) is the most widely used method in clinical research and is recommended by international guidelines as the reference standard for muscle mass evaluation in sarcopenia. However, its accessibility in routine clinical practice is limited. Bioelectrical impedance analysis (BIA) is a validated method for assessing body composition due to its affordability, ease of use and non-invasive nature. Nevertheless, variability across devices and assessment protocols may influence measurement accuracy, underscoring the need for validation in specific clinical populations. This study compared body composition measured by BIA and DXA and evaluated the diagnostic accuracy of BIA for detecting myopenia in SSc.

methodsIn this cross-sectional study, patients with SSc underwent body composition assessment by BIA (InBody 370 s) and DXA (Lunar Prodigy Primo). Fat mass (FM), fat mass index (FMI), fat-free mass (FFM), fat-free mass index (FFMI), appendicular skeletal muscle mass (ASM), appendicular skeletal muscle mass index (ASMI) and ASM adjusted by body mass index (ASM/BMI) were assessed. Myopenia was defined according to established muscle mass criteria. Agreement was evaluated using Bland-Altman analysis and Lin's concordance correlation coefficient (CCC). Diagnostic performance was assessed using receiver operating characteristic (ROC) curves.

resultsOne hundred patients with SSc were included (91% women; mean age 60.1 ± 11.5 years; median disease duration 11.5 [5.0-20.3] years). Disease subtypes comprised 23% diffuse cutaneous, 61% limited cutaneous and 16% sine scleroderma. BIA demonstrated excellent agreement with DXA (CCC > 0.900) for ASM/BMI [Δ = 0.032; 95% CI 0.019-0.045], FM (Δ = -0.401; 95% CI -0.804 to 0.003), FMI (Δ = -0.190; 95% CI -0.366 to -0.015) and FFM (Δ = -0.010; 95% CI -0.415 to 0.395). Good concordance (CCC 0.750-0.900) was observed for ASM (Δ = 0.803; 95% CI 0.518-1.088). In women, ROC analysis showed high discriminative ability, with AUCs of 0.956 (95% CI 0.908-1.000) for ASM, 0.878 (95% CI 0.763-0.993) for ASMI and 0.969 (95% CI 0.935-1.000) for ASM/BMI. The optimal ASM/BMI cut-off (0.506) yielded 100% sensitivity and 90.1% specificity (PPV 55.6%, NPV 100%).

conclusionBIA showed high agreement with DXA and strong diagnostic accuracy for detecting myopenia in SSc, particularly in women. These findings support BIA as an accessible tool for body composition assessment in SSc when standardized conditions and validated sex-specific cut-offs are applied.

Indexed as

Body CompositionElectric ImpedanceScleroderma, SystemicAbsorptiometry, PhotonAdultAgedCross-Sectional StudiesFemaleHumansMaleMiddle AgedReproducibility of ResultsROC Curveagreementbioelectrical impedance analysisbioimpedance (BIA)body compositioncut‐off pointfat‐free massfat massmuscle massmyopeniasystemic sclerosis (SSc)

Identifiers

PMID41889160
PMCPMC13054670

What Socratic 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 Socratic graph.