Evidence map›Paper›PMID 40972870›Full record

ArticleThe American journal of clinical nutrition2025

Relationship between skeletal muscle indicators and clinical outcomes in cystic fibrosis is modified by adiposity and CFTR modulator use: a cross-sectional analysis.

Lucia A Gonzalez Ramirez, Pichatorn Suppakitjanusant, Tasha M Burley, Swati Zaveri, Arlene A Stecenko, William R Hunt, Ryan A Harris, Virginia A Stallings, Elizabeth A Ivie, Chris Driggers and 3 more

Abstract read
In one paragraph

Article in The American journal of clinical nutrition, 2025. 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
–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

1 citing paper in PubMed.

  1. 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

13 authors.

Lucia A Gonzalez RamirezNutrition and Health Sciences Doctoral Program, Laney Graduate School, Emory University, Atlanta, GA, United States.
Pichatorn SuppakitjanusantDepartment of Neurology, Texas Tech University Health Sciences Center, El Paso, TX, United States.
Tasha M BurleyDivision of Endocrinology, Metabolism, and Lipids, Department of Medicine, Emory University, Atlanta, GA, United States.
Swati ZaveriDivision of Endocrinology, Metabolism, and Lipids, Department of Medicine, Emory University, Atlanta, GA, United States.
Arlene A StecenkoDivision of Pulmonary, Asthma, Cystic Fibrosis and Sleep, Department of Pediatrics, Emory University, Atlanta, GA, United States.
William R HuntDivision of Pulmonary, Allergy, Critical Care and Sleep Medicine, Department of Medicine, Emory University, Atlanta, GA, United States.
Ryan A HarrisDepartment of Medicine, Georgia Prevention Institute, Augusta University, Augusta, GA, United States.
Virginia A StallingsDivision of Gastroenterology, Hepatology, and Nutrition, Children's Hospital of Philadelphia, Philadelphia, PA, United States.
Elizabeth A IvieDivision of Endocrinology, Metabolism, and Lipids, Department of Medicine, Emory University, Atlanta, GA, United States.
Chris DriggersDivision of Pulmonary, Asthma, Cystic Fibrosis and Sleep, Department of Pediatrics, Emory University, Atlanta, GA, United States.
Jose N BinongoDepartment of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, Atlanta, GA, United States.
Thomas R ZieglerNutrition and Health Sciences Doctoral Program, Laney Graduate School, Emory University, Atlanta, GA, United States; Division of Endocrinology, Metabolism, and Lipids, Department of Medicine, Emory University, Atlanta, GA, United States.
Jessica A AlvarezNutrition and Health Sciences Doctoral Program, Laney Graduate School, Emory University, Atlanta, GA, United States; Division of Endocrinology, Metabolism, and Lipids, Department of Medicine, Emory University, Atlanta, GA, United States. Electronic address: jessica.alvarez@emory.edu.

Funding

Implementing a Maternal health and PRegnancy Outcomes Vision for Everyone (IMPROVE)UL1TR002378 · NCATS · EMORY UNIVERSITY · PI Andres J Garcia, Elizabeth O. Ofili · 2017 to 2026
$92.1M
Pilot & Feasibility CoreP30DK125013 · NIDDK · EMORY UNIVERSITY · PI NAEL A MCCARTY, Arlene A Stecenko · 2020 to 2026
$6.7M
A Dietary Intervention to Improve Glucose Tolerance in Adults with Cystic FibrosisR01DK133523 · NIDDK · EMORY UNIVERSITY · PI Jessica Alejandra Alvarez · 2022 to 2026
$3.2M
Integration of Nutritional Metabolomics with Bioenergetics in Cystic FibrosisK01DK102851 · NIDDK · EMORY UNIVERSITY · PI ALVAREZ, JESSICA ALEJANDRA · 2014 to 2018
$614k
NCATS NIH HHS UL1 TR002378NIDDK NIH HHS K01 DK102851NIDDK NIH HHS P30 DK125013NIDDK NIH HHS R01 DK133523
6 · The paper itself

Abstract

backgroundMuscle mass predicts clinical outcomes in people with cystic fibrosis (PwCF), but muscle quality remains insufficiently characterized. Furthermore, although CFTR modulators promote weight gain, their impact on the relationship between muscle and clinical outcomes is unknown.

objectivesTo quantify the relationships between skeletal muscle indicators and clinical outcomes in adults with cystic fibrosis (CF) and determine whether CFTR modulators and/or adiposity influence the relationships.

methodsThis cross-sectional study included 75 adults with CF and 73 controls without CF. Body composition [appendicular skeletal muscle mass index (ASMI), visceral fat, and total body fat] was measured by dual-energy X-ray absorptiometry. Muscle quality (via phase angle) was assessed using bioelectrical impedance analysis. Clinical outcomes included physical functionality [hand grip (HG) strength and 1-min sit-to-stand test result], lung function, and an oral glucose tolerance test result. Sarcopenia was defined as having low muscle mass and low HG strength. Statistical analyses included testing for effect modification in the relationships between variables.

resultsFive PwCF had sarcopenia compared with none of the controls. Despite similar BMI, PwCF had lower ASMI [β: -0.46; 95% confidence interval (CI): -0.88, -0.05; P = 0.02], HG strength (β: -3.6; 95% CI: -6.6, -0.61; P = 0.02), and muscle quality (β: -0.57; 95% CI: -0.93, -0.21; P = 0.01) compared with controls. In PwCF, lung function was positively associated with ASMI among people not taking CFTR modulators but not among users (interaction; β: -9.21; 95% CI: -16.87, -1.55; P = 0.01). Muscle quality (r = 0.35; 95% CI: 0.04, 0.59; P = 0.02) and HG strength (r = 0.36; 95% CI: 0.05, 0.60; P = 0.02) were positively related to insulin sensitivity. The positive relationship between ASMI and physical functionality was only significant among PwCF with low adiposity (interaction; β: -1.9; 95% CI: -3.51, -0.35; P = 0.02).

conclusionsMuscle mass, strength, and quality are lower in PwCF than in controls, with muscle strength and quality linked to glucose tolerance. Lung function relationships with muscle mass differ by CFTR modulator use, and excess adiposity attenuates strength-related functional benefits. This study highlights the need for personalized approaches to CF management.

Indexed as

AdiposityCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorMuscle, SkeletalAbsorptiometry, PhotonAdultBody CompositionCross-Sectional StudiesFemaleHumansMaleMuscle StrengthSarcopeniaYoung AdultCFTR protein, humanCystic Fibrosis Transmembrane Conductance Regulatorbody compositioncystic fibrosisglucose tolerancemuscle massphase angle

Identifiers

PMID40972870
PMCPMC12700035

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LicenceCC BY-NC-ND
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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.