Publication:
Usefulness of Muscle Ultrasonography in the Nutritional Assessment of Adult Patients with Cystic Fibrosis.

dc.contributor.authorSánchez-Torralvo, Francisco José
dc.contributor.authorPorras, Nuria
dc.contributor.authorRuiz-García, Ignacio
dc.contributor.authorMaldonado-Araque, Cristina
dc.contributor.authorGarcía-Olivares, María
dc.contributor.authorGirón, María Victoria
dc.contributor.authorGonzalo-Marín, Montserrat
dc.contributor.authorOlveira, Casilda
dc.contributor.authorOlveira, Gabriel
dc.date.accessioned2024-02-27T15:10:18Z
dc.date.available2024-02-27T15:10:18Z
dc.date.issued2022-08-17
dc.description.abstractBackground: Muscle ultrasonography of the quadriceps rectus femoris (QRF) is a technique on the rise in the assessment of muscle mass in application of nutritional assessment. The aim of the present study is to assess the usefulness of muscle ultrasonography in patients with cystic fibrosis, comparing the results with other body composition techniques such as anthropometry, bioelectrical impedance analysis (BIA), dual-energy X-ray absorptiometry (DXA), and handgrip strength (HGS). At the same time, we intend to assess the possible association with the nutritional and respiratory status. Methods: This was a prospective observational study in adult patients with cystic fibrosis in a clinically stable situation. Muscle ultrasonography of the QRF was performed, and the results were compared with other measures of body composition: anthropometry, BIA, and DXA. HGS was used to assess muscle function. Respiratory parameters were collected, and nutritional status was assessed using Global Leadership Initiative on Malnutrition (GLIM) criteria. Results: A total of 48 patients were included, with a mean age of 34.1 ± 8.8 years. In total, 24 patients were men, and 24 patients were women. Mean BMI was 22.5 ± 3.8 kg/m2. Mean muscular area rectus anterior (MARA) was 4.09 ± 1.5 cm2, and mean muscular circumference rectus was 8.86 ± 1.61 cm. A positive correlation was observed between the MARA and fat-free mass index (FFMI) determined by anthropometry (r = 0.747; p < 0.001), BIA (r = 0.780; p < 0.001), and DXA (r = 0.678; p < 0.001), as well as muscle function (HGS: r = 0.790; p < 0.001) and respiratory parameters (FEV1; r = 0.445, p = 0.005; FVC: r = 0.376, p = 0.02; FEV1/FVC: r = 0.344, p = 0.037). A total of 25 patients (52.1%) were diagnosed with malnutrition according to GLIM criteria. Differences were observed when comparing the MARA based on the diagnosis of malnutrition (4.75 ± 1.65 cm2 in normo-nourished vs. 3.37 ± 1.04 in malnourished; p = 0.014). Conclusions: In adults with cystic fibrosis, the measurements collected by muscle ultrasound of the QRF correlate adequately with body composition techniques such as anthropometry, BIA, DXA, and handgrip strength. Muscle ultrasound measurements, particularly the MARA, are related to the nutritional status and respiratory function of these patients.
dc.format.number16es_ES
dc.format.volume14es_ES
dc.identifier.doi10.3390/nu14163377
dc.identifier.e-issn2072-6643es_ES
dc.identifier.journalNutrientses_ES
dc.identifier.otherhttp://hdl.handle.net/10668/21495
dc.identifier.pubmedID36014883es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/18740
dc.language.isoeng
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectGLIM criteria
dc.subjectcystic fibrosis
dc.subjectmalnutrition
dc.subjectmuscle mass
dc.subjectmuscle ultrasound
dc.subjectultrasonography
dc.subject.meshAbsorptiometry, Photon
dc.subject.meshAdult
dc.subject.meshBody Composition
dc.subject.meshBody Mass Index
dc.subject.meshCystic Fibrosis
dc.subject.meshElectric Impedance
dc.subject.meshFemale
dc.subject.meshHand Strength
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshMalnutrition
dc.subject.meshNutrition Assessment
dc.subject.meshNutritional Status
dc.subject.meshQuadriceps Muscle
dc.subject.meshUltrasonography
dc.titleUsefulness of Muscle Ultrasonography in the Nutritional Assessment of Adult Patients with Cystic Fibrosis.
dc.typeresearch article
dc.type.hasVersionVoR
dspace.entity.typePublication

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