Identificador persistente para citar o vincular este elemento: https://accedacris.ulpgc.es/jspui/handle/10553/153716
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dc.contributor.authorIglesias Hernandez, Natalia Covadongaen_US
dc.contributor.authorRamos Carrasco, Aracelien_US
dc.contributor.authorDe Luis Roman, Daniel Antonioen_US
dc.contributor.authorDe Pablos Velasco, Pedro Luisen_US
dc.contributor.authorCalanas Continente, Alfonsoen_US
dc.contributor.authorRodriguez Soto, Miren Josuneen_US
dc.contributor.authorLopez-Gomez, Juan Joseen_US
dc.contributor.authorComi Diaz, Cristinaen_US
dc.contributor.authorGarcia-Rey, Silviaen_US
dc.contributor.authorPerez-Rambla, Claraen_US
dc.contributor.authorGarcia-Luna, Pedro Pabloen_US
dc.date.accessioned2025-12-16T16:33:07Z-
dc.date.available2025-12-16T16:33:07Z-
dc.date.issued2025en_US
dc.identifier.issn2296-861Xen_US
dc.identifier.otherWoS-
dc.identifier.urihttps://accedacris.ulpgc.es/jspui/handle/10553/153716-
dc.description.abstractBackground and aims The recent global trend toward reducing the consumption of animal-derived products has contributed to a growing demand for plant-based oral nutritional supplement (pbONS) options. PbONS, in addition to achieving good compliance, have an improvement in nutritional status (increased energy and protein intake, body weight, and BMI) on malnourished patients. However, there is no evidence of their impact compared to animal-based ONS (aONS). Methods A multicenter, open-label, and non-inferiority trial (NCT06055543) was conducted in 5 tertiary hospitals in Spain. Adult malnourished outpatients requiring high-energy ONS for at least 12 weeks (1.5 kcal/ml;200 ml, 2 bottles/day), having signed informed consent, were recruited and randomly assigned (1:1) to receive pbONS or aONS. Randomization was performed using a pre-generated list embedded in the electronic data entry platform. The total number of participants randomized was 149, 75 patients in aONS group and 74 in pONS group. Baseline and final characteristics of the two groups were described and compared in terms of sociodemographic, clinical, compliance, and satisfaction variables. Results A total of 129 patients who received pbONS (66) or aONS (74) were included. Weight increased significantly from 55.1 +/- 12.7 kg to 57.4 +/- 13.1 kg (p-value < 0.001) in the aONS group, and from 55.0 +/- 10.7 kg to 57.1 +/- 10.7 kg (p-value < 0.001) in the pbONS group, with no significant differences between groups (p = 0.659). It was further confirmed that pbONS is not inferior to aONS in terms of body weight gain. According to GLIM criteria, patients improved their nutritional status 92.1% (58/63) in the aONS group and 95.5% (63/66) in the pbONS group with no statistical difference between groups (p-value = 0.425). Functional strength was increased after 12 weeks: 55.6% (35/63) in aONS and 60.6% (40/66) in pbONS, with no significant difference between groups (p-value = 0.346). Gastrointestinal Symptom Rating Scale (GSRS) scores were lower in both groups at 12 weeks, indicating a reduction in symptom severity. Conclusion PbONS are as effective and well-tolerated as traditional ONS in improving nutritional outcomes, with high patient satisfaction in malnourished patients. This study provides valuable evidence for integrating pbONS into routine clinical practice for the tailored management of patients.en_US
dc.languageengen_US
dc.relation.ispartofFrontiers In Nutritionen_US
dc.sourceFrontiers In Nutrition[ISSN 2296-861X],v. 12, (Noviembre 2025)en_US
dc.subject32 Ciencias médicasen_US
dc.subject3206 Ciencias de la nutriciónen_US
dc.subject.otherOlder-Adultsen_US
dc.subject.otherHigh-Proteinen_US
dc.subject.otherImpacten_US
dc.subject.otherTasteen_US
dc.subject.otherRisken_US
dc.subject.otherMalnourished Patientsen_US
dc.subject.otherOral Nutritional Supplementen_US
dc.subject.otherNutritional Statusen_US
dc.subject.otherPlant-Based Dieten_US
dc.subject.otherGastrointestinal Toleranceen_US
dc.titleEffect of a new plant-based high-energy oral nutritional supplement in adult malnourished patients: an open-label, randomized clinical trialen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.3389/fnut.2025.1667954en_US
dc.identifier.isi001631021200001-
dc.relation.volume12en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.contributor.daisngidNo ID-
dc.contributor.daisngid29714358-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngid6835100-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.description.numberofpages15en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Hernández, NCI-
dc.contributor.wosstandardWOS:Carrasco, AR-
dc.contributor.wosstandardWOS:Román, DAD-
dc.contributor.wosstandardWOS:de Pablos-Velasco, PL-
dc.contributor.wosstandardWOS:Continente, AC-
dc.contributor.wosstandardWOS:Soto, MJR-
dc.contributor.wosstandardWOS:Lopez-Gomez, JJ-
dc.contributor.wosstandardWOS:Comi-Díaz, C-
dc.contributor.wosstandardWOS:García-Rey, S-
dc.contributor.wosstandardWOS:Pérez-Rambla, C-
dc.contributor.wosstandardWOS:García-Luna, PP-
dc.date.coverdateNoviembre 2025en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr0,828
dc.description.jcr4,0
dc.description.sjrqQ1
dc.description.jcrqQ2
dc.description.esciESCI
dc.description.miaricds8,3
item.grantfulltextopen-
item.fulltextCon texto completo-
crisitem.author.deptGIR IUIBS: Rendimiento humano, ejercicio físico y salud-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.orcid0000-0002-9190-2581-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameDe Pablos Velasco, Pedro Luis-
Colección:Artículos
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