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dc.contributor.authorRamos-Hernández, Rafael
dc.contributor.authorMiguel Ortega, Alvaro
dc.contributor.authorMartínez Ferrán, María
dc.contributor.authorFernández-Lázaro, Diego
dc.contributor.authorBusto Vázquez, Natalia 
dc.contributor.authorMielgo Ayuso, Juan 
dc.date.accessioned2026-01-13T12:57:16Z
dc.date.available2026-01-13T12:57:16Z
dc.date.issued2025-10
dc.identifier.issn2509-2715
dc.identifier.urihttps://hdl.handle.net/10259/11211
dc.description.abstractSarcopenia is a major contributor to frailty and functional decline among older adults. Combining exercise with nutritional strategies such as creatine monohydrate (CRE) and β-hydroxy-β-methylbutyrate (HMB) supplementation may help to preserve strength and independence. To evaluate the effects of 6-week CRE + HMB supplementation combined with an integral physical conditioning (IPC) program on functional strength and body composition in physically active older adults. In a randomized, double-blind, placebo-controlled crossover trial, 30 older adults (20 men, 10 women; ≥ 60 years) completed two 6-week intervention periods (CRE + HMB or placebo) separated by a 3-week washout. The IPC program performed in both conditions consisted of four supervised weekly sessions combining strength, power, multicomponent circuits, high-intensity interval and moderate intensity continuous training), performed at 40–100% training heart rate (THR) and 20–90% one-repetition maximum (1RM) and structured as warm-up, main part and cooldown. Functional strength and body composition (bioelectrical impedance analysis) were assessed pre- and post-intervention, respectively. Significant time × group interactions were observed for fat mass, fat-free mass, total muscle mass, skeletal muscle mass, appendicular skeletal muscle mass, muscle mass index, skeletal muscle index and ALM/BMI (all p < 0.05). The CRE + HMB group showed reductions in fat mass and body fat percentage, with slight numerical increases in muscle parameters, whereas the placebo group exhibited opposite trends. However, within-group changes were not statistically significant. In contrast, CRE + HMB significantly improved multiple functional strength outcomes, including leg/back strength, arm flexion strength, upper-body endurance (dumbbell flexion, push-ups, isometric hold) and core endurance (crunches). Regression analyses suggested that these improvements were largely independent of changes in muscle mass, supporting a potential neuromuscular mechanism. Six weeks of CRE + HMB supplementation combined with IPC enhanced functional strength and endurance in active older adults, largely independent of changes in muscle mass. This combined approach represents a promising strategy for preserving functional capacity and promoting healthy ageing.en
dc.description.sponsorshipOpen access funding provided by FEDER European Funds and the Junta de Castilla y León under the Research and Innovation Strategy for Smart Specialization (RIS3) of Castilla y León 2021-2027. This research did not receive any specific grants from funding agencies in the public, commercial, or notfor-profit sectors.en
dc.format.mimetypeapplication/pdf
dc.language.isoenges
dc.publisherSpringeres
dc.relation.ispartofGeroScience. 2025es
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectCreatine monohydrateen
dc.subjectβ-Hydroxy-βmethylbutyrateen
dc.subjectFunctional strengthen
dc.subjectSarcopeniaen
dc.subjectOlder adultsen
dc.subjectMulticomponent exerciseen
dc.subjectMuscle qualityen
dc.subjectNeuromuscular adaptationsen
dc.subjectHealthy agingen
dc.subjectBody compositionen
dc.subject.otherFisiología del ejercicioes
dc.subject.otherExercise-Physiological aspectsen
dc.subject.otherSuplementos nutricionaleses
dc.subject.otherDietary supplementsen
dc.titleCombined creatine and HMB co-supplementation improves functional strength independent of muscle mass in physically active older adults: a randomized crossover trialen
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.relation.publisherversionhttps://doi.org/10.1007/s11357-025-01889-yes
dc.identifier.doi10.1007/s11357-025-01889-y
dc.identifier.essn2509-2723
dc.journal.titleGeroSciencees
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones


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