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dc.contributor.authorMuñoz-Muñoz, M
dc.contributor.authorBond, B
dc.contributor.authorSánchez-Martín, C
dc.contributor.authorRodríguez-Gómez, I
dc.contributor.authorWeston, M
dc.contributor.authorGarcía-Aguirre, M
dc.contributor.authorMorin-Martin, MM
dc.contributor.authorAlegre Durán, L
dc.contributor.authorLeal-Martin, J
dc.contributor.authorAlcazar, J
dc.contributor.authorAra, I
dc.contributor.authorGarcía-García, FJ
dc.date.accessioned2024-07-12T09:18:26Z
dc.date.issued2024-07-24
dc.date.updated2024-07-09T15:54:47Z
dc.description.abstractExcess adipose tissue may promote chronic systemic inflammation and oxidative stress, causing endothelial damage. Early evidence indicates that obesity may be associated with poorer cerebral perfusion. The purpose of this study was to examine the relationship between body composition and cerebral hemodynamics. A total of 248 middle-aged adults (50-58 years old; 55% women) underwent a ramp test on a cycle-ergometer until volitional exhaustion. Gas exchange was assessed on a breath-by-breath basis. Mean middle cerebral artery velocity (MCAv) was measured using transcranial Doppler, and pulsatility index (PI) calculated. Body composition was assessed by dual X-ray absorptiometry. Statistical analyses were performed using a compositional data approach including a three-compartment model for body composition (trunk fat mass, extremities fat mass, and fat-free mass). The unadjusted models for the whole sample showed that trunk fat mass relative to other compartments was negatively associated with MCAvrest, MCAvmax, and gain, and positively associated with PImax; extremities fat mass relative to other compartments was positively associated with MCAvrest and MCAvmax, and negatively associated with PImax; and fat-free mass relative to other compartments was positively associated with PImax. These associations were sex-dependent, remaining in the women’s subgroup. However, after adjusting for confounders, these associations became non-significant, except for PImax in the whole sample and women’s subgroup. These findings suggest a possible association between cerebral hemodynamics and body composition in middle-aged adults, highlighting sex-specific differences. Moreover, our results indicate that higher trunk fat mass relative to other compartments may negatively impact cerebral hemodynamics, reducing MCAv and increasing PImax.en_GB
dc.description.sponsorshipInstituto de Salud Carlos III, Carlos III Health Instituteen_GB
dc.description.sponsorshipConsorcio Centro de Investigación Biomédica en Red (CIBER)en_GB
dc.description.sponsorshipInstituto de Salud Carlos III, Ministerio de Ciencia e Innovaciónen_GB
dc.description.sponsorshipMinisterio de Ciencia e Innovación y Universidadesen_GB
dc.description.sponsorshipUniversity of Castilla-La Mancha, Toledo, Spainen_GB
dc.identifier.citationPublished online 24 July 2024en_GB
dc.identifier.doi10.1093/gerona/glae182
dc.identifier.grantnumberPI18/00972en_GB
dc.identifier.grantnumberCB16/10/00477en_GB
dc.identifier.grantnumberCB16/10/00456en_GB
dc.identifier.grantnumberFPU19/01276en_GB
dc.identifier.grantnumber2019-PREDUCLM-11385en_GB
dc.identifier.grantnumber2020- 506 PREDUCLM-14936en_GB
dc.identifier.grantnumberCD23/00236en_GB
dc.identifier.urihttp://hdl.handle.net/10871/136695
dc.identifierORCID: 0000-0003-3597-8562 (Bond, Bert)
dc.language.isoenen_GB
dc.publisherOxford University Press (OUP) / The Gerontological Society of Americaen_GB
dc.rights.embargoreasonUnder embargo until 24 July 2025 in compliance with publisher policyen_GB
dc.rights© The Author(s) 2024. Published by Oxford University Press on behalf of The Gerontological Society of America
dc.subjectcerebrovasculatureen_GB
dc.subjectcardiovascularen_GB
dc.subjectadiposeen_GB
dc.subjectcerebral hemodynamicsen_GB
dc.subjectexercise testingen_GB
dc.subjectcardiovascular risken_GB
dc.subjectfat distributionen_GB
dc.titleRelationship of body composition with middle cerebral artery hemodynamic using compositional data analysis in middle-age adults from Toledo Study for Healthy Ageingen_GB
dc.typeArticleen_GB
dc.date.available2024-07-12T09:18:26Z
dc.identifier.issn1079-5006
dc.descriptionThis is the author accepted manuscript. The final version is available from Oxford University Press via the DOI in this recorden_GB
dc.identifier.eissn1758-535X
dc.identifier.journalThe Journals of Gerontology, Series A: Biological Sciences and Medical Sciencesen_GB
dc.rights.urihttp://www.rioxx.net/licenses/all-rights-reserveden_GB
dcterms.dateAccepted2024-07-09
dcterms.dateSubmitted2024-03-01
rioxxterms.versionAMen_GB
rioxxterms.licenseref.startdate2024-07-09
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2024-07-09T15:54:49Z
refterms.versionFCDAM
refterms.panelAen_GB
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