Näytä suppeat kuvailutiedot

dc.contributor.authorOwen, Patrick J.
dc.contributor.authorDaly, Robin M.
dc.contributor.authorDalla Via, Jack
dc.contributor.authorMundell, Niamh L.
dc.contributor.authorLivingston, Patricia M.
dc.contributor.authorRantalainen, Timo
dc.contributor.authorFraser, Steve F.
dc.date.accessioned2019-09-18T06:12:05Z
dc.date.available2019-09-18T06:12:05Z
dc.date.issued2019
dc.identifier.citationOwen, P. J., Daly, R. M., Dalla Via, J., Mundell, N. L., Livingston, P. M., Rantalainen, T., & Fraser, S. F. (2019). Does Use of Androgen Deprivation Therapy (ADT) in Men with Prostate Cancer Increase the Risk of Sarcopenia?. <i>Calcified Tissue International</i>, <i>105</i>(4), 403-411. <a href="https://doi.org/10.1007/s00223-019-00586-1" target="_blank">https://doi.org/10.1007/s00223-019-00586-1</a>
dc.identifier.otherCONVID_32138298
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/65536
dc.description.abstractAndrogen deprivation therapy (ADT) for prostate cancer (PCa) can compromise muscle health. Hence, we aimed to quantify the prevalence of sarcopenia (i.e., compromised lean mass, muscle strength, and physical function) in ADT-treated (> 12 week) men (n = 70) compared to similarly aged non-ADT-treated PCa (n = 52) and healthy controls (n = 70). Lean and fat mass were quantified by dual-energy X-ray absorptiometry. Muscle strength and function were measured using handgrip dynamometry and gait speed, respectively. Sarcopenia was defined as low adjusted appendicular lean mass [ALM; height-adjusted (ALMI), body mass index-adjusted (ALMBMI) and height and fat mass-adjusted (ALMHFM)] with weak handgrip strength and/or slow gait speed according to the following criteria: European Working Group on Sarcopenia in Older People [EWGSOP; both 2010 (EWGSOP1) and 2018 (EWGSOP2)], Foundation for the National Institutes of Health (FNIH) and International Working Group on Sarcopenia (IWGS). Overall the prevalence of sarcopenia was low and did not differ between the three groups. Only two (3.2%) ADT-treated men presented with sarcopenia as per EWGSOP1 and FNIH criteria, whereas no cases were observed using EWGSOP2 and IWGS criteria. The prevalence of low ALMBMI was greater in ADT-treated men (32%) compared to PCa (15%; P = 0.037) and healthy controls (7.1%; P < 0.001). Similarly, low ALMHFM was greater in ADT-treated men (29%) compared to healthy controls only (13%; P = 0.019). There was also a low prevalence of weak muscle strength and slow gait speed (0.0–11%) in all men, with no differences between the groups. Based on these findings, an adiposity-based adjustment of ALM is recommended to quantify risk of adverse outcomes associated with ADT in these men.en
dc.format.mimetypeapplication/pdf
dc.languageeng
dc.language.isoeng
dc.publisherSpringer New York LLC
dc.relation.ispartofseriesCalcified Tissue International
dc.rightsCC BY 4.0
dc.subject.otheratrofia
dc.subject.otherkasvaimet
dc.subject.othereturauhanen
dc.subject.otherkehonkoostumus
dc.subject.otherlihakset
dc.subject.otherlihavuus
dc.titleDoes Use of Androgen Deprivation Therapy (ADT) in Men with Prostate Cancer Increase the Risk of Sarcopenia?
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201909184183
dc.contributor.laitosLiikuntatieteellinen tiedekuntafi
dc.contributor.laitosFaculty of Sport and Health Sciencesen
dc.contributor.oppiaineGerontologia ja kansanterveysfi
dc.contributor.oppiaineGerontologian tutkimuskeskusfi
dc.contributor.oppiaineHyvinvoinnin tutkimuksen yhteisöfi
dc.contributor.oppiaineGerontology and Public Healthen
dc.contributor.oppiaineGerontology Research Centeren
dc.contributor.oppiaineSchool of Wellbeingen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange403-411
dc.relation.issn0171-967X
dc.relation.numberinseries4
dc.relation.volume105
dc.type.versionpublishedVersion
dc.rights.copyright© The Authors, 2019
dc.rights.accesslevelopenAccessfi
dc.subject.ysolihakset
dc.subject.ysoeturauhanen
dc.subject.ysokasvaimet
dc.subject.ysokehonkoostumus
dc.subject.ysolihavuus
dc.subject.ysoatrofia
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p2784
jyx.subject.urihttp://www.yso.fi/onto/yso/p20465
jyx.subject.urihttp://www.yso.fi/onto/yso/p2299
jyx.subject.urihttp://www.yso.fi/onto/yso/p26989
jyx.subject.urihttp://www.yso.fi/onto/yso/p823
jyx.subject.urihttp://www.yso.fi/onto/yso/p20904
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1007/s00223-019-00586-1
jyx.fundinginformationThis research did not receive any specific grant from any funding agency in the public, commercial or not-for-profit sector.
dc.type.okmA1


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