Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/34828
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dc.contributor.authorRamchand, Sabashini K-
dc.contributor.authorHoermann, Rudolf-
dc.contributor.authorWhite, Shane-
dc.contributor.authorYeo, Belinda-
dc.contributor.authorFrancis, Prudence A-
dc.contributor.authorXu, Cecilia L H-
dc.contributor.authorZajac, Jeffrey D-
dc.contributor.authorSeeman, Ego-
dc.contributor.authorGrossmann, Mathis-
dc.date2024-
dc.date.accessioned2024-01-11T01:55:20Z-
dc.date.available2024-01-11T01:55:20Z-
dc.date.issued2024-01-05-
dc.identifier.citationThe Journal of Clinical Endocrinology and Metabolism 2024-01-05en_US
dc.identifier.issn1945-7197-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/34828-
dc.description.abstractMenopause is associated with changes in musculoskeletal, body composition, and metabolic parameters that may be amplified in premenopausal women receiving estradiol suppression for breast cancer. Denosumab offsets deleterious skeletal effects of estradiol suppression and has been reported to have effects on body composition and metabolic parameters in pre-clinical and observational studies, though evidence from double-blind randomized controlled trials is limited. To assess the effect of denosumab on body composition and metabolic parameters. In a pre-specified secondary analysis of a 12-month randomized, double-blind, placebo-controlled trial, 68 premenopausal women with breast cancer initiating ovarian function suppression and aromatase inhibition were randomized to denosumab 60-mg or placebo administered at baseline and 6 months. Outcome measures were total and regional fat and lean mass (DXA), body mass index (BMI), waist and hip circumference, fasting glucose, HOMA-IR, and lipid profile. Using a mixed model, between-group mean adjusted differences, MAD, [95% confidence interval], over time are reported. Over 12 months, relative to placebo, android and gynoid fat mass decreased in the denosumab group (-266 g [95%CI -453 to -79], P = 0.02, and -452 g [95%CI -783 to -122], P = 0.03, respectively). Total fat mass and waist circumference were lower in the denosumab group but not significantly so (-1792g [95% CI -3346 to -240], P = 0.08 and (- 3.77 cm [95% CI -6.76 to -0.79], P = 0.06, respectively). No significant treatment effects were detected in lean mass, BMI, hip circumference, fasting glucose, HOMA-IR, or lipid profile. In premenopausal women receiving estradiol suppression, denosumab decreases some measures of fat mass with no detectable effects on other measures of body composition or metabolic parameters.en_US
dc.language.isoeng-
dc.subjectbody compositionen_US
dc.subjectbreast canceren_US
dc.subjectdenosumaben_US
dc.subjectestradiol suppressionen_US
dc.subjectglucose metabolismen_US
dc.subjectlipidsen_US
dc.titleCardiometabolic Effects of Denosumab in Premenopausal Women with Breast Cancer Receiving Estradiol Suppression: RCT.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleThe Journal of Clinical Endocrinology and Metabolismen_US
dc.identifier.affiliationMedicine (University of Melbourne)en_US
dc.identifier.affiliationDepartment of Medicine, Austin Health, University of Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationOlivia Newton-John Cancer Wellness and Research Centreen_US
dc.identifier.affiliationDepartment of Medicine, Austin Health, University of Melbourne, Victoria, Australia.;Olivia Newton-John Cancer & Wellness Centre, Austin Health, Victoria, Australia.en_US
dc.identifier.affiliationPeter MacCallum Cancer Centre, Sir Peter MacCallum Department of Oncology, University of Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationDepartment of Medicine, Austin Health, University of Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationDepartment of Medicine, Austin Health, University of Melbourne, Victoria, Australia.;Department of Endocrinology, Austin Health, Victoria, Australia.en_US
dc.identifier.affiliationDepartment of Medicine, Austin Health, University of Melbourne, Victoria, Australia.;Department of Endocrinology, Austin Health, Victoria, Australia.en_US
dc.identifier.affiliationDepartment of Medicine, Austin Health, University of Melbourne, Victoria, Australia.;Department of Endocrinology, Austin Health, Victoria, Australia.en_US
dc.identifier.doi10.1210/clinem/dgae003en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-6755-8469en_US
dc.identifier.orcid0000-0001-8261-3457en_US
dc.identifier.pubmedid38181438-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptEndocrinology-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
crisitem.author.deptMedical Oncology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptEndocrinology-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptEndocrinology-
crisitem.author.deptEndocrinology-
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