{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T16:02:29Z","timestamp":1785427349636,"version":"3.56.0"},"reference-count":45,"publisher":"American Medical Association (AMA)","issue":"7","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Netw Open"],"abstract":"<jats:sec id=\"ab-zoi260726-4\">\n                    <jats:title>Importance<\/jats:title>\n                    <jats:p>Aromatase inhibitors (AIs) profoundly suppress estrogen synthesis and accelerate bone loss in postmenopausal women with early breast cancer (EBC). Although body mass index (BMI)\u2013defined obesity has been considered protective for skeletal health, emerging evidence suggests a paradoxical association with fracture risk.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260726-5\">\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>To evaluate whether fat mass percentage (FM%) greater than 40.8%, measured by dual-energy x-ray absorptiometry (DXA), is associated with vertebral fracture (VF) progression in patients with EBC receiving AIs.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260726-6\">\n                    <jats:title>Design, Settings, and Participants<\/jats:title>\n                    <jats:p>This retrospective cohort study included consecutive postmenopausal women with EBC (stages I-III) recruited in a single referral center between September 2014 and June 2024. All patients received adjuvant endocrine therapy and underwent serial DXA assessments. Patients treated with tamoxifen or with major comorbidities affecting skeletal fragility were excluded.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260726-7\">\n                    <jats:title>Exposures<\/jats:title>\n                    <jats:p>Body composition and bone fragility parameters evaluated by DXA at baseline and at 18, 24, and 30 months.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260726-8\">\n                    <jats:title>Main Outcomes and Measures<\/jats:title>\n                    <jats:p>Adiposity excess was defined as FM% greater than 40.8%, and VF progression was defined as new incident fractures and\/or worsening by at least 1 Genant grade at a previously fractured vertebral level. Their association was evaluated using a joint model; time-dependent associations were evaluated using extended Cox regression. Secondary analyses explored associations with bone mineral density, trabecular bone score (TBS), appendicular lean mass index (ALMI), and traditional fracture risk factors.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260726-9\">\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      A total of 769 White women (median [range] age, 63 [30-87] years; median [range] BMI, 24.6 [15.6-46.1]) entered the study. During follow-up, 69 patients (9.0%) experienced VF progression. FM% greater than 40.8% was independently associated with increased VF progression (adjusted hazard ratio [HR], 2.00; 95% CI, 1.44-2.82;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001). Higher ALMI (HR, 0.38; 95% CI, 0.22-0.65;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001) and BMD (HR, 0.79; 95% CI, 0.66-0.94;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009=\u2009.01) were associated with lower risk of VF progression.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260726-10\">\n                    <jats:title>Conclusions and Relevance<\/jats:title>\n                    <jats:p>In this retrospective cohort study of patients with EBC receiving AIs, adiposity excess was identified as a novel fracture risk factor, whereas higher muscle mass was protective. These findings support incorporating body-composition assessment into fracture-risk evaluation and preventive strategies for patients undergoing AI therapy.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1001\/jamanetworkopen.2026.26450","type":"journal-article","created":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T15:30:26Z","timestamp":1785425426000},"page":"e2626450","source":"Crossref","is-referenced-by-count":0,"title":["Adiposity Excess and Vertebral Fractures in Patients With Breast Cancer Taking Aromatase Inhibitors"],"prefix":"10.1001","volume":"9","author":[{"given":"Greta","family":"Schivardi","sequence":"first","affiliation":[{"name":"Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health (DSMC), University of Brescia, Brescia, Italy"},{"name":"Medical Oncology Unit, ASST Spedali Civili di Brescia Comprehensive Cancer Center, Brescia, 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