Accelerated Bone Loss in Older Men With Severe Abdominal Aortic Calcification—the Prospective MINOS Study

Author:

Szulc Pawel1ORCID,Lewis Joshua R23,Chapurlat Roland1

Affiliation:

1. INSERM UMR 1033, University of Lyon, Hospices Civils de Lyon , 69437, Lyon , France

2. Institute for Nutrition Research, Edith Cowan University , Joondalup, Perth, WA 6027 , Australia

3. Medical School, the University of Western Australia , Perth, WA 6009 , Australia

Abstract

Abstract Context Data on the association between the severity of abdominal aortic calcification (AAC) and bone loss are discordant. Objective Our aim was to assess the association between baseline AAC and prospectively assessed bone loss in older men. Methods This prospective cohort study started in 1995 (MINOS). Men aged 50 to 85 years (n = 778) had AAC assessed on the lateral radiograph of the spine using Kauppila's semiquantitative score and was followed prospectively for 7.5 years. Bone mineral density (BMD) and bone mineral content (BMC) were measured by dual-energy x-ray absorptiometry every 18 months. Statistical analysis was performed using linear mixed models. Results In comparison to men without AAC (AAC = 0), severe AAC (>6) was associated with more rapid bone loss at the total hip (−0.62 ± 0.06 vs −0.32 ± 0.04%/year; P < .001), trochanter, and distal forearm (−0.72 ± 0.06 vs −0.45 ± 0.03%/year; P < .001). The highest decile (AAC >10) was associated with more rapid bone loss at the femoral neck, whole body, and ultradistal radius (−0.86 ± 0.12 vs −0.34 ± 0.05%/year; P < .001). The results were similar for BMD and for BMC. The patterns were similar in sensitivity analyses (eg, after excluding men with abdominal obesity, after excluding current smokers, after excluding men with ischemic heart disease or with diabetes mellitus, after excluding men with abnormal concentrations of lipids, bioavailable 17β-estradiol or 25-hydroxycholecalciferol, after excluding men with glomerular filtration rate <60 mL/min). Conclusion Severe AAC is associated with faster bone loss in older men and may contribute to the higher fracture risk observed in this population.

Funder

Merck Sharp & Dohme Chibret

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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