Associations of Osteocalcin Forms With Metabolic Syndrome and Its Individual Components in Older Men: The Health In Men Study

Author:

Liu Xiaoying1ORCID,Yeap Bu B23ORCID,Brock Kaye E1,Levinger Itamar45ORCID,Golledge Jonathan67ORCID,Flicker Leon28ORCID,Brennan-Speranza Tara C19

Affiliation:

1. School of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Sydney, New South Wales, Australia

2. Medical School, University of Western Australia, Perth, Western Australia, Australia

3. Department of Endocrinology and Diabetes, Fiona Stanley Hospital, Perth, Western Australia, Australia

4. Institute for Health and Sport (IHES), Victoria University, Melbourne, Victoria, Australia

5. Australian Institute for Musculoskeletal Science (AIMSS), Department of Medicine-Western Health, Melbourne Medical School, The University of Melbourne, Melbourne, Victoria, Australia

6. Queensland Research Centre for Peripheral Vascular Disease, James Cook University, Townsville, Queensland, Australia

7. Department of Vascular and Endovascular Surgery, Townsville University Hospital, Townsville, Queensland, Australia

8. Western Australian Centre for Health and Ageing, University of Western Australia, Perth, Western Australia, Australia

9. School of Public Health, Faculty of Medicine and Health, The University of Sydney, Sydney, New South Wales, Australia

Abstract

Abstract Context The osteoblast-derived polypeptide, osteocalcin (OC), has been associated with lower risk of type 2 diabetes and metabolic syndrome (MetS) in several epidemiological studies. Animal studies have indicated the undercarboxylated form of OC (ucOC) drives its association with metabolic outcomes. Objective We compared associations of ucOC and carboxylated OC (cOC) with MetS and its components in older men. Methods A cross-sectional analysis of 2575 men aged ≥70 years and older resident in Perth, Western Australia. ucOC was assayed using a hydroxyapatite-binding method, and cOC calculated by subtracting ucOC from total OC. Main outcome measures were MetS and its components. Results Both lower serum ucOC and cOC levels, and the proportion of cOC (%cOC) were associated with less favorable metabolic parameters (higher waist circumference, triglyceride, glucose, blood pressure, and lower high-density lipoprotein cholesterol), whereas inverse associations were found with %ucOC. Men in the lowest quintile of ucOC had higher risk of MetS compared to men in the highest quintile (Q1 ≤ 7.7 vs Q5 > 13.8 ng/mL; OR = 2.4; 95% CI, 1.8-3.2). Men in the lowest quintile of cOC had higher risk of MetS compared to those in the highest quintile (≤ 5.8 vs > 13.0 ng/mL; OR = 2.4; 95% CI, 1.8-3.2). Conclusion Lower concentrations of serum ucOC or cOC were associated with less favorable metabolic parameters and a higher risk of MetS. In contrast, a lower proportion of ucOC was associated with better metabolic parameters and lower MetS risk. Further research is warranted to determine whether ucOC and cOC are suitable biomarkers for cardiometabolic risk in men.

Funder

National Heart Foundation of Australia

National Health and Medical Research Council of Australia

Publisher

The Endocrine Society

Subject

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

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