Osteoglycin Across the Adult Lifespan

Author:

Woessner Mary N1ORCID,Hiam Danielle2,Smith Cassandra13ORCID,Lin Xuzhu1,Zarekookandeh Navabeh1,Tacey Alexander13,Parker Lewan2,Landen Shanie1,Jacques Macsue1,Lewis Joshua R456ORCID,Brennan-Speranza Tara7,Voisin Sarah1,Duque Gustavo38ORCID,Eynon Nir1,Levinger Itamar13ORCID

Affiliation:

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

2. Institute for Physical Activity and Nutrition (IPAN), Deakin University, Geelong, VIC, Australia

3. Australian Institute for Musculoskeletal Science (AIMSS), The University of Melbourne and Western Health, Melbourne, VIC, Australia

4. Institute for Nutrition Research, School of Medical and Health Sciences, Edith Cowan University, Joondalup, WA, Australia

5. Medical School, Royal Perth Hospital Unit, The University of Western Australia, Perth, WA, Australia

6. The University of Sydney, School of Public Health, Sydney Medical School, Centre for Kidney Research, Children’s Hospital  at Westmead, NSW, Australia

7. Department of Physiology, University of Sydney, Sydney, NSW, Australia

8. Department of Medicine-Western Health, Melbourne Medical School, The University of Melbourne, Melbourne, VIC, Australia

Abstract

Abstract Context Osteoglycin (OGN) is a proteoglycan released from bone and muscle which has been associated with markers of metabolic health. However, it is not clear whether the levels of circulating OGN change throughout the adult lifespan or if they are associated with clinical metabolic markers or fitness. Objective We aimed to identify the levels of circulating OGN across the lifespan and to further explore the relationship between OGN and aerobic capacity as well as OGN’s association with glucose and HOMA-IR. Methods 107 individuals (46 males and 61 females) aged 21-87 years were included in the study. Serum OGN levels, aerobic capacity (VO2peak), glucose, and homeostatic model assessment for insulin resistance (HOMA-IR) were assessed. T-tests were used to compare participant characteristics between sexes. Regression analyses were performed to assess the relationship between OGN and age, and OGN and fitness and metabolic markers. Results OGN displayed a nonlinear, weak “U-shaped” relationship with age across both sexes. Men had higher levels of OGN than women across the lifespan (β = 0.23, P = .03). Age and sex explained 16% of the variance in OGN (adjusted R2 = 0.16; P < .001). Higher OGN was associated with higher VO2peak (β = 0.02, P = .001); however, those aged <50 showed a stronger positive relationship than those aged >50. A higher OGN level was associated with a higher circulating glucose level (β = 0.17, P < .01). No association was observed between OGN and HOMA-IR. Conclusion OGN was characterized by a U-shaped curve across the lifespan which was similar between sexes. Those with a higher aerobic capacity or higher glucose concentration had higher OGN levels. Our data suggest an association between OGN and aerobic fitness and glucose regulation. Future studies should focus on exploring the potential of OGN as a biomarker for chronic disease.

Funder

Victoria University Planetary Health Grant

National Heart Foundation Early Career Fellowship

National Health and Medical Research Council

Early Career Research Fellowship

Career Development Fellowship

Investigator Grant

National Heart Foundation of Australia Future Leader Fellowship

Australian Research Council

Publisher

The Endocrine Society

Subject

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

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