Journal article icon

Journal article

Associations of Markers of Inflammatory Status and Adiposity with Bone Phenotype at Age 60–64 Years: Findings from the MRC National Survey of Health and Development

Alternative title:
Associations of Markers of Inflammatory Status and Adiposity with Bone Phenotype at Age 60–64 Years
Abstract:
This study investigated associations between markers of inflammatory status and adiposity (interleukin-6 [IL-6], adiponectin and leptin) and measures of bone phenotype and fractures. The Medical Research Council (MRC) National Survey of Health and Development (NSHD) is a British birth cohort study. Participants (born during the same week in 1946) with complete data on DXA and pQCT parameters, markers of inflammatory status and adiposity, and potential confounders (498 men and 474 women) were included in cross-sectional analyses. At age 60–64 years, bone phenotype was assessed by DXA and pQCT. Fractures were self-reported at ages 60–64 and 68–70 years. Multiple linear regression was used to determine associations of IL-6, adiponectin and leptin with bone phenotype (adjusted for fat and lean mass and lifestyle confounders). Standard deviation (SD) differences in outcomes per SD increases in exposures were estimated. Higher IL-6 levels were associated with lower total volumetric bone mineral density (vBMD) (− 0.10[− 0.19, 0.00]) in men, and higher areal BMD (aBMD) at the spine (0.12[0.03, 0.22]) and whole body (0.11[0.01, 0.20]) in women. Higher levels of adiponectin were associated with lower aBMD and trabecular vBMD. In women, higher leptin levels were associated with higher cortical vBMD (0.11[0.02, 0.20]). Higher adiponectin was associated with moderately increased odds of having a fragility fracture during adulthood in women (OR 1.16 [95% CI 0.94, 1.43, p = 0.18]). Our results highlight non-mechanical associations between markers of inflammatory status and adiposity with BMD and, in women, fractures. Ensuring inflammaging is minimised may be important in healthy bone ageing.
Publication status:
Published
Peer review status:
Peer reviewed

Actions

Access Document

Files:
Publisher copy:
10.1007/s00223-025-01380-y

Authors

More by this author
Role:
Author
ORCID:
0000-0002-5914-2180
More by this author
Role:
Author
ORCID:
0000-0003-3486-8353
More by this author
Role:
Author
ORCID:
0000-0001-7386-2857
More by this author
Role:
Author
ORCID:
0000-0003-3370-5720
More by this author
Role:
Author
ORCID:
0000-0002-3048-4961


More from this funder
Funder identifier:
https://ror.org/03x94j517
More from this funder
Funder identifier:
https://ror.org/044m9mw93


Publisher:
Springer
Journal:
Calcified Tissue International and Musculoskeletal Research More from this journal
Volume:
116
Issue:
1
Pages:
71
Article number:
71
Publication date:
2025-05-06
Acceptance date:
2025-04-20
DOI:
EISSN:
1432-0827
ISSN:
0171967X, 0171-967X


Language:
English
Keywords:
Pubs id:
2124284
UUID:
uuid_758587c9-e7cb-4b1e-a08a-978cc981737b
Local pid:
pubs:2124284
Source identifiers:
3604213
Deposit date:
2025-12-26
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

Terms of use


Views and Downloads






If you are the owner of this record, you can report an update to it here: Report update to this record

TO TOP