Evidence map›Paper›PMID 40329072›Full record

ArticleCalcified tissue international2025

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.

Ruth Durdin, Camille Pearse, Diana Kuh, Rachel Cooper, Elaine M Dennison, Cyrus Cooper, Kate A Ward

Abstract read
In one paragraph

Article in Calcified tissue international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Ruth DurdinMRC Lifecourse Epidemiology Centre, University of Southampton, Southampton General Hospital, Southampton, UK.ORCID http://orcid.org/0000-0002-5914-2180
Camille PearseMRC Lifecourse Epidemiology Centre, University of Southampton, Southampton General Hospital, Southampton, UK.ORCID http://orcid.org/0000-0003-3486-8353
Diana KuhMRC Unit for Lifelong Health and Ageing, University College London, London, UK.ORCID http://orcid.org/0000-0001-7386-2857
Rachel CooperAGE Research Group, Translational and Clinical Research Institute, Newcastle University, Newcastle Upon Tyne, UK.ORCID http://orcid.org/0000-0003-3370-5720
Elaine M DennisonMRC Lifecourse Epidemiology Centre, University of Southampton, Southampton General Hospital, Southampton, UK.ORCID http://orcid.org/0000-0002-3048-4961
Cyrus CooperMRC Lifecourse Epidemiology Centre, University of Southampton, Southampton General Hospital, Southampton, UK.ORCID http://orcid.org/0000-0003-3510-0709
Kate A WardMRC Lifecourse Epidemiology Centre, University of Southampton, Southampton General Hospital, Southampton, UK. kw@mrc.soton.ac.uk.ORCID http://orcid.org/0000-0001-7034-6750

Funding

Medical Research Council MC_PC_21001Medical Research Council MC_PC_21003Medical Research Council MC_UU_00019/1Medical Research Council MC_UU_00019/4National Institute for Health and Care Research NIHR203319NIHR Newcastle Biomedical Research Centre NIHR203309
6 · The paper itself

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.

Indexed as

AdiposityBone and BonesInflammationAdiponectinAgedBiomarkersBone DensityCohort StudiesCross-Sectional StudiesFemaleFractures, BoneHumansInterleukin-6LeptinMaleMiddle AgedAdiponectinBiomarkersInterleukin-6LeptinAgeingBody compositionBone mineral densityDual energy X-ray absorptiometryInflammationPeripheral quantitative computed tomography

Identifiers

PMID40329072
PMCPMC12055629

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.