Fracture risk based on HR-pQCT measures does not vary with age in older adults - the bone microarchitecture international consortium (BoMIC) prospective cohort study.

Fracture risk cohort study high resolution peripheral quantitative computed tomography osteoporosis

Journal

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
ISSN: 1523-4681
Titre abrégé: J Bone Miner Res
Pays: England
ID NLM: 8610640

Informations de publication

Date de publication:
03 Mar 2024
Historique:
received: 02 08 2023
revised: 25 01 2024
medline: 13 3 2024
pubmed: 13 3 2024
entrez: 13 3 2024
Statut: aheadofprint

Résumé

Fracture risk increases with lower areal BMD (aBMD); however, aBMD-related estimate of risk may decrease with age. This may depend on technical limitations of 2-dimensional (2D) DXA which are reduced with 3D high-resolution peripheral quantitative computed tomography (HR-pQCT). Our aim was to examine whether the predictive utility of HR-pQCT measures with fracture varies with age. We analyzed associations of HR-pQCT measures at the distal radius and distal tibia with two outcomes: incident fractures and major osteoporotic fractures. We censored follow-up time at first fracture, death, last contact or 8 years after baseline. We estimated hazard ratios (HR) and 95%CI for the association between bone traits and fracture incidence across age quintiles. Among 6835 men and women (ages 40-96) with at least one valid baseline HR-pQCT scan who were followed prospectively for a median of 48.3 months, 681 sustained fractures. After adjustment for confounders, bone parameters at both the radius and tibia were associated with higher fracture risk. The estimated HRs for fracture did not vary significantly across age quintiles for any HR-pQCT parameter measured at either the radius or tibia. In this large cohort, the homogeneity of the associations between the HR-pQCT measures and fracture risk across age groups persisted for all fractures and for major osteoporotic fractures. The patterns were similar regardless of the HR-pQCT measure, the type of fracture, or the statistical models. The stability of the associations between HR-pQCT measures and fracture over a broad age range shows that bone deficits or low volumetric density remain major determinants of fracture risk regardless of age group. The lower risk for fractures across measures of aBMD in older adults in other studies may be related to factors which interfere with DXA but not with HR-pQCT measures.

Identifiants

pubmed: 38477737
pii: 7618444
doi: 10.1093/jbmr/zjae033
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the American Society for Bone and Mineral Research. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Pawel Szulc (P)

INSERM UMR1033, University of Lyon, Hôpital Edouard Herriot, Lyon, France.

Alyssa B Dufour (AB)

Hinda and Arthur Marcus Institute for Aging Research, Hebrew SeniorLife, and Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States.

Marian T Hannan (MT)

Hinda and Arthur Marcus Institute for Aging Research, Hebrew SeniorLife, and Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States.

Douglas P Kiel (DP)

Hinda and Arthur Marcus Institute for Aging Research, Hebrew SeniorLife, and Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States.

Roland Chapurlat (R)

INSERM UMR1033, University of Lyon, Hôpital Edouard Herriot, Lyon, France.

Elisabeth Sornay-Rendu (E)

INSERM UMR1033, University of Lyon, Hôpital Edouard Herriot, Lyon, France.

Blandine Merle (B)

INSERM UMR1033, University of Lyon, Hôpital Edouard Herriot, Lyon, France.

Steven K Boyd (SK)

McCaig Institute for Bone and Joint Health, University of Calgary, Calgary AB, Canada.

Danielle E Whittier (DE)

McCaig Institute for Bone and Joint Health, University of Calgary, Calgary AB, Canada.

David A Hanley (DA)

McCaig Institute for Bone and Joint Health, University of Calgary, Calgary AB, Canada.

David Goltzman (D)

Departments of Medicine, McGill University and McGill University Health Centre, Montreal, Quebec, Canada.

Andy Kin On Wong (AKO)

Joint Department of Medical Imaging, University Health Network; and Division of Epidemiology, Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.

Eric Lespessailles (E)

Department of Rheumatology and PRIMMO, University Hospital of Orléans, Orléans, France.

Sundeep Khosla (S)

Division of Endocrinology and Kogod Center on Aging, Mayo Clinic, Rochester, MN, United States.

Serge Ferrari (S)

Division of Bone Diseases, Geneva University Hospitals and Faculty of Medicine, University of Geneva.

Emmanuel Biver (E)

Division of Bone Diseases, Geneva University Hospitals and Faculty of Medicine, University of Geneva.

Mary L Bouxsein (ML)

Dept of Orthopedic Surgery, Harvard Medical School, Center for Advanced Orthopedic Studies, BIDMC, Boston, MA, United States.

Elizabeth J Samelson (EJ)

Hinda and Arthur Marcus Institute for Aging Research, Hebrew SeniorLife, and Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States.

Classifications MeSH