Short-term risk of fracture is increased by deficits in cortical and trabecular bone microarchitecture independent of DXA BMD and FRAX: bone microarchitecture international consortium (BoMIC) prospective cohorts.

bone microarchitecture bone mineral density high resolution peripheral quantitative computed tomography osteoporosis short-term fracture risk

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:
05 Sep 2024
Historique:
received: 14 12 2023
revised: 14 08 2024
accepted: 04 09 2024
medline: 5 9 2024
pubmed: 5 9 2024
entrez: 5 9 2024
Statut: aheadofprint

Résumé

Identifying individuals at risk for short-term fracture is essential to offer prompt beneficial treatment, especially since many fractures occur in those without osteoporosis by DXA-aBMD. We evaluated whether deficits in bone microarchitecture and density predict short-term fracture risk independent of the clinical predictors, DXA-BMD and FRAX. We combined data from eight cohorts to conduct a prospective study of bone microarchitecture at the distal radius and tibia (by HR-pQCT) and 2-year incidence of fracture (non-traumatic and traumatic) in 7327 individuals (4824 women, 2503 men, mean 69 ± 9 years). We estimated sex-specific hazard ratios (HR) for associations between bone measures and 2-year fracture incidence, adjusted for age, cohort, height and weight, and then additionally adjusted for femoral neck (FN) aBMD or FRAX for major osteoporotic fracture. Only 7% of study participants had FN T-score ≤ -2.5, whereas 53% had T-scores between -1.0 to -2.5 and 37% had T-scores ≥-1.0. Two-year cumulative fracture incidence was 4% (296/7327). Each SD decrease in radius cortical bone measures increased fracture risk by 38%-76% for women and men. After additional adjustment for FN-aBMD, risks remained increased by 28%-61%. Radius trabecular measures were also associated with 2-year fracture risk independently of FN-aBMD in women (HRs range: 1.21 per SD for trabecular separation to 1.55 for total vBMD). Decreased failure load was associated with increased fracture risk in both women and men (FN-aBMD ranges of adjusted HR = 1.47-2.42). Tibia measurement results were similar to radius results. Findings were also similar when models were adjusted for FRAX. In older adults, failure load and HR-pQCT measures of cortical and trabecular bone microarchitecture and density with strong associations to short-term fractures improved fracture prediction beyond aBMD and FRAX. Thus, HR-pQCT may be a useful adjunct to traditional assessment of short-term fracture risk in older adults, including those with T-scores above the osteoporosis range. Identifying individuals at risk for short-term fracture (within 2-years) is essential to offer prompt treatment. We examined bone microarchitecture at arm and lower leg for prediction of short-term fractures in 7327 older adults, independent of the common clinical practice measures — DXA-BMD and FRAX. After adjusting for other factors, we found that measures of failure load, cortical and trabecular bone microarchitecture and density predicted short-term risk of fracture beyond the usual clinical measures of DXA and FRAX. These measures of bone that indicate deficits in microarchitecture may be a useful adjunct to traditional assessment of fracture risk in older adults.

Autres résumés

Type: plain-language-summary (eng)
Identifying individuals at risk for short-term fracture (within 2-years) is essential to offer prompt treatment. We examined bone microarchitecture at arm and lower leg for prediction of short-term fractures in 7327 older adults, independent of the common clinical practice measures — DXA-BMD and FRAX. After adjusting for other factors, we found that measures of failure load, cortical and trabecular bone microarchitecture and density predicted short-term risk of fracture beyond the usual clinical measures of DXA and FRAX. These measures of bone that indicate deficits in microarchitecture may be a useful adjunct to traditional assessment of fracture risk in older adults.

Identifiants

pubmed: 39236248
pii: 7749959
doi: 10.1093/jbmr/zjae143
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.

Auteurs

Marine Sarfati (M)

INSERM UMR1033, Université de Lyon, Hôpital Edouard Herriot, Lyon, France.

Roland Chapurlat (R)

INSERM UMR1033, Université de Lyon, Hôpital Edouard Herriot, Lyon, France.

Alyssa B Dufour (AB)

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

Elisabeth Sornay-Rendu (E)

INSERM UMR1033, Université de Lyon, Hôpital Edouard Herriot, Lyon, France.

Blandine Merle (B)

INSERM UMR1033, Université de 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.

Pawel Szulc (P)

INSERM UMR1033, Université de Lyon, Hôpital Edouard Herriot, Lyon, France.

Andy Kin On Wong (AKO)

Toronto General Hospital and University Health Network; and Dept of Epidemiology, Dalla Lana School of Public Health, University of Toronto, Toronto, CA.

Eric Lespessailles (E)

Regional University Hospital of Orléans, PRIMMO, 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.

Claes Ohlsson (C)

Sahlgrenska Osteoporosis Centre, Centre for Bone & Arthritis Research, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

Mattias Lorentzon (M)

Sahlgrenska Osteoporosis Centre, Department of Internal Medicine and Clinical Nutrition, Institute of Medicine, University of Gothenburg, Gothenburg, Sweden.
Region Västra Götaland, Department of Geriatric Medicine, Sahlgrenska University Hospital, Mölndal, Sweden.

Dan Mellström (D)

Sahlgrenska Osteoporosis Centre, Centre for Bone & Arthritis Research, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

Maria Nethander (M)

Sahlgrenska Osteoporosis Centre, Centre for Bone & Arthritis Research, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Bioinformatics and Data Center, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

Elizabeth J Samelson (EJ)

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

Mary L Bouxsein (ML)

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

Classifications MeSH