A Fracture Risk Assessment Tool for High Resolution Peripheral Quantitative Computed Tomography.

BONE MICROARCHITECTURE FRACTURE PREDICTION HIGH RESOLUTION PERIPHERAL QUANTITATIVE COMPUTED TOMOGRAPHY MACHINE LEARNING OSTEOPOROSIS RISK ASSESSMENT

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: United States
ID NLM: 8610640

Informations de publication

Date de publication:
09 2023
Historique:
revised: 10 02 2023
received: 13 04 2022
accepted: 21 03 2023
pmc-release: 01 09 2024
medline: 25 9 2023
pubmed: 3 5 2023
entrez: 3 5 2023
Statut: ppublish

Résumé

Most fracture risk assessment tools use clinical risk factors combined with bone mineral density (BMD) to improve assessment of osteoporosis; however, stratifying fracture risk remains challenging. This study developed a fracture risk assessment tool that uses information about volumetric bone density and three-dimensional structure, obtained using high-resolution peripheral quantitative compute tomography (HR-pQCT), to provide an alternative approach for patient-specific assessment of fracture risk. Using an international prospective cohort of older adults (n = 6802) we developed a tool to predict osteoporotic fracture risk, called μFRAC. The model was constructed using random survival forests, and input predictors included HR-pQCT parameters summarizing BMD and microarchitecture alongside clinical risk factors (sex, age, height, weight, and prior adulthood fracture) and femoral neck areal BMD (FN aBMD). The performance of μFRAC was compared to the Fracture Risk Assessment Tool (FRAX) and a reference model built using FN aBMD and clinical covariates. μFRAC was predictive of osteoporotic fracture (c-index = 0.673, p < 0.001), modestly outperforming FRAX and FN aBMD models (c-index = 0.617 and 0.636, respectively). Removal of FN aBMD and all clinical risk factors, except age, from μFRAC did not significantly impact its performance when estimating 5-year and 10-year fracture risk. The performance of μFRAC improved when only major osteoporotic fractures were considered (c-index = 0.733, p < 0.001). We developed a personalized fracture risk assessment tool based on HR-pQCT that may provide an alternative approach to current clinical methods by leveraging direct measures of bone density and structure. © 2023 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).

Identifiants

pubmed: 37132542
doi: 10.1002/jbmr.4808
pmc: PMC10523935
mid: NIHMS1886053
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1234-1244

Subventions

Organisme : NIAMS NIH HHS
ID : R01 AR027065
Pays : United States
Organisme : NHLBI NIH HHS
ID : N01 HC025195
Pays : United States
Organisme : NHLBI NIH HHS
ID : N01HC25195
Pays : United States
Organisme : NIAMS NIH HHS
ID : R01 AR061445
Pays : United States
Organisme : NIAMS NIH HHS
ID : R01 AR041398
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2023 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).

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Auteurs

Danielle E Whittier (DE)

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

Elizabeth J Samelson (EJ)

Hinda and Arthur Marcus Institute for Aging Research, Hebrew Senior Life, Harvard Medical School, Boston, MA, USA.
Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.

Marian T Hannan (MT)

Hinda and Arthur Marcus Institute for Aging Research, Hebrew Senior Life, Harvard Medical School, Boston, MA, USA.
Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.

Lauren A Burt (LA)

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

David A Hanley (DA)

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

Emmanuel Biver (E)

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

Pawel Szulc (P)

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

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.

Roland Chapurlat (R)

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

Eric Lespessailles (E)

Regional Hospital of Orleans, PRIMMO and EA 4708-I3MTO, University of Orleans, Orleans, France.

Andy Kin On Wong (AKO)

Joint Department of Medical Imaging, University Health Network, Dalla Lana School of Public Health, University of Toronto, Toronto, CA, USA.
Department of Epidemiology, Dalla Lana School of Public Health, University of Toronto, Toronto, CA, USA.

David Goltzman (D)

Department of Medicine, McGill University and McGill University Health Centre, Montreal, QC, Canada.

Sundeep Khosla (S)

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

Serge Ferrari (S)

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

Mary L Bouxsein (ML)

Center for Advanced Orthopedic Studies, BIDMC, Harvard Medical School, Boston, MA, USA.
Endocrine Unit, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Department of Orthopedic Surgery, Harvard Medical School, Boston, MA, USA.

Douglas P Kiel (DP)

Hinda and Arthur Marcus Institute for Aging Research, Hebrew Senior Life, Harvard Medical School, Boston, MA, USA.
Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.

Steven K Boyd (SK)

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

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Classifications MeSH