Ultrasound-Based Estimates of Cortical Bone Thickness and Porosity Are Associated With Nontraumatic Fractures in Postmenopausal Women: A Pilot Study.


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 2019
Historique:
received: 18 09 2018
revised: 21 02 2019
accepted: 10 03 2019
pubmed: 27 3 2019
medline: 23 9 2020
entrez: 27 3 2019
Statut: ppublish

Résumé

Recent ultrasound (US) axial transmission techniques exploit the multimode waveguide response of long bones to yield estimates of cortical bone structure characteristics. This pilot cross-sectional study aimed to evaluate the performance at the one-third distal radius of a bidirectional axial transmission technique (BDAT) to discriminate between fractured and nonfractured postmenopausal women. Cortical thickness (Ct.Th) and porosity (Ct.Po) estimates were obtained for 201 postmenopausal women: 109 were nonfractured (62.6 ± 7.8 years), 92 with one or more nontraumatic fractures (68.8 ± 9.2 years), 17 with hip fractures (66.1 ± 10.3 years), 32 with vertebral fractures (72.4 ± 7.9 years), and 17 with wrist fractures (67.8 ± 9.6 years). The areal bone mineral density (aBMD) was obtained using DXA at the femur and spine. Femoral aBMD correlated weakly, but significantly with Ct.Th (R = 0.23, p < 0.001) and Ct.Po (R = -0.15, p < 0.05). Femoral aBMD and both US parameters were significantly different between the subgroup of all nontraumatic fractures combined and the control group (p < 0.05). The main findings were that (1) Ct.Po was discriminant for all nontraumatic fractures combined (OR = 1.39; area under the receiver operating characteristic curve [AUC] equal to 0.71), for vertebral (OR = 1.96; AUC = 0.84) and wrist fractures (OR = 1.80; AUC = 0.71), whereas Ct.Th was discriminant for hip fractures only (OR = 2.01; AUC = 0.72); there was a significant association (2) between increased Ct.Po and vertebral and wrist fractures when these fractures were not associated with any measured aBMD variables; (3) between increased Ct.Po and all nontraumatic fractures combined independently of aBMD neck; and (4) between decreased Ct.Th and hip fractures independently of aBMD femur. BDAT variables showed comparable performance to that of aBMD neck with all types of fractures (OR = 1.48; AUC = 0.72) and that of aBMD femur with hip fractures (OR = 2.21; AUC = 0.70). If these results are confirmed in prospective studies, cortical BDAT measurements may be considered useful for assessing fracture risk in postmenopausal women. © 2019 American Society for Bone and Mineral Research.

Identifiants

pubmed: 30913320
doi: 10.1002/jbmr.3733
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1585-1596

Subventions

Organisme : Azalée
Pays : International
Organisme : Fondation pour la Recherche Médicale
ID : DBS201311228444
Pays : International
Organisme : MSD
Pays : International

Informations de copyright

© 2019 American Society for Bone and Mineral Research.

Auteurs

J-G Minonzio (JG)

Laboratoire d'Imagerie Biomédicale, Sorbonne Université, CNRS, INSERM, Paris, France.

N Bochud (N)

Laboratoire d'Imagerie Biomédicale, Sorbonne Université, CNRS, INSERM, Paris, France.

Q Vallet (Q)

Laboratoire d'Imagerie Biomédicale, Sorbonne Université, CNRS, INSERM, Paris, France.

D Ramiandrisoa (D)

Laboratoire d'Imagerie Biomédicale, Sorbonne Université, CNRS, INSERM, Paris, France.

A Etcheto (A)

Department of Rheumatology, Cochin Hospital, Epidemiology and Biostatistics Sorbonne Paris Cité, Research Center, INSERM U1153, Paris Descartes University, Paris, France.

K Briot (K)

Department of Rheumatology, Cochin Hospital, Epidemiology and Biostatistics Sorbonne Paris Cité, Research Center, INSERM U1153, Paris Descartes University, Paris, France.

S Kolta (S)

Department of Rheumatology, Cochin Hospital, Epidemiology and Biostatistics Sorbonne Paris Cité, Research Center, INSERM U1153, Paris Descartes University, Paris, France.

C Roux (C)

Department of Rheumatology, Cochin Hospital, Epidemiology and Biostatistics Sorbonne Paris Cité, Research Center, INSERM U1153, Paris Descartes University, Paris, France.

P Laugier (P)

Laboratoire d'Imagerie Biomédicale, Sorbonne Université, CNRS, INSERM, Paris, France.

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Classifications MeSH