DXA-Based Bone Strain Index: A New Tool to Evaluate Bone Quality in Primary Hyperparathyroidism.


Journal

The Journal of clinical endocrinology and metabolism
ISSN: 1945-7197
Titre abrégé: J Clin Endocrinol Metab
Pays: United States
ID NLM: 0375362

Informations de publication

Date de publication:
13 07 2021
Historique:
received: 02 12 2020
pubmed: 9 5 2021
medline: 21 10 2021
entrez: 8 5 2021
Statut: ppublish

Résumé

Primary hyperparathyroidism (PHPT) is associated with impaired bone quality and increased fracture risk. Reliable tools for the evaluation of bone quality parameters are not yet clinically available. Bone Strain Index (BSI) is a new metric for bone strength based on Finite Element Analysis from lumbar spine and femoral neck dual-energy x-ray absorptiometry (DXA) images. To assess the lumbar spine (LS), femoral neck (FN), and total hip (TH) BSI in PHPT patients compared with controls and to investigate the association of BSI with vertebral fractures (VFs) in PHPT. This case-control study enrolled 50 PHPT patients and 100 age- and sex-matched control subjects from an outpatient clinic. The main outcome measures were LS-BSI, FN-BSI, and TH-BSI. FN bone mineral density (BMD) and one-third distal radius BMD were lower in the PHPT group than in controls (FN 0.633 ± 0.112 vs 0.666 ± 0.081, P = 0.042; radius 0.566 ± 0.07 vs 0.625 ± 0.06, P < 0.001). PHPT group has significant lower TBS score compared with controls (1.24 ± 0.09 vs 1.30 ± 0.10, P < 0.001). BSI was significantly higher at LS (2.28 ± 0.59 vs 2.02 ± 0.43, P = 0.009), FN (1.72 ± 0.41 vs 1.49 ± 0.35, P = 0.001), and TH (1.51 ± 0.33 vs 1.36 ± 0.25, P = 0.002) in PHPT. LS-BSI showed moderate accuracy for discriminating VFs (AUC 0.667; 95% CI, 0.513-0.820). LS-BSI ≥ 2.2 and was a statistically significant independent predictor of VFs, with an adjusted odds ratio ranging from 5.7 to 15.1. BSI, a DXA-derived bone quality index, is impaired in PHPT and may help to identify PHPT subjects at high risk of fractures.

Identifiants

pubmed: 33963754
pii: 6272395
doi: 10.1210/clinem/dgab317
pmc: PMC8599893
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

2304-2312

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Auteurs

Gaia Tabacco (G)

Unit of Endocrinology and Diabetes, Campus Bio-Medico University of Rome, Rome, Italy.

Anda M Naciu (AM)

Unit of Endocrinology and Diabetes, Campus Bio-Medico University of Rome, Rome, Italy.

Carmelo Messina (C)

IRCCS Istituto Ortopedico Galeazzi, Milan, Italy.
Department of Biomedical Sciences for Health, Università degli Studi di Milano, Milano, Italy.

Gianfranco Sanson (G)

School of Nursing, Clinical Department of Medical, Surgical and Health Sciences, University of Trieste, Trieste, Italy.

Luca Rinaudo (L)

TECHNOLOGIC Srl, Torino, Italy.

Roberto Cesareo (R)

UOS Malattie Metaboliche, Santa Maria Goretti Hospital, Latina, Italy.

Stefania Falcone (S)

Unit of Endocrinology and Metabolic Diseases, CTO A. Alesini Hospital, University Tor Vergata, Rome, Italy.

Silvia Manfrini (S)

Unit of Endocrinology and Diabetes, Campus Bio-Medico University of Rome, Rome, Italy.

Nicola Napoli (N)

Unit of Endocrinology and Diabetes, Campus Bio-Medico University of Rome, Rome, Italy.

John P Bilezikian (JP)

Department of Medicine, Division of Endocrinology, Vagelos College of Physicians & Surgeons, Columbia University, New York, New York 10032, USA.

Fabio M Ulivieri (FM)

U.O. Medicina Nucleare, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milano, Italy.

Andrea Palermo (A)

Unit of Endocrinology and Diabetes, Campus Bio-Medico University of Rome, Rome, Italy.

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