Influence of soft tissue on bone density and microarchitecture measurements by high-resolution peripheral quantitative computed tomography.


Journal

Bone
ISSN: 1873-2763
Titre abrégé: Bone
Pays: United States
ID NLM: 8504048

Informations de publication

Date de publication:
07 2019
Historique:
received: 15 03 2019
revised: 11 04 2019
accepted: 13 04 2019
pubmed: 19 4 2019
medline: 30 7 2020
entrez: 19 4 2019
Statut: ppublish

Résumé

High-resolution peripheral quantitative computed tomography (HR-pQCT) is a non-invasive method of measuring volumetric bone mineral density (vBMD) and microarchitecture at the distal radius and tibia. With increasing use of this technology, it is crucial to understand the potential impact of overlying soft tissue on the accuracy of HR-pQCT measures. Thus, we examined the effects of a simulated increase in adiposity (via 6- and 12-mm thick layers of overlying circumferential fat) on HR-pQCT measures of a hydroxyapatite (HA) phantom and in women (n = 20, aged 18-75 years). In the phantom, increasing the amount of overlying fat tissue led to a corresponding decrease in the mean measured density for each HA rod. In women, fat-layering led to a decrease in total vBMD (-2.9 to -3.7%, p < 0.001), cortical vBMD (-1.4% to -5.5%, p < 0.001), and estimated failure load (-1.4 to -5.7%, p = 0.002) at the radius, with similar changes in the tibia. Trabecular microarchitectural measurements were also impacted by simulated adiposity, with fat-layering leading to decreased trabecular thickness and separation and increased trabecular number at the radius (Δ's = 5 to 12%) with more pronounced differences at the tibia (Δ's = 14 to 40%). At the tibia, fat-layering also led to decreased cortical thickness and increased cortical porosity. Altogether, these results demonstrate that overlying adipose tissue can lead to artifacts in bone measurements by HR-pQCT, resulting in an underestimation of vBMD and generally, an overestimation of bone microarchitecture impairment. Therefore, soft tissue artifact should be considered when interpreting HR-pQCT results, particularly in those with high BMI and/or marked changes in adiposity.

Identifiants

pubmed: 30998999
pii: S8756-3282(19)30136-X
doi: 10.1016/j.bone.2019.04.008
pii:
doi:

Substances chimiques

Durapatite 91D9GV0Z28

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

47-52

Subventions

Organisme : NCRR NIH HHS
ID : S10 RR023405
Pays : United States

Informations de copyright

Published by Elsevier Inc.

Auteurs

Signe Caksa (S)

Endocrine Unit, Massachusetts General Hospital, 50 Blossom Street, THR-1051 Boston, MA, USA.

Amy Yuan (A)

Endocrine Unit, Massachusetts General Hospital, 50 Blossom Street, THR-1051 Boston, MA, USA.

Sara E Rudolph (SE)

Endocrine Unit, Massachusetts General Hospital, 50 Blossom Street, THR-1051 Boston, MA, USA.

Elaine W Yu (EW)

Endocrine Unit, Massachusetts General Hospital, 50 Blossom Street, THR-1051 Boston, MA, USA; Harvard Medical School, 25 Shattuck St., Boston, MA, USA.

Kristin L Popp (KL)

Endocrine Unit, Massachusetts General Hospital, 50 Blossom Street, THR-1051 Boston, MA, USA; United States Army Research Institute of Environmental Medicine, 10 General Greene Ave, Natick, MA, USA; Harvard Medical School, 25 Shattuck St., Boston, MA, USA. Electronic address: kpopp@mgh.harvard.edu.

Mary L Bouxsein (ML)

Endocrine Unit, Massachusetts General Hospital, 50 Blossom Street, THR-1051 Boston, MA, USA; Harvard Medical School, 25 Shattuck St., Boston, MA, USA; Center for Advanced Orthopedic Studies, Beth Israel Deaconess Medical Center, One Overland Street, Boston, MA, USA.

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Classifications MeSH