Peripheral quantitative computed tomography in the assessment of bone mineral density in anti-TNF-treated rheumatoid arthritis and ankylosing spondylitis patients.

Ankylosing spondylitis Biologics Bone density Osteoporosis Peripheral quantitative computed tomography Rheumatoid arthritis

Journal

BMC musculoskeletal disorders
ISSN: 1471-2474
Titre abrégé: BMC Musculoskelet Disord
Pays: England
ID NLM: 100968565

Informations de publication

Date de publication:
23 Sep 2021
Historique:
received: 08 04 2021
accepted: 11 09 2021
entrez: 24 9 2021
pubmed: 25 9 2021
medline: 28 9 2021
Statut: epublish

Résumé

Rheumatoid arthritis (RA) and ankylosing spondylitis (AS) are associated with osteoporosis. There have not been many peripheral quantitative computed tomography (QCT) studies in patients receiving biologics. We assessed volumetric and areal bone mineral density (BMD) by forearm QCT and dual-energy X-ray absorptiometry (DXA), respectively in addition to laboratory biomarkers in these arthritides. Forty RA and AS patients treated with either etanercept (ETN) or certolizumab pegol (CZP) were undergoing follow-ups for one year. Volumetric and areal BMD, as well as parathyroid hormone (PTH), osteocalcin, RANKL, 25-hydroxyvitamin D (VITD), P1NP, CTX, sclerostin (SOST), Dickkopf 1 (DKK-1) and cathepsin K (CATHK) were determined. We did not observe any further bone loss during the 12-month treatment period. Volumetric and areal BMD showed significant correlations with each other (p<0.017 after Bonferroni's correction). Trabecular QCT BMD at baseline (p=0.015) and cortical QCT BMD after 12 months (p=0.005) were inversely determined by disease activity at baseline in the full cohort. Trabecular QCT BMD at baseline also correlated with CTX (p=0.011). In RA, CRP negatively (p=0.014), while SOST positively (p=0.013) correlated with different QCT parameters. In AS, RANKL at baseline (p=0.014) and after 12 months (p=0.007) correlated with cortical QCT BMD. In the full cohort, 12-month change in QTRABBMD was related to TNF inhibition together with elevated VITD-0 levels (p=0.031). Treatment and lower CATHK correlated with QCORTBMD changes (p=0.006). In RA, TNF inhibition together with VITD-0 (p<0.01) or CATHK-0 (p=0.002), while in AS, treatment and RANKL-0 (p<0.05) determined one-year changes in QCT BMD. BMD as determined by QCT did not change over one year of anti-TNF treatment. Disease activity, CATHK, RANKL and VITD may be associated with the effects of anti-TNF treatment on QCT BMD changes. RA and AS may differ in this respect.

Identifiants

pubmed: 34556105
doi: 10.1186/s12891-021-04708-5
pii: 10.1186/s12891-021-04708-5
pmc: PMC8461899
doi:

Substances chimiques

Tumor Necrosis Factor Inhibitors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

817

Informations de copyright

© 2021. The Author(s).

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Auteurs

Balázs Juhász (B)

Department of Oncology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Katalin Gulyás (K)

Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Nagyerdei str. 98, Debrecen, 4032, Hungary.

Ágnes Horváth (Á)

Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Nagyerdei str. 98, Debrecen, 4032, Hungary.

Edit Végh (E)

Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Nagyerdei str. 98, Debrecen, 4032, Hungary.

Anita Pusztai (A)

Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Nagyerdei str. 98, Debrecen, 4032, Hungary.

Ágnes Szentpétery (Á)

Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Nagyerdei str. 98, Debrecen, 4032, Hungary.
Department of Rheumatology, Uppsala University Hospital, Uppsala, Sweden.
Conway Institute for Biomolecular Research, University College Dublin, Dublin, Ireland.

Zsófia Pethő (Z)

Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Nagyerdei str. 98, Debrecen, 4032, Hungary.

Nóra Bodnár (N)

Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Nagyerdei str. 98, Debrecen, 4032, Hungary.

Attila Hamar (A)

Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Nagyerdei str. 98, Debrecen, 4032, Hungary.

Levente Bodoki (L)

Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Nagyerdei str. 98, Debrecen, 4032, Hungary.

Harjit Pal Bhattoa (HP)

Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Éva Szekanecz (É)

Department of Oncology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Katalin Hodosi (K)

Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Nagyerdei str. 98, Debrecen, 4032, Hungary.

Andrea Domján (A)

Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Nagyerdei str. 98, Debrecen, 4032, Hungary.

Szilvia Szamosi (S)

Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Nagyerdei str. 98, Debrecen, 4032, Hungary.

Csaba Horváth (C)

First Department of Medicine, Semmelweis University, Budapest, Hungary.

Sándor Szántó (S)

Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Nagyerdei str. 98, Debrecen, 4032, Hungary.
Department of Sports Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Gabriella Szűcs (G)

Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Nagyerdei str. 98, Debrecen, 4032, Hungary.

Hennie G Raterman (HG)

Department of Rheumatology, Northwest Clinics, Alkmaar, The Netherlands.

Willem F Lems (WF)

Amsterdam Rheumatology and Immunology Centre, Amsterdam, The Netherlands.

Oliver FitzGerald (O)

Conway Institute for Biomolecular Research, University College Dublin, Dublin, Ireland.

Zoltán Szekanecz (Z)

Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Nagyerdei str. 98, Debrecen, 4032, Hungary. szekanecz.zoltan@med.unideb.hu.

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