Bony proliferations in rheumatoid arthritis, psoriatic arthritis and osteoarthritis using high‐resolution peripheral quantitative computed tomography—A systematic literature review

Author:

Moen Haakon Vilstrup12ORCID,Hänel Mathias23ORCID,Therkildsen Josephine23ORCID,Klose‐Jensen Rasmus23ORCID,Keller Kresten Krarup23ORCID,Hauge Ellen Margrethe23ORCID

Affiliation:

1. Department of Internal Medicine Gødstrup Regional Hospital Gødstrup Denmark

2. Department of Clinical Medicine Aarhus University Aarhus Denmark

3. Department of Rheumatology Aarhus University Hospital Aarhus Denmark

Abstract

AbstractPurposeOsteoarthritis (OA), rheumatoid arthritis (RA), and psoriatic arthritis (PsA) can all lead to the formation of bony proliferations (BP). This systematic review aimed to examine the characteristics of BPs in patients with RA, PsA, OA, and healthy controls (HC) using high‐resolution peripheral quantitative computed tomography (HR‐pQCT). Secondarily, we examined any treatment‐related effect on BP number and size.MethodsA systematic literature search was conducted in PubMed and Embase, and a total of 15 studies were included.ResultsSeven studies demonstrated a disease‐specific variation in BP location. One study showed no difference in the number of BPs between patients with PsA and OA. The number of BPs was greater in patients with PsA compared to RA in one study, and to HC in another study, while one study documented no difference in the number of BPs between patients with RA and HC. Five studies showed larger BPs in patients with PsA compared to HC, and one study larger BPs in patients with PsA compared to RA. One study showed no difference in BP size between patients with PsA and OA. Secukinumab may have a potential effect on arresting BP progression. Otherwise, no other treatment was reported to influence BP size and progression. No standard definitions or measurement techniques for BPs using HR‐pQCT have been identified.ConclusionBPs showed disease‐specific variations in location, size, and number. Results regarding treatment‐related effects are sparse. An agreement on the definition and measurement technique for BPs using HR‐pQCT is warranted for diagnostic accuracy, disease comparability, and monitoring potential.

Publisher

Wiley

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