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. 2017 Oct 24;19(1):243.
doi: 10.1186/s13075-017-1448-0.

Ultrasound verified inflammation and structural damage in patients with hereditary haemochromatosis-related arthropathy

Affiliations

Ultrasound verified inflammation and structural damage in patients with hereditary haemochromatosis-related arthropathy

Christian Dejaco et al. Arthritis Res Ther. .

Abstract

Background: Chronic arthropathy occurs in approximately two thirds of patients with hereditary haemochromatosis (HH). The aim was to study inflammatory and structural lesions in patients with HH with (HH-A) and without arthropathy (HH-WA) using ultrasonography.

Methods: This was a cross-sectional study of 26 patients with HH-A, 24 with HH-WA and 37 with hand osteoarthritis (HOA). Clinical examination was performed in 68 joints, and we retrieved data on hand function, pain and global disease activity (all using a visual analogue scale (VAS)), morning stiffness and ferritin levels. Standard x-ray and ultrasound were conducted in 36 joints (hands, hips, knees and ankles), and we graded grey scale synovitis (GSS), power Doppler ultrasound (PD), osteophytes, erosions, tenosynovitis and cartilage damage semi-quantitatively in accordance with prior publications.

Results: Ultrasound revealed a high proportion of inflammatory changes in HH-A; GSS was found in 96.2% and PD signals in 80.8% of patients (median GSS score 9, PD score 2.5). The frequency of these findings was similar in HOA. Inflammation was also common in HH-WA, yielding GSS in 83.3% and PD signals in 50.0% of patients. Cartilage damage was most prominent in HH-A as compared to HH-WA and HOA (median scores 11.0, 2.5 and 2.0, respectively). The prevalence and extent of erosions and osteophytes were similar in all groups. None of the ultrasound scores was associated with pain or function; GSS, PD, osteophyte and cartilage scores correlated with x-ray-verified structural damage.

Conclusion: A high prevalence of ultrasound-verified inflammation and cartilage damage was found in HH-A, and to a lesser extent in HH-WA. These findings were associated with x-ray-verified damage but not with clinical scores of pain and function.

Keywords: Arthritis; Haemochromatosis; Hand osteoarthritis; Ultrasonography.

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Conflict of interest statement

Ethics approval and consent to participate

This study was approved by the institutional review boards of the Medical University Graz (24-142 ex 11/12), the Land Salzburg (415-E/1262/2-2010) and the city of Vienna (EK-12-005-VK), and written informed consent of each patient was obtained.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Figures

Fig. 1
Fig. 1
Ultrasound image examples of patients with hereditary haemochromatosis. a Longitudinal dorsal scan of a metacarpophalangeal (MCP) joint (left = proximal) indicating an extensive proximal osteophyte (arrow) and a smaller osteophyte in the distal part of the joint (broken arrow). b, c Longitudinal dorsal scan of MCP joints indicating a proximal osteophyte (arrow), grey scale synovitis (arrow heads) and power Doppler signals (asterix). d Transverse suprapatellar scan of a knee indicating calcium pyrophosphate deposition in the hyaline cartilage (arrow)
Fig. 2
Fig. 2
Ultrasound scores in patients with hereditary haemochromatosis and hand osteoarthritis. Total grey scale synovitis (GSS) and power Doppler (PD) scores are shown in patients with hereditary haemochromatosis without arthropathy (HH-WA), haemochromatosis with arthropathy (HH-A) and hand osteoarthritis (HOA). p < 0.1 and *p < 0.05 for analysis using the Mann-Whitney U test (p values are not adjusted for multiple testing)

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