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Inflammatory osteoarthritis of the hand

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Inflammatory or erosive are terms used interchangeably to define a clinical subset of osteoarthritis of the hand (HOA), targeting interphalangeal joints and characterised by an abrupt onset, marked pain and functional impairment, inflammatory symptoms and signs, including stiffness, soft tissue swelling, erythema, paraesthesiae, mildly elevated C-reactive protein and a worse outcome than non-erosive HOA. This subset is defined radiographically by subchondral erosion, cortical destruction and subsequent reparative change, which may include bony ankylosis. Although the presence of both clinical and radiographic aspects are very suggestive for the diagnosis in most cases, doubts have been recently raised from some studies which, by means of sensitive imaging techniques such as magnetic resonance imaging (MRI) and sonography, had found erosive changes in most patients with HOA, including those without signs of erosions at conventional radiography. However, many findings suggest that subjects with erosive HOA exhibit more inflammatory features than those with non-erosive HOA in different ways, including clinical, laboratory and sonographic aspects. Thus, it is probably preferable to use the double term inflammatory/erosive to better define this particular subset of HOA.

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Inflammatory/erosive HOA: the difficult to search an identity

There is still no general consensus on the definition of IE-HOA. In time, its identity has been discussed and variously proposed as a subset of HOA [11], *[12], *[13], variant of HOA [14], severe form of HOA [15], inflammatory phase of HOA [16] and an entity distinct from OA [17]. These doubts have influenced many aspects of research in this particular field of HOA, therefore, leading to many difficulties in the interpretation of available data.

Since 1961, Crain underlined the existence of “a

Epidemiological and clinical features of inflammatory/erosive HOA

In absence of a true disease definition, no exact epidemiological data are available, especially concerning prevalence. Therefore, there are some discrepancies among old studies suggesting that IE-HOA was a rare disease and those, more recent, claiming that this variant is very frequent. Pattrick et al. found 10 cases of erosive HOA among 67 patients attending their Rheumatology Unit with polyarticular HOA [24]. In a prospective study of 500 consecutive patients attending a rheumatology clinic

Radiography

Although the main hallmark of IE-HOA is the presence of erosion at CR, the precise definition of erosion in IE-HOA is still a matter for debate. Classically, as stated in the EULAR recommendations, erosive HOA is defined radiographically by subchondral erosion, cortical destruction and subsequent reparative change, which may include bony ankylosis [13]. These apparently simple observations need to be carefully specified.

The erosions in HOA are seen in DIPs and PIPs and may occur within both the

The inflammation of inflammatory/erosive HOA

Besides clinical features, signs of inflammation in IE-HOA subset may also be evident by other ways (Table 2). In a recent US study performed in IE-HOA using a power Doppler, the findings of synovial membrane thickening and increased vascularity indicative of active synovitis were found in the vast majority of patients with erosive HOA, thus consistent with the term “inflammatory form of OA” that has been attributed to erosive HOA [23]. The percentages of DIPs and PIPs with active synovitis on

Pathogenetic hypotheses concerning the role of inflammation in erosive/inflammatory HOA

The first attempt to investigate the pathogenesis of IE-HOA was by Utsinger et al. to evaluate the possibility that immune mechanisms may have a role [46]. They compared some immunologic parameters in erosive HOA and RA. Changes in levels of IgG, lymphocytotoxic antibodies and cryoglobulins were found almost exclusively in RA [46]. In another study, the same authors observed that synovial fluid and synovial membrane from patients with erosive HOA, similarly to RA, had increased number of Ia+ T

Therapy: is an anti-inflammatory therapy justified?

Treatment of IE-HOA remains still unsatisfactory. In contrast to non-IE-HOA, paracetamol and even non-steroidal anti-inflammatory drugs (NSAIDs) are ineffective in a significant number of cases of IE-HOA [11], *[12], [46], *[51]. Intra-articular injections of corticosteroids seem to be more effective in controlling symptoms, although there is no demonstration that they are able to reduce the development of erosions or accelerate their healing [46]. Thus, other substances have been proposed, not

References (62)

  • T. Silvestri et al.

    Analysis of cartilage biomarkers in erosive and non-erosive osteoarthritis of the hands

    Osteoarthr Cartil

    (2004)
  • R. Ramonda et al.

    Coll2–1, Coll2-1NO2 and myeloperoxydase serum levels in erosive and non erosive osteoarthritis of the hands

    Osteoarthr Cartil

    (2008)
  • A.G. Stern et al.

    Association of erosive hand osteoarthritis with a single nucleotide polymorphism on the gene encoding interleukin-1 beta

    Osteoarthr Cartil

    (2003)
  • G. Verbruggen et al.

    Chondroitin sulfate: S/DMOAD (structure/disease-modifying anti-osteoarthritis drug) in the treatment of finger joint OA

    Osteoarthr Cartil

    (1998)
  • J. Bondeson et al.

    Antimalarial drugs inhibit phospholipase A2 activation and induction of interleukin 1beta and tumor necrosis factor alpha in macrophages: implications for their mode of action in rheumatoid arthritis

    Gen Pharmacol

    (1998)
  • J.P. Pelletier et al.

    Osteoarthritis, an inflammatory disease: potential implication for the selection of new therapeutic targets

    Arthritis Rheum

    (2001)
  • M.B. Goldring et al.

    Osteoarthritis

    J Cell Physiol

    (2007)
  • F. Iannone et al.

    The pathophysiology of osteoarthritis

    Aging Clin Exp Res

    (2003)
  • C. Melchiorri et al.

    Enhanced and coordinated in vivo expression of inflammatory cytokines and nitric oxide synthase by chondrocytes from patients with osteoarthritis

    Arthritis Rheum

    (1998)
  • L.C. Tetlow et al.

    Matrix metalloproteinase and proinflammatory cytokine production by chondrocytes of human osteoarthritic cartilage

    Arthritis Rheum

    (2001)
  • C. Valvason et al.

    Influence of glucosamine sulphate on oxidative stress in human osteoarthritic chondrocytes: effects on HO-1, p22Phox and iNOS expression

    Rheumatology

    (2008)
  • S.J. Millward-Sadler et al.

    Integrin-dependent signal cascades in chondrocyte mechanotransduction

    Ann Biomed Eng

    (2004)
  • L. Punzi et al.

    New biochemical insights into the pathogenesis of osteoarthritis and the role of laboratory investigations in clinical assessment

    Crit Rev Clin Lab Sci

    (2005)
  • W. Zhang et al.

    EULAR evidence based recommendations for the diagnosis of hand osteoarthritis - report of a task force of the EULAR Standing Committee for International Clinical Studies Including Therapeutics (ESCISIT)

    Ann Rheum Dis

    (2009)
  • D.C. Crain et al.

    Interphalangeal osteoarthritis characterised by painful, inflammatory episodes resulting in deformity of the proximal and distal articulations

    J Am Med Assoc

    (1961)
  • J.B. Peter et al.

    Erosive osteoarthritis of the hands

    Arthritis Rheum

    (1966)
  • G.E. Ehrlich

    Osteoarthritis beginning with inflammation. Definitions and correlations

    J Am Med Assoc

    (1975)
  • J.H. Kellgren et al.

    Generalised osteoarthritis and Heberden's nodes

    Br Med J

    (1952)
  • M. Doherty et al.

    Osteoarthritis

  • A.J. Grainger et al.

    MR imaging of erosions in interphalangeal joint osteoarthritis: is all osteoarthritis erosive?

    Skeletal Radiol

    (2007)
  • M. Vlychou et al.

    Ultrasonographic evidence of inflammation is frequent in hands of patients with erosive osteoarthritis

    Osteoarthr Cartil

    (2009 May 7)
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