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Normal circulating serum amyloid P component concentration in systemic sclerosis

Tennent, G.A.; Dziadzio, M.; Triantafillidou, E.; Davies, P.; Gallimore, J.R.; Denton, C.P.; Pepys, M.B.; (2007) Normal circulating serum amyloid P component concentration in systemic sclerosis. Arthritis and Rheumatism , 56 (6) pp. 2013-2017. 10.1002/art.22694.

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Objective: The observation of reduced circulating concentrations of the constitutive plasma pentraxin protein, serum amyloid P component (SAP), in serum samples obtained from a small number of patients with systemic sclerosis (SSc) has been reported as confirmation of an antifibrotic role of this protein. Because neither sustained SAP depletion in humans nor SAP deficiency in mice is associated with fibrosis, we sought to establish rigorously the serum SAP concentration in well-characterized patients with SSc. Methods: Serum concentrations of SAP were measured by electroimmunoassay in a cross-sectional cohort of 20 patients with diffuse cutaneous SSc and 12 patients with limited cutaneous SSc, and in a separate 12-month longitudinal cohort of 13 patients with diffuse disease and 37 patients with limited disease. The extent and severity of disease were characterized in detail at the time of serum sampling. Serum concentrations of the classic acute-phase reactants, C-reactive protein and serum amyloid A protein, were measured by immunonephelometric assays. Results: SAP values were entirely within the normal range, regardless of the extent and severity of disease, apart from a very few isolated raised values associated with acute intercurrent complications causing major acute-phase responses. Conclusion: We observed no reduced circulating concentrations of SAP in patients with SSc, nor any evidence of an association between SAP levels and the extent or severity of fibrosis.

Type: Article
Title: Normal circulating serum amyloid P component concentration in systemic sclerosis
DOI: 10.1002/art.22694
Publisher version: http://dx.doi.org/10.1002/art.22694
Language: English
UCL classification: UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Div of Medicine > Inflammation
URI: http://discovery.ucl.ac.uk/id/eprint/7990
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