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Hypocomplementemia in systemic sclerosis--clinical and serological correlations.

Hypocomplementemia in systemic sclerosis--clinical and serological correlations. Research Abstract Details 

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  • Hypocomplementemia in systemic sclerosis--clinical and serological correlations. Abstract Text:

    marie hudsonMarie Hudson,jennifer g walkerJennifer G Walker,marvin fritzlerMarvin Fritzler,suzanne tailleferSuzanne Taillefer,murray baronMurray Baron,marie hudsonMarie Hudson,jennifer g walkerJennifer G Walker,marvin fritzlerMarvin Fritzler,suzanne tailleferSuzanne Taillefer,murray baronMurray Baron,

    OBJECTIVE: Although complement fixation is not commonly thought to be part of the pathogenesis of systemic sclerosis (SSc), hypocomplementemia has been associated with SSc. We hypothesized that hypocomplementemia in SSc might indicate the presence of overlap disease. We investigated if SSc patients with hypocomplementemia had more features of overlap disease than those with normal complement levels. METHODS: Study subjects consisted of those enrolled in the Canadian Scleroderma Research Group Registry. Patients were divided into 2 groups: those with normal complement levels (normal C3 and C4) and those with hypocomplementemia (low C3 or C4). Evidence of overlap disease was defined as physician reports of other specific rheumatic conditions. Autoantibodies were assayed. Differences in rates of concomitant diseases and in antibody profiles were compared between groups. RESULTS: Our study included 321 patients (88% women, mean age 56 +/- 13 yrs, mean disease duration 11 +/- 9 yrs). Of these, 276 (86%) had normal complements and 45 (14%) had hypocomplementemia. Patients with hypocomplementemia were significantly more likely to have physician-reported inflammatory myositis (27% vs 12%; p < 0.008) and vasculitis (11% vs 2%; p < 0.011) than those with normal complement. There was also a trend toward more antichromatin antibodies (18% vs 9%; p = 0.051) in patients with hypocomplementemia compared to normals. CONCLUSION: Hypocomplementemia may identify a particular subgroup of SSc patients who have overlap disease.

    Hypocomplementemia in systemic sclerosis--clinical and serological correlations. Publishing Authors By Initials

    m hudsonM Hudson,jg walkerJG Walker,m fritzlerM Fritzler,s tailleferS Taillefer,m baronM Baron,m hudsonM Hudson,jg walkerJG Walker,m fritzlerM Fritzler,s tailleferS Taillefer,m baronM Baron,

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    Hypocomplementemia in systemic sclerosis--clinical and serological correlations. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: The Journal of rheumatology

    VOLUME: 34

    Page Numbers: 2218-23

    Journal Abbreviation: J. Rheumatol.

    ISSN: 0315-162X

    DAY: 15

    MONTH: 10

    YEAR: 2007

    Hypocomplementemia in systemic sclerosis--clinical and serological correlations. Information

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    LANGUAGE: eng

    NlmUniqueID: 7501984

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    AFFILIATION: SMBD-Jewish General Hospital and McGill University, 3755 Cote Sainte-Catherine Road, Montreal, Quebec, Canada. marie.hudson@mcgill.ca

    Country: Canada

    Canada Research PublicationCanada Research Publication

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    MEDLINETA: J Rheumatol

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