Racial Differences in the Frequencies of Scleroderma‐Related Autoantibodies

Objective. To determine demographic differences in scleroderma‐related autoantibodies. Methods. One hundred fifty‐six patients with systemic sclerosis were prospectively examined for anticentromere antibodies (ACA), anti—topoisomerase I (anti—topo I, or Scl‐70), antinucleolar, and anti—U1 RNP autoan...

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Veröffentlicht in:Arthritis and rheumatism 1992-02, Vol.35 (2), p.216-218
Hauptverfasser: Reveille, John D., Durban, Egon, Goldstein, Rose, Moreda, Ramon, Arnett, Frank C.
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container_end_page 218
container_issue 2
container_start_page 216
container_title Arthritis and rheumatism
container_volume 35
creator Reveille, John D.
Durban, Egon
Goldstein, Rose
Moreda, Ramon
Arnett, Frank C.
description Objective. To determine demographic differences in scleroderma‐related autoantibodies. Methods. One hundred fifty‐six patients with systemic sclerosis were prospectively examined for anticentromere antibodies (ACA), anti—topoisomerase I (anti—topo I, or Scl‐70), antinucleolar, and anti—U1 RNP autoantibodies. Results. ACA was found in 36% of Caucasians and 4% of American blacks (P = 0.002, odds ratio [OR] 15). Anti—topo I was found in 37% of American blacks, compared with 17% of Caucasians (P = 0.04, OR 3). No significant differences in the frequencies of antinucleolar and anti—U1 RNP autoantibodies were found. Conclusion. These data suggest important demographic differences in scleroderma‐associated autoantibodies.
doi_str_mv 10.1002/art.1780350215
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To determine demographic differences in scleroderma‐related autoantibodies. Methods. One hundred fifty‐six patients with systemic sclerosis were prospectively examined for anticentromere antibodies (ACA), anti—topoisomerase I (anti—topo I, or Scl‐70), antinucleolar, and anti—U1 RNP autoantibodies. Results. ACA was found in 36% of Caucasians and 4% of American blacks (P = 0.002, odds ratio [OR] 15). Anti—topo I was found in 37% of American blacks, compared with 17% of Caucasians (P = 0.04, OR 3). No significant differences in the frequencies of antinucleolar and anti—U1 RNP autoantibodies were found. Conclusion. These data suggest important demographic differences in scleroderma‐associated autoantibodies.</description><identifier>ISSN: 0004-3591</identifier><identifier>EISSN: 1529-0131</identifier><identifier>DOI: 10.1002/art.1780350215</identifier><identifier>PMID: 1734910</identifier><identifier>CODEN: ARHEAW</identifier><language>eng</language><publisher>New York: John Wiley &amp; Sons, Inc</publisher><subject>African Continental Ancestry Group - genetics ; Autoantibodies - genetics ; Biological and medical sciences ; European Continental Ancestry Group - genetics ; Hispanic Americans ; Humans ; Medical sciences ; Nuclear Proteins - immunology ; Prospective Studies ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. 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To determine demographic differences in scleroderma‐related autoantibodies. Methods. One hundred fifty‐six patients with systemic sclerosis were prospectively examined for anticentromere antibodies (ACA), anti—topoisomerase I (anti—topo I, or Scl‐70), antinucleolar, and anti—U1 RNP autoantibodies. Results. ACA was found in 36% of Caucasians and 4% of American blacks (P = 0.002, odds ratio [OR] 15). Anti—topo I was found in 37% of American blacks, compared with 17% of Caucasians (P = 0.04, OR 3). No significant differences in the frequencies of antinucleolar and anti—U1 RNP autoantibodies were found. Conclusion. 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Vasculitis</topic><topic>Scleroderma, Systemic - ethnology</topic><topic>Scleroderma, Systemic - immunology</topic><toplevel>online_resources</toplevel><creatorcontrib>Reveille, John D.</creatorcontrib><creatorcontrib>Durban, Egon</creatorcontrib><creatorcontrib>Goldstein, Rose</creatorcontrib><creatorcontrib>Moreda, Ramon</creatorcontrib><creatorcontrib>Arnett, Frank C.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Arthritis and rheumatism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Reveille, John D.</au><au>Durban, Egon</au><au>Goldstein, Rose</au><au>Moreda, Ramon</au><au>Arnett, Frank C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Racial Differences in the Frequencies of Scleroderma‐Related Autoantibodies</atitle><jtitle>Arthritis and rheumatism</jtitle><addtitle>Arthritis Rheum</addtitle><date>1992-02</date><risdate>1992</risdate><volume>35</volume><issue>2</issue><spage>216</spage><epage>218</epage><pages>216-218</pages><issn>0004-3591</issn><eissn>1529-0131</eissn><coden>ARHEAW</coden><abstract>Objective. To determine demographic differences in scleroderma‐related autoantibodies. Methods. One hundred fifty‐six patients with systemic sclerosis were prospectively examined for anticentromere antibodies (ACA), anti—topoisomerase I (anti—topo I, or Scl‐70), antinucleolar, and anti—U1 RNP autoantibodies. Results. ACA was found in 36% of Caucasians and 4% of American blacks (P = 0.002, odds ratio [OR] 15). Anti—topo I was found in 37% of American blacks, compared with 17% of Caucasians (P = 0.04, OR 3). No significant differences in the frequencies of antinucleolar and anti—U1 RNP autoantibodies were found. Conclusion. These data suggest important demographic differences in scleroderma‐associated autoantibodies.</abstract><cop>New York</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>1734910</pmid><doi>10.1002/art.1780350215</doi><tpages>3</tpages></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete; Alma/SFX Local Collection
subjects African Continental Ancestry Group - genetics
Autoantibodies - genetics
Biological and medical sciences
European Continental Ancestry Group - genetics
Hispanic Americans
Humans
Medical sciences
Nuclear Proteins - immunology
Prospective Studies
Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis
Scleroderma, Systemic - ethnology
Scleroderma, Systemic - immunology
title Racial Differences in the Frequencies of Scleroderma‐Related Autoantibodies
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