Abstract:
STUDY OBJECTIVES:To determine whether African-American race is independently associated with lung disease in scleroderma. DESIGN:Retrospective review. SETTING:University medical center in Baltimore. PATIENTS:One hundred one patients with diffuse cutaneous scleroderma with available serum samples. MEASUREMENTS:Patients underwent lung function testing as part of their routine clinical care. Percent predicted values adjusted for race were calculated for FVC, single-breath carbon monoxide diffusing capacity (Dco), and FEV1. Serum samples were assayed for the presence of antibodies to topoisomerase I and RNA polymerase II. RESULTS:Scleroderma patients of African-American race had lower percent predicted values than white patients for FVC (p<0.002), Dco (p<0.0001), and FEV1 (p<0.0001). Antibodies to topoisomerase I but not antibodies to RNA polymerase II were also associated with lung function. African-American scleroderma patients were distinct from white patients in having younger age of onset and higher prevalence of antibodies to topoisomerase I. In multivariate analyses accounting for sex, age, smoking history, years of scleroderma symptoms, and RNA polymerase II antibody status, African-American race and topoisomerase I antibody status independently predicted lower lung function. CONCLUSION:African-American race and antibodies to topoisomerase I are independent risk factors for scleroderma lung disease.
journal_name
Chestjournal_title
Chestauthors
Greidinger EL,Flaherty KT,White B,Rosen A,Wigley FM,Wise RAdoi
10.1378/chest.114.3.801subject
Has Abstractpub_date
1998-09-01 00:00:00pages
801-7issue
3eissn
0012-3692issn
1931-3543pii
S0012-3692(16)32584-3journal_volume
114pub_type
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