ObjectiveTo estimate and identify factors associated with the incidence of all-cause end-stage renal disease (ESRD) among newly diagnosed systemic lupus erythematosus (SLE) patients. MethodsData from a national registry of treated ESRD were linked to data from a lupus registry of SLE patients who were newly diagnosed and living in Atlanta, Georgia, 2002-2004 (median followup 7.8 years). Cumulative incidence and incidence rates (ESRD treatment initiations per 1,000 patient-years) were calculated, and age- and race-adjusted Poisson models were used to calculate incidence rate ratios (IRRs). ResultsAmong 344 newly diagnosed SLE patients, 29 initiated ESRD treatment over 2,603.8 years of followup. Incidence rates were 13.8 (95% confidence interval [95% CI] 9.4-20.3) among black patients and 3.3 (95% CI 0.8-13.0) among white patients, per 1,000 patient-years; corresponding 5-year cumulative incidence was 6.4% and 2.5% among black and white patients, respectively. Lupus nephritis documented prior to 2005, which occurred in 80% of those who progressed to ESRD, was the strongest risk factor for incident ESRD (IRR 6.7 [95% CI 2.7-16.8]; incidence rate 27.6 per 1,000 patient-years). Results suggested that patients who were black versus white (IRR 3.9 [95% CI 0.9-16.4]) or <18 years old (versus 30 years old) at diagnosis (IRR 2.1 [95% CI 0.9-5.3]) may be more likely to progress to ESRD, but incidence did not differ by sex or other characteristics. ConclusionThe incidence of all-cause ESRD among patients with a recent diagnosis of SLE is high in Georgia. Interventions to decrease ESRD incidence among newly diagnosed SLE patients should target young and black patients, as well as patients with lupus nephritis.
机构:
Augusta Univ, Dept Internal Med, Med Coll Georgia, Augusta, GA USA
Charlie Norwood VA Med Ctr, Augusta, GA USAAugusta Univ, Dept Internal Med, Med Coll Georgia, Augusta, GA USA
Le, B.
Waller, J. L.
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Augusta Univ, Dept Biostat & Epidemiol, Augusta, GA USAAugusta Univ, Dept Internal Med, Med Coll Georgia, Augusta, GA USA
Waller, J. L.
Radhakrishnan, R.
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Augusta Univ, Sch Med, Med Coll Georgia, Augusta, GA USAAugusta Univ, Dept Internal Med, Med Coll Georgia, Augusta, GA USA
Radhakrishnan, R.
Oh, S. J.
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Augusta Univ, Div Rheumatol, Dept Internal Med, Med Coll Georgia, Augusta, GA USAAugusta Univ, Dept Internal Med, Med Coll Georgia, Augusta, GA USA
Oh, S. J.
Kheda, M. F.
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Southwest Georgia Nephrol Clin, PC, Albany, GA USAAugusta Univ, Dept Internal Med, Med Coll Georgia, Augusta, GA USA
Kheda, M. F.
Nahman, N. S.
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Augusta Univ, Dept Internal Med, Med Coll Georgia, Augusta, GA USA
Charlie Norwood VA Med Ctr, Augusta, GA USA
Augusta Univ, Div Nephrol, Dept Internal Med, Med Coll Georgia, Augusta, GA USAAugusta Univ, Dept Internal Med, Med Coll Georgia, Augusta, GA USA
Nahman, N. S.
Carbone, L.
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Augusta Univ, Dept Internal Med, Med Coll Georgia, Augusta, GA USA
Charlie Norwood VA Med Ctr, Augusta, GA USA
Augusta Univ, Div Rheumatol, Dept Internal Med, Med Coll Georgia, Augusta, GA USAAugusta Univ, Dept Internal Med, Med Coll Georgia, Augusta, GA USA