The Association between Pathologic Features from Renal Biopsies and End-Stage Renal Disease in Lupus Nephritis Patients Pubblico
Patel, Deesha (2012)
Abstract
Background: Systemic lupus erythematosus (SLE) is a
multisystem autoimmune disease.
SLE can potentially be fatal, especially when major organs are
affected. About two-thirds
of SLE patients may develop inflammation of the kidneys, or lupus
nephritis. Lupus
nephritis can progress to end-stage renal disease (ESRD), which
requires dialysis or renal
transplant. Lupus nephritis is currently classified through
pathologic features from renal
biopsies, which are categorized by the World Health Organization
(WHO) morphologic
classification of lupus nephritis (1995) or the International
Society of Nephrology/Renal
Pathology Society Classification (ISN/RPS) of Lupus Nephritis
(2003). The aim of this
study was to determine the association between pathologic findings
from renal biopsies
and ESRD in lupus nephritis patients, as well as to determine if
the WHO classification
of proliferative lupus nephritis was associated with ESRD.
Methods: 237 patients were selected from the Georgia Lupus
Registry, a population-
based registry of diagnosed SLE in metropolitan Atlanta. Inclusion
criteria included
validated diagnosis of SLE, a pathology report of an abnormal renal
biopsy (WHO
classes II-V), ESRD diagnosis after renal biopsy, and African
American or White race.
Final predictors, and potential confounders, were determined based
on previous research
and clinical relevance; proliferative lupus nephritis was
determined using WHO
classification. Univariate and multivariate analyses were conducted
to determine if
pathologic features and proliferative lupus nephritis were
associated with ESRD.
Results: The final predictors of interstitial damage,
glomerular damage, greater than 25%
glomeruli sclerosed, arteriosclerosis or arteriolosclerosis, and
tubuloreticular bodies
combined were predictive of ESRD (aOR = 8.73, 95% CI: 1.19, 63.76).
Glomerular
damage and greater than 25% glomeruli sclerosed were statistically
significantly
associated with ESRD in univariate and multivariate analyses;
tubuloreticular bodies
were a statistically significant protective factor for ESRD in both
analyses. Proliferative
lupus nephritis was not associated with ESRD in either analysis,
producing almost a null
effect.
Conclusion: When combined together, the selected pathologic
features were greatly
associated with ESRD. However, only half of those features were
associated with ESRD
individually. Proliferative lupus nephritis was not associated with
ESRD. This study
indicates the potential of pathologic features in predicting ESRD
in lupus nephritis
patients.
Table of Contents
Background...1
Methods...9
Results...15
Discussion...18
References...21
Tables...25
Figures...30
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