We retrospectively evaluated the prevalence of primary glomerular lesi
ons in adults who had a renal biopsy for nephrotic proteinuria. From J
uly 1975 to May 1994, 340 patients undergoing renal biopsies evaluated
at Rush-Presbyterian-St Lukes Medical Center had the primary glomerul
ar lesions of minimal-change disease, focal segmental glomerular scler
osis (FSGS), membranous glomerulonephritis (MGN), membranoproliferativ
e glomerulonephropathy, immunoglobulin A nephropathy, and immunotactoi
d glomenrulopathy. The patients had a mean age of 43 +/- 17 years, 57%
were male, and 50% were white, 36% were black, 7% were of other race,
and 7% were of unknown race, The distribution of lesions for black pa
tients was minimal-change disease 14%, FSGS 57%, MGN 24%, membranoprol
iferative glomerulonephritis 2%, immunoglobulin A 2%, and immunotactoi
d glomerulopathy 1%; for white patients, the distribution of lesions w
as minimal-change disease 20%, FSGS 23%, MGN 36%, membranoproliferativ
e glomerulonephropathy 6%, immunoglobulin A 8%, and immunotactoid glom
erulopathy 6%, The prevalence of FSGS was significantly greater (P < 0
.0001) and that for MON, immunoglobulin A, and immunotactoid glomerulo
pathy was significantly less (P < 0.05) for black patients compared wi
th white patients, In a logistic regression analysis, race remained th
e only significant predictor of FSGS (P = 0.0001), with black patients
four times as likely to have FSGS as white patients, The distribution
of lesions among white patients was similar based on gender, age, and
biopsy period. For black patients the distribution was also similar b
ased on gender and age, but over 20 years the incidence of FSGS increa
sed from 39% (1975 to 1984) to 64% (1985 to 1994) (P < 0.01). Thus, si
gnificant racial differences in the distribution of primary glomerular
lesions exists, This has important prognostic and therapeutic implica
tions for nephrotic adults. (C) 1996 by the National Kidney Foundation
, Inc.