Jb. Buckheit et al., MODELING OF PROGRESSIVE GLOMERULAR INJURY IN HUMANS WITH LUPUS NEPHRITIS, American journal of physiology. Renal, fluid and electrolyte physiology, 42(1), 1997, pp. 158-169
We studied glomerular function longitudinally for 36-120 mo in 21 pati
ents undergoing treatment for diffuse, proliferative lupus nephritis.
We determined glomerular filtration rate (GFR) and glomerular oncotic
pressure (Pi(GC)) and computed the two-kidney ultrafiltration coeffici
ent (K-f) at 6- to 12-mo intervals. The relationships and cross talk a
mong the three variables over time were then analyzed by eigenfunction
regression and canonical correlations. We also performed a morphometr
ic analysis of serial biopsies and computed single-nephron K-f in pate
nt glomeruli at baseline and after 36-94 mo of follow-up. Patients wer
e divisible into progressors (n = 12) or nonprogressors (n = 9) accord
ing to the presence or absence, respectively, of an irrevocable declin
e in GFR over time. Examination of longitudinal variables revealed GFR
to be strongly related to K-f in all patients and inversely related t
o Pi(GC) in progressors. By serial morphometric analysis we observed a
threefold increase in the prevalence of global sclerosis in progresso
rs but unchanged prevalence in nonprogressors. Whereas single-nephron
K-f of remnant glomeruli increased to supernormal levels in nonprogres
sors, the absence of this compensatory phenomenon in progressors permi
tted GFR and K-f to decline in parallel with the declining number of f
unctional glomeruli.