MODELING OF PROGRESSIVE GLOMERULAR INJURY IN HUMANS WITH LUPUS NEPHRITIS

Citation
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
Citations number
29
Categorie Soggetti
Physiology
ISSN journal
03636127
Volume
42
Issue
1
Year of publication
1997
Pages
158 - 169
Database
ISI
SICI code
0363-6127(1997)42:1<158:MOPGII>2.0.ZU;2-6
Abstract
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.