Thin GBM nephropathy: premature glomerular obsolescence is associated with hypertension and late onset renal failure. Export

@article{citeulike:3150140, abstract = {Thin glomerular basement membrane (GBM) nephropathy, also called familial benign hematuria, is characterized by chronic hematuria and uniform thinning of the lamina densa of the glomerular basement membrane. It generally holds an excellent renal prognosis. Alport syndrome in early stages can also show attenuation of the GBM; conversely, renal insufficiency has been reported in familial benign hematuria. To discern early Alport syndrome from thin GBM nephropathy, we carried out a prospective epidemiological study in which 19 normotensive and non-azotemic adult patients with chronic microscopic (18 of 19) and macroscopic (1 of 19) hematuria and biopsy-proven thin GBM nephropathy were followed for a median of 12 years (range 9 to 15 years). Renal biopsies of thin GBM patients at entry showed an increased incidence of focal global glomerulosclerosis when compared to disease controls as IgA nephropathy (P = 0.047) and normal renal tissue (P = 0.0075). All renal biopsies showed the presence of the Goodpasture antigen when tested immunohistochemically. Presence of Alport syndrome was excluded clinically as none of the patients had complaints of hearing loss or abnormalities by audiography and ophthalmology. At the end of follow-up, the incidence of hypertension in thin GBM nephropathy (35\%) exceeded that of healthy clinical controls (P = 0.048), and one hypertensive patient developed mild renal failure. In the normotensive patients, the glomerular filtration rate at follow-up as measured by inulin clearance was reduced in three out of seven; these were over 50 years of age. Although no family members were known to have renal disease at inclusion, within four families six elderly first degree relatives had developed unexplained renal insufficiency at the end of follow-up. Thus, thin GBM nephropathy predisposes to premature glomerular obsolescence, leading in time to increased incidences of hypertension and late onset renal insufficiency.}, address = {Department of Immunology, University Hospital Maastricht, The Netherlands.}, author = {Nieuwhof, C. M. and de Heer, F. and de Leeuw, P. and van Breda Vriesman, P. J.}, citeulike-article-id = {3150140}, citeulike-linkout-0 = {http://view.ncbi.nlm.nih.gov/pubmed/9150478}, citeulike-linkout-1 = {http://www.hubmed.org/display.cgi?uids=9150478}, issn = {0085-2538}, journal = {Kidney international}, keywords = {thin-basement-membrane-nephropathy}, month = {May}, number = {5}, pages = {1596--1601}, posted-at = {2008-08-22 23:56:01}, priority = {2}, title = {Thin GBM nephropathy: premature glomerular obsolescence is associated with hypertension and late onset renal failure.}, url = {http://view.ncbi.nlm.nih.gov/pubmed/9150478}, volume = {51}, year = {1997} }

TY - JOUR ID - citeulike:3150140 L3 - citeulike-article-id:3150140 N2 - Thin glomerular basement membrane (GBM) nephropathy, also called familial benign hematuria, is characterized by chronic hematuria and uniform thinning of the lamina densa of the glomerular basement membrane. It generally holds an excellent renal prognosis. Alport syndrome in early stages can also show attenuation of the GBM; conversely, renal insufficiency has been reported in familial benign hematuria. To discern early Alport syndrome from thin GBM nephropathy, we carried out a prospective epidemiological study in which 19 normotensive and non-azotemic adult patients with chronic microscopic (18 of 19) and macroscopic (1 of 19) hematuria and biopsy-proven thin GBM nephropathy were followed for a median of 12 years (range 9 to 15 years). Renal biopsies of thin GBM patients at entry showed an increased incidence of focal global glomerulosclerosis when compared to disease controls as IgA nephropathy (P = 0.047) and normal renal tissue (P = 0.0075). All renal biopsies showed the presence of the Goodpasture antigen when tested immunohistochemically. Presence of Alport syndrome was excluded clinically as none of the patients had complaints of hearing loss or abnormalities by audiography and ophthalmology. At the end of follow-up, the incidence of hypertension in thin GBM nephropathy (35%) exceeded that of healthy clinical controls (P = 0.048), and one hypertensive patient developed mild renal failure. In the normotensive patients, the glomerular filtration rate at follow-up as measured by inulin clearance was reduced in three out of seven; these were over 50 years of age. Although no family members were known to have renal disease at inclusion, within four families six elderly first degree relatives had developed unexplained renal insufficiency at the end of follow-up. Thus, thin GBM nephropathy predisposes to premature glomerular obsolescence, leading in time to increased incidences of hypertension and late onset renal insufficiency. IS - 5 JF - Kidney international SN - 0085-2538 AD - Department of Immunology, University Hospital Maastricht, The Netherlands. EP - 1601 TI - Thin GBM nephropathy: premature glomerular obsolescence is associated with hypertension and late onset renal failure. VL - 51 SP - 1596 KW - thin-basement-membrane-nephropathy AU - Nieuwhof, CM AU - de Heer, F AU - de Leeuw, P AU - van Breda Vriesman, PJ PY - 1997/05// UR - http://view.ncbi.nlm.nih.gov/pubmed/9150478 ER -