8 607 38.4 933 38.9 Renal graft 90 11.0 171 10.8 261 10.9 Membranous nephropathy
74 9.0 128 8.1 202 8.4 Minor glomerular abnormalities 52 6.3 143 9.0 195 8.1 Crescentic SC79 and necrotizing glomerulonephritis 32 3.9 87 5.5 119 5.0 Nephrosclerosis 38 4.6 77 4.9 115 4.8 Focal segmental glomerulosclerosis 32 3.9 65 4.1 97 4.0 Membranoproliferative glomerulonephritis (type I and III) 20 2.4 32 2.0 52 2.2 Chronic interstitial nephritis 24 2.9 21 1.3 45 1.9 Endocapillary proliferative glomerulonephritis 18 2.2 27 1.7 45 1.9 Sclerosing glomerulonephritis 10 1.2 33 2.1 43 1.8 Acute interstitial nephritis 7 0.9 18 1.1 25 1.0 Acute tubular necrosis 5 0.6 6 0.4 11 0.5 Dense deposit disease 1 0.1 5 0.3 6 0.3 Others 89 10.8 162 10.2 251 10.5 Total 818 100.0 1582 100.0 2400 100.0 In the pathological click here diagnoses as classified by histopathology, mesangial proliferative glomerulonephritis was primarily observed in 2007 and 2008 (Table 4). Selleck ACY-738 In the present cohort, except for renal grafts, the frequency
of mesangial proliferative glomerulonephritis was the highest followed by MN, minor glomerular abnormalities, nephrosclerosis, and crescentic and necrotizing glomerulonephritis in 2007 (Table 4). In 2008, mesangial proliferative glomerulonephritis was the most frequently diagnosed, with minor glomerular abnormalities being the second, and MN being the third (Table 4). Primary glomerular disease (except IgAN) and nephrotic syndrome In the cohort of primary glomerular disease as classified by pathogenesis, MN was predominant, followed by mesangial proliferative GPX6 glomerulonephritis, minor glomerular
abnormalities, and FSGS in 2007 (Table 5). In 2008, MN was still the most frequently diagnosed, present at the same frequency as minor glomerular abnormalities (Table 5). Table 5 Frequency of pathological diagnoses as classified by histopathology in primary glomerular disease (except IgA nephropathy) Classification 2007 2008 Total n % n % n % Membranous nephropathy 60 31.4 95 25.7 155 27.7 Minor glomerular abnormalities 33 17.3 95 25.7 128 22.9 Mesangial proliferative glomerulonephritis 45 23.6 82 22.2 127 22.7 Focal segmental glomerulosclerosis 24 12.6 53 14.4 77 13.8 Membranoproliferative glomerulonephritis (type I and III) 13 6.8 19 5.1 32 5.7 Crescentic and necrotizing glomerulonephritis 5 2.6 6 1.6 11 2.0 Endocapillary proliferative glomerulonephritis 1 0.5 6 1.6 7 1.3 Nephrosclerosis 2 1.0 4 1.1 6 1.1 Dense deposit disease 1 0.5 3 0.8 4 0.7 Sclerosing glomerulonephritis 2 1.0 1 0.3 3 0.5 Others 5 2.6 5 1.4 10 1.8 Total 191 100.0 369 100.0 560 100.0 In nephrotic syndrome as classified by clinical diagnosis, primary glomerular disease (except IgAN) was predominant, followed by diabetic nephropathy, amyloid nephropathy, IgAN, and lupus nephritis in 2007 (Table 6). A similar ordering of the disease frequencies was noted in 2008 (Table 6).