Quantitative morphometry of renal biopsies prior to cyclosporine in nephrotic syndrome

被引:7
作者
Smoyer, WE [1 ]
Gregory, MJ [1 ]
Bajwa, RS [1 ]
Johnson, KJ [1 ]
Bunchman, TE [1 ]
机构
[1] Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA
关键词
interstitial fibrosis; glomerulosclerosis; focal segmental glomerulosclerosis; IgM nephropathy;
D O I
10.1007/s004670050536
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Use of cyclosporine (CsA) in the management of children with steroid-resistant (SRNS) and steroid-dependent (SDNS) nephrotic syndrome has become increasingly popular in recent years. Although most children receive a renal biopsy prior to initiation of CsA, the relationship between initial renal histology and the subsequent clinical response to CsA is not known. We analyzed the correlation between pre-CsA segmental and global glomerular scarring and interstitial fibrosis and the subsequent response to CsA in 23 children (5.6 +/-1.0 years, Mean+/-SEM) with SDNS (n=8) and SRNS (n=15) treated with CsA for 24.2+/-3.8 months and followed for 28.0+/-4.1 months. Complete remission was obtained in 78% of patients within 67.6+/-16 days, while 18% had a partial response and 4% no response. Quantitative histological analysis revealed a trend toward partial rather than complete response with increasing segmental glomerular (P=0.13), global glomerular (P=0.05), and interstitial (P=0.08) scarring, and among patients with minimal change nephrotic syndrome versus IgM nephropathy versus focal segmental glomerulosclerosis. Among complete responders, linear regression analyses revealed no correlation between time to response and pre-CsA glomerular or interstitial scarring. We conclude that increased glomerular or interstitial scarring on a pre-CsA renal biopsy tends to correlate with a partial, rather than complete, response to CsA in childhood nephrotic syndrome.
引用
收藏
页码:737 / 743
页数:7
相关论文
共 24 条
[1]   CYCLOSPORIN-A TREATMENT IN CHILDREN WITH MINIMAL CHANGE NEPHROTIC SYNDROME AND FOCAL SEGMENTAL GLOMERULOSCLEROSIS [J].
BRODEHL, J ;
BRANDIS, M ;
HELMCHEN, U ;
HOYER, PF ;
BURGHARD, R ;
EHRICH, JHH ;
ZIMMERHACKL, RB ;
KLEIN, W ;
WONIGEIT, K .
KLINISCHE WOCHENSCHRIFT, 1988, 66 (22) :1126-1137
[2]  
CAPODICASA G, 1986, INT J PED NEPHROL, V7, P69
[3]  
Gregory MJ, 1996, J AM SOC NEPHROL, V7, P543
[4]  
HABIB R, 1994, CLIN NEPHROL, V42, P141
[5]   STEROID-RESISTANT, CYCLOSPORINE-RESPONSIVE, RELAPSING NEPHROTIC SYNDROME [J].
HYMES, LC .
PEDIATRIC NEPHROLOGY, 1995, 9 (02) :137-139
[6]   RACIAL-DIFFERENCES IN THE INCIDENCE AND RENAL OUTCOME OF IDIOPATHIC FOCAL SEGMENTAL GLOMERULOSCLEROSIS IN CHILDREN [J].
INGULLI, E ;
TEJANI, A .
PEDIATRIC NEPHROLOGY, 1991, 5 (04) :393-397
[7]  
INGULLI E, 1995, J AM SOC NEPHROL, V5, P1820
[8]  
ITTEL TH, 1995, CLIN NEPHROL, V44, P156
[9]  
LEE HY, 1995, CLIN NEPHROL, V43, P375
[10]   LONG-TERM CYCLOSPORINE-A TREATMENT OF STEROID-RESISTANT AND STEROID-DEPENDENT NEPHROTIC SYNDROME [J].
MELOCOTON, TL ;
KAMIL, ES ;
COHEN, AH ;
FINE, RN .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1991, 18 (05) :583-588