메뉴 건너뛰기




Volumn 28, Issue 5, 2013, Pages 699-709

New developments in steroid-resistant nephrotic syndrome

Author keywords

Genetics; Nephrin; Nephrotic; Podocin; Podocyte circulating factors

Indexed keywords

ACTIN; ALPHA ACTININ 4; CALCIUM CHANNEL; CD2 ASSOCIATED PROTEIN; CYCLOSPORIN A; DEXAMETHASONE; NEPHRIN; PODOCIN; RITUXIMAB; TRANSIENT RECEPTOR POTENTIAL CHANNEL 6; WT1 PROTEIN;

EID: 84880573499     PISSN: 0931041X     EISSN: 1432198X     Source Type: Journal    
DOI: 10.1007/s00467-012-2239-0     Document Type: Review
Times cited : (42)

References (80)
  • 1
    • 34247891468 scopus 로고    scopus 로고
    • Idiopathic nephrotic syndrome in New Zealand children, demographic, clinical features, initial management and outcome after twelve-month follow-up: Results of a three-year national surveillance study
    • 17489822 10.1111/j.1440-1754.2007.01077.x
    • Wong W (2007) Idiopathic nephrotic syndrome in New Zealand children, demographic, clinical features, initial management and outcome after twelve-month follow-up: results of a three-year national surveillance study. J Paediatr Child Health 43:337-341
    • (2007) J Paediatr Child Health , vol.43 , pp. 337-341
    • Wong, W.1
  • 4
    • 75749101016 scopus 로고    scopus 로고
    • Nephrin-signature molecule of the glomerular podocyte?
    • 19950250 1:CAS:528:DC%2BC3cXhvFWqtro%3D
    • Welsh GI, Saleem MA (2010) Nephrin-signature molecule of the glomerular podocyte? J Pathol 220:328-337
    • (2010) J Pathol , vol.220 , pp. 328-337
    • Welsh, G.I.1    Saleem, M.A.2
  • 5
    • 0034034757 scopus 로고    scopus 로고
    • NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
    • 10742096 10.1038/74166 1:CAS:528:DC%2BD3cXisVCjsb4%3D
    • Boute N, Gribouval O, Roselli S, Benessy F, Lee H, Fuchshuber A, Dahan K, Gubler MC, Niaudet P, Antignac C (2000) NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome. Nat Genet 24:349-354
    • (2000) Nat Genet , vol.24 , pp. 349-354
    • Boute, N.1    Gribouval, O.2    Roselli, S.3    Benessy, F.4    Lee, H.5    Fuchshuber, A.6    Dahan, K.7    Gubler, M.C.8    Niaudet, P.9    Antignac, C.10
  • 7
    • 0038136885 scopus 로고    scopus 로고
    • CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility
    • 12764198 10.1126/science.1081068 1:CAS:528:DC%2BD3sXktFGkt7s%3D
    • Kim JM, Wu H, Green G, Winkler CA, Kopp JB, Miner JH, Unanue ER, Shaw AS (2003) CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility. Science 300:1298-1300
    • (2003) Science , vol.300 , pp. 1298-1300
    • Kim, J.M.1    Wu, H.2    Green, G.3    Winkler, C.A.4    Kopp, J.B.5    Miner, J.H.6    Unanue, E.R.7    Shaw, A.S.8
  • 10
    • 0032922319 scopus 로고    scopus 로고
    • Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis. International collaborative group for the study of familial focal segmental glomerulosclerosis
    • 10200986 10.1046/j.1523-1755.1999.00384.x 1:STN:280:DyaK1M3hslSnsQ%3D%3D
    • Winn MP, Conlon PJ, Lynn KL, Howell DN, Gross DA, Rogala AR, Smith AH, Graham FL, Bembe M, Quarles LD, Pericak-Vance MA, Vance JM (1999) Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis. International collaborative group for the study of familial focal segmental glomerulosclerosis. Kidney Int 55:1241-1246
    • (1999) Kidney Int , vol.55 , pp. 1241-1246
    • Winn, M.P.1    Conlon, P.J.2    Lynn, K.L.3    Howell, D.N.4    Gross, D.A.5    Rogala, A.R.6    Smith, A.H.7    Graham, F.L.8    Bembe, M.9    Quarles, L.D.10    Pericak-Vance, M.A.11    Vance, J.M.12
  • 12
    • 0025288793 scopus 로고
    • An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor
    • 2163761 10.1016/0092-8674(90)90690-G 1:CAS:528:DyaK3cXltFSgsLo%3D
    • Haber DA, Buckler AJ, Glaser T, Call KM, Pelletier J, Sohn RL, Douglass EC, Housman DE (1990) An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor. Cell 61:1257-1269
    • (1990) Cell , vol.61 , pp. 1257-1269
    • Haber, D.A.1    Buckler, A.J.2    Glaser, T.3    Call, K.M.4    Pelletier, J.5    Sohn, R.L.6    Douglass, E.C.7    Housman, D.E.8
  • 16
    • 3242795082 scopus 로고    scopus 로고
    • NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence
    • 15253708 10.1111/j.1523-1755.2004.00776.x 1:CAS:528:DC%2BD2cXmvVegsLw%3D
    • Weber S, Gribouval O, Esquivel EL, Moriniere V, Tete MJ, Legendre C, Niaudet P, Antignac C (2004) NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence. Kidney Int 66:571-579
    • (2004) Kidney Int , vol.66 , pp. 571-579
    • Weber, S.1    Gribouval, O.2    Esquivel, E.L.3    Moriniere, V.4    Tete, M.J.5    Legendre, C.6    Niaudet, P.7    Antignac, C.8
  • 21
    • 77954534482 scopus 로고    scopus 로고
    • Successful treatment of steroid-resistant nephrotic syndrome associated with WT1 mutations
    • 20191369 10.1007/s00467-010-1468-3
    • Gellermann J, Stefanidis CJ, Mitsioni A, Querfeld U (2010) Successful treatment of steroid-resistant nephrotic syndrome associated with WT1 mutations. Pediatr Nephrol 25:1285-1289
    • (2010) Pediatr Nephrol , vol.25 , pp. 1285-1289
    • Gellermann, J.1    Stefanidis, C.J.2    Mitsioni, A.3    Querfeld, U.4
  • 25
    • 33845232634 scopus 로고    scopus 로고
    • Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations
    • 17186472 10.1086/510023 1:CAS:528:DC%2BD28Xht1yksr%2FE
    • Lopez LC, Schuelke M, Quinzii CM, Kanki T, Rodenburg RJ, Naini A, Dimauro S, Hirano M (2006) Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations. Am J Hum Genet 79:1125-1129
    • (2006) Am J Hum Genet , vol.79 , pp. 1125-1129
    • Lopez, L.C.1    Schuelke, M.2    Quinzii, C.M.3    Kanki, T.4    Rodenburg, R.J.5    Naini, A.6    Dimauro, S.7    Hirano, M.8
  • 27
    • 45949099527 scopus 로고    scopus 로고
    • Early coenzyme Q10 supplementation in primary coenzyme Q10 deficiency
    • 18579827 10.1056/NEJMc0800582 1:CAS:528:DC%2BD1cXnvFGjtL8%3D
    • Montini G, Malaventura C, Salviati L (2008) Early coenzyme Q10 supplementation in primary coenzyme Q10 deficiency. N Engl J Med 358:2849-2850
    • (2008) N Engl J Med , vol.358 , pp. 2849-2850
    • Montini, G.1    Malaventura, C.2    Salviati, L.3
  • 28
    • 78649941274 scopus 로고    scopus 로고
    • Genetics in clinical practice: Nephrotic and proteinuric syndromes
    • 21071976 10.1159/000320878
    • McCarthy HJ, Saleem MA (2011) Genetics in clinical practice: nephrotic and proteinuric syndromes. Nephron Exp Nephrol 118:e1-e8
    • (2011) Nephron Exp Nephrol , vol.118
    • McCarthy, H.J.1    Saleem, M.A.2
  • 31
    • 84455169599 scopus 로고    scopus 로고
    • The podocyte cytoskeleton-key to a functioning glomerulus in health and disease
    • 10.1038/nrneph.2011.151 1:CAS:528:DC%2BC3MXhs1CqurnE
    • Welsh GI, Saleem MA (2012) The podocyte cytoskeleton-key to a functioning glomerulus in health and disease. Nat Rev Nephrol 8:14-21
    • (2012) Nat Rev Nephrol , vol.8 , pp. 14-21
    • Welsh, G.I.1    Saleem, M.A.2
  • 32
    • 80052333245 scopus 로고    scopus 로고
    • Activation of RhoA in podocytes induces focal segmental glomerulosclerosis
    • 21804090 10.1681/ASN.2010111146 1:CAS:528:DC%2BC3MXht1GktL%2FL
    • Zhu L, Jiang R, Aoudjit L, Jones N, Takano T (2011) Activation of RhoA in podocytes induces focal segmental glomerulosclerosis. J Am Soc Nephrol 22:1621-1630
    • (2011) J Am Soc Nephrol , vol.22 , pp. 1621-1630
    • Zhu, L.1    Jiang, R.2    Aoudjit, L.3    Jones, N.4    Takano, T.5
  • 33
    • 78149355567 scopus 로고    scopus 로고
    • A high-powered view of the filtration barrier
    • 20576805 10.1681/ASN.2010040378
    • Peti-Peterdi J, Sipos A (2010) A high-powered view of the filtration barrier. J Am Soc Nephrol 21:1835-1841
    • (2010) J Am Soc Nephrol , vol.21 , pp. 1835-1841
    • Peti-Peterdi, J.1    Sipos, A.2
  • 37
    • 77949541746 scopus 로고    scopus 로고
    • Proteinuria: An enzymatic disease of the podocyte?
    • 19924101 10.1038/ki.2009.424 1:CAS:528:DC%2BC3cXjtFSntbc%3D
    • Mundel P, Reiser J (2010) Proteinuria: an enzymatic disease of the podocyte? Kidney Int 77:571-580
    • (2010) Kidney Int , vol.77 , pp. 571-580
    • Mundel, P.1    Reiser, J.2
  • 38
    • 33744969296 scopus 로고    scopus 로고
    • Synaptopodin orchestrates actin organization and cell motility via regulation of RhoA signalling
    • 16622418 10.1038/ncb1400 1:CAS:528:DC%2BD28XksVGnur0%3D
    • Asanuma K, Yanagida-Asanuma E, Faul C, Tomino Y, Kim K, Mundel P (2006) Synaptopodin orchestrates actin organization and cell motility via regulation of RhoA signalling. Nat Cell Biol 8:485-491
    • (2006) Nat Cell Biol , vol.8 , pp. 485-491
    • Asanuma, K.1    Yanagida-Asanuma, E.2    Faul, C.3    Tomino, Y.4    Kim, K.5    Mundel, P.6
  • 44
    • 0031563832 scopus 로고    scopus 로고
    • Rearrangements of the cytoskeleton and cell contacts induce process formation during differentiation of conditionally immortalized mouse podocyte cell lines
    • 9344605 10.1006/excr.1997.3739 1:CAS:528:DyaK2sXms1Grsr0%3D
    • Mundel P, Reiser J, Zuniga Mejia Borja A, Pavenstadt H, Davidson GR, Kriz W, Zeller R (1997) Rearrangements of the cytoskeleton and cell contacts induce process formation during differentiation of conditionally immortalized mouse podocyte cell lines. Exp Cell Res 236:248-258
    • (1997) Exp Cell Res , vol.236 , pp. 248-258
    • Mundel, P.1    Reiser, J.2    Zuniga Mejia Borja, A.3    Pavenstadt, H.4    Davidson, G.R.5    Kriz, W.6    Zeller, R.7
  • 46
    • 32844469380 scopus 로고    scopus 로고
    • Glucocorticoids protect and enhance recovery of cultured murine podocytes via actin filament stabilization
    • 16316324 10.1111/j.1523-1755.2005.00723.x 1:CAS:528: DC%2BD28XhslSmuw%3D%3D
    • Ransom RF, Lam NG, Hallett MA, Atkinson SJ, Smoyer WE (2005) Glucocorticoids protect and enhance recovery of cultured murine podocytes via actin filament stabilization. Kidney Int 68:2473-2483
    • (2005) Kidney Int , vol.68 , pp. 2473-2483
    • Ransom, R.F.1    Lam, N.G.2    Hallett, M.A.3    Atkinson, S.J.4    Smoyer, W.E.5
  • 48
    • 84857115704 scopus 로고    scopus 로고
    • Short-term efficacy of rituximab versus tacrolimus in steroid-dependent nephrotic syndrome
    • 21922213 10.1007/s00467-011-1997-4
    • Sinha A, Bagga A, Gulati A, Hari P (2012) Short-term efficacy of rituximab versus tacrolimus in steroid-dependent nephrotic syndrome. Pediatr Nephrol 27:235-241
    • (2012) Pediatr Nephrol , vol.27 , pp. 235-241
    • Sinha, A.1    Bagga, A.2    Gulati, A.3    Hari, P.4
  • 53
    • 33747266807 scopus 로고    scopus 로고
    • The bioactivity of plasma factors in focal segmental glomerulosclerosis
    • 16707909 10.1159/000093259
    • Marszal J, Saleem MA (2006) The bioactivity of plasma factors in focal segmental glomerulosclerosis. Nephron Exp Nephrol 104:e1-e5
    • (2006) Nephron Exp Nephrol , vol.104
    • Marszal, J.1    Saleem, M.A.2
  • 57
    • 73349125115 scopus 로고    scopus 로고
    • SuPAR: The molecular crystal ball
    • 19893210
    • Thuno M, Macho B, Eugen-Olsen J (2009) suPAR: the molecular crystal ball. Dis Markers 27:157-172
    • (2009) Dis Markers , vol.27 , pp. 157-172
    • Thuno, M.1    Macho, B.2    Eugen-Olsen, J.3
  • 58
    • 20544465220 scopus 로고    scopus 로고
    • Nephrotic plasma alters slit diaphragm-dependent signaling and translocates nephrin, Podocin, and CD2 associated protein in cultured human podocytes
    • 15659563 10.1681/ASN.2004030172 1:CAS:528:DC%2BD2MXis12gurc%3D
    • Coward RJ, Foster RR, Patton D, Ni L, Lennon R, Bates DO, Harper SJ, Mathieson PW, Saleem MA (2005) Nephrotic plasma alters slit diaphragm-dependent signaling and translocates nephrin, Podocin, and CD2 associated protein in cultured human podocytes. J Am Soc Nephrol 16:629-637
    • (2005) J Am Soc Nephrol , vol.16 , pp. 629-637
    • Coward, R.J.1    Foster, R.R.2    Patton, D.3    Ni, L.4    Lennon, R.5    Bates, D.O.6    Harper, S.J.7    Mathieson, P.W.8    Saleem, M.A.9
  • 59
    • 18444373239 scopus 로고    scopus 로고
    • Serum glomerular permeability activity in patients with podocin mutations (NPHS2) and steroid-resistant nephrotic syndrome
    • 12089392 10.1097/01.ASN.0000016445.29513.AB 1:CAS:528: DC%2BD38XlvVSqtL4%3D
    • Carraro M, Caridi G, Bruschi M, Artero M, Bertelli R, Zennaro C, Musante L, Candiano G, Perfumo F, Ghiggeri GM (2002) Serum glomerular permeability activity in patients with podocin mutations (NPHS2) and steroid-resistant nephrotic syndrome. J Am Soc Nephrol 13:1946-1952
    • (2002) J Am Soc Nephrol , vol.13 , pp. 1946-1952
    • Carraro, M.1    Caridi, G.2    Bruschi, M.3    Artero, M.4    Bertelli, R.5    Zennaro, C.6    Musante, L.7    Candiano, G.8    Perfumo, F.9    Ghiggeri, G.M.10
  • 64
    • 0031747153 scopus 로고    scopus 로고
    • Limb and kidney defects in Lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndrome
    • 9590288 10.1038/ng0598-51
    • Chen H, Lun Y, Ovchinnikov D, Kokubo H, Oberg KC, Pepicelli CV, Gan L, Lee B, Johnson RL (1998) Limb and kidney defects in Lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndrome. Nat Genet 19:51-55
    • (1998) Nat Genet , vol.19 , pp. 51-55
    • Chen, H.1    Lun, Y.2    Ovchinnikov, D.3    Kokubo, H.4    Oberg, K.C.5    Pepicelli, C.V.6    Gan, L.7    Lee, B.8    Johnson, R.L.9
  • 65
    • 0031800728 scopus 로고    scopus 로고
    • Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome
    • 9590287 10.1038/ng0598-47 1:CAS:528:DyaK1cXislWqurc%3D
    • Dreyer SD, Zhou G, Baldini A, Winterpacht A, Zabel B, Cole W, Johnson RL, Lee B (1998) Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome. Nat Genet 19:47-50
    • (1998) Nat Genet , vol.19 , pp. 47-50
    • Dreyer, S.D.1    Zhou, G.2    Baldini, A.3    Winterpacht, A.4    Zabel, B.5    Cole, W.6    Johnson, R.L.7    Lee, B.8
  • 72
    • 0031774828 scopus 로고    scopus 로고
    • A case of mitochondrial cytopathy with a typical point mutation for MELAS, presenting with severe focal-segmental glomerulosclerosis as main clinical manifestation
    • 9845835 10.1159/000013406 1:STN:280:DyaK1M%2FmtlKgtw%3D%3D
    • Kurogouchi F, Oguchi T, Mawatari E, Yamaura S, Hora K, Takei M, Sekijima Y, Ikeda S, Kiyosawa K (1998) A case of mitochondrial cytopathy with a typical point mutation for MELAS, presenting with severe focal-segmental glomerulosclerosis as main clinical manifestation. Am J Nephrol 18:551-556
    • (1998) Am J Nephrol , vol.18 , pp. 551-556
    • Kurogouchi, F.1    Oguchi, T.2    Mawatari, E.3    Yamaura, S.4    Hora, K.5    Takei, M.6    Sekijima, Y.7    Ikeda, S.8    Kiyosawa, K.9
  • 74
    • 33748329411 scopus 로고    scopus 로고
    • Focal segmental glomerulosclerosis in patients with mandibuloacral dysplasia owing to ZMPSTE24 deficiency
    • 17152860 10.2310/6650.2006.05068
    • Agarwal AK, Zhou XJ, Hall RK, Nicholls K, Bankier A, Van Esch H, Fryns JP, Garg A (2006) Focal segmental glomerulosclerosis in patients with mandibuloacral dysplasia owing to ZMPSTE24 deficiency. J Investig Med 54:208-213
    • (2006) J Investig Med , vol.54 , pp. 208-213
    • Agarwal, A.K.1    Zhou, X.J.2    Hall, R.K.3    Nicholls, K.4    Bankier, A.5    Van Esch, H.6    Fryns, J.P.7    Garg, A.8
  • 75
    • 0027296792 scopus 로고
    • Galloway-Mowat syndrome of abnormal gyral patterns and glomerulopathy
    • 8213914 10.1002/ajmg.1320470221 1:STN:280:DyaK2c%2FislWlsg%3D%3D
    • Cooperstone BG, Friedman A, Kaplan BS (1993) Galloway-Mowat syndrome of abnormal gyral patterns and glomerulopathy. Am J Med Genet 47:250-254
    • (1993) Am J Med Genet , vol.47 , pp. 250-254
    • Cooperstone, B.G.1    Friedman, A.2    Kaplan, B.S.3
  • 76
    • 0029830491 scopus 로고    scopus 로고
    • Congenital nephrotic syndrome: A novel phenotype of type i carbohydrate-deficient glycoprotein syndrome
    • 8982953 10.1007/BF01799174
    • van der Knaap MS, Wevers RA, Monnens L, Jakobs C, Jaeken J, van Wijk JA (1996) Congenital nephrotic syndrome: a novel phenotype of type I carbohydrate-deficient glycoprotein syndrome. J Inherit Metab Dis 19:787-791
    • (1996) J Inherit Metab Dis , vol.19 , pp. 787-791
    • Van Der Knaap, M.S.1    Wevers, R.A.2    Monnens, L.3    Jakobs, C.4    Jaeken, J.5    Van Wijk, J.A.6
  • 80
    • 77950515351 scopus 로고    scopus 로고
    • Genetics of nephrotic syndrome: Connecting molecular genetics to podocyte physiology
    • 19808795 10.1093/hmg/ddp328 1:CAS:528:DC%2BD1MXhtlCqu7nP
    • Machuca E, Benoit G, Antignac C (2009) Genetics of nephrotic syndrome: connecting molecular genetics to podocyte physiology. Hum Mol Genet 18:R185-R194
    • (2009) Hum Mol Genet , vol.18
    • Machuca, E.1    Benoit, G.2    Antignac, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.