Histological prognostic factors in children with Henoch-Schönlein purpura nephritis

Springer Science and Business Media LLC - Tập 35 - Trang 313-320 - 2019
Jean-Daniel Delbet1,2, Guillaume Geslain1, Martin Auger1, Julien Hogan3,4, Rémi Salomon5, Michel Peuchmaur3, Georges Deschênes3,4, David Buob6, Cyrielle Parmentier1, Tim Ulinski1,2
1Pediatric Nephrology unit, Trousseau Hospital, APHP.6, DMU Origyne, Paris, France
2Sorbonne Université, Paris, France
3Pediatric Nephrology, Robert Debré Hospital, APHP, Paris, France
4University Paris Diderot, Paris, France
5Pediatric Nephrology, Necker Enfants Malades, APHP, Paris, France
6Pathology Department, Tenon Hospital, APHP, Paris, France

Tóm tắt

The management of IgA vasculitis with nephritis (IgAVN) remains controversial because of the difficulty to identify prognostic factors. This study reports the prognosis of children with IgAVN in relation to histological parameters. All children with IgAVN diagnosed between 2000 and 2015 in three pediatric nephrology centers were included. The following histological parameters were analyzed: mesangial proliferation (MP), endocapillary proliferation (EP), crescents, active, or chronic tubular and interstitial lesions (TIa lesions/TIc lesions), and segmental glomerulosclerosis (GS). Clinical and biological data were collected at the time of renal biopsy. The primary endpoint was IgAVN remission defined as a proteinuria < 200 mg/l without renal failure. One hundred fifty-nine children were included with a median age of 7.6 years. Acute glomerular or TI lesions including MP, EP, crescents, and TIa lesions were observed, respectively, in 81%, 86%, 49%, and 21% of patients. Chronic glomerular lesions including GS and TIc lesions were observed in 6 and 7% of patients. Median initial proteinuria was 330 mg/mmol, albuminemia 32 g/l, and eGFR 110 ml/min/1.73 m2. One hundred twelve (70%) patients were in remission at the end of a median follow-up of 37.4 months. Chronic lesions were significantly associated with the absence of remission in multivariate analysis, whereas EP, crescents and TIa were not associated with a poor prognosis. Of children with IgAVN, 30% present a persistent renal disease at the end of a 3-year follow-up. Chronic histological lesions, but not EP or crescents, are associated with a bad prognosis and must be evaluated in IgAVN histological classification.

Tài liệu tham khảo

Chartapisak W, Opastirakul S, Hodson EM, Willis NS, Craig JC (2009) Interventions for preventing and treating kidney disease in Henoch-Schönlein Purpura (HSP). In: The Cochrane collaboration (ed) cochrane database of systematic reviews. John Wiley & Sons, Ltd, Chichester, UK Stewart M, Savage JM, Bell B, McCord B (1988) Long term renal prognosis of Henoch-Schönlein purpura in an unselected childhood population. Eur J Pediatr 147:113–115 Ronkainen J, Ala-Houhala M, Huttunen NP, Jahnukainen T, Koskimies O, Ormälä T, Nuutinen M (2003) Outcome of Henoch-Schoenlein nephritis with nephrotic-range proteinuria. Clin Nephrol 60:80–84 Goldstein AR, White RH, Akuse R, Chantler C (1992) Long-term follow-up of childhood Henoch-Schönlein nephritis. Lancet Lond Engl 339:280–282 Tudorache E, Azema C, Hogan J, Wannous H, Aoun B, Decramer S, Deschênes G, Ulinski T (2015) Even mild cases of paediatric Henoch-Schönlein purpura nephritis show significant long-term proteinuria. Acta Paediatr Oslo Nor 1992 104:843–848. https://doi.org/10.1111/apa.12723 Coppo R, Mazzucco G, Cagnoli L, Lupo A, Schena FP (1997) Long-term prognosis of Henoch-Schönlein nephritis in adults and children. Italian Group of Renal Immunopathology Collaborative Study on Henoch-Schönlein purpura. Nephrol Dial Transplant 12:2277–2283 Soylemezoglu O, Ozkaya O, Ozen S, Bakkaloglu A, Dusunsel R, Peru H, Cetinyurek A, Yildiz N, Donmez O, Buyan N, Mir S, Arisoy N, Gur-Guven A, Alpay H, Ekim M, Aksu N, Soylu A, Gok F, Poyrazoglu H, Sonmez F, Turkish Pediatric Vasculitis Study Group (2009) Henoch-Schönlein nephritis: a nationwide study. Nephron Clin Pract 112:c199–c204. https://doi.org/10.1159/000218109 Davin JC, Weening JJ (2001) Henoch-Schönlein purpura nephritis: an update. Eur J Pediatr 160:689–695 A Working Group of the International IgA Nephropathy Network and the Renal Pathology Society, Cattran DC, Coppo R, Cook HT, Feehally J, ISD R, Troyanov S, Alpers CE, Amore A, Barratt J, Berthoux F, Bonsib S, Bruijn JA, D’Agati V, D’ Amico G, Emancipator S, Emma F, Ferrario F, Fervenza FC, Florquin S, Fogo A, Geddes CC, Groene H-J, Haas M, Herzenberg AM, Hill PA, Hogg RJ, Hsu SI, Jennette JC, Joh K, Julian BA, Kawamura T, Lai FM, Leung CB, Li L-S, PKT L, Liu Z-H, Mackinnon B, Mezzano S, Schena FP, Tomino Y, Walker PD, Wang H, Weening JJ, Yoshikawa N, Zhang H (2009) The Oxford classification of IgA nephropathy: rationale, clinicopathological correlations, and classification. Kidney Int 76:534–545. https://doi.org/10.1038/ki.2009.243 Kim CH, Lim BJ, Bae YS, Kwon YE, Kim YL, Nam KH, Park KS, An SY, Koo HM, Doh FM, Lee MJ, Oh HJ, Yoo T-H, Kang S-W, Choi KH, Jeong HJ, Han SH (2014) Using the Oxford classification of IgA nephropathy to predict long-term outcomes of Henoch-Schönlein purpura nephritis in adults. Mod Pathol Off J U S Can Acad Pathol Inc 27:972–982. https://doi.org/10.1038/modpathol.2013.222 Goldstein AR, White RH, Akuse R, Chantler C (2010) EULAR/PRINTO/PRES criteria for Henoch-Schonlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part II: final classification criteria. Ann Rheum Dis 69:798–806. https://doi.org/10.1136/ard.2009.116657 Goldstein AR, White RH, Akuse R, Chantler C (1992) Long-term follow-up of childhood Henoch-Schönlein nephritis. Lancet Lond Engl 339:280–282 Edström Halling S, Söderberg MP, Berg UB (2010) Predictors of outcome in Henoch-Schönlein nephritis. Pediatr Nephrol Berl Ger 25:1101–1108. https://doi.org/10.1007/s00467-010-1444-y Mir S, Yavascan O, Mutlubas F, Yeniay B, Sonmez F (2007) Clinical outcome in children with Henoch-Schönlein nephritis. Pediatr Nephrol Berl Ger 22:64–70. https://doi.org/10.1007/s00467-006-0278-0 A Working Group of the International IgA Nephropathy Network and the Renal Pathology Society, Cattran DC, Coppo R, Cook HT, Feehally J, ISD R, Troyanov S, Alpers CE, Amore A, Barratt J, Berthoux F, Bonsib S, Bruijn JA, D’Agati V, D’ Amico G, Emancipator S, Emma F, Ferrario F, Fervenza FC, Florquin S, Fogo A, Geddes CC, Groene H-J, Haas M, Herzenberg AM, Hill PA, Hogg RJ, Hsu SI, Jennette JC, Joh K, Julian BA, Kawamura T, Lai FM, Leung CB, Li L-S, PKT L, Liu Z-H, Mackinnon B, Mezzano S, Schena FP, Tomino Y, Walker PD, Wang H, Weening JJ, Yoshikawa N, Zhang H (2009) The Oxford classification of IgA nephropathy: rationale, clinicopathological correlations, and classification. Kidney Int 76:534–545. https://doi.org/10.1038/ki.2009.243 Hennies I, Gimpel C, Gellermann J, Möller K, Mayer B, Dittrich K, Büscher AK, Hansen M, Aulbert W, Wühl E, Nissel R, Schalk G, Weber LT, Pohl M, Wygoda S, Beetz R, Klaus G, Fehrenbach H, König S, Staude H, Beringer O, Bald M, Walden U, von Schnakenburg C, Bertram G, Wallot M, Häffner K, Wiech T, Hoyer PF, Pohl M, German Society of Pediatric Nephrology (2018) Presentation of pediatric Henoch-Schönlein purpura nephritis changes with age and renal histology depends on biopsy timing. Pediatr Nephrol Berl Ger 33:277–286. https://doi.org/10.1007/s00467-017-3794-1 (2012) Chapter 11: Henoch-Schönlein purpura nephritis. Kidney Int (Suppl 2):218–220. https://doi.org/10.1038/kisup.2012.24 Niaudet P, Habib R (1998) Methylprednisolone pulse therapy in the treatment of severe forms of Schönlein-Henoch purpura nephritis. Pediatr Nephrol Berl Ger 12:238–243 Davin J-C, Coppo R (2013) Pitfalls in recommending evidence-based guidelines for a protean disease like Henoch–Schönlein purpura nephritis. Pediatr Nephrol 28:1897–1903. https://doi.org/10.1007/s00467-013-2550-4 Kim CH, Lim BJ, Bae YS, Kwon YE, Kim YL, Nam KH, Park KS, An SY, Koo HM, Doh FM, Lee MJ, Oh HJ, Yoo T-H, Kang S-W, Choi KH, Jeong HJ, Han SH (2014) Using the Oxford classification of IgA nephropathy to predict long-term outcomes of Henoch-Schönlein purpura nephritis in adults. Mod Pathol Off J U S Can Acad Pathol Inc 27:972–982. https://doi.org/10.1038/modpathol.2013.222 Inagaki K, Kaihan AB, Hachiya A, Ozeki T, Ando M, Kato S, Yasuda Y, Maruyama S (2018) Clinical impact of endocapillary proliferation according to the Oxford classification among adults with Henoch-Schönlein purpura nephritis: a multicenter retrospective cohort study. BMC Nephrol 19:208. https://doi.org/10.1186/s12882-018-1009-z Shima Y, Nakanishi K, Hama T, Mukaiyama H, Togawa H, Hashimura Y, Kaito H, Sako M, Iijima K, Yoshikawa N (2012) Validity of the Oxford classification of IgA nephropathy in children. Pediatr Nephrol Berl Ger 27:783–792. https://doi.org/10.1007/s00467-011-2061-0 Ronkainen J, Nuutinen M, Koskimies O (2002) The adult kidney 24 years after childhood Henoch-Schönlein purpura: a retrospective cohort study. Lancet Lond Engl 360:666–670. https://doi.org/10.1016/S0140-6736(02)09835-5 Butani L, Morgenstern BZ (2007) Long-term outcome in children after Henoch-Schonlein purpura nephritis. Clin Pediatr (Phila) 46:505–511. https://doi.org/10.1177/0009922806298896 Halling SFE, Söderberg MP, Berg UB (2005) Henoch Schönlein nephritis: clinical findings related to renal function and morphology. Pediatr Nephrol Berl Ger 20:46–51. https://doi.org/10.1007/s00467-004-1650-6 Delbet JD, Hogan J, Aoun B, Stoica I, Salomon R, Decramer S, Brocheriou I, Deschênes G, Ulinski T (2017) Clinical outcomes in children with Henoch-Schönlein purpura nephritis without crescents. Pediatr Nephrol Berl Ger 32:1193–1199. https://doi.org/10.1007/s00467-017-3604-9 Coppo R, Andrulli S, Amore A, Gianoglio B, Conti G, Peruzzi L, Locatelli F, Cagnoli L (2006) Predictors of outcome in Henoch-Schönlein nephritis in children and adults. Am J Kidney Dis Off J Natl Kidney Found 47:993–1003. https://doi.org/10.1053/j.ajkd.2006.02.178