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Is IgA nephropathy the same disease in different parts of the world?

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Abstract

Since it was first described in 1968, immunoglobulin A nephropathy (IgAN) is understood to be the most common form of glomerulonephritis worldwide. The diagnosis of IgAN depends on the presence of dominant mesangial IgA1 deposition by renal biopsy. To date, a wide spectrum of clinical and pathologic features of IgAN have been observed, implying that IgAN might not be the same disease across the world. Here, we review the characteristics of IgAN from perspectives of epidemiology, clinical-pathological patterns, disease pathogenesis, and treatment response across different ethnic populations. Overall, IgAN is most prevalent in Asians, followed by Caucasians, and relatively rare in Africans. More severe clinical presentation and higher risk of disease progression have been reported in Asians than Europeans. Moreover, active lesions, such as endocapillary hypercellularity and crescents, are more commonly reported in Asians than Europeans. Response to corticosteroid/immunosuppression therapy is variably reported, with greater apparent efficacy reported in Asian than European studies. Although a multi-hit hypothesis has been suggested for IgAN, the relative importance of each “hit” may vary in different ethnic populations and this variation underlies the differences in presentation of IgAN. In the future, a better understanding of pathogenic pathways operating in different ethnic populations may help provide better biomarkers of disease and more precise targeting of treatment strategies for IgAN.

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References

  1. D’Amico G (2004) Natural history of idiopathic IgA nephropathy and factors predictive of disease outcome. Semin Nephrol 24(3):179–196

    Article  PubMed  Google Scholar 

  2. Roberts IS (2014) Pathology of IgA nephropathy. Nat Rev Nephrol 10(8):445–454

    Article  CAS  PubMed  Google Scholar 

  3. Yeo SC, Goh SM, Barratt J (2019) Is immunoglobulin A nephropathy different in different ethnic populations? Nephrology (Carlton) 24(9):885–895

    Google Scholar 

  4. Lai KN, Tang SC, Schena FP, Novak J, Tomino Y, Fogo AB, Glassock RJ (2016) IgA nephropathy Nat Rev Dis Primers 2:16001

    Article  PubMed  Google Scholar 

  5. Schena FP, Nistor I (2018) Epidemiology of IgA nephropathy: a global perspective. Semin Nephrol 38(5):435–442

    Article  PubMed  Google Scholar 

  6. Moriyama T (2019) Clinical and histological features and therapeutic strategies for IgA nephropathy. Clin Exp Nephrol 23(9):1089–1099

    Article  PubMed  Google Scholar 

  7. Fennelly NK, Kennedy C, Jenkinson AC, Connaughton DM, Stapleton C, Dorman AM, Doyle B, Conlon PJ (2018) Clinical heterogeneity in familial IgA nephropathy. Nephron 139(1):63–69

    Article  CAS  PubMed  Google Scholar 

  8. Barbour SJ, Cattran DC, Kim SJ, Levin A, Wald R, Hladunewich MA, Reich HN (2013) Individuals of Pacific Asian origin with IgA nephropathy have an increased risk of progression to end-stage renal disease. Kidney Int 84(5):1017–1024

    Article  CAS  PubMed  Google Scholar 

  9. Suzuki H, Kiryluk K, Novak J, Moldoveanu Z, Herr AB, Renfrow MB, Wyatt RJ, Scolari F, Mestecky J, Gharavi AG et al (2011) The pathophysiology of IgA nephropathy. J Am Soc Nephrol 22(10):1795–1803

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Kiryluk K, Julian BA, Wyatt RJ, Scolari F, Zhang H, Novak J, Gharavi AG (2010) Genetic studies of IgA nephropathy: past, present, and future. Pediatr Nephrol 25(11):2257–2268

    Article  PubMed  PubMed Central  Google Scholar 

  11. Waldherr R, Rambausek M, Duncker WD, Ritz E (1989) Frequency of mesangial IgA deposits in a non-selected autopsy series. Nephrol Dial Transplant 4(11):943–946

    Article  CAS  PubMed  Google Scholar 

  12. Hall YN, Fuentes EF, Chertow GM, Olson JL (2004) Race/ethnicity and disease severity in IgA nephropathy. BMC Nephrol 5:10

    Article  PubMed  PubMed Central  Google Scholar 

  13. Riansuwan T, Kanjanabuch T, Lewsuwan S, Eiam-Ong S (2006) Clinical characteristics and histopathological findings in 120 IgA nephropathy patients in Thailand. J Med Assoc Thai 89(Suppl 2):S163-167

    PubMed  Google Scholar 

  14. Li PK, Ho KK, Szeto CC, Yu L, Lai FM (2002) Prognostic indicators of IgA nephropathy in the Chinese–clinical and pathological perspectives. Nephrol Dial Transplant 17(1):64–69

    Article  CAS  PubMed  Google Scholar 

  15. Schena FP (1990) A retrospective analysis of the natural history of primary IgA nephropathy worldwide. Am J Med 89(2):209–215

    Article  CAS  PubMed  Google Scholar 

  16. Gutierrez E, Zamora I, Ballarin JA, Arce Y, Jimenez S, Quereda C, Olea T, Martinez-Ara J, Segarra A, Bernis C et al (2012) Long-term outcomes of IgA nephropathy presenting with minimal or no proteinuria. J Am Soc Nephrol 23(10):1753–1760

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Bartosik LP, Lajoie G, Sugar L, Cattran DC (2001) Predicting progression in IgA nephropathy. Am J Kidney Dis 38(4):728–735

    Article  CAS  PubMed  Google Scholar 

  18. Szeto CC, Lai FM, To KF, Wong TY, Chow KM, Choi PC, Lui SF, Li PK (2001) The natural history of immunoglobulin a nephropathy among patients with hematuria and minimal proteinuria. Am J Med 110(6):434–437

    Article  CAS  PubMed  Google Scholar 

  19. Li L (1996) End-stage renal disease in China. Kidney Int 49(1):287–301

    Article  CAS  PubMed  Google Scholar 

  20. Koyama A, Igarashi M, Kobayashi M (1997) Natural history and risk factors for immunoglobulin A nephropathy in Japan. Research Group on Progressive Renal Diseases. Am J Kidney Dis 29(4):526–532

  21. Working Group of the International Ig ANN, the Renal Pathology S, Roberts IS, Cook HT, Troyanov S, Alpers CE, Amore A, Barratt J, Berthoux F, Bonsib S, et al (2009) The Oxford classification of IgA nephropathy: pathology definitions, correlations, and reproducibility. Kidney Int 76(5):546–556

    Article  Google Scholar 

  22. Working Group of the International Ig ANN, the Renal Pathology S, Cattran DC, Coppo R, Cook HT, Feehally J, Roberts IS, Troyanov S, Alpers CE, Amore A, et al (2009) The Oxford classification of IgA nephropathy: rationale, clinicopathological correlations, and classification. Kidney Int 76(5):534–545

    Article  Google Scholar 

  23. Trimarchi H, Barratt J, Cattran DC, Cook HT, Coppo R, Haas M, Liu ZH, Roberts IS, Yuzawa Y, Zhang H et al (2017) Oxford Classification of IgA nephropathy 2016: an update from the IgA Nephropathy Classification Working Group. Kidney Int 91(5):1014–1021

    Article  PubMed  Google Scholar 

  24. Alamartine E, Sauron C, Laurent B, Sury A, Seffert A, Mariat C (2011) The use of the Oxford classification of IgA nephropathy to predict renal survival. Clin J Am Soc Nephrol 6(10):2384–2388

    Article  PubMed  PubMed Central  Google Scholar 

  25. Edstrom Halling S, Soderberg MP, Berg UB (2012) Predictors of outcome in paediatric IgA nephropathy with regard to clinical and histopathological variables (Oxford classification). Nephrol Dial Transplant 27(2):715–722

    Article  PubMed  CAS  Google Scholar 

  26. El Karoui K, Hill GS, Karras A, Moulonguet L, Caudwell V, Loupy A, Bruneval P, Jacquot C, Nochy D (2011) Focal segmental glomerulosclerosis plays a major role in the progression of IgA nephropathy. II. Light microscopic and clinical studies. Kidney Int 79(6):643–654

  27. Zeng CH, Le W, Ni Z, Zhang M, Miao L, Luo P, Wang R, Lv Z, Chen J, Tian J et al (2012) A multicenter application and evaluation of the oxford classification of IgA nephropathy in adult chinese patients. Am J Kidney Dis 60(5):812–820

    Article  PubMed  Google Scholar 

  28. Katafuchi R, Ninomiya T, Nagata M, Mitsuiki K, Hirakata H (2011) Validation study of oxford classification of IgA nephropathy: the significance of extracapillary proliferation. Clin J Am Soc Nephrol 6(12):2806–2813

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. Kang SH, Choi SR, Park HS, Lee JY, Sun IO, Hwang HS, Chung BH, Park CW, Yang CW, Kim YS et al (2012) The Oxford classification as a predictor of prognosis in patients with IgA nephropathy. Nephrol Dial Transplant 27(1):252–258

    Article  PubMed  Google Scholar 

  30. Shi SF, Wang SX, Jiang L, Lv JC, Liu LJ, Chen YQ, Zhu SN, Liu G, Zou WZ, Zhang H et al (2011) Pathologic predictors of renal outcome and therapeutic efficacy in IgA nephropathy: validation of the oxford classification. Clin J Am Soc Nephrol 6(9):2175–2184

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. 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 27(5):783–792

    Article  PubMed  Google Scholar 

  32. Kataoka H, Ohara M, Shibui K, Sato M, Suzuki T, Amemiya N, Watanabe Y, Honda K, Mochizuki T, Nitta K (2012) Overweight and obesity accelerate the progression of IgA nephropathy: prognostic utility of a combination of BMI and histopathological parameters. Clin Exp Nephrol 16(5):706–712

    Article  CAS  PubMed  Google Scholar 

  33. Moriyama T, Nakayama K, Iwasaki C, Ochi A, Tsuruta Y, Itabashi M, Tsukada M, Takei T, Uchida K, Nitta K (2012) Severity of nephrotic IgA nephropathy according to the Oxford classification. Int Urol Nephrol 44(4):1177–1184

    Article  PubMed  Google Scholar 

  34. Lee H, Yi SH, Seo MS, Hyun JN, Jeon JS, Noh H, Han DC, Hwang SD, Jin SY, Kwon SH (2012) Validation of the Oxford classification of IgA nephropathy: a single-center study in Korean adults. Korean J Intern Med 27(3):293–300

    Article  PubMed  PubMed Central  Google Scholar 

  35. Le W, Zeng CH, Liu Z, Liu D, Yang Q, Lin RX, Xia ZK, Fan ZM, Zhu G, Wu Y et al (2012) Validation of the Oxford classification of IgA nephropathy for pediatric patients from China. BMC Nephrol 13:158

    Article  PubMed  PubMed Central  Google Scholar 

  36. Herzenberg AM, Fogo AB, Reich HN, Troyanov S, Bavbek N, Massat AE, Hunley TE, Hladunewich MA, Julian BA, Fervenza FC et al (2011) Validation of the Oxford classification of IgA nephropathy. Kidney Int 80(3):310–317

    Article  PubMed  Google Scholar 

  37. Yau T, Korbet SM, Schwartz MM, Cimbaluk DJ (2011) The Oxford classification of IgA nephropathy: a retrospective analysis. Am J Nephrol 34(5):435–444

    Article  CAS  PubMed  Google Scholar 

  38. Alexander S, Varughese S, Franklin R, Roy S, Rebekah G, David VG, Mohapatra A, Valson AT, Jacob S, Koshy PM et al (2021) Epidemiology, baseline characteristics and risk of progression in the first South-Asian prospective longitudinal observational IgA nephropathy cohort. Kidney Int Rep 6(2):414–428

    Article  PubMed  Google Scholar 

  39. Hsu SI (2008) Racial and genetic factors in IgA nephropathy. Semin Nephrol 28(1):48–57

    Article  PubMed  Google Scholar 

  40. Feehally J, Farrall M, Boland A, Gale DP, Gut I, Heath S, Kumar A, Peden JF, Maxwell PH, Morris DL et al (2010) HLA has strongest association with IgA nephropathy in genome-wide analysis. J Am Soc Nephrol 21(10):1791–1797

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  41. Gharavi AG, Kiryluk K, Choi M, Li Y, Hou P, Xie J, Sanna-Cherchi S, Men CJ, Julian BA, Wyatt RJ et al (2011) Genome-wide association study identifies susceptibility loci for IgA nephropathy. Nat Genet 43(4):321–327

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Yu XQ, Li M, Zhang H, Low HQ, Wei X, Wang JQ, Sun LD, Sim KS, Li Y, Foo JN et al (2011) A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy. Nat Genet 44(2):178–182

    Article  PubMed  CAS  Google Scholar 

  43. Kiryluk K, Li Y, Scolari F, Sanna-Cherchi S, Choi M, Verbitsky M, Fasel D, Lata S, Prakash S, Shapiro S et al (2014) Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens. Nat Genet 46(11):1187–1196

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  44. Li M, Foo JN, Wang JQ, Low HQ, Tang XQ, Toh KY, Yin PR, Khor CC, Goh YF, Irwan ID et al (2015) Identification of new susceptibility loci for IgA nephropathy in Han Chinese. Nat Commun 6:7270

    Article  CAS  PubMed  Google Scholar 

  45. Li M, Wang L, Shi DC, Foo JN, Zhong Z, Khor CC, Lanzani C, Citterio L, Salvi E, Yin PR et al (2020) Genome-wide meta-analysis identifies three novel susceptibility loci and reveals ethnic heterogeneity of genetic susceptibility for IgA nephropathy. J Am Soc Nephrol 31(12):2949–2963

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  46. Allen AC, Harper SJ, Feehally J (1995) Galactosylation of N- and O-linked carbohydrate moieties of IgA1 and IgG in IgA nephropathy. Clin Exp Immunol 100(3):470–474

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  47. Hastings MC, Moldoveanu Z, Julian BA, Novak J, Sanders JT, McGlothan KR, Gharavi AG, Wyatt RJ (2010) Galactose-deficient IgA1 in African Americans with IgA nephropathy: serum levels and heritability. Clin J Am Soc Nephrol 5(11):2069–2074

    Article  PubMed  PubMed Central  Google Scholar 

  48. Allen AC, Bailey EM, Barratt J, Buck KS, Feehally J (1999) Analysis of IgA1 O-glycans in IgA nephropathy by fluorophore-assisted carbohydrate electrophoresis. J Am Soc Nephrol 10(8):1763–1771

    Article  CAS  PubMed  Google Scholar 

  49. Mestecky J, Tomana M, Crowley-Nowick PA, Moldoveanu Z, Julian BA, Jackson S (1993) Defective galactosylation and clearance of IgA1 molecules as a possible etiopathogenic factor in IgA nephropathy. Contrib Nephrol 104:172–182

    Article  CAS  PubMed  Google Scholar 

  50. Gale DP, Molyneux K, Wimbury D, Higgins P, Levine AP, Caplin B, Ferlin A, Yin P, Nelson CP, Stanescu H et al (2017) Galactosylation of IgA1 Is associated with common variation in C1GALT1. J Am Soc Nephrol 28(7):2158–2166

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  51. Kiryluk K, Li Y, Moldoveanu Z, Suzuki H, Reily C, Hou P, Xie J, Mladkova N, Prakash S, Fischman C, et al. (2017) GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway. PLoS Genet 13(2):e1006609

  52. Suzuki H, Fan R, Zhang Z, Brown R, Hall S, Julian BA, Chatham WW, Suzuki Y, Wyatt RJ, Moldoveanu Z et al (2009) Aberrantly glycosylated IgA1 in IgA nephropathy patients is recognized by IgG antibodies with restricted heterogeneity. J Clin Invest 119(6):1668–1677

    CAS  PubMed  PubMed Central  Google Scholar 

  53. Yanagihara T, Brown R, Hall S, Moldoveanu Z, Goepfert A, Tomana M, Julian BA, Mestecky J, Novak J (2012) In vitro-generated immune complexes containing galactose-deficient IgA1 stimulate proliferation of mesangial cells. Results Immunol 2:166–172

    Article  PubMed  PubMed Central  Google Scholar 

  54. Yanagawa H, Suzuki H, Suzuki Y, Kiryluk K, Gharavi AG, Matsuoka K, Makita Y, Julian BA, Novak J, Tomino Y (2014) A panel of serum biomarkers differentiates IgA nephropathy from other renal diseases. PLoS One 9(5):e98081

  55. van der Boog PJ, De Fijter JW, Van Kooten C, Van Der Holst R, Van Seggelen A, Van Es LA, Daha MR (2003) Complexes of IgA with FcalphaRI/CD89 are not specific for primary IgA nephropathy. Kidney Int 63(2):514–521

    Article  PubMed  Google Scholar 

  56. Launay P, Grossetete B, Arcos-Fajardo M, Gaudin E, Torres SP, Beaudoin L, Patey-Mariaud de Serre N, Lehuen A, Monteiro RC (2000) Fcalpha receptor (CD89) mediates the development of immunoglobulin A (IgA) nephropathy (Berger’s disease). Evidence for pathogenic soluble receptor-Iga complexes in patients and CD89 transgenic mice. J Exp Med 191(11):1999–2009

  57. Wu H, Wang X, Yang Z, Zhao Q, Wen Y, Li X, Zhang W, Gao R (2020) Serum Soluble CD89-IgA Complexes are elevated in IgA nephropathy without immunosuppressant history. Dis Markers 2020:8393075

    PubMed  PubMed Central  Google Scholar 

  58. Evans DJ, Williams DG, Peters DK, Sissons JG, Boulton-Jones JM, Ogg CS, Cameron JS, Hoffbrand BI (1973) Glomerular deposition of properdin in Henoch-Schonlein syndrome and idiopathic focal nephritis. Br Med J 3(5875):326–328

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  59. Zhai YL, Meng SJ, Zhu L, Shi SF, Wang SX, Liu LJ, Lv JC, Yu F, Zhao MH, Zhang H (2016) Rare variants in the complement factor H-related protein 5 gene contribute to genetic susceptibility to IgA nephropathy. J Am Soc Nephrol 27(9):2894–2905

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  60. Medjeral-Thomas NR, Lomax-Browne HJ, Beckwith H, Willicombe M, McLean AG, Brookes P, Pusey CD, Falchi M, Cook HT, Pickering MC (2017) Circulating complement factor H-related proteins 1 and 5 correlate with disease activity in IgA nephropathy. Kidney Int 92(4):942–952

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  61. Zhu L, Guo WY, Shi SF, Liu LJ, Lv JC, Medjeral-Thomas NR, Lomax-Browne HJ, Pickering MC, Zhang H (2018) Circulating complement factor H-related protein 5 levels contribute to development and progression of IgA nephropathy. Kidney Int 94(1):150–158

    Article  CAS  PubMed  Google Scholar 

  62. Rauterberg EW, Lieberknecht HM, Wingen AM, Ritz E (1987) Complement membrane attack (MAC) in idiopathic IgA-glomerulonephritis. Kidney Int 31(3):820–829

    Article  CAS  PubMed  Google Scholar 

  63. Roos A, Rastaldi MP, Calvaresi N, Oortwijn BD, Schlagwein N, van Gijlswijk-Janssen DJ, Stahl GL, Matsushita M, Fujita T, van Kooten C et al (2006) Glomerular activation of the lectin pathway of complement in IgA nephropathy is associated with more severe renal disease. J Am Soc Nephrol 17(6):1724–1734

    Article  CAS  PubMed  Google Scholar 

  64. Guo WY, Zhu L, Meng SJ, Shi SF, Liu LJ, Lv JC, Zhang H (2017) Mannose-binding lectin levels could predict prognosis in IgA nephropathy. J Am Soc Nephrol 28(11):3175–3181

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  65. Lv J, Zhang H, Wong MG, Jardine MJ, Hladunewich M, Jha V, Monaghan H, Zhao M, Barbour S, Reich H et al (2017) Effect of oral methylprednisolone on clinical outcomes in patients with IgA nephropathy: the TESTING randomized clinical trial. JAMA 318(5):432–442

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  66. Rauen T, Eitner F, Fitzner C, Sommerer C, Zeier M, Otte B, Panzer U, Peters H, Benck U, Mertens PR et al (2015) Intensive supportive care plus immunosuppression in IgA nephropathy. N Engl J Med 373(23):2225–2236

    Article  CAS  PubMed  Google Scholar 

  67. Tang S, Leung JC, Chan LY, Lui YH, Tang CS, Kan CH, Ho YW, Lai KN (2005) Mycophenolate mofetil alleviates persistent proteinuria in IgA nephropathy. Kidney Int 68(2):802–812

    Article  CAS  PubMed  Google Scholar 

  68. Tang SC, Tang AW, Wong SS, Leung JC, Ho YW, Lai KN (2010) Long-term study of mycophenolate mofetil treatment in IgA nephropathy. Kidney Int 77(6):543–549

    Article  CAS  PubMed  Google Scholar 

  69. Maes BD, Oyen R, Claes K, Evenepoel P, Kuypers D, Vanwalleghem J, Van Damme B, Vanrenterghem YF (2004) Mycophenolate mofetil in IgA nephropathy: results of a 3-year prospective placebo-controlled randomized study. Kidney Int 65(5):1842–1849

    Article  CAS  PubMed  Google Scholar 

  70. Frisch G, Lin J, Rosenstock J, Markowitz G, D’Agati V, Radhakrishnan J, Preddie D, Crew J, Valeri A, Appel G (2005) Mycophenolate mofetil (MMF) vs placebo in patients with moderately advanced IgA nephropathy: a double-blind randomized controlled trial. Nephrol Dial Transplant 20(10):2139–2145

    Article  CAS  PubMed  Google Scholar 

  71. Hogg RJ, Bay RC, Jennette JC, Sibley R, Kumar S, Fervenza FC, Appel G, Cattran D, Fischer D, Hurley RM et al (2015) Randomized controlled trial of mycophenolate mofetil in children, adolescents, and adults with IgA nephropathy. Am J Kidney Dis 66(5):783–791

    Article  CAS  PubMed  Google Scholar 

  72. Du B, Jia Y, Zhou W, Min X, Miao L, Cui W (2017) Efficacy and safety of mycophenolate mofetil in patients with IgA nephropathy: an update meta-analysis. BMC Nephrol 18(1):245

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  73. Xie Y, Nishi S, Ueno M, Imai N, Sakatsume M, Narita I, Suzuki Y, Akazawa K, Shimada H, Arakawa M et al (2003) The efficacy of tonsillectomy on long-term renal survival in patients with IgA nephropathy. Kidney Int 63(5):1861–1867

    Article  PubMed  Google Scholar 

  74. Komatsu H, Fujimoto S, Hara S, Sato Y, Yamada K, Kitamura K (2008) Effect of tonsillectomy plus steroid pulse therapy on clinical remission of IgA nephropathy: a controlled study. Clin J Am Soc Nephrol 3(5):1301–1307

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  75. Yuzawa Y, Yamamoto R, Takahashi K, Katafuchi R, Tomita M, Fujigaki Y, Kitamura H, Goto M, Yasuda T, Sato M et al (2016) Evidence-based clinical practice guidelines for IgA nephropathy 2014. Clin Exp Nephrol 20(4):511–535

    Article  PubMed  PubMed Central  Google Scholar 

  76. Rasche FM, Schwarz A, Keller F (1999) Tonsillectomy does not prevent a progressive course in IgA nephropathy. Clin Nephrol 51(3):147–152

    CAS  PubMed  Google Scholar 

  77. Piccoli A, Codognotto M, Tabbi MG, Favaro E, Rossi B (2010) Influence of tonsillectomy on the progression of mesangioproliferative glomerulonephritis. Nephrol Dial Transplant 25(8):2583–2589

    Article  PubMed  Google Scholar 

  78. Feehally J, Coppo R, Troyanov S, Bellur SS, Cattran D, Cook T, Roberts IS, Verhave JC, Camilla R, Vergano L et al (2016) Tonsillectomy in a European cohort of 1,147 patients with IgA nephropathy. Nephron 132(1):15–24

    Article  CAS  PubMed  Google Scholar 

  79. Smerud HK, Barany P, Lindstrom K, Fernstrom A, Sandell A, Pahlsson P, Fellstrom B (2011) New treatment for IgA nephropathy: enteric budesonide targeted to the ileocecal region ameliorates proteinuria. Nephrol Dial Transplant 26(10):3237–3242

    Article  CAS  PubMed  Google Scholar 

  80. Fellstrom BC, Barratt J, Cook H, Coppo R, Feehally J, de Fijter JW, Floege J, Hetzel G, Jardine AG, Locatelli F et al (2017) Targeted-release budesonide versus placebo in patients with IgA nephropathy (NEFIGAN): a double-blind, randomised, placebo-controlled phase 2b trial. Lancet 389(10084):2117–2127

    Article  PubMed  Google Scholar 

  81. Han SS, Yang SH, Choi M, Kim HR, Kim K, Lee S, Moon KC, Kim JY, Lee H, Lee JP et al (2016) The role of TNF superfamily member 13 in the progression of IgA nephropathy. J Am Soc Nephrol 27(11):3430–3439

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  82. Lafayette RA, Rovin BH, Reich HN, Tumlin JA, Floege J, Barratt J (2020) Safety, tolerability and efficacy of narsoplimab, a Novel MASP-2 inhibitor for the treatment of IgA nephropathy. Kidney Int Rep 5(11):2032–2041

    Article  PubMed  PubMed Central  Google Scholar 

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This study was funded by the National Natural Science Foundation of China (grant number 82070733).

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This article is a contribution to the Special issue on: The IgA system, IgA nephropathy and IgA vasculitis - Guest Editors: Jürgen Floege & Jonathan Barratt

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Zhang, H., Barratt, J. Is IgA nephropathy the same disease in different parts of the world?. Semin Immunopathol 43, 707–715 (2021). https://doi.org/10.1007/s00281-021-00884-7

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