浏览全部资源
扫码关注微信
扫 描 看 全 文
1.中南大学湘雅二医院肾脏移植科,长沙 410011
2.湖南省器官移植临床医学研究中心,长沙 410011
3.中南大学临床免疫研究中心,长沙 410011
TANG Zhouqi, Email: tzq0510@csu.edu.cn, ORCID: 0009-0004-7939-0730
LI Tengfang, Email: ltf120316@163.com, ORCID: 0000-0001-6345-6716
DAI Helong, Email: helong68888@csu.edu.cn, ORCID: 0000-0002-0696-3081
纸质出版日期: 2023-07-28 ,
收稿日期: 2023-03-06 ,
汤周琦, 李腾芳, 冯晨, 彭龙开, 谢续标, 彭风华, 蓝恭斌, 余少杰, 王彧, 代贺龙. 81例成人IgA肾病肾移植的临床疗效[J]. 中南大学学报(医学版), 2023, 48(7): 1017-1025.
TANG Zhouqi, LI Tengfang, FENG Chen, PENG Longkai, XIE Xubiao, PENG Fenghua, LAN Gongbin, YU Shaojie, WANG Yu, DAI Helong. Clinical outcomes for kidney transplantation in 81 adults with IgA nephropathy[J]. Journal of Central South University. Medical Science, 2023, 48(7): 1017-1025.
汤周琦, 李腾芳, 冯晨, 彭龙开, 谢续标, 彭风华, 蓝恭斌, 余少杰, 王彧, 代贺龙. 81例成人IgA肾病肾移植的临床疗效[J]. 中南大学学报(医学版), 2023, 48(7): 1017-1025. DOI:10.11817/j.issn.1672-7347.2023.230079
TANG Zhouqi, LI Tengfang, FENG Chen, PENG Longkai, XIE Xubiao, PENG Fenghua, LAN Gongbin, YU Shaojie, WANG Yu, DAI Helong. Clinical outcomes for kidney transplantation in 81 adults with IgA nephropathy[J]. Journal of Central South University. Medical Science, 2023, 48(7): 1017-1025. DOI:10.11817/j.issn.1672-7347.2023.230079
目的
2
免疫球蛋白A肾病(immunoglobulin A nephropathy,IgAN)是最常见的肾病类型之一,肾移植手术是终末期肾病最有效的治疗手段。本研究旨在分析成人IgA肾病肾移植的临床疗效,探讨IgA肾病肾移植围手术期及中远期的有效性与安全性。
方法
2
回顾性纳入2018年1月至2022年1月中南大学湘雅二医院实施的所有81例成人IgA肾病肾移植的临床资料和随访数据。受者年龄(34.1±9.9)岁,其中男性47例(58.0%),体重指数为(20.8±3.2) kg/m
2
,人白细胞抗原错配数为(3.5±1.2)个。总结受者肾移植手术后第1、5、7天以及出院时的估算肾小球滤过率(estimated glomerular filtration rate,eGFR)及每日24 h尿量情况,综合评估其移植肾恢复情况以及并发症发生情况。评估随访第6、12、24、36、48个月的eGFR、尿蛋白、尿隐血等指标。
结果
2
随访(25.7±15.8)个月。围手术期所有患者均未发生原发性移植肾无功能,51例(62.9%)患者属于移植物功能立即恢复,16例(19.8%)患者属于移植物功能缓慢恢复,两者占总数的82.7%;14例患者出现了移植物功能延迟恢复,占17.3%。共发生19例围手术期并发症,包括急性排斥反应9例、尿瘘5例、双下肢血管血栓1例、淋巴瘘4例。随访第6、12、24、36及48个月的eGFR分别为(65.3±22.9)、(67.6±23.0)、(64.3±21.8)、(65.9±24.7)及(68.7±31.2) mL/(min·1.73 m
2
)。中长期随访eGFR均保持较高水平,最长随访至56个月,eGFR波动仍较小;末次随访尿蛋白阳性率与尿隐血阳性率较低。移植肾IgAN复发4例,占总患者的4.94%,未出现严重肾功能不全。3例患者因重症肺炎、排斥反应、移植肾结石出现移植肾失功能,总体移植肾存活率达95%以上,随访至2022年1月所有患者存活率100%。
结论
2
成人IgAN肾病肾移植近期效果显著,受者受益明显,中远期效果良好,IgAN复发率较低,且很少引起严重肾功能损害。
Objective
2
Immunoglobulin A nephropathy (IgAN) is one of the most common types of kidney disease
and kidney transplantation is the most effective treatment for end-stage renal disease. This study aims to analyze the clinical curative effect of renal transplantation for adults with IgAN and to discuss the efficacy and safety of kidney transplantation for IgAN at the perioperative period and medium- and long-term follow-up.
Methods
2
This retrospective study included the clinical and follow-up data of 81 adult patients with IgAN who underwent kidney transplantation at the Second Xiangya Hospital
Central South University from January 2018 to January 2022. Of the 81 patients whose age at (34.1±9.9) years old
47 (58.0%) were male. The body mass index was (20.8±3.2) kg/m
2
and the human leukocyte antigen (HLA) mismatch number was 3.5±1.2. The estimated glomerular filtration rate (eGFR) and daily 24-hour urine output for the recipients on the 1st
5th
and 7th day after kidney transplantation and when they were discharged were analyzed. The recovery of the transplanted kidney and occurrence of complications were comprehensively evaluated. The eGFR
urinary protein
and occult blood were evaluated at the 6th
12th
24th
36th
and 48th month and at the last follow-up.
Results
2
The follow-up time was (25.7±15.8) months. No primary non-function occurred in any patient during the perioperative period time. Fifty-one (63.0%) patients had immediate graft function recovery
and 16 (19.8%) patients had slow graft function recovery. Delayed recovery of graft function was observed in 14 (17.3%) patients. A total of 19 perioperative complications occurred
including 9 patients with acute rejection
5 patients with urinary fistula
1 thrombosis in both lower limbs
and 4 lymphatic fistula. The eGFR at 6th
12th
24th
36th
and 48th month of follow-up were (65.3±22.9)
(67.6±23.0)
(64.3±21.8)
(65.9±24.7)
and (68.7±31.2) mL/(min·1.73 m
2
)
respectively. The eGFR remained high during the medium- and long-term follow-ups. At the longest follow-up of 56 months
eGFR fluctuation was still mild
and the positive rate of urine protein and occult blood was low. IgAN recurred in 4 transplanted kidneys
accounting for 4.94% of the total patients
without severe renal insufficiency. Three patients had kidney dysfunction due to severe pneumonia
rejection
and stone in the transplanted kidney. The overall survival rate of the transplanted kidney was higher than 95%
and the survival rate of all patients was 100% till Januray 2022.
Conclusion
2
Renal transplantation for adults with IgAN had a remarkable short-term effect. The recipients can be beneficial significantly to favorable midium- and long-term outcomes. IgAN recurrence is infrequent and rarely causes severe renal function damage.
IgA肾病肾移植疗效
immunoglobulin A nephropathykidney transplantationoutcomes
Penfold RS, Prendecki M, McAdoo S, et al. Primary IgA nephropathy: current challenges and future prospects[J]. Int J Nephrol Renovasc Dis, 2018, 11: 137-148. https://doi.org/10. 2147/IJNRD.S129227https://doi.org/10.2147/IJNRD.S129227.
Li LS, Liu ZH. Epidemiologic data of renal diseases from a single unit in China: analysis based on 13, 519 renal biopsies[J]. Kidney Int, 2004, 66(3): 920-923. https://doi.org/10.1111/j.1523-1755.2004.00837.xhttps://doi.org/10.1111/j.1523-1755.2004.00837.x.
Uffing A, Pérez-Saéz MJ, Jouve T, et al. Recurrence of IgA nephropathy after kidney transplantation in adults[J]. Clin J Am Soc Nephrol, 2021, 16(8): 1247-1255. https://doi.org/10.2215/CJN.00910121https://doi.org/10.2215/CJN.00910121.
Magistroni R, D’Agati VD, Appel GB, et al. New developments in the genetics, pathogenesis, and therapy of IgA nephropathy[J]. Kidney Int, 2015, 88(5): 974-989. https://doi.org/10.1038/ki.2015.252https://doi.org/10.1038/ki.2015.252.
D’Amico G. Natural history of idiopathic IgA nephropathy: role of clinical and histological prognostic factors[J]. Am J Kidney Dis, 2000, 36(2): 227-237. https://doi.org/10.1053/ajkd.2000.8966https://doi.org/10.1053/ajkd.2000.8966.
Dai HL, Peng LK, Peng FH, et al. A novel technique for en bloc kidney transplantation from infant donors with extremely low body weight by using the distal abdominal aorta as an outflow tract[J]. Am J Transplant, 2018, 18(9): 2200-2207. https://doi.org/10.1111/ajt.14692https://doi.org/10.1111/ajt.14692.
Tang ZQ, Li TF, Dai HL, et al. Drug-induced Fanconi syndrome in patients with kidney allograft transplantation[J]. Front Immunol, 2022, 13: 979983. https://doi.org/10.3389/fimmu.2022.979983https://doi.org/10.3389/fimmu.2022.979983.
Eder M, Kozakowski N, Omic H, et al. Glomerular C4d in post-transplant IgA nephropathy is associated with decreased allograft survival[J]. J Nephrol, 2021, 34(3): 839-849. https://doi.org/10.1007/s40620-020-00914-xhttps://doi.org/10.1007/s40620-020-00914-x.
Lai KN, Tang SC, Schena FP, et al. IgA nephropathy[J]. Nat Rev Dis Primers, 2016, 2: 16001. https://doi.org/10.1038/nrdp.2016.1https://doi.org/10.1038/nrdp.2016.1.
Jarrick S, Lundberg S, Welander A, et al. Mortality in IgA nephropathy: a nationwide population-based cohort study[J]. J Am Soc Nephrol, 2019, 30(5): 866-876. https://doi.org/10.1681/ASN.2018101017https://doi.org/10.1681/ASN.2018101017.
Otsuka Y, Takeda A, Horike K, et al. Early recurrence of active IgA nephropathy after kidney transplantation[J]. Nephrology (Carlton), 2014, 19(Suppl 3): 45-48. https://doi.org/10.1111/nep.12252https://doi.org/10.1111/nep.12252.
Rodas LM, Ruiz-Ortiz E, Garcia-Herrera A, et al. IgA nephropathy recurrence after kidney transplantation: role of recipient age and human leukocyte antigen-B mismatch[J]. Am J Nephrol, 2020, 51(5): 357-365. https://doi.org/10.1159/000506853https://doi.org/10.1159/000506853.
Nijim S, Vujjini V, Alasfar S, et al. Recurrent IgA nephropathy after kidney transplantation[J]. Transplant Proc, 2016, 48(8): 2689-2694. https://doi.org/10.1016/j.transproceed.2016.08.011https://doi.org/10.1016/j.transproceed.2016.08.011.
Wyld Melanie L, Chadban Steven J. Recurrent IgA nephropathy after kidney transplantation[J]. Transplantation, 2016, 100(9): 1827-32. https://doi.org/10.1097/TP.0000000000001093https://doi.org/10.1097/TP.0000000000001093.
Berger J, Yaneva H, Nabarra B, et al. Recurrence of mesangial deposition of IgA after renal transplantation[J]. Kidney Int, 1975, 7(4): 232-241. https://doi.org/10.1038/ki.1975.35https://doi.org/10.1038/ki.1975.35.
Jäger C, Stampf S, Molyneux K, et al. Recurrence of IgA nephropathy after kidney transplantation: experience from the Swiss transplant cohort study[J]. BMC Nephrol, 2022, 23(1): 178. https://doi.org/10.1186/s12882-022-02802-xhttps://doi.org/10.1186/s12882-022-02802-x.
Lionaki S, Panagiotellis K, Melexopoulou C, et al. The clinical course of IgA nephropathy after kidney transplantation and its management[J]. Transplant Rev (Orlando), 2017, 31(2): 106-114. https://doi.org/10.1016/j.trre.2017.01.005https://doi.org/10.1016/j.trre.2017.01.005.
Chailimpamontree W, Dmitrienko S, Li GY, et al. Probability, predictors, and prognosis of posttransplantation glomer-ulonephritis[J]. J Am Soc Nephrol, 2009, 20(4): 843-851. https://doi.org/10.1681/ASN.2008050454https://doi.org/10.1681/ASN.2008050454.
Seeman T. Management of proteinuria in the transplanted patient[J]. Pediatr Nephrol, 2015, 30(6): 889-903. https://doi.org/10.1007/s00467-014-2876-6https://doi.org/10.1007/s00467-014-2876-6.
Zhang J, Qiu J, Chen GD, et al. Etiological analysis of graft dysfunction following living kidney transplantation: a report of 366 biopsies[J]. Ren Fail, 2018, 40(1): 219-225. https://doi.org/10.1080/0886022X.2018.1455592https://doi.org/10.1080/0886022X.2018.1455592.
朱兰, 冯豪, 贾金东, 等. 扁桃体切除对肾移植术后IgA肾病复发的影响[J]. 中华医学杂志, 2018, 98(3): 176-180. https://doi.org/10.3760/cma.j.issn.0376-2491.2018.03.004https://doi.org/10.3760/cma.j.issn.0376-2491.2018.03.004.
ZHU Lan, FENG Hao, JIA Jindong, et al. Clinical efficacy of tonsillectomy in renal transplant patients with recurrent IgA nephropathy[J]. National Medical Journal of China, 2018, 98(3): 176-180. https://doi.org/10.3760/cma.j.issn.0376-2491.2018. 03.004https://doi.org/10.3760/cma.j.issn.0376-2491.2018.03.004.
0
浏览量
153
下载量
0
CSCD
关联资源
相关文章
相关作者
相关机构