Citation: | Fang Yiling, Miao Yun. Primary hyperoxaluria type II and organ transplantation[J]. ORGAN TRANSPLANTATION, 2023, 14(6): 804-809. doi: 10.3969/j.issn.1674-7445.2023145 |
[1] |
王心悦, 詹浩苏, 孙丽莹. 中国大陆原发性高草酸尿症1型临床特点及诊治情况总结[J]. 器官移植, 2022, 13(2): 232-239. DOI: 10.3969/j.issn.1674-7445.2022.02.012.
WANG XY, ZHAN HS, SUN LY. Summary of clinical characteristics, diagnosis and treatment of primary hyperoxaluria type 1 in mainland China[J]. Organ Transplant, 2022, 13(2): 232-239. DOI: 10.3969/j.issn.1674-7445.2022.02.012.
|
[2] |
SINGH P, VIEHMAN JK, MEHTA RA, et al. Clinical characterization of primary hyperoxaluria type 3 in comparison with types 1 and 2[J]. Nephrol Dial Transplant, 2022, 37(5): 869-875. DOI: 10.1093/ndt/gfab027.
|
[3] |
SHEE K, STOLLER ML. Perspectives in primary hyperoxaluria - historical, current and future clinical interventions[J]. Nat Rev Urol, 2022, 19(3): 137-146. DOI: 10.1038/s41585-021-00543-4.
|
[4] |
MANDRILE G, PELLE A, SCIANNAMEO V, et al. Primary hyperoxaluria in Italy: the past 30 years and the near future of a (not so) rare disease[J]. J Nephrol, 2022, 35(3): 841-850. DOI: 10.1007/s40620-022-01258-4.
|
[5] |
SIKORA P, ZANIEW M, GRENDA R, et al. Still diagnosed too late and under-recognized? the first comprehensive report on primary hyperoxaluria in Poland[J]. Pol Arch Intern Med, 2020, 130(12): 1053-1063. DOI: 10.20452/pamw.15698.
|
[6] |
CRIVELLI JJ, MITCHELL T, KNIGHT J, et al. Contribution of dietary oxalate and oxalate precursors to urinary oxalate excretion[J]. Nutrients, 2020, 13(1): 62. DOI: 10.3390/nu13010062.
|
[7] |
CAPOLONGO G, FERRARO PM, UNWIN R. Inflammation and kidney stones: cause and effect?[J]. Curr Opin Urol, 2023, 33(2): 129-135. DOI: 10.1097/MOU.0000000000001066.
|
[8] |
DEMOULIN N, AYDIN S, GILLION V, et al. Pathophysiology and management of hyperoxaluria and oxalate nephropathy: a review[J]. Am J Kidney Dis, 2022, 79(5): 717-727. DOI: 10.1053/j.ajkd.2021.07.018.
|
[9] |
PIJNENBURG L, CAILLARD S, BOIVIN G, et al. Type 1 primary hyperoxaluria: a case report and focus on bone impairment of systemic oxalosis[J]. Morphologie, 2018, 102(336): 48-53. DOI: 10.1016/j.morpho.2017.09.004.
|
[10] |
BIRTEL J, DIEDEREN RM, HERRMANN P, et al. The retinal phenotype in primary hyperoxaluria type 2 and 3[J]. Pediatr Nephrol, 2023, 38(5): 1485-1490. DOI: 10.1007/s00467-022-05765-1.
|
[11] |
LEE DH, KASPROWICZ T, MORALES A, et al. A case of infiltrative cardiomyopathy secondary to primary hyperoxaluria type 2 - utilization of multimodality imaging[J]. Cureus, 2021, 13(9): e17914. DOI: 10.7759/cureus.17914.
|
[12] |
DEVRESSE A, COCHAT P, GODEFROID N, et al. Transplantation for primary hyperoxaluria type 1: designing new strategies in the era of promising therapeutic perspectives[J]. Kidney Int Rep, 2020, 5(12): 2136-2145. DOI: 10.1016/j.ekir.2020.09.022.
|
[13] |
COCHAT P, RUMSBY G. Primary hyperoxaluria[J]. N Engl J Med, 2013, 369(7): 649-658. DOI: 10.1056/NEJMra1301564.
|
[14] |
GARRELFS SF, RUMSBY G, PETERS-SENGERS H, et al. Patients with primary hyperoxaluria type 2 have significant morbidity and require careful follow-up[J]. Kidney Int, 2019, 96(6): 1389-1399. DOI: 10.1016/j.kint.2019.08.018.
|
[15] |
HOSAAGRAHARA RAMAKRISHNA S, HASSAN A, KASALA MB, et al. Pediatric combined living donor liver and kidney transplantation for primary hyperoxaluria type 2[J]. Am J Transplant, 2023, 23(10): 1622-1625. DOI: 10.1016/j.ajt.2023.05.006.
|
[16] |
MANDRILE G, BECK B, ACQUAVIVA C, et al. Genetic assessment in primary hyperoxaluria: why it matters[J]. Pediatr Nephrol, 2023, 38(3): 625-634. DOI: 10.1007/s00467-022-05613-2.
|
[17] |
詹睿超, 葛玉成, 张道新, 等. 原发性高草酸尿症基因型与表型的研究进展[J]. 国际外科学杂志, 2021, 48(3): 203-207. DOI: 10.3760/cma.j.cn115396-20200319-00072.
ZHAN RC, GE YC, ZHANG DX, et al. Research progress on genotype and phenotype of primary hyperoxaluria[J]. Int J Surg, 2021, 48(3): 203-207. DOI: 10.3760/cma.j.cn115396-20200319-00072.
|
[18] |
GROOTHOFF JW, METRY E, DEESKER L, et al. Clinical practice recommendations for primary hyperoxaluria: an expert consensus statement from ERKNet and OxalEurope[J]. Nat Rev Nephrol, 2023, 19(3): 194-211. DOI: 10.1038/s41581-022-00661-1.
|
[19] |
ZHAO F, BERGSTRALH EJ, MEHTA RA, et al. Predictors of incident ESRD among patients with primary hyperoxaluria presenting prior to kidney failure[J]. Clin J Am Soc Nephrol, 2016, 11(1): 119-126. DOI: 10.2215/CJN.02810315.
|
[20] |
INJEYAN M, BIDAULT V, BACCHETTA J, et al. Hydration and nephrolithiasis in pediatric populations: specificities and current recommendations[J]. Nutrients, 2023, 15(3): 728. DOI: 10.3390/nu15030728.
|
[21] |
冯潇雨, 程娜, 张荣军, 等. 儿童原发性高草酸尿症1型1例并文献复习[J]. 中国临床研究, 2021, 34(9): 1245-1249. DOI: 10.13429/j.cnki.cjcr.2021.09.021.
FENG XY, CHENG N, ZHANG RJ, et al. A case of primary hyperoxaluria type 1 in children and literature review[J]. Chin J Clin Res, 2021, 34(9): 1245-1249. DOI: 10.13429/j.cnki.cjcr.2021.09.021.
|
[22] |
BHASIN B, ÜREKLI HM, ATTA MG. Primary and secondary hyperoxaluria: understanding the enigma[J]. World J Nephrol, 2015, 4(2): 235-244. DOI: 10.5527/wjn.v4.i2.235.
|
[23] |
BOSE KS, SARMA RH. Delineation of the intimate details of the backbone conformation of pyridine nucleotide coenzymes in aqueous solution[J]. Biochem Biophys Res Commun, 1975, 66(4): 1173-1179. DOI: 10.1016/0006-291x(75)90482-9.
|
[24] |
MASSY ZA, DRUEKE TB. Running interference: lumasiran and other RNA interference therapeutics for kidney diseases[J]. Kidney Int, 2022, 101(2): 208-211. DOI: 10.1016/j.kint.2021.05.027.
|
[25] |
METRY EL, VAN DIJK LMM, PETERS-SENGERS H, et al. Transplantation outcomes in patients with primary hyperoxaluria: a systematic review[J]. Pediatr Nephrol, 2021, 36(8): 2217-2226. DOI: 10.1007/s00467-021-05043-6.
|
[26] |
CORNELL LD, AMER H, VIEHMAN JK, et al. Posttransplant recurrence of calcium oxalate crystals in patients with primary hyperoxaluria: incidence, risk factors, and effect on renal allograft function[J]. Am J Transplant, 2022, 22(1): 85-95. DOI: 10.1111/ajt.16732.
|
[27] |
GUPTA A, SOMERS MJG, BAUM MA. Treatment of primary hyperoxaluria type 1[J]. Clin Kidney J, 2022, 15(Suppl 1): i9-i13. DOI: 10.1093/ckj/sfab232.
|
[28] |
LAM CW, YUEN YP, LAI CK, et al. Novel mutation in the GRHPR gene in a Chinese patient with primary hyperoxaluria type 2 requiring renal transplantation from a living related donor[J]. Am J Kidney Dis, 2001, 38(6): 1307-1310. DOI: 10.1053/ajkd.2001.29229.
|
[29] |
NADERI G, LATIF A, TABASSOMI F, et al. Failure of isolated kidney transplantation in a pediatric patient with primary hyperoxaluria type 2[J]. Pediatr Transplant, 2014, 18(3): E69-E73. DOI: 10.1111/petr.12240.
|
[30] |
LIU S, GAO B, WANG G, et al. Recurrent primary hyperoxaluria type 2 leads to early post-transplant renal function loss: a case report[J]. Exp Ther Med, 2018, 15(4): 3169-3172. DOI: 10.3892/etm.2018.5841.
|
[31] |
DHONDUP T, LORENZ EC, MILLINER DS, et al. Combined liver-kidney transplantation for primary hyperoxaluria type 2: a case report[J]. Am J Transplant, 2018, 18(1): 253-257. DOI: 10.1111/ajt.14418.
|
[32] |
DEL BELLO A, COINTAULT O, DELAS A, et al. Recurrence of oxalate nephropathy after isolated kidney transplantation for primary hyperoxaluria type 2[J]. Am J Transplant, 2018, 18(2): 525-526. DOI: 10.1111/ajt.14550.
|
[33] |
DEL BELLO A, COINTAULT O, DELAS A, et al. Primary hyperoxaluria type 2 successfully treated with combined liver-kidney transplantation after failure of isolated kidney transplantation[J]. Am J Transplant, 2020, 20(6): 1752-1753. DOI: 10.1111/ajt.15829.
|
[34] |
JIA Z, ZHONG Q, LIN T, et al. Subsequent liver transplantation did not reverse recurrence of oxalate nephropathy after isolated kidney transplantation for primary type 2 hyperoxaluria[J]. Asian J Surg, 2022, 45(1): 483-485. DOI: 10.1016/j.asjsur.2021.08.066.
|
[35] |
GENENA KM, SAS DJ, MILLINER DS, et al. Successful treatment of primary hyperoxaluria type 2 with a combined liver and kidney transplant[J]. Kidney Int Rep, 2023, 8(7): 1469-1472. DOI: 10.1016/j.ekir.2023.03.013.
|
[36] |
YAU AA, HINDI J, URIBARRI J. Recurrent nephrolithiasis causing kidney failure[J]. Am J Kidney Dis, 2021, 77(4): A18-A21. DOI: 10.1053/j.ajkd.2020.04.020.
|
[37] |
MONICO CG, MILLINER DS. Combined liver-kidney and kidney-alone transplantation in primary hyperoxaluria[J]. Liver Transpl, 2001, 7(11): 954-963. DOI: 10.1053/jlts.2001.28741.
|
[38] |
SHASHA-LAVSKY H, AVNI A, PAZ Z, et al. Long-term outcomes after pre-emptive liver transplantation in primary hyperoxaluria type 1[J]. Pediatr Nephrol, 2023, 38(6): 1811-1820. DOI: 10.1007/s00467-022-05803-y.
|