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本文引用的文献

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Successful skipping of abnormal pseudoexon by antisense oligonucleotides in vitro for a patient with beta-propeller protein-associated neurodegeneration.体外反义寡核苷酸成功跳过β-三叶螺旋蛋白相关神经退行性变患者的异常假外显子。
Sci Rep. 2024 Mar 18;14(1):6506. doi: 10.1038/s41598-024-56704-z.
2
Comprehensive genetic diagnosis of Japanese patients with severe proteinuria.对日本严重蛋白尿患者进行全面的基因诊断。
Sci Rep. 2020 Jan 14;10(1):270. doi: 10.1038/s41598-019-57149-5.
3
Effectiveness of integrated interpretation of exome and corresponding transcriptome data for detecting splicing variants of genes associated with autosomal recessive disorders.外显子组与相应转录组数据综合解读在检测常染色体隐性遗传病相关基因剪接变异中的有效性
Mol Genet Metab Rep. 2019 Oct 23;21:100531. doi: 10.1016/j.ymgmr.2019.100531. eCollection 2019 Dec.
4
Predicting Splicing from Primary Sequence with Deep Learning.深度学习预测剪接。
Cell. 2019 Jan 24;176(3):535-548.e24. doi: 10.1016/j.cell.2018.12.015. Epub 2019 Jan 17.
5
The Calcium-Dependent Protease Calpain-1 Links TRPC6 Activity to Podocyte Injury.钙依赖性蛋白酶钙蛋白酶-1 将 TRPC6 活性与足细胞损伤联系起来。
J Am Soc Nephrol. 2018 Aug;29(8):2099-2109. doi: 10.1681/ASN.2016111248. Epub 2018 Jun 28.
6
Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome.中国激素抵抗型肾病综合征患儿的基因突变谱
Pediatr Nephrol. 2017 Jul;32(7):1181-1192. doi: 10.1007/s00467-017-3590-y. Epub 2017 Feb 15.
7
Minimal Change Disease.微小病变性肾病。
Clin J Am Soc Nephrol. 2017 Feb 7;12(2):332-345. doi: 10.2215/CJN.05000516. Epub 2016 Dec 9.
8
Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid-Resistant Nephrotic Syndrome.非遗传性与遗传性激素抵抗型肾病综合征对环孢素A的快速反应及良好肾脏转归
Clin J Am Soc Nephrol. 2016 Feb 5;11(2):245-53. doi: 10.2215/CJN.07370715. Epub 2015 Dec 14.
9
Genetic Interactions Between TRPC6 and NPHS1 Variants Affect Posttransplant Risk of Recurrent Focal Segmental Glomerulosclerosis.TRPC6与NPHS1基因变异之间的遗传相互作用影响移植后局灶节段性肾小球硬化复发风险。
Am J Transplant. 2015 Dec;15(12):3229-38. doi: 10.1111/ajt.13378. Epub 2015 Jul 3.
10
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.序列变异解读的标准与指南:美国医学遗传学与基因组学学会和分子病理学协会的联合共识推荐
Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

成人起病的类固醇抵抗性肾病综合征伴TRPC6新型剪接供体位点变异的有效钙调神经磷酸酶抑制剂治疗:一例报告

Effective calcineurin inhibitor treatment in adult-onset steroid-resistant nephrotic syndrome with a novel splice donor site variant of TRPC6: a case report.

作者信息

Nagasaka Tomoki, Uchiyama Kiyotaka, Hama Eriko Yoshida, Kojima Daiki, Kaneko Kenji, Yoshimoto Norifumi, Yasuda Itaru, Yamada Mamiko, Miya Fuyuki, Suzuki Hisato, Tajima Takaya, Yamaguchi Shintaro, Hayashi Kaori, Kanda Takeshi, Hashiguchi Akinori, Kosaki Kenjiro, Itoh Hiroshi

机构信息

Department of Endocrinology, Metabolism and Nephrology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan.

Department of Nephrology, International University of Health and Welfare Narita Hospital, 852, Hatakeda, Narita, Chiba, 286-0124, Japan.

出版信息

CEN Case Rep. 2025 Apr;14(2):208-216. doi: 10.1007/s13730-024-00935-6. Epub 2024 Sep 30.

DOI:10.1007/s13730-024-00935-6
PMID:39349897
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11958860/
Abstract

Transient receptor potential canonical 6 (TRPC6) variants, which were initially detected in adult-onset familial focal segmental glomerulosclerosis (FSGS), were also identified in pediatric-onset one. Here, we present a patient with adult-onset steroid-resistant nephrotic syndrome (SRNS) who harbored a likely pathogenic TRPC6 variant and partially responded to calcineurin inhibitors (CNIs). A 44-year-old woman with stable rheumatoid arthritis, systemic lupus erythematosus, and Sjögren's syndrome was presented with nephrotic syndrome. Her renal biopsy results showed minor glomerular abnormalities. Upon admission, she was treated with steroids for around 4 weeks, but it was ineffective. After 1-2 weeks of cyclosporine A (CyA) administration, urine output increased, renal function improved without a decrease in proteinuria, and she was discharged. Her renal function was maintained for 2 months, but after a CyA dose reduction, she was again admitted to the hospital due to relapsing edema, decreased urine output, and worsening renal function. CyA was replaced by tacrolimus (TAC). A second renal biopsy showed nearly the same findings as the first except for tubulointerstitial lesions. After 1-2 weeks of TAC administration, urine output increased, and renal function improved. However, urinary protein levels did not decrease as before. After discharge, a whole exome analysis revealed a heterozygous splice donor site variant NM_004621.6;c.2644 + 1G > A in TRPC6. Genetic testing identified a novel splice donor site variant of TRPC6 in a patient with adult-onset SRNS, which prevented unnecessary steroid continuation. The safety and efficacy of CNI in TRPC6 glomerulopathy must be evaluated in future larger studies with longer follow-up.

摘要

瞬时受体电位香草酸亚型6(TRPC6)变异最初是在成人发病的家族性局灶节段性肾小球硬化(FSGS)中检测到的,在儿童发病的FSGS中也有发现。在此,我们报告一名患有成人发病的类固醇抵抗性肾病综合征(SRNS)的患者,该患者携带一种可能致病的TRPC6变异,并对钙调神经磷酸酶抑制剂(CNIs)有部分反应。一名患有稳定类风湿关节炎、系统性红斑狼疮和干燥综合征的44岁女性出现肾病综合征。她的肾活检结果显示肾小球仅有轻微异常。入院后,她接受了约4周的类固醇治疗,但无效。在给予环孢素A(CyA)1 - 2周后,尿量增加,肾功能改善,但蛋白尿没有减少,随后她出院了。她的肾功能维持了2个月,但在CyA剂量减少后,她因水肿复发、尿量减少和肾功能恶化再次入院。CyA被他克莫司(TAC)替代。第二次肾活检显示除肾小管间质病变外,结果与第一次几乎相同。在给予TAC 1 - 2周后,尿量增加,肾功能改善。然而,尿蛋白水平没有像之前那样下降。出院后,全外显子组分析显示TRPC6基因存在一个杂合剪接供体位点变异NM_004621.6;c.2644 + 1G > A。基因检测在一名成人发病的SRNS患者中发现了一种新的TRPC6剪接供体位点变异,这避免了不必要的类固醇持续使用。未来必须通过更大规模、更长随访时间的研究来评估CNI在TRPC6肾小球病中的安全性和有效性。