• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

新生儿期和中度尿素循环障碍的早期肝移植可能导致正常的神经发育。

Early liver transplantation in neonatal-onset and moderate urea cycle disorders may lead to normal neurodevelopment.

机构信息

Department of Pediatrics, Graduate School of Medical Sciences, Kumamoto University, 1-1-1 Honjo, Kumamoto City, Kumamoto Prefecture, 860-8556, Japan.

出版信息

Metab Brain Dis. 2018 Oct;33(5):1517-1523. doi: 10.1007/s11011-018-0259-6. Epub 2018 Jun 11.

DOI:10.1007/s11011-018-0259-6
PMID:29948653
Abstract

Urea cycle disorders (UCDs) are inherited metabolic diseases that lead to hyperammonemia. Neurodevelopmental outcomes of patients with UCDs depend on the maximum ammonia concentration (MAC) in the blood during onset. MAC ≥360 μM is a marker of poor neurodevelopmental outcomes. We investigated the neurodevelopmental outcomes and MAC at onset for 177 patients with UCDs in Japan (median age, 8 years and 2 months; range, 10 days-72 years), including 57 patients with male ornithine transcarbamylase (OTCD), 59 patients with female OTCD, 23 patients with carbamoyl-phosphate synthetase 1 deficiency (CPSD), 28 patients with arginosuccinate synthetase deficiency, 9 patients with arginosuccinate lyase deficiency (ALD), and 1 patient with arginase 1 deficiency. Neurodevelopmental outcomes of patients with CPSD and ALD were poor because most had neonatal onset with blood MAC ≥300 μM at onset. Although OTCD, particularly female late-onset OTCD, has good neurodevelopmental outcomes among those with UCDs, it is not necessarily a mild disease with good long-term outcomes. Patients with severe UCDs and MAC ≥300 μM at onset should undergo liver transplantation (LT). Moreover, this study suggested that if the onset of UCD began during the neonatal period, then even UCD patients with MAC <300 μM at onset should undergo LT to protect the brain.

摘要

尿素循环障碍(UCDs)是导致高氨血症的遗传性代谢疾病。UCD 患者的神经发育结局取决于发病时血液中最大氨浓度(MAC)。MAC≥360μM 是神经发育不良结局的标志。我们研究了日本 177 例 UCD 患者的神经发育结局和发病时的 MAC(中位数年龄为 8 岁 2 个月;范围 10 天-72 岁),包括 57 例男性鸟氨酸转氨甲酰酶(OTCD)患者、59 例女性 OTCD 患者、23 例氨甲酰磷酸合成酶 1 缺乏症(CPSD)患者、28 例精氨酸合成酶缺乏症患者、9 例精氨酸琥珀酸裂解酶缺乏症(ALD)患者和 1 例精氨酸酶 1 缺乏症患者。CPSD 和 ALD 患者的神经发育结局较差,因为大多数患者在发病时具有新生儿发病,MAC≥300μM。尽管 OTCD,尤其是女性迟发性 OTCD,在 UCD 患者中具有良好的神经发育结局,但它并不一定是一种具有良好长期结局的轻度疾病。发病时伴有严重 UCD 和 MAC≥300μM 的患者应进行肝移植(LT)。此外,本研究表明,如果 UCD 的发病始于新生儿期,那么即使发病时 MAC<300μM 的 UCD 患者也应进行 LT 以保护大脑。

相似文献

1
Early liver transplantation in neonatal-onset and moderate urea cycle disorders may lead to normal neurodevelopment.新生儿期和中度尿素循环障碍的早期肝移植可能导致正常的神经发育。
Metab Brain Dis. 2018 Oct;33(5):1517-1523. doi: 10.1007/s11011-018-0259-6. Epub 2018 Jun 11.
2
Role of liver transplantation in urea cycle disorders: Report from a nationwide study in Japan.肝移植在尿素循环障碍中的作用:来自日本全国性研究的报告。
J Inherit Metab Dis. 2021 Nov;44(6):1311-1322. doi: 10.1002/jimd.12415. Epub 2021 Jul 13.
3
Liver transplantation may prevent neurodevelopmental deterioration in high-risk patients with urea cycle disorders.肝移植可能会预防尿素循环障碍高危患者的神经发育恶化。
Pediatr Transplant. 2017 Sep;21(6). doi: 10.1111/petr.12987. Epub 2017 Jun 12.
4
Long-term outcome of urea cycle disorders: Report from a nationwide study in Japan.尿素循环障碍的长期预后:来自日本一项全国性研究的报告。
J Inherit Metab Dis. 2021 Jul;44(4):826-837. doi: 10.1002/jimd.12384. Epub 2021 Apr 18.
5
Clinical outcomes of neonatal onset proximal versus distal urea cycle disorders do not differ.新生儿期近端型与远端型尿素循环障碍的临床结局无差异。
J Pediatr. 2013 Feb;162(2):324-9.e1. doi: 10.1016/j.jpeds.2012.06.065. Epub 2012 Aug 15.
6
Clinical course of 63 patients with neonatal onset urea cycle disorders in the years 2001-2013.2001年至2013年期间63例新生儿期发病的尿素循环障碍患者的临床病程。
Orphanet J Rare Dis. 2016 Aug 19;11(1):116. doi: 10.1186/s13023-016-0493-0.
7
Long-term outcome and intervention of urea cycle disorders in Japan.日本尿素循环障碍的长期预后和干预措施。
J Inherit Metab Dis. 2012 Sep;35(5):777-85. doi: 10.1007/s10545-011-9427-0. Epub 2011 Dec 14.
8
Neonatal factors related to survival and intellectual and developmental outcome of patients with early-onset urea cycle disorders.与早发性尿素循环障碍患者生存及智力和发育结局相关的新生儿因素。
Mol Genet Metab. 2020 Jun;130(2):110-117. doi: 10.1016/j.ymgme.2020.03.003. Epub 2020 Mar 19.
9
Citrulline for urea cycle disorders in Japan.日本用于尿素循环障碍的瓜氨酸。
Pediatr Int. 2017 Apr;59(4):422-426. doi: 10.1111/ped.13163. Epub 2016 Dec 22.
10
Physical, cognitive, and social status of patients with urea cycle disorders in Japan.日本尿素循环障碍患者的身体、认知和社会状况。
Mol Genet Metab Rep. 2021 Feb 7;27:100724. doi: 10.1016/j.ymgmr.2021.100724. eCollection 2021 Jun.

引用本文的文献

1
Clinical characteristics and long-term outcomes of 101 patients with urea cycle disorders in China.中国101例尿素循环障碍患者的临床特征及长期预后
Orphanet J Rare Dis. 2025 Aug 13;20(1):432. doi: 10.1186/s13023-025-03985-w.
2
Pathogenic variants of ornithine transcarbamylase deficiency: Nation-wide study in Japan and literature review.鸟氨酸转氨甲酰酶缺乏症的致病变体:日本全国性研究及文献综述
Front Genet. 2022 Oct 11;13:952467. doi: 10.3389/fgene.2022.952467. eCollection 2022.
3
Liver transplantation for late-onset ornithine transcarbamylase deficiency: A case report.

本文引用的文献

1
Liver transplantation may prevent neurodevelopmental deterioration in high-risk patients with urea cycle disorders.肝移植可能会预防尿素循环障碍高危患者的神经发育恶化。
Pediatr Transplant. 2017 Sep;21(6). doi: 10.1111/petr.12987. Epub 2017 Jun 12.
2
Hyperammonemia crisis following parturition in a female patient with ornithine transcarbamylase deficiency.一名患有鸟氨酸转氨甲酰酶缺乏症的女性患者产后发生高氨血症危象。
World J Hepatol. 2017 Feb 28;9(6):343-348. doi: 10.4254/wjh.v9.i6.343.
3
Age at disease onset and peak ammonium level rather than interventional variables predict the neurological outcome in urea cycle disorders.
迟发性鸟氨酸转氨甲酰酶缺乏症的肝移植:一例报告。
World J Clin Cases. 2022 Jun 26;10(18):6156-6162. doi: 10.12998/wjcc.v10.i18.6156.
4
Mitochondrial hepatopathy: Anticipated difficulties in management of fatty acid oxidation defects and urea cycle defects.线粒体肝病:脂肪酸氧化缺陷和尿素循环缺陷管理中预期的困难。
World J Hepatol. 2022 Jan 27;14(1):180-194. doi: 10.4254/wjh.v14.i1.180.
5
Hyperammonemia in Inherited Metabolic Diseases.遗传性代谢病中的高血氨症。
Cell Mol Neurobiol. 2022 Nov;42(8):2593-2610. doi: 10.1007/s10571-021-01156-6. Epub 2021 Oct 19.
6
Outcomes After Living Donor Liver Transplantation in Pediatric Patients with Inherited Metabolic Diseases.遗传代谢性疾病患儿活体肝移植的结局。
Ann Transplant. 2021 Oct 1;26:e932994. doi: 10.12659/AOT.932994.
7
Clinical Practice Guidelines for Liver Transplantation in Saudi Arabia.沙特阿拉伯肝脏移植临床实践指南。
Saudi Med J. 2021 Sep;42(9):927-968. doi: 10.15537/smj.2021.42.9.20210126.
8
Neurophysiological characteristics in argininemia: a case report.精氨酸血症的神经生理学特征:一例报告
Transl Pediatr. 2021 Jul;10(7):1947-1951. doi: 10.21037/tp-21-112.
9
Physical, cognitive, and social status of patients with urea cycle disorders in Japan.日本尿素循环障碍患者的身体、认知和社会状况。
Mol Genet Metab Rep. 2021 Feb 7;27:100724. doi: 10.1016/j.ymgmr.2021.100724. eCollection 2021 Jun.
10
Considering Proximal Urea Cycle Disorders in Expanded Newborn Screening.在扩大新生儿筛查中考虑近端尿素循环障碍
Int J Neonatal Screen. 2020 Oct 8;6(4):77. doi: 10.3390/ijns6040077.
疾病发作年龄和血氨峰值而非干预变量可预测尿素循环障碍的神经学转归。
J Inherit Metab Dis. 2016 Sep;39(5):661-672. doi: 10.1007/s10545-016-9938-9. Epub 2016 Apr 22.
4
The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype.有机酸尿症和尿素循环障碍的表型谱。第2部分:不断演变的临床表型。
J Inherit Metab Dis. 2015 Nov;38(6):1059-74. doi: 10.1007/s10545-015-9840-x. Epub 2015 Apr 15.
5
The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation.有机酸血症和尿素循环障碍的表型谱。第1部分:初始表现。
J Inherit Metab Dis. 2015 Nov;38(6):1041-57. doi: 10.1007/s10545-015-9839-3. Epub 2015 Apr 15.
6
Living donor liver transplantation for pediatric patients with metabolic disorders: the Japanese multicenter registry.日本多中心登记处:小儿代谢紊乱患者的活体供肝肝移植
Pediatr Transplant. 2014 Feb;18(1):6-15. doi: 10.1111/petr.12196. Epub 2013 Nov 28.
7
Long-term outcome and intervention of urea cycle disorders in Japan.日本尿素循环障碍的长期预后和干预措施。
J Inherit Metab Dis. 2012 Sep;35(5):777-85. doi: 10.1007/s10545-011-9427-0. Epub 2011 Dec 14.
8
A series of pregnancies in women with inherited metabolic disease.一系列遗传性代谢疾病女性的妊娠。
J Inherit Metab Dis. 2012 May;35(3):419-24. doi: 10.1007/s10545-011-9389-2. Epub 2011 Sep 15.
9
Establishing a consortium for the study of rare diseases: The Urea Cycle Disorders Consortium.建立一个罕见病研究联盟:尿素循环障碍联盟。
Mol Genet Metab. 2010;100 Suppl 1(Suppl 1):S97-105. doi: 10.1016/j.ymgme.2010.01.014. Epub 2010 Feb 10.
10
Intellectual, adaptive, and behavioral functioning in children with urea cycle disorders.尿素循环障碍患儿的智力、适应能力及行为功能
Pediatr Res. 2009 Jul;66(1):96-101. doi: 10.1203/PDR.0b013e3181a27a16.