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本文引用的文献

1
Sodium phenylbutyrate decreases plasma branched-chain amino acids in patients with urea cycle disorders.苯丁酸钠可降低尿素循环障碍患者的血浆支链氨基酸水平。
Mol Genet Metab. 2014 Sep-Oct;113(1-2):131-5. doi: 10.1016/j.ymgme.2014.06.005. Epub 2014 Jul 3.
2
Significant hepatic involvement in patients with ornithine transcarbamylase deficiency.精氨酸代琥珀酸合成酶缺乏症患者的显著肝脏受累。
J Pediatr. 2014 Apr;164(4):720-725.e6. doi: 10.1016/j.jpeds.2013.12.024. Epub 2014 Jan 30.
3
Infectious precipitants of acute hyperammonemia are associated with indicators of increased morbidity in patients with urea cycle disorders.急性高血氨的感染性诱因与尿素循环障碍患者发病率增加的指标相关。
J Pediatr. 2013 Dec;163(6):1705-1710.e1. doi: 10.1016/j.jpeds.2013.08.029. Epub 2013 Sep 29.
4
Nitric-oxide supplementation for treatment of long-term complications in argininosuccinic aciduria.补充一氧化氮治疗精氨琥珀酸尿症的长期并发症。
Am J Hum Genet. 2012 May 4;90(5):836-46. doi: 10.1016/j.ajhg.2012.03.018. Epub 2012 Apr 26.
5
Hepatocellular carcinoma in a research subject with ornithine transcarbamylase deficiency.研究对象患有鸟氨酸转氨甲酰酶缺乏症合并肝细胞癌。
Mol Genet Metab. 2012 Feb;105(2):263-5. doi: 10.1016/j.ymgme.2011.10.016. Epub 2011 Nov 7.
6
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.
7
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.
8
Relationship between carbamoyl-phosphate synthetase genotype and systemic vascular function.氨甲酰磷酸合成酶基因型与全身血管功能之间的关系。
Hypertension. 2004 Feb;43(2):186-91. doi: 10.1161/01.HYP.0000112424.06921.52. Epub 2004 Jan 12.
9
Metabolic and neuropsychological phenotype in women heterozygous for ornithine transcarbamylase deficiency.鸟氨酸转氨甲酰酶缺乏症杂合子女性的代谢和神经心理学表型
Ann Neurol. 2004 Jan;55(1):80-6. doi: 10.1002/ana.10794.
10
Alternative pathway therapy for urea cycle disorders: twenty years later.尿素循环障碍的替代途径疗法:二十年后
J Pediatr. 2001 Jan;138(1 Suppl):S46-54; discussion S54-5. doi: 10.1067/mpd.2001.111836.

尿素循环障碍的纵向研究。

A longitudinal study of urea cycle disorders.

作者信息

Batshaw Mark L, Tuchman Mendel, Summar Marshall, Seminara Jennifer

机构信息

Children's Research Institute, Children's National Health System, 111 Michigan Ave. NW, Washington, DC 20010, USA; Department of Pediatrics, George Washington University School of Medicine and Health Sciences, USA.

出版信息

Mol Genet Metab. 2014 Sep-Oct;113(1-2):127-30. doi: 10.1016/j.ymgme.2014.08.001. Epub 2014 Aug 10.

DOI:10.1016/j.ymgme.2014.08.001
PMID:25135652
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4178008/
Abstract

The Urea Cycle Disorders Consortium (UCDC) is a member of the NIH funded Rare Diseases Clinical Research Network and is performing a longitudinal study of 8 urea cycle disorders (UCDs) with initial enrollment beginning in 2006. The consortium consists of 14 sites in the U.S., Canada and Europe. This report summarizes data mining studies of 614 patients with UCDs enrolled in the UCDC's longitudinal study protocol. The most common disorder is ornithine transcarbamylase deficiency, accounting for more than half of the participants. We calculated the overall prevalence of urea cycle disorders to be 1/35,000, with 2/3rds presenting initial symptoms after the newborn period. We found the mortality rate to be 24% in neonatal onset cases and 11% in late onset cases. The most common precipitant of clinical hyperammonemic episodes in the post-neonatal period was intercurrent infections. Elevations in both blood ammonia and glutamine appeared to be biomarkers for neurocognitive outcome. In terms of chronic treatment, low protein diet appeared to result in normal weight but decreased linear growth while N-scavenger therapy with phenylbutyrate resulted in low levels of branched chain amino acids. Finally, we found an unexpectedly high risk for hepatic dysfunction in patients with ornithine transcarbamylase deficiency. This natural history study illustrates how a collaborative study of a rare genetic disorder can result in an improved understanding of morbidity and disease outcome.

摘要

尿素循环障碍协会(UCDC)是美国国立卫生研究院资助的罕见病临床研究网络的成员,正在对8种尿素循环障碍(UCD)进行纵向研究,初始入组于2006年开始。该协会由美国、加拿大和欧洲的14个研究点组成。本报告总结了对参与UCDC纵向研究方案的614例尿素循环障碍患者的数据挖掘研究。最常见的疾病是鸟氨酸转氨甲酰酶缺乏症,占参与者的一半以上。我们计算出尿素循环障碍的总体患病率为1/35000,其中三分之二在新生儿期后出现初始症状。我们发现新生儿期发病病例的死亡率为24%,晚发病例的死亡率为11%。新生儿期后临床高氨血症发作最常见的诱因是并发感染。血氨和谷氨酰胺升高似乎是神经认知结局的生物标志物。在慢性治疗方面,低蛋白饮食似乎能使体重正常,但会降低线性生长,而用苯丁酸钠进行氮清除疗法会导致支链氨基酸水平降低。最后,我们发现鸟氨酸转氨甲酰酶缺乏症患者出现肝功能障碍的风险出乎意料地高。这项自然史研究说明了对一种罕见遗传病的合作研究如何能够增进对发病率和疾病结局的理解。