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早发性尿素循环障碍患儿的新生儿死亡率及1岁末的转归——对35年多来发表的观察性研究的综述与荟萃分析

Neonatal mortality and outcome at the end of the first year of life in early onset urea cycle disorders--review and meta-analysis of observational studies published over more than 35 years.

作者信息

Burgard Peter, Kölker Stefan, Haege Gisela, Lindner Martin, Hoffmann Georg F

机构信息

Centre for Paediatric and Adolescent Medicine, Division for Neuropaediatrics and Metabolic Medicine, Heidelberg University Hospital, Im Neuenheimer Feld 430, D-69120, Heidelberg, Germany.

University Hospital Frankfurt, Children's Hospital, Theodor-Stern-Kai 7, D-60590, Frankfurt am Main, Germany.

出版信息

J Inherit Metab Dis. 2016 Mar;39(2):219-29. doi: 10.1007/s10545-015-9901-1. Epub 2015 Dec 3.

Abstract

BACKGROUND

For urea cycle disorders (UCD), proportions and mortality of early onset (EO) patients, as well as outcome at one year of life show large variability. We aimed to integrate available evidence to create benchmarks for new diagnostic and therapeutic strategies.

METHODS

Medline search for reports published between 1978 and Dec 22, 2014 was completed by hand search. Random effects meta-analysis was done for four UCDs, deficiency of carbamylphosphate synthetase 1 (CPS1D), male/female ornithine transcarbamylase (OTCDm/f), argininosuccinate synthetase (ASSD) and lyase (ASLD). Effects of publication year and geographic area were analysed by meta-regression.

RESULTS

Twenty-four publications report onset time (n = 1542 patients), survival of EO (n = 665 patients) and outcome at one year of life (n = 172 patients). Proportions for EO manifestation (95% confidence interval) were: CPS1D = 0.75 (0.61;0.88); OTCDm = 0.52 (0.39;0.65); OTCDf = 0.07 (0.03;0.11); ASSD = 0.65 (0.57;0.73); ASLD = 0.60 (0.44;0.77); for surviving EO patients: CPS1D = 0.64 (0.50;0.79); OTCDm = 0.40 (0.16;0.64); OTCDf = 0.57 (0.29;0.85); ASSD = 0.67 (0.48;0.86); ASLD = 0.81 (0.68;0.94); and for normal outcome at one year for survivors: CPS1D = 0.20 (0.07;0.38); OTCDm = 0.15 (0.00;0.39); OTCDf no data; ASSD = 0.36 (0.13;0.60); ASLD = 0.36 (0.17;0.58). Between study variation was large. Year of publication had no effect. Studies from Europe showed lower survival rates than those from Japan or USA.

CONCLUSIONS

UCDs, except for OTCDf, have high risks of EO disease manifestation and, except for ASLD, of neonatal death. No improvement of survival was observed over more than three decades. Geographic variation remains to be explained. This comprehensive description of the natural history of EO UCDs should be considered by scientists, clinicians, health policy makers and guideline developers.

摘要

背景

对于尿素循环障碍(UCD),早发型(EO)患者的比例、死亡率以及一岁时的预后差异很大。我们旨在整合现有证据,为新的诊断和治疗策略制定基准。

方法

通过手工检索完成了对1978年至2014年12月22日发表的报告的Medline检索。对四种尿素循环障碍进行了随机效应荟萃分析,即氨甲酰磷酸合成酶1缺乏症(CPS1D)、男性/女性鸟氨酸转氨甲酰酶缺乏症(OTCDm/f)、精氨琥珀酸合成酶缺乏症(ASSD)和裂解酶缺乏症(ASLD)。通过荟萃回归分析了发表年份和地理区域的影响。

结果

24篇出版物报告了发病时间(n = 1542例患者)、早发型患者的生存情况(n = 665例患者)以及一岁时的预后(n = 172例患者)。早发型表现的比例(95%置信区间)为:CPS1D = 0.75(0.61;0.88);OTCDm = 0.52(0.39;0.65);OTCDf = 0.07(0.03;0.11);ASSD = 0.65(0.57;0.73);ASLD = 0.60(0.44;0.77);早发型存活患者的比例为:CPS1D = 0.64(0.50;0.79);OTCDm = 0.40(0.16;0.64);OTCDf = 0.57(0.29;0.85);ASSD = 0.67(0.48;0.86);ASLD = 0.81(0.68;0.94);存活者一岁时正常预后的比例为:CPS1D = 0.20(0.07;0.38);OTCDm = 0.15(0.00;0.39);OTCDf无数据;ASSD = 0.36(0.13;0.60);ASLD = 0.36(0.17;0.58)。研究间的差异很大。发表年份没有影响。来自欧洲的研究显示生存率低于来自日本或美国的研究。

结论

除OTCDf外,尿素循环障碍有很高的早发型疾病表现风险,除ASLD外,有新生儿死亡风险。三十多年来未观察到生存率的改善。地理差异仍有待解释。科学家、临床医生、卫生政策制定者和指南制定者应考虑对早发型尿素循环障碍自然史的这一全面描述。

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