• 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

荷兰11年枫糖尿症新生儿筛查评估及文献系统综述:优化策略

Evaluation of 11 years of newborn screening for maple syrup urine disease in the Netherlands and a systematic review of the literature: Strategies for optimization.

作者信息

Stroek Kevin, Boelen Anita, Bouva Marelle J, De Sain-van der Velden Monique, Schielen Peter C J I, Maase Rose, Engel Henk, Jakobs Bernadette, Kluijtmans Leo A J, Mulder Margot F, Rubio-Gozalbo M E, van Spronsen Francjan J, Visser Gepke, de Vries Maaike C, Williams Monique, Heijboer Annemieke C, Kemper Evelien A, Bosch Annet M

机构信息

Endocrinology Laboratory, Department of Clinical Chemistry Amsterdam Gastroenterology & Metabolism, Amsterdam UMC, University of Amsterdam Amsterdam The Netherlands.

Reference Laboratory Neonatal Screening, Center for Health protection National Institute for Public Health and the Environment Bilthoven The Netherlands.

出版信息

JIMD Rep. 2020 May 13;54(1):68-78. doi: 10.1002/jmd2.12124. eCollection 2020 Jul.

DOI:10.1002/jmd2.12124
PMID:32685353
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7358668/
Abstract

Maple syrup urine disease (MSUD) leads to severe neurological deterioration unless diagnosed early and treated immediately. We have evaluated the effectiveness of 11 years of MSUD newborn screening (NBS) in the Netherlands (screening >72 hours, referral if both total leucine (Xle) and valine ≥400 μmol/L blood) and have explored possibilities for improvement by combining our data with a systematic literature review and data from Collaborative Laboratory Integrated Reports (CLIR). Dutch MSUD NBS characteristics and accuracy were determined. The hypothetical referral numbers in the Dutch population of additional screening markers suggested by CLIR were calculated. In a systematic review, articles reporting NBS leucine concentrations of confirmed patients were included. Our data showed that NBS of 1 963 465 newborns identified 4 MSUD patients and led to 118 false-positive referrals (PPV 3.28%; incidence 1:491 000 newborns). In literature, leucine is the preferred NBS parameter. Total leucine (Xle) concentrations (mass-spectrometry) of 53 detected and 8 false-negative patients (sampling age within 25 hours in 3 patients) reported in literature ranged from 288 to 3376 (median 900) and 42 to 325 (median 209) μmol/L blood respectively. CLIR showed increasing Xle concentrations with sampling age and early NBS sampling and milder variant MSUD phenotypes with (nearly) normal biochemical profiles are causes of false-negative NBS results. We evaluated the effect of additional screening markers and established the Xle/phenylalanine ratio as a promising additional marker ratio for increasing the PPV, while maintaining high sensitivity in the Dutch MSUD NBS.

摘要

枫糖尿症(MSUD)如不及早诊断并立即治疗,会导致严重的神经功能恶化。我们评估了荷兰11年的MSUD新生儿筛查(NBS)的有效性(筛查时间>72小时,若血总亮氨酸(Xle)和缬氨酸均≥400μmol/L则转诊),并通过将我们的数据与系统文献综述及协作实验室综合报告(CLIR)的数据相结合,探索改进的可能性。确定了荷兰MSUD NBS的特征和准确性。计算了CLIR建议的荷兰人群中其他筛查标志物的假设转诊数量。在一项系统综述中,纳入了报告确诊患者NBS亮氨酸浓度的文章。我们的数据显示,对1963465名新生儿进行的NBS筛查出4例MSUD患者,并导致118例假阳性转诊(阳性预测值3.28%;发病率1:491000新生儿)。在文献中,亮氨酸是首选的NBS参数。文献报道的53例检测到的患者和8例假阴性患者(3例患者的采样年龄在25小时内)的血总亮氨酸(Xle)浓度(质谱法)分别为288至3376(中位数900)和42至325(中位数209)μmol/L。CLIR显示,随着采样年龄的增加,Xle浓度升高,早期NBS采样以及(几乎)具有正常生化特征的较轻变异型MSUD表型是NBS假阴性结果的原因。我们评估了额外筛查标志物的效果,并确定Xle/苯丙氨酸比值是一种有前景的额外标志物比值,可提高荷兰MSUD NBS的阳性预测值,同时保持高灵敏度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c24/7358668/f847b1b5e131/JMD2-54-68-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c24/7358668/f847b1b5e131/JMD2-54-68-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c24/7358668/f847b1b5e131/JMD2-54-68-g001.jpg

相似文献

1
Evaluation of 11 years of newborn screening for maple syrup urine disease in the Netherlands and a systematic review of the literature: Strategies for optimization.荷兰11年枫糖尿症新生儿筛查评估及文献系统综述:优化策略
JIMD Rep. 2020 May 13;54(1):68-78. doi: 10.1002/jmd2.12124. eCollection 2020 Jul.
2
Newborn screening of maple syrup urine disease and the effect of early diagnosis.新生儿枫糖尿症筛查及早期诊断效果。
Clin Chim Acta. 2023 Aug 1;548:117483. doi: 10.1016/j.cca.2023.117483. Epub 2023 Jul 6.
3
Maple syrup urine disease: further evidence that newborn screening may fail to identify variant forms.枫糖尿症:进一步的证据表明,新生儿筛查可能无法识别变异形式。
Mol Genet Metab. 2010 Jun;100(2):136-42. doi: 10.1016/j.ymgme.2009.11.010. Epub 2009 Dec 5.
4
Second-tier test for quantification of alloisoleucine and branched-chain amino acids in dried blood spots to improve newborn screening for maple syrup urine disease (MSUD).用于定量干血斑中别异亮氨酸和支链氨基酸的二线检测,以改进枫糖尿症(MSUD)的新生儿筛查。
Clin Chem. 2008 Mar;54(3):542-9. doi: 10.1373/clinchem.2007.098434. Epub 2008 Jan 4.
5
Evolution of maple syrup urine disease in patients diagnosed by newborn screening versus late diagnosis.新生儿筛查诊断与延迟诊断的枫糖尿症患者的病情演变
Eur J Paediatr Neurol. 2015 Nov;19(6):652-9. doi: 10.1016/j.ejpn.2015.07.009. Epub 2015 Jul 20.
6
Exploratory Untargeted Metabolomics of Dried Blood Spot Samples from Newborns with Maple Syrup Urine Disease.新生儿枫糖尿症干血斑样本的探索性非靶向代谢组学研究。
Int J Mol Sci. 2024 May 24;25(11):5720. doi: 10.3390/ijms25115720.
7
Rapid diagnosis of maple syrup urine disease in blood spots from newborns by tandem mass spectrometry.通过串联质谱法对新生儿血斑中的枫糖尿症进行快速诊断。
Clin Chem. 1995 Jan;41(1):62-8.
8
Treatment Outcomes for Maple Syrup Urine Disease Detected by Newborn Screening.新生儿筛查发现的枫糖尿症治疗结局。
Pediatrics. 2024 Aug 1;154(2). doi: 10.1542/peds.2023-064370.
9
Diagnosis of maple syrup urine disease by determination of L-valine, L-isoleucine, L-leucine and L-phenylalanine in neonatal blood spots by gas chromatography-mass spectrometry.通过气相色谱-质谱法测定新生儿血斑中的L-缬氨酸、L-异亮氨酸、L-亮氨酸和L-苯丙氨酸来诊断枫糖尿症。
J Chromatogr B Analyt Technol Biomed Life Sci. 2003 Jul 25;792(2):261-8. doi: 10.1016/s1570-0232(03)00270-8.
10
Maple syrup urine disease: favourable effect of early diagnosis by newborn screening on the neonatal course of the disease.枫糖尿症:新生儿筛查早期诊断对该疾病新生儿病程的有利影响。
J Inherit Metab Dis. 2006 Aug;29(4):532-7. doi: 10.1007/s10545-006-0315-y.

引用本文的文献

1
Exploring molecular spectrum in thai patients with maple syrup urine disease: unveiling a common variant.探讨泰国枫糖尿症患者的分子谱:揭示一种常见变异。
Orphanet J Rare Dis. 2024 Oct 25;19(1):396. doi: 10.1186/s13023-024-03411-7.
2
The Value of Reducing Inconclusive and False-Positive Newborn Screening Results for Congenital Hypothyroidism, Congenital Adrenal Hyperplasia and Maple Syrup Urine Disease in The Netherlands.降低荷兰先天性甲状腺功能减退症、先天性肾上腺皮质增生症和枫糖尿症新生儿筛查结果的不确定性和假阳性的价值
Int J Neonatal Screen. 2024 Oct 8;10(4):70. doi: 10.3390/ijns10040070.
3
Current Status of Newborn Bloodspot Screening Worldwide 2024: A Comprehensive Review of Recent Activities (2020-2023).

本文引用的文献

1
Challenges in the management of patients with maple syrup urine disease diagnosed by newborn screening in a developing country.发展中国家通过新生儿筛查诊断出的枫糖尿症患者管理中的挑战。
J Community Genet. 2017 Jan;8(1):9-15. doi: 10.1007/s12687-016-0281-5. Epub 2016 Oct 6.
2
Pilot study of newborn screening of inborn error of metabolism using tandem mass spectrometry in Malaysia: outcome and challenges.马来西亚使用串联质谱法进行先天性代谢缺陷新生儿筛查的试点研究:结果与挑战
J Pediatr Endocrinol Metab. 2016 Sep 1;29(9):1031-9. doi: 10.1515/jpem-2016-0028.
3
Genetic cause and prevalence of hydroxyprolinemia.
《2024年全球新生儿血斑筛查现状:2020 - 2023年近期活动综合回顾》
Int J Neonatal Screen. 2024 May 23;10(2):38. doi: 10.3390/ijns10020038.
4
Future of Dutch NGS-Based Newborn Screening: Exploring the Technical Possibilities and Assessment of a Variant Classification Strategy.荷兰基于下一代测序技术的新生儿筛查的未来:探索技术可能性及变异分类策略评估
Int J Neonatal Screen. 2024 Mar 7;10(1):20. doi: 10.3390/ijns10010020.
5
Multivariate Independent Component Analysis Identifies Patients in Newborn Screening Equally to Adjusted Reference Ranges.多变量独立成分分析在新生儿筛查中识别患者的能力与调整后的参考范围相当。
Int J Neonatal Screen. 2023 Oct 20;9(4):60. doi: 10.3390/ijns9040060.
6
Optimizing the Dutch newborn screening for congenital hypothyroidism by incorporating amino acids and acylcarnitines in a machine learning-based model.基于机器学习模型纳入氨基酸和酰基肉碱来优化荷兰先天性甲状腺功能减退症新生儿筛查。
Eur Thyroid J. 2023 Nov 3;12(6). doi: 10.1530/ETJ-23-0141. Print 2023 Dec 1.
7
A functional group-guided approach to aptamers for small molecules.基于功能基团的小分子适体筛选方法。
Science. 2023 Jun 2;380(6648):942-948. doi: 10.1126/science.abn9859. Epub 2023 Jun 1.
8
Maple syrup urine disease due to a paracentric inversion of chr 19 that disrupts : A case report.因19号染色体臂间倒位导致的枫糖尿症:一例报告。
JIMD Rep. 2022 Sep 20;63(6):575-580. doi: 10.1002/jmd2.12333. eCollection 2022 Nov.
9
Diagnosis of inborn errors of metabolism within the expanded newborn screening in the Madrid region.马德里地区扩大新生儿筛查中先天性代谢缺陷的诊断
JIMD Rep. 2022 Jan 27;63(2):146-161. doi: 10.1002/jmd2.12265. eCollection 2022 Mar.
10
Real-world management of maple syrup urine disease (MSUD) metabolic decompensations with branched chain amino acid-free formulas in France and Germany: A retrospective observational study.法国和德国使用无支链氨基酸配方对枫糖尿症(MSUD)代谢失代偿进行的真实世界管理:一项回顾性观察研究。
JIMD Rep. 2021 Mar 6;59(1):110-119. doi: 10.1002/jmd2.12207. eCollection 2021 May.
羟脯氨酸血症的遗传病因及患病率
J Inherit Metab Dis. 2016 Sep;39(5):625-632. doi: 10.1007/s10545-016-9940-2. Epub 2016 May 2.
4
Inborn errors of metabolism detectable by tandem mass spectrometry in Egypt: The first newborn screening pilot study.埃及可通过串联质谱检测的先天性代谢缺陷:首次新生儿筛查试点研究。
J Med Screen. 2016 Sep;23(3):124-9. doi: 10.1177/0969141315618229. Epub 2016 Jan 20.
5
Evolution of maple syrup urine disease in patients diagnosed by newborn screening versus late diagnosis.新生儿筛查诊断与延迟诊断的枫糖尿症患者的病情演变
Eur J Paediatr Neurol. 2015 Nov;19(6):652-9. doi: 10.1016/j.ejpn.2015.07.009. Epub 2015 Jul 20.
6
Nutrition management guideline for maple syrup urine disease: an evidence- and consensus-based approach.枫糖尿症的营养管理指南:循证与共识方法。
Mol Genet Metab. 2014 Jul;112(3):210-7. doi: 10.1016/j.ymgme.2014.05.006. Epub 2014 May 17.
7
Postanalytical tools improve performance of newborn screening by tandem mass spectrometry.分析后工具可提高串联质谱法新生儿筛查的性能。
Genet Med. 2014 Dec;16(12):889-95. doi: 10.1038/gim.2014.62. Epub 2014 May 29.
8
Reduction in newborn screening metabolic false-positive results following a new collection protocol.采用新的采集方案后新生儿筛查代谢假阳性结果的减少
Genet Med. 2014 Jun;16(6):477-83. doi: 10.1038/gim.2013.171. Epub 2013 Oct 31.
9
Cerebral edema in maple syrup urine disease despite newborn screening diagnosis and early initiation of treatment.尽管进行了新生儿筛查诊断并早期开始治疗,但枫糖尿症仍出现脑水肿。
JIMD Rep. 2012;3:103-6. doi: 10.1007/8904_2011_69. Epub 2011 Sep 22.
10
Application of liquid chromatography-tandem mass spectrometry in the diagnosis and follow-up of maple syrup urine disease in a Chinese population.液相色谱-串联质谱法在中国人群枫糖尿症诊断及随访中的应用
J Pediatr Endocrinol Metab. 2013;26(5-6):433-9. doi: 10.1515/jpem-2012-0343.