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Flexible mixture modeling via the multivariate t distribution with the Box-Cox transformation: an alternative to the skew-t distribution.通过具有Box-Cox变换的多元t分布进行灵活混合建模:偏t分布的一种替代方法。
Stat Comput. 2012 Jan 1;22(1):33-52. doi: 10.1007/s11222-010-9204-1.
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Metabolomics in neonatology and pediatrics.新生儿学与儿科学中的代谢组学。
Clin Biochem. 2011 May;44(7):452-454. doi: 10.1016/j.clinbiochem.2011.03.006.
3
1H NMR-based metabolomic analysis of urine from preterm and term neonates.基于1H核磁共振的早产儿和足月儿尿液代谢组学分析。
Front Biosci (Elite Ed). 2011 Jun 1;3(3):1005-12. doi: 10.2741/e306.
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Altered metabolism and newborn screening using tandem mass spectrometry: lessons learned from the bench to bedside.串联质谱技术改变代谢物检测和新生儿筛查:从实验室到临床的经验教训。
Curr Pharm Biotechnol. 2011 Jul;12(7):965-75. doi: 10.2174/138920111795909104.
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Metabolomics: the "new clinical chemistry" for personalized neonatal medicine.代谢组学:个性化新生儿医学的“新临床化学”。
Minerva Pediatr. 2010 Jun;62(3 Suppl 1):145-8.
6
Effect of temperature changes on the occurrence of congenital hypothyroidism.温度变化对先天性甲状腺功能减退症发生的影响。
J Med Screen. 2010;17(3):121-4. doi: 10.1258/jms.2010.010026.
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Metabolomics: a new tool for the neonatologist.代谢组学:新生儿科医生的新工具。
J Matern Fetal Neonatal Med. 2009;22 Suppl 3:50-3. doi: 10.1080/14767050903181500.
8
Functional glucocorticoid receptor gene variants do not underlie the high variability of 17-hydroxyprogesterone screening values in healthy newborns.功能性糖皮质激素受体基因变异并非健康新生儿17-羟孕酮筛查值高度变异的基础。
Eur J Endocrinol. 2009 Apr;160(4):667-73. doi: 10.1530/EJE-08-0639. Epub 2009 Jan 27.
9
Clarification of laboratory and clinical variables that influence cystic fibrosis newborn screening with initial analysis of immunoreactive trypsinogen.通过对免疫反应性胰蛋白酶原的初步分析,阐明影响囊性纤维化新生儿筛查的实验室和临床变量。
Pediatrics. 2009 Feb;123(2):e338-46. doi: 10.1542/peds.2008-1681.
10
Determination of the reference range of endogenous plasma carnitines in healthy adults.健康成年人内源性血浆肉碱参考范围的测定。
Ann Clin Biochem. 2008 Nov;45(Pt 6):585-92. doi: 10.1258/acb.2008.008045. Epub 2008 Sep 9.

用于新生儿筛查的代谢生物标志物的临床和环境影响。

Clinical and environmental influences on metabolic biomarkers collected for newborn screening.

机构信息

Department of Pediatrics, University of Iowa Hospitals and Clinics, Iowa City, IA 52242, USA.

出版信息

Clin Biochem. 2013 Jan;46(1-2):133-8. doi: 10.1016/j.clinbiochem.2012.09.013. Epub 2012 Sep 23.

DOI:10.1016/j.clinbiochem.2012.09.013
PMID:23010448
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3534803/
Abstract

OBJECTIVES

Identifying common clinical and environmental factors that influence newborn metabolic biomarkers will improve the utilization of metabolite panels for clinical diagnostic medicine.

DESIGN AND METHODS

Environmental effects including gender, season of birth, gestational age, birth weight, feeding method and age at time of collection were evaluated for over 50 metabolites collected by the Iowa Neonatal Metabolic Screening Program on 221,788 newborns over a six year period.

RESULTS

We replicated well known observations that low birth weight and preterm infants have higher essential amino acids and lower medium and long chain acylcarnitine levels than their term counterparts. Smaller, but still significant, differences were observed for gender and timing of sample collection, specifically the season in which the infant was born. Most intriguing were our findings of higher thyroid stimulating hormone in the winter months (P<1×10(-40)) which correlated with an increased false positive rate of congenital hypothyroidism in the winter (0.9%) compared to summer (0.6%). Previous studies, conducted globally, have identified an increased prevalence of suspected and confirmed cases of congenital hypothyroidism in the winter months. We found that the percentage of unresolved suspected cases were slightly higher in the winter (0.3% vs. 0.2%).

CONCLUSIONS

We identified differences in metabolites by gestational age, birth weight, gender and season. Some are widely reported such as gestational age and birth weight, while others such as the effect of seasonality are not as well studied.

摘要

目的

确定影响新生儿代谢生物标志物的常见临床和环境因素,将有助于提高代谢物谱在临床诊断医学中的应用。

设计与方法

本研究评估了爱荷华州新生儿代谢筛查计划在六年期间收集的 50 多种代谢物,这些代谢物受到环境因素的影响,包括性别、出生季节、胎龄、出生体重、喂养方式和采集时间。

结果

我们复制了一些众所周知的观察结果,即低出生体重和早产儿的必需氨基酸水平较高,而中长链酰基辅酶 A 水平较低,与足月婴儿相比。性别和样本采集时间也存在较小但仍显著的差异,具体来说,就是婴儿出生的季节。最有趣的是我们发现冬季的促甲状腺激素水平较高(P<1×10(-40)),这与冬季(0.9%)先天性甲状腺功能减退症的假阳性率高于夏季(0.6%)相关。先前的全球研究已经确定了冬季先天性甲状腺功能减退症的疑似和确诊病例的患病率增加。我们发现冬季未解决的疑似病例百分比略高(0.3%比 0.2%)。

结论

我们确定了代谢物与胎龄、出生体重、性别和季节的差异。有些差异是广泛报道的,如胎龄和出生体重,而其他差异,如季节性的影响,尚未得到充分研究。