Applications of quantitative metabolomics to revolutionize early diagnosis of inborn errors of metabolism in India

IF 3 Q2 CHEMISTRY, ANALYTICAL Analytical science advances Pub Date : 2021-08-05 DOI:10.1002/ansa.202100010
Jisha Chandran, Anikha Bellad, Madan Gopal Ramarajan, Kannan Rangiah
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引用次数: 1

Abstract

Inborn errors of metabolism (IEMs) are a group of disorders caused by disruption of metabolic pathways, which leads to accumulation, decreased circulating levels, or increased excretion of metabolites as a consequence of the underlying genetic defects. These heterogeneous groups of disorders cause significant neonatal and infant mortality across the whole world and it is of utmost concern for developing countries like India owing to lack of awareness and standard preventive strategies like newborn screening (NBS). Though the predictive cumulative incidence of IEMs is said to be ∼1:800 newborns, data pertaining to the true prevalence of individual IEMs is not available in the context of Indian population. There is a need for a large population-based study to get a clear picture of the prevalence of different IEMs. One of the best ways to screen for IEMs is by applying advanced liquid chromatography-mass spectrometry (LC-MS) technology using a quantitative metabolomics approaches such as selected or multiple reaction monitoring (SRM or MRM). Recent developments in LC-MS/MRM based quantification of marker metabolites in newborns have opened a novel opportunity to screen multiple disorders simultaneously from a minuscule volume of biological fluids. In this review article, we have highlighted how LC-MS/MRM based metabolomics approach with its high sensitivity and diagnostic capability can make an impact on the nation's public health through NBS programs.

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定量代谢组学应用于印度先天性代谢错误的早期诊断
先天性代谢错误(IEMs)是一组由代谢途径中断引起的疾病,由于潜在的遗传缺陷导致代谢物的积累、循环水平降低或排泄增加。这些异质群体的疾病在全世界造成严重的新生儿和婴儿死亡率,由于缺乏认识和新生儿筛查等标准预防战略,这是印度等发展中国家最为关注的问题。虽然IEMs的预测累积发病率据说是约1:800新生儿,但在印度人口的背景下,没有关于个体IEMs真实患病率的数据。有必要进行大规模的以人群为基础的研究,以清楚地了解不同传染病的流行情况。筛选IEMs的最佳方法之一是应用先进的液相色谱-质谱(LC-MS)技术,使用定量代谢组学方法,如选择或多重反应监测(SRM或MRM)。基于LC-MS/MRM的新生儿标记物代谢物定量分析的最新进展为从微小体积的生物液体中同时筛选多种疾病提供了新的机会。在这篇综述文章中,我们强调了基于LC-MS/MRM的代谢组学方法如何以其高灵敏度和诊断能力,通过NBS计划对国家公共卫生产生影响。
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