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利用宏基因组学了解营养不良的遗传基础。

Use of metagenomics to understand the genetic basis of malnutrition.

机构信息

International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.

出版信息

Nutr Rev. 2009 Nov;67 Suppl 2:S201-6. doi: 10.1111/j.1753-4887.2009.00241.x.

Abstract

Childhood malnutrition is not just due to lack of nutrients, it can also be caused by enteric infections leading to intestinal inflammation and malabsorption of nutrients. Human genetic polymorphisms can alter host genes that affect nutrient absorption and metabolism. Changes in intestinal microbial ecology and the microbiome (the collective genome of the intestinal microbiota) can also affect the harvest of nutrients from the diet. A substantial proportion of malnourished children fail to recover due to inappropriate treatment. However, there may be other causes for treatment failure, including changes in the microbiome and infection with an enteropathogen, and a genetic predisposition to malnutrition may exist. It is, therefore, logical to undertake the following: 1) investigate genetic predisposition to malnutrition, 2) determine the genetic markers and biomarkers that can help identify children at risk of malnutrition, and 3) look for new treatment modalities that can improve the clinical management of children with malnutrition.

摘要

儿童期营养不良不仅是由于缺乏营养物质所致,还可能由肠道感染引起,导致肠道炎症和营养物质吸收不良。人类遗传多态性可改变宿主基因,影响营养物质的吸收和代谢。肠道微生物生态和微生物组(肠道微生物群落的集体基因组)的变化也会影响从饮食中获取营养物质的效果。相当一部分营养不良的儿童由于治疗不当而无法康复。然而,治疗失败可能还有其他原因,包括微生物组的变化和肠病原体感染,并且可能存在营养不良的遗传易感性。因此,有必要进行以下研究:1)调查营养不良的遗传易感性,2)确定有助于识别营养不良风险儿童的遗传标记物和生物标志物,3)寻找可改善营养不良儿童临床管理的新治疗方法。

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