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环境、代谢和炎症因素在儿童中重度急性营养不良的发病机制中汇聚:一项观察性队列研究。

Environmental, Metabolic, and Inflammatory Factors Converge in the Pathogenesis of Moderate Acute Malnutrition in Children: An Observational Cohort Study.

机构信息

1Department of Internal Medicine and Infectious Disease, University of Texas Medical Branch, Galveston, Texas.

2Centre for Clinical Research, Kenya Medical Research Institute, Nairobi, Kenya.

出版信息

Am J Trop Med Hyg. 2021 Mar 22;104(5):1877-1888. doi: 10.4269/ajtmh.20-0963.

DOI:10.4269/ajtmh.20-0963
PMID:33755580
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8103470/
Abstract

Acute malnutrition affects more than 50 million children worldwide. These children are at an increased risk of morbidity and mortality from infectious disease. However, the pathogenesis of acute malnutrition and mechanisms underlying the increased risk and poor outcomes from infection are not well understood. Our objective was to identify differences in inflammation and inflammatory responses between children with moderate acute malnutrition (MAM) and healthy controls (HCs), and search for environmental, pathophysiological, and metabolic factors that may influence this response. Sixteen children with MAM and 16 HCs aged 18-36 months were studied in Nairobi, Kenya. None of the children had symptoms of an infectious disease (fever, diarrhea, or cough) in the 2 weeks before enrollment and sample collection. Demographic and health data were provided by their primary caregivers. Blood samples were collected to measure various biomarkers and the response to an inflammatory stimulus. Children with MAM were more frequently from households with contaminated water, crowding, and unstable income sources. They also had increases in basal inflammation, circulating bacterial lipopolysaccharide (LPS), markers of intestinal damage, and an exaggerated whole blood inflammatory response to LPS. Metabolic changes in children with MAM led to increased plasma levels of long-chain fatty acids, which were found to contribute to the pro-inflammatory state. These exploratory findings suggest convergence of multiple factors to promote dysregulated inflammatory responses and prompt several mechanistic hypotheses that can be pursued to better understand the pathogenesis of MAM.

摘要

全球有超过 5000 万儿童患有急性营养不良。这些儿童罹患传染病的发病率和死亡率增加。然而,急性营养不良的发病机制以及感染风险增加和不良结局的机制尚不清楚。我们的目的是确定患有中度急性营养不良 (MAM) 的儿童与健康对照 (HC) 之间在炎症和炎症反应方面的差异,并寻找可能影响这种反应的环境、病理生理和代谢因素。在肯尼亚内罗毕研究了 16 名患有 MAM 的儿童和 16 名年龄在 18-36 个月的 HCs。在入组和样本采集前的 2 周内,没有儿童出现传染病的症状(发热、腹泻或咳嗽)。其主要照顾者提供了人口统计学和健康数据。采集血样以测量各种生物标志物和对炎症刺激的反应。患有 MAM 的儿童更频繁地来自于饮用水受到污染、拥挤和收入来源不稳定的家庭。他们的基础炎症、循环细菌脂多糖 (LPS)、肠道损伤标志物以及全血对 LPS 的炎症反应也会增加。MAM 患儿的代谢变化导致长链脂肪酸的血浆水平升高,这被发现导致促炎状态。这些探索性发现表明,多种因素的融合会促进失调的炎症反应,并提出了一些可以进一步研究以更好地理解 MAM 发病机制的机制假设。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3027/8103470/8202bd5bb71d/tpmd200963f6.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3027/8103470/8202bd5bb71d/tpmd200963f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3027/8103470/65a929259d58/tpmd200963f1.jpg
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