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微量营养素和肠功能障碍评估工具的验证,以及评估马里幼儿生长迟缓与疫苗接种失败的生物标志物风险因素。

Validation of the Micronutrient and Environmental Enteric Dysfunction Assessment Tool and evaluation of biomarker risk factors for growth faltering and vaccine failure in young Malian children.

机构信息

PATH, Seattle, Washington, United States of America.

Department of Global Health, University of Washington, United States of America.

出版信息

PLoS Negl Trop Dis. 2020 Sep 30;14(9):e0008711. doi: 10.1371/journal.pntd.0008711. eCollection 2020 Sep.

Abstract

Environmental enteric dysfunction (EED) is an intestinal disorder common among children in low-resource settings and is associated with increased risk of growth stunting, cognitive deficits, and reduced oral vaccine immunogenicity. The Micronutrient and EED Assessment Tool (MEEDAT) is a multiplexed immunoassay that measures biomarkers previously associated with child growth faltering and/or oral vaccine immunogenicity: intestinal fatty acid-binding protein (I-FABP), soluble CD14 (sCD14), insulin-like growth factor 1 (IGF-1), and fibroblast growth factor 21 (FGF21). MEEDAT also measures systemic inflammation (α1-acid glycoprotein, C-reactive protein), ferritin, soluble transferrin receptor, retinol binding protein 4, thyroglobulin, and Plasmodium falciparum antigenemia (histidine-rich protein 2). The performance of MEEDAT was compared with commercially available enzyme-linked immunosorbent assays (ELISAs) using 300 specimens from Malian infant clinical trial participants. Regression methods were used to test if MEEDAT biomarkers were associated with seroconversion to meningococcal A conjugate vaccine (MenAV), yellow fever vaccine (YFV), and pentavalent rotavirus vaccine (PRV) after 28 days, or with growth faltering over 12 weeks. The Pearson correlations between the MEEDAT and ELISA results were 0.97, 0.86, 0.80, and 0.97 for serum I-FABP, sCD14, IGF-1, and FGF21, respectively. There were significant associations between I-FABP concentration and the probability of PRV IgG seroconversion and between IGF-1 concentration and the probability of YFV seroconversion. In multivariable models neither association remained significant, however there was a significant negative association between AGP concentration and YFV seroconversion. GLP-2 and sCD14 concentrations were significantly negatively associated with 12-week change in weight-for-age z-score and weight-for-height z-score in multivariable models. MEEDAT performed well in comparison to commercially-available ELISAs for the measurement of four analytes for EED and growth hormone resistance. Adoption of MEEDAT in low-resource settings could help accelerate the identification of interventions that prevent or treat child stunting and interventions that boost the immunogenicity of child vaccinations.

摘要

环境肠道功能障碍 (EED) 是一种常见于资源匮乏环境中儿童的肠道疾病,与生长迟缓、认知缺陷和口服疫苗免疫原性降低的风险增加有关。微量营养素和 EED 评估工具 (MEEDAT) 是一种多重免疫测定法,可测量先前与儿童生长迟缓相关的生物标志物和/或口服疫苗免疫原性:肠脂肪酸结合蛋白 (I-FABP)、可溶性 CD14 (sCD14)、胰岛素样生长因子 1 (IGF-1) 和成纤维细胞生长因子 21 (FGF21)。MEEDAT 还测量全身炎症 (α1-酸性糖蛋白、C 反应蛋白)、铁蛋白、可溶性转铁蛋白受体、视黄醇结合蛋白 4、甲状腺球蛋白和恶性疟原虫抗原血症 (富含组氨酸蛋白 2)。使用来自马里婴儿临床试验参与者的 300 份标本比较了 MEEDAT 的性能与商业上可用的酶联免疫吸附测定 (ELISA)。回归方法用于测试 MEEDAT 生物标志物是否与脑膜炎球菌 A 结合疫苗 (MenAV)、黄热病疫苗 (YFV) 和五价轮状病毒疫苗 (PRV) 在 28 天后的血清转化率或 12 周内的生长迟缓相关。MEEDAT 和 ELISA 结果之间的 Pearson 相关系数分别为血清 I-FABP、sCD14、IGF-1 和 FGF21 的 0.97、0.86、0.80 和 0.97。I-FABP 浓度与 PRV IgG 血清转化率之间存在显著相关性,IGF-1 浓度与 YFV 血清转化率之间存在显著相关性。然而,在多变量模型中,这两种相关性均不显著,AGP 浓度与 YFV 血清转化率之间存在显著负相关。GLP-2 和 sCD14 浓度在多变量模型中与体重年龄 z 评分和体重身高 z 评分的 12 周变化呈显著负相关。MEEDAT 在测量 EED 和生长激素抵抗的四种分析物方面与商业上可用的 ELISA 相比表现良好。在资源匮乏的环境中采用 MEEDAT 可以帮助加速识别预防或治疗儿童发育迟缓的干预措施,以及增强儿童疫苗免疫原性的干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8831/7549819/0301d539b5b8/pntd.0008711.g001.jpg

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