Narvaez-Rivas Monica, Setchell Kenneth D R, Galandi Stephanie L, Zhao Xueheng, Iqbal Najeeha Talat, Ahmed Sheraz, Iqbal Junaid, Syed Sana, Ali Syed Asad, Moore Sean R
Division of Pathology & Laboratory Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45229, USA.
Metabolites. 2023 Mar 29;13(4):489. doi: 10.3390/metabo13040489.
Environmental enteric dysfunction (EED) is characterized by intestinal inflammation, malabsorption and growth-faltering in children with heightened exposure to gut pathogens. The aim of this study was to characterize serum non-esterified fatty acids (NEFA), in association with childhood undernutrition and EED, as potential biomarkers to predict growth outcomes. The study comprised a cohort of undernourished rural Pakistani infants ( = 365) and age-matched controls followed prospectively up to 24 months of age. Serum NEFA were quantified at ages 3-6 and 9 months and correlated with growth outcomes, serum bile acids and EED histopathological biomarkers. Serum NEFA correlated with linear growth-faltering and systemic and gut biomarkers of EED. Undernourished children exhibited essential fatty acid deficiency (EFAD), with low levels of linoleic acid and total n-6 polyunsaturated fatty acids, compensated by increased levels of oleic acid and increased elongase and desaturase activities. EFAD correlated with reduced anthropometric Z scores at 3-6 and 9 months of age. Serum NEFA also correlated with elevated BA and liver dysfunction. Essential fatty acid depletion and altered NEFA metabolism were highly prevalent and associated with acute and chronic growth-faltering in EED. The finding suggests that targeting early interventions to correct EFAD and promote FA absorption in children with EED may facilitate childhood growth in high-risk settings.
环境肠道功能障碍(EED)的特征是肠道炎症、吸收不良以及肠道病原体暴露增加的儿童生长发育迟缓。本研究的目的是将血清非酯化脂肪酸(NEFA)与儿童期营养不良和EED相关联,作为预测生长结局的潜在生物标志物进行特征描述。该研究包括一组营养不良的巴基斯坦农村婴儿(n = 365)和年龄匹配的对照组,前瞻性随访至24个月龄。在3 - 6个月和9个月龄时对血清NEFA进行定量,并与生长结局、血清胆汁酸和EED组织病理学生物标志物相关联。血清NEFA与线性生长迟缓以及EED的全身和肠道生物标志物相关。营养不良的儿童表现出必需脂肪酸缺乏(EFAD),亚油酸和总n - 6多不饱和脂肪酸水平较低,通过油酸水平升高以及延长酶和去饱和酶活性增加来代偿。EFAD与3 - 6个月和9个月龄时人体测量Z评分降低相关。血清NEFA也与胆汁酸升高和肝功能障碍相关。必需脂肪酸耗竭和NEFA代谢改变非常普遍,并与EED中的急性和慢性生长迟缓相关。这一发现表明,针对EED儿童进行早期干预以纠正EFAD并促进脂肪酸吸收,可能有助于高危环境下儿童的生长。