加蓬儿童发热性疾病的铁稳态和细胞因子反应。

IF 5.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Wolfram Mayr, Paulin E Ndong, Ayodele Alabi, Lumeka A Kabwende, Günter Weiss, Selidji T Agnandji
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引用次数: 0

摘要

背景:缺铁、贫血和传染病在很大程度上造成了撒哈拉以南非洲儿童的疾病负担。准确评估铁状态及其与感染的关系对于完善铁补充策略至关重要。方法:我们回顾性分析了一项横断面研究的数据,该研究来自加蓬lambar尼什纳(NCT03047642)的2-17岁急性发热性疾病(发烧≤7天)儿童。基于症状的微生物检测确定了感染病因。血细胞计数、c反应蛋白、铁参数和细胞因子水平评估缺铁、贫血和免疫激活。结果:经筛查的415例急性发热性疾病患儿中,197例血红蛋白、铁参数正常。其中145例(73.6%)为贫血:53例(36.6%)为炎症性贫血(AI), 11例(7.6%)为缺铁性贫血(IDA), 29例(20.0%)为AI/IDA合并贫血。其他被归类为多因素,主要是小细胞性贫血,转铁蛋白饱和度(TSAT)≥20%和不同的铁蛋白水平。在疟疾阳性组中,TSAT与IL-10、IL-6和IL-2呈负相关,IL-10也与寄生虫计数呈正相关。在病原体未确定的疟疾阴性儿童中,IFN-γ和IL-4水平与TSAT和铁蛋白呈正相关。结论:这些发现强调了感染性疾病中的铁平衡失调,并证实了铁的可利用性与对病原体的免疫激活之间的联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Iron homeostasis and cytokine responses in Gabonese children with febrile illness.

Background: Iron deficiency, anemia, and infectious diseases contribute largely to the disease burden among children in Sub-Saharan Africa. Accurate assessment of iron status and its relationship with infections is essential for refining iron supplementation strategies.

Methods: We report retrospectively analyzed data from a cross-sectional study of children aged 2-17 years with acute febrile illness (fever ≤7 days) in Lambaréné, Gabon (NCT03047642). Symptom-based microbiological testing identified infection etiology. Blood count, C-reactive protein, iron parameters, and cytokines levels assessed iron deficiency, anemia, and immune activation.

Results: Among 415 screened children with acute febrile illness, hemoglobin and iron parameters are available in 197. Of those, 145 (73.6%) are anemic: 53 (36.6%) show anemia of inflammation (AI), 11 (7.6%) iron-deficiency anemia (IDA), and 29 (20.0%) combined AI/IDA. Others are categorized as multifactorial, with mostly microcytic anemia, transferrin saturation (TSAT) ≥ 20% and varying ferritin levels. TSAT is negatively associated with IL-10, IL-6, and IL-2 in the malaria-positive group, with IL-10 also showing a positive correlation with parasitemia counts. In malaria-negative children with undetermined pathogens, IFN-γ and IL-4 levels are positively associated with TSAT and ferritin.

Conclusions: These findings highlight iron dyshomeostasis in infectious diseases and confirm associations between iron availability and immune activation to causative pathogens.

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