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肝脏维生素 A 浓度与儿童死亡感染性病因的关系。

Hepatic Vitamin A Concentrations and Association with Infectious Causes of Child Death.

机构信息

Hubert Department of Global Health, Rollins School of Public Health, Emory University, Atlanta, GA.

Global Health Center, Centers for Disease Control and Prevention, Atlanta, GA.

出版信息

J Pediatr. 2024 Feb;265:113816. doi: 10.1016/j.jpeds.2023.113816. Epub 2023 Nov 4.

Abstract

OBJECTIVES

To assess postmortem vitamin A (VA) concentrations in children under 5 years of age and evaluate the association between VA deficiency (VAD) and infectious causes of death (CoD).

STUDY DESIGN

In this cross-sectional study from the Child Health and Mortality Prevention Surveillance (CHAMPS) Network, liver biopsies collected within 72 hours of death were analyzed from 405 stillbirths and children under 5 years in Kenya and South Africa. Total liver VA (TLVA) concentrations were quantified using ultra-performance liquid chromatography, and cutoffs of ≤0.1 μmol/g, >0.1 to <0.7 μmol/g, ≥0.7 to <1.0 μmol/g, and ≥1.0 μmol/g were used to define VAD, adequate VA status, high VA, and hypervitaminosis A, respectively. CoD were determined by expert panel review.

RESULTS

Among 366 liver samples with viable extraction, pooled prevalences of VAD, adequacy, high VA, and hypervitaminosis were 34.2%, 51.1%, 6.0%, and 8.7%, respectively. VAD was more common among neonates compared with stillbirths, infants, or children, and among those with low birthweight (LBW), underweight, or stunting (P < .05). When adjusting for site, age, and sex, there was no significant association of VAD with increased infectious CoD (OR 1.9, 95% confidence interval [CI] 0.9, 3.8, P = .073). In stratified analyses, VA deficient boys, but not girls, had an increased risk of infectious CoD (OR 3.4, 95% CI 1.3, 10.3, P = .013).

CONCLUSIONS

Definitive postmortem assessment of VA status identified both VAD and VA excess among children under 5 years of age in Kenya and South Africa. VAD in boys was associated with increased risk of infectious mortality. Our findings may inform a transition from universal VA supplementation (VAS) to targeted strategies in certain countries.

摘要

目的

评估 5 岁以下儿童死后维生素 A(VA)浓度,并评估 VA 缺乏(VAD)与感染性死因(CoD)之间的关系。

研究设计

本研究为横断面研究,来自儿童健康与死亡率监测(CHAMPS)网络,对肯尼亚和南非的 405 例死产儿和 5 岁以下儿童的肝活检组织进行了分析。使用超高效液相色谱法定量测定总肝 VA(TLVA)浓度,将≤0.1μmol/g、>0.1 至<0.7μmol/g、≥0.7 至<1.0μmol/g 和≥1.0μmol/g 分别定义为 VAD、VA 充足状态、VA 高值和高维甲酸血症。通过专家小组审查确定 CoD。

结果

在 366 份具有可提取活性的肝样本中,VAD、充足、VA 高值和高维甲酸血症的总体患病率分别为 34.2%、51.1%、6.0%和 8.7%。与死产儿、婴儿或儿童相比,新生儿 VAD 更为常见,与低出生体重(LBW)、体重不足或发育迟缓者相比,VAD 也更为常见(P<0.05)。在校正地点、年龄和性别后,VAD 与感染性 CoD 增加无关(比值比 1.9,95%置信区间[CI]0.9,3.8,P=0.073)。在分层分析中,VA 缺乏的男孩,而不是女孩,感染性 CoD 的风险增加(比值比 3.4,95%CI 1.3,10.3,P=0.013)。

结论

对 VA 状态进行明确的死后评估,发现肯尼亚和南非 5 岁以下儿童中既有 VAD,也有 VA 过量。男孩的 VAD 与感染性死亡率增加有关。我们的研究结果可能为某些国家从普遍 VA 补充(VAS)向有针对性的策略转变提供信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d84d/10869935/2fedca73fa0b/gr1.jpg

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