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HIV 感染孕妇早产的代谢组学特征分析。

Metabolomic profiling of preterm birth in pregnant women living with HIV.

机构信息

Division of Infectious Diseases, Department of Pediatrics, David Geffen School of Medicine at the University of California, Los Angeles, CA, USA.

Department of Obstetrics and Gynecology, David Geffen School of Medicine at the University of California, Los Angeles, CA, USA.

出版信息

Metabolomics. 2023 Oct 25;19(11):91. doi: 10.1007/s11306-023-02055-1.

Abstract

BACKGROUND

Preterm birth is a leading cause of death in children under the age of five. The risk of preterm birth is increased by maternal HIV infection as well as by certain antiretroviral regimens, leading to a disproportionate burden on low- and medium-income settings where HIV is most prevalent. Despite decades of research, the mechanisms underlying spontaneous preterm birth, particularly in resource limited areas with high HIV infection rates, are still poorly understood and accurate prediction and therapeutic intervention remain elusive.

OBJECTIVES

Metabolomics was utilized to identify profiles of preterm birth among pregnant women living with HIV on two different antiretroviral therapy (ART) regimens.

METHODS

This pilot study comprised 100 mother-infant dyads prior to antiretroviral initiation, on zidovudine monotherapy or on protease inhibitor-based antiretroviral therapy. Pregnancies that resulted in preterm births were matched 1:1 with controls by gestational age at time of sample collection. Maternal plasma and blood spots at 23-35 weeks gestation and infant dried blood spots at birth, were assayed using an untargeted metabolomics method. Linear regression and random forests classification models were used to identify shared and treatment-specific markers of preterm birth.

RESULTS

Classification models for preterm birth achieved accuracies of 95.5%, 95.7%, and 80.7% in the untreated, zidovudine monotherapy, and protease inhibitor-based treatment groups, respectively. Urate, methionine sulfone, cortisone, and 17α-hydroxypregnanolone glucuronide were identified as shared markers of preterm birth. Other compounds including hippurate and N-acetyl-1-methylhistidine were found to be significantly altered in a treatment-specific context.

CONCLUSION

This study identified previously known as well as novel metabolomic features of preterm birth in pregnant women living with HIV. Validation of these models in a larger, independent cohort is necessary to ascertain whether they can be utilized to predict preterm birth during a stage of gestation that allows for therapeutic intervention or more effective resource allocation.

摘要

背景

早产是五岁以下儿童死亡的主要原因。艾滋病毒感染以及某些抗逆转录病毒方案会增加早产的风险,导致艾滋病毒流行率最高的中低收入环境中负担不成比例。尽管进行了数十年的研究,但自发性早产的机制,特别是在艾滋病毒感染率高的资源有限地区,仍知之甚少,准确的预测和治疗干预仍然难以实现。

目的

利用代谢组学鉴定接受两种不同抗逆转录病毒疗法(ART)方案的艾滋病毒感染孕妇的早产特征。

方法

本研究包括 100 对母婴对,在开始抗逆转录病毒治疗前,接受齐多夫定单药治疗或基于蛋白酶抑制剂的抗逆转录病毒治疗。根据样本采集时的妊娠周龄,将早产妊娠与对照组按 1:1 匹配。在 23-35 周妊娠时检测母体血浆和血斑,以及婴儿出生时的干血斑,采用非靶向代谢组学方法进行检测。使用线性回归和随机森林分类模型来识别早产的共同和治疗特异性标志物。

结果

未治疗、齐多夫定单药治疗和基于蛋白酶抑制剂的治疗组早产的分类模型的准确率分别为 95.5%、95.7%和 80.7%。尿酸、甲硫氨酸亚砜、皮质酮和 17α-羟孕烯醇酮葡萄糖醛酸苷被鉴定为早产的共同标志物。其他化合物,包括马尿酸和 N-乙酰-1-甲基组氨酸,在特定的治疗环境中发现明显改变。

结论

本研究鉴定了艾滋病毒感染孕妇早产的先前已知和新的代谢组学特征。在更大的独立队列中验证这些模型,以确定它们是否可用于预测妊娠晚期的早产,以便进行治疗干预或更有效的资源分配。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49a2/10600291/2c977edc1b41/11306_2023_2055_Fig1_HTML.jpg

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