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撒哈拉以南非洲新生儿败血症宿主反应特征的前瞻性多中心研究。

Prospective multicentre study of host response signatures in neonatal sepsis in Sub Saharan Africa.

机构信息

Open Innovation & Partnerships Lyon Sud (OI&P), bioMérieux, Marcy-l'Étoile, France.

Institute of Integrative Biology of the Cell (I2BC), CNRS, CEA, University Paris Saclay, Gif-sur-Yvette, France.

出版信息

Sci Rep. 2022 Dec 12;12(1):21458. doi: 10.1038/s41598-022-25892-x.

Abstract

Few biomarkers for sepsis diagnosis are commonly used in neonatal sepsis. While the role of host response is increasingly recognized in sepsis pathogenesis and prognosis, there is a need for evaluating new biomarkers targeting host response in regions where sepsis burden is high and medico-economic resources are scarce. The objective of the study is to evaluate diagnostic and prognostic accuracy of biomarkers of neonatal sepsis in Sub Saharan Africa. This prospective multicentre study included newborn infants delivered in the Abomey-Calavi region in South Benin and their follow-up from birth to 3 months of age. Accuracy of transcriptional (CD74, CX3CR1), proteic (PCT, IL-6, IL-10, IP-10) biomarkers and clinical characteristics to diagnose and prognose neonatal sepsis were measured. At delivery, cord blood from all consecutive newborns were sampled and analysed, and infants were followed for a 12 weeks' period. Five hundred and eighty-one newborns were enrolled. One hundred and seventy-two newborns developed neonatal sepsis (29.6%) and death occurred in forty-nine infants (8.4%). Although PCT, IL-6 and IP-10 levels were independently associated with sepsis diagnosis, diagnostic accuracy of clinical variables combinations was similar to combinations with biomarkers and superior to biomarkers alone. Nonetheless, CD74, being the only biomarkers independently associated with mortality, showed elevated prognosis accuracy (AUC > 0.9) either alone or in combination with other biomarkers (eg. CD74/IP-10) or clinical criterion (eg. Apgar 1, birth weight). These results suggest that cord blood PCT had a low accuracy for diagnosing early onset neonatal sepsis in Sub Saharan African neonates, while association of clinical criterion showed to be more accurate than any biomarkers taken independently. At birth, CD74, either associated with IP-10 or clinical criterion, had the best accuracy in prognosing sepsis mortality.Trial registration Clinicaltrial.gov registration number: NCT03780712. Registered 19 December 2018. Retrospectively registered.

摘要

在新生儿败血症中,很少有生物标志物被广泛用于诊断。虽然宿主反应在败血症的发病机制和预后中的作用越来越受到重视,但在败血症负担高且医疗经济资源匮乏的地区,需要评估针对宿主反应的新生物标志物。本研究的目的是评估生物标志物在撒哈拉以南非洲新生儿败血症中的诊断和预后准确性。这是一项前瞻性多中心研究,纳入了在贝宁南部阿波美-卡拉维地区分娩的新生儿及其从出生到 3 个月的随访。测量了转录(CD74、CX3CR1)、蛋白(PCT、IL-6、IL-10、IP-10)生物标志物和临床特征对新生儿败血症的诊断和预后的准确性。在分娩时,对所有连续出生的新生儿进行脐带血采样和分析,并对婴儿进行了 12 周的随访。共纳入 581 名新生儿。172 名新生儿发生新生儿败血症(29.6%),49 名婴儿死亡(8.4%)。虽然 PCT、IL-6 和 IP-10 水平与败血症诊断独立相关,但临床变量组合的诊断准确性与生物标志物组合相似,且优于单独使用生物标志物。尽管 CD74 是唯一与死亡率独立相关的生物标志物,但无论单独使用还是与其他生物标志物(如 CD74/IP-10)或临床标准(如 Apgar 1、出生体重)联合使用,其预后准确性均较高(AUC>0.9)。这些结果表明,在撒哈拉以南非洲新生儿中,脐带血 PCT 对早期发病的新生儿败血症的诊断准确性较低,而联合临床标准比任何单独使用的生物标志物都更准确。在出生时,CD74 与 IP-10 或临床标准联合使用,对预测败血症死亡率的准确性最高。

试验注册

Clinicaltrial.gov 注册号:NCT03780712。注册于 2018 年 12 月 19 日。回顾性注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24d6/9744733/1b63ccdc7076/41598_2022_25892_Fig1_HTML.jpg

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