Evidence map›Paper›PMID 40380203›Full record

ArticleBMC pediatrics2025

Complement levels and their diagnostic utility in neonatal sepsis.

Fuqiang Diao, Feng Zhong, Lingling Tang, Chunming Gu, Junfei Guo, Lihong Wu, Weixiang Wu, Mingyong Luo

Abstract read
In one paragraph

Article in BMC pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Fuqiang DiaoDepartment of Clinical Laboratory, Guangdong Women and Children Hospital, Guangzhou, 511443, China.
Feng ZhongDepartment of Clinical Laboratory, Guangdong Women and Children Hospital, Guangzhou, 511443, China.
Lingling TangDepartment of Clinical Laboratory, Guangdong Women and Children Hospital, Guangzhou, 511443, China.
Chunming GuDepartment of Clinical Laboratory, Guangdong Women and Children Hospital, Guangzhou, 511443, China.
Junfei GuoDepartment of Clinical Laboratory, Guangdong Women and Children Hospital, Guangzhou, 511443, China.
Lihong WuDepartment of Clinical Laboratory, Guangdong Women and Children Hospital, Guangzhou, 511443, China.
Weixiang WuDepartment of Clinical Laboratory, Guangdong Women and Children Hospital, Guangzhou, 511443, China. samwoowu@163.com.
Mingyong LuoDepartment of Clinical Laboratory, Guangdong Women and Children Hospital, Guangzhou, 511443, China. luo-my@163.com.

Funding

National Natural Science Foundation of China 42207492Natural Science Foundation of Guangdong Province of China 2022A1515012226
6 · The paper itself

Abstract

backgroundThis study evaluated the diagnostic value of complement levels in neonatal sepsis and their roles in disease progression.

methodsThis diagnostic accuracy study, conducted in Guangdong Province, China (January 2021-February 2022), involved 41 neonates with sepsis and 41 controls matched by sex and gestational age. Cases included neonates with culture-positive or clinically diagnosed sepsis, while controls consisted of neonates hospitalized for non-septic conditions, confirmed by negative blood cultures. Ten complement components (C1q, C3, C3c, C3b, C4, C5, C5a, H, B, mannose-binding lectin [MBL]) were quantified using residual specimens from routine clinical tests. Descriptive statistics, logistic regression, ROC curve analysis, and correlation assessments were introduced in this study.

resultsThe neonatal sepsis group had significantly higher levels of C3c (0.68 vs. 0.49 ng/mL, P = 0.007) and MBL (518.81 vs. 397.06 pg/mL, P < 0.001) compared to controls. In contrast, C5a levels were significantly lower in neonates with sepsis (51.18 vs. 57.25 ng/mL, P = 0.042). C5a demonstrated limited individual performance (AUC = 0.63, 95% CI: 0.51-0.75; sensitivity = 65.9%, specificity = 65.9% at 55.63 ng/mL), while MBL showed moderate accuracy (AUC = 0.75, 95% CI: 0.64-0.85; specificity = 90.2%, sensitivity = 53.7% at 512.86 pg/mL). Notably, their combined C5a + MBL indicator achieved exceptional discrimination (AUC = 0.92, 95% CI: 0.85-0.99) with 85.4% sensitivity and 97.6% specificity, yielding 97.2% positive predictive value (PPV) and 87.0% negative predictive value (NPV).Positive correlations were found between C4 levels and C-reactive protein (CRP), and C3 levels and neutrophil percentage (Neut%), while negative correlations were observed between C5 and MBL levels and total cholesterol (TCH).

conclusionsThis study highlights the diagnostic significance of combined C5a + MBL indicator in neonatal sepsis and underscores the association between complement levels and disease progression.

Indexed as

Complement System ProteinsNeonatal SepsisBiomarkersCase-Control StudiesChinaFemaleHumansInfant, NewbornMaleMannose-Binding LectinROC CurveBiomarkersComplement System ProteinsMannose-Binding LectinComplementDiagnostic valueMannose-binding lectinNeonatal sepsis

Identifiers

PMID40380203
PMCPMC12085051

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.