Evidence map›Paper›PMID 40052388›Full record

ArticleEuropean journal of clinical investigation2025

Mid-regional pro-adrenomedullin: A rapid sepsis biomarker for diagnosing spontaneous bacterial peritonitis in cirrhosis.

Abderrahim Oussalah, Vincent Haghnejad, Maël Silva Rodriguez, Anne-Sophie Lagneaux, Tom Alix, Pierre Filhine-Tresarrieu, Janina Ferrand, Jean Jung, Julien Broseus, Sylvain Salignac and 8 more

Abstract readValidation Study
In one paragraph

Article in European journal of clinical investigation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

18 authors.

Abderrahim OussalahDepartment of Genomic Medicine, Division of Biochemistry, Molecular Biology and Nutrition, University Hospital of Nancy, Nancy, France.ORCID https://orcid.org/0000-0002-9731-4529
Vincent HaghnejadDepartment of Gastroenterology and Hepatology, University Hospital of Nancy, Nancy, France.
Maël Silva RodriguezDepartment of Genomic Medicine, Division of Biochemistry, Molecular Biology and Nutrition, University Hospital of Nancy, Nancy, France.ORCID https://orcid.org/0009-0007-6191-7452
Anne-Sophie LagneauxDepartment of Bacteriology, University Hospital of Nancy, Nancy, France.
Tom AlixDepartment of Genomic Medicine, Division of Biochemistry, Molecular Biology and Nutrition, University Hospital of Nancy, Nancy, France.
Pierre Filhine-TresarrieuDepartment of Genomic Medicine, Division of Biochemistry, Molecular Biology and Nutrition, University Hospital of Nancy, Nancy, France.
Janina FerrandDepartment of Bacteriology, University Hospital of Nancy, Nancy, France.
Jean JungDepartment of Genomic Medicine, Division of Biochemistry, Molecular Biology and Nutrition, University Hospital of Nancy, Nancy, France.
Julien BroseusUniversity of Lorraine, INSERM UMR_S 1256, Nutrition, Genetics, and Environmental Risk Exposure (NGERE), Faculty of Medicine of Nancy, Nancy, France.
Sylvain SalignacLaboratory of Hematology, University Hospital of Nancy, Nancy, France.
Amandine LucMethodology, Data Management and Statistics Unit, University Hospital of Nancy, Nancy, France.
Cédric BaumannMethodology, Data Management and Statistics Unit, University Hospital of Nancy, Nancy, France.
Philipp SchuetzMedical University Clinic, Department of Internal and Emergency Medicine and Department of Endocrinology, Diabetology and Clinical Nutrition, Kantonsspital Aarau, Aarau, Switzerland.
Alain LozniewskiDepartment of Bacteriology, University Hospital of Nancy, Nancy, France.
Katell Peoc'hLaboratory of Biochemistry, Beaujon Hospital, University of Paris, Clichy, France.
Hervé PuyInflammation Research Center, University of Paris, INSERM, CNRS, 75018 Paris, France. Laboratory of Excellence GR-EX, Paris, France.
Jean-Louis GuéantDepartment of Genomic Medicine, Division of Biochemistry, Molecular Biology and Nutrition, University Hospital of Nancy, Nancy, France.
Jean-Pierre BronowickiUniversity of Lorraine, INSERM UMR_S 1256, Nutrition, Genetics, and Environmental Risk Exposure (NGERE), Faculty of Medicine of Nancy, Nancy, France.

Funding

Department of Genomic Medicine, Division of Biochemistry, Molecular Biology, Nutrition, and Metabolism, University Hospital of Nancy, F-54000 Nancy, FranceINSERM UMR_S 1256, Nutrition, Genetics, and Environmental Risk Exposure, F-54000 Nancy, FranceThermo Fisher Scientific (Asnières-sur-Seine, France) generously provided the B.R.A.H.M.S. Sensitive KRYPTOR™ immunofluorescence assays used to measure procalcitonin and mid-regional pro-adrenomedullin concentrations in ascitic fluids. The funding sources had no involvement in the study design, conduct, data collection, management, analysis, interpretation, manuscript preparation, review, approval, or the decision to submit the manuscript for publication
6 · The paper itself

Abstract

backgroundSpontaneous bacterial peritonitis (SBP) is a frequent and life-threatening complication of cirrhosis, contributing to considerable morbidity and mortality.

methodsA cross-sectional derivation study was conducted to assess the diagnostic accuracy of two sepsis-related calcitonin peptide family biomarkers, mid-regional pro-adrenomedullin (MR-pro-ADM) and procalcitonin, in ascitic fluid for identifying bacteriologically confirmed SBP (BC-SBP). In a subsequent validation study, the diagnostic performance of the 'SBP score' was evaluated in an independent patient cohort using an absolute polymorphonuclear (PMN) leukocyte count threshold of ≥250 cells/mm

resultsIn the derivation study, the concentration of MR-pro-ADM in ascitic fluid was significantly higher in patients with BC-SBP compared to those without BC-SBP (3.14 nmol/L [IQR, 2.39-6.74] vs. 1.91 nmol/L [IQR, 1.33-2.80]; p = .0002). Bayesian ANOVA indicated that MR-pro-ADM was highly discriminative for diagnosing BC-SBP, with a substantial Bayes factor (BFM = 2505), whereas procalcitonin exhibited poor discriminatory performance. Receiver-operating characteristic (ROC) analysis identified an optimal MR-pro-ADM cut-off of ≥2.50 nmol/L for diagnosing BC-SBP, with an area under the ROC curve (AUROC) of 0.746 (95% CI, 0.685-0.801; p < .0001). Multivariable logistic regression identified three independent predictors of BC-SBP, which were subsequently incorporated into the 'SBP score' (MR-pro-ADM ≥2.5 nmol/L, absolute PMN count ≥250 cells/mm

conclusionMR-pro-ADM in ascitic fluid emerges as a promising biomarker for SBP diagnosis. Combining MR-pro-ADM with absolute PMN count and Child-Pugh score in the 'SBP score' greatly improves the diagnostic accuracy of SBP.

Indexed as

AdrenomedullinAscitic FluidBacterial InfectionsLiver CirrhosisPeritonitisProcalcitoninProtein PrecursorsSepsisAgedBayes TheoremBiomarkersCross-Sectional StudiesFemaleHumansLeukocyte CountMaleAdrenomedullinBiomarkersmid-regional pro-adrenomedullin, humanPeptide FragmentsProcalcitoninProtein Precursorscirrhosismid‐regional pro‐adrenomedullinrapid assay biomarkerspontaneous bacterial peritonitis

Identifiers

PMID40052388
PMCPMC12066915

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