# Mid-Regional Pro-Adrenomedullin as a Translational Biomarker of Microcirculatory Dysfunction in Sepsis: A Prospective Observational Study

**Authors:** Rachael Cusack, Alexis Garduno, Sanja Cumpf, Pramila Reyes-Morales, Marc Leone, Alfonso Blanco Fernández, Alejandro Rodriguez, Ignacio Martin-Loeches

PMC · DOI: 10.3390/medsci14010117 · Medical Sciences · 2026-03-02

## TL;DR

This study shows that a biomarker called MR-proADM is linked to microcirculatory issues in sepsis patients, suggesting it could help monitor their condition.

## Contribution

The study demonstrates MR-proADM's dynamic correlation with microvascular dysfunction in sepsis, supporting its use as a translational biomarker.

## Key findings

- Higher MR-proADM levels at ICU admission correlate with impaired microvascular perfusion.
- Rising MR-proADM levels over time are strongly linked to worsening microvascular perfusion.
- MR-proADM predicts the need for renal replacement therapy in sepsis patients.

## Abstract

Background/Objectives: Mid-regional pro-adrenomedullin (MR-proADM) is a biomarker of endothelial dysfunction in sepsis. Its relationship with real-time microcirculatory alterations in critically ill patients remains insufficiently characterised. Methods: In a prospective cohort of 59 ICU patients with sepsis, serial sublingual microcirculation assessments were performed using sidestream dark field (SDF) imaging. Serum MR-proADM concentrations were measured with BRAHMS Kryptor assays. Automated software quantified microvascular structure and flow. Associations with disease severity and outcomes were evaluated using correlation, regression, and receiver operating characteristic (ROC) analyses (ClinicalTrials.gov Identifier: NCT05357339). Results: Higher MR-proADM concentrations at ICU admission were modestly associated with impaired microvascular perfusion (perfused number of crossings [PNOC]: ρ = −0.32; perfused De Backer density [PDBD]: ρ = −0.32; consensus proportion of perfused vessels [CPPV]: ρ = −0.26; all p < 0.05). Rising MR-proADM levels over time were strongly associated with worsening perfusion (ΔPDBD: ρ = 0.52; ΔPNOC: ρ = 0.54). MR-proADM correlated with SOFA and APACHE II scores and predicted the need for renal replacement therapy (AUC = 0.799, p = 0.041), but not ICU length of stay or hospital mortality. Conclusions: MR-proADM correlates with in vivo microcirculatory dysfunction in sepsis. Its dynamic association with microvascular impairment supports its potential role as a translational biomarker for monitoring endothelial and microcirculatory failure in critically ill patients.

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, PNOC (prepronociceptin) [NCBI Gene 5368] {aka N/OFQ, NOP, OFQ, PPNOC, ppN/OFQ}, ADM (adrenomedullin) [NCBI Gene 133] {aka AM, PAMP}
- **Diseases:** Endothelial dysfunction (MESH:D014652), multiorgan failure (MESH:D051437), Inflammatory (MESH:D007249), MR (MESH:D008944), hypoxia (MESH:D000860), Sepsis (MESH:D018805), shock (MESH:D012769), AKIN (MESH:D058186), multi-organ failure (MESH:D009102), microvascular dysfunction (MESH:D017566), Bacteraemia (MESH:C531821), capillary leak (MESH:D019559), vasoplegia (MESH:D056987), septic (MESH:D001170), critical illness (MESH:D016638), Dysfunction (MESH:D006331), kidney injury (MESH:D007674), death (MESH:D003643), endothelial injury (MESH:D057772), hypotension (MESH:D007022), injury to (MESH:D014947), leukocytosis (MESH:D007964), septic shock (MESH:D012772), infection (MESH:D007239)
- **Chemicals:** creatinine (MESH:D003404), noradrenaline (MESH:D009638), lactate (MESH:D019344), cyclic AMP (MESH:D000242), oxygen (MESH:D010100), citrate (MESH:D019343), MR-proADM (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13028104/full.md

## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC13028104/full.md

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Source: https://tomesphere.com/paper/PMC13028104