# Association of fibrinogen to albumin ratio with sepsis-associated acute kidney injury: A retrospective cohort study based on the MIMIC-IV database

**Authors:** Tuan Li, Muyan Diao, Feng Lu, Zhuojian Zeng, Zhiwen Chen, Shengyuan Su, Yuehui Zhang

PMC · DOI: 10.1371/journal.pone.0343549 · 2026-03-06

## TL;DR

This study found that a high fibrinogen-to-albumin ratio is linked to increased risk of kidney injury in sepsis patients, especially after three days in the ICU.

## Contribution

The study identifies fibrinogen-to-albumin ratio as a potential biomarker for predicting sepsis-associated acute kidney injury.

## Key findings

- High FAR (≥110.74) is associated with increased risk of SA-AKI in patients without COPD and hypertension.
- The association becomes significant only after ICU day 3.
- Combining FAR with SOFA improves prediction of SA-AKI compared to SOFA alone.

## Abstract

Sepsis-associated acute kidney injury (SA-AKI) is a critical complication associated with negative outcomes. However, the effective prevention of SA-AKI is limited. This retrospective cohort study, which used the MIMIC-IV database, investigated the association between fibrinogen-to-albumin ratio (FAR) and SA-AKI.

The retrospective cohort study involved 1,771 sepsis patients in MIMIC-IV database. Multivariable logistic and Cox regression models were used to estimate ORs/HRs with 95% CIs for incident SA-AKI. Sensitivity analyses, including stratified analyses and RCS curve, assessed the strength of the association. The predictive performance was compared to other marker using ROC curves and AUCs.

An elevated FAR level (≥110.74) was found to be associated with an elevated risk of SA-AKI (adjusted OR 1.55, 95%CI 1.11–2.18, P = 0.011), but the association was timing, it reached statistical significance only when SA-AKI occurred after ICU day 3 (adjusted HR 5.17, 95%CI 1.81–14.72, P = 0.002). Subgroup analyses indicated that chronic obstructive pulmonary disease (COPD) and hypertension interacted in this association. In sepsis patients without COPD and hypertension, high FAR (≥110.74) was linked to SA-AKI (adjusted OR 2.31, 95%CI 1.40–3.82, P = 0.001), with statistical significance also occurring 3 days after ICU admission (adjusted HR 8.57, 95%CI 1.88–38.94, P = 0.005). The RCS curve showed a linear relationship between FAR and SA-AKI (P for non-linearity: 0.415). ROC analyses showed that FAR combined with SOFA slightly outperformed SOFA alone (AUC 0.697 vs. 0.678, P = 0.004).

An elevated FAR level was associated with an increased incidence of SA-AKI in patients without COPD and hypertension. However, this association reached statistical significance only when SA-AKI occurred after ICU day 3. Further research is needed to investigate this association.

## Linked entities

- **Proteins:** FGB (fibrinogen beta chain), LOC100189571 (uncharacterized LOC100189571)
- **Diseases:** acute kidney injury (MONDO:0002492), chronic obstructive pulmonary disease (MONDO:0005002)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, MBP (myelin basic protein) [NCBI Gene 4155], FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}
- **Diseases:** perinatal disease (MESH:C564306), biliary cirrhosis (MESH:D008105), RCS (MESH:D002313), DIC (MESH:D004211), Sepsis (MESH:D018805), Kidney Disease (MESH:D007674), heart failure (MESH:D006333), hepatic sclerosis (MESH:D056486), thromboembolic complications (MESH:D013923), liver dysfunction (MESH:D017093), cardiovascular disease (MESH:D002318), peritonitis (MESH:D010538), ascites (MESH:D001201), malnutrition (MESH:D044342), hypertension (MESH:D006973), alcoholic cirrhosis of liver (MESH:D008104), SA (MESH:D013615), MV (MESH:D053717), systemic lupus erythematosus (MESH:D008180), hypoxia (MESH:D000860), systemic sclerosis (MESH:D012595), hypoxic (MESH:D002534), SOFA (MESH:D009102), COPD (MESH:D029424), AKI (MESH:D058186), failure (MESH:D051437), cancer (MESH:D009369), diabetes (MESH:D003920), cirrhosis of liver (MESH:D008103), MIMIC (MESH:C000657744), CKD (MESH:D051436), inflammation (MESH:D007249), platelet aggregation (MESH:D001791), alcoholic fibrosis (MESH:D005355), nephrotic syndrome (MESH:D009404), acute coronary syndrome (MESH:D054058)
- **Chemicals:** dopamine (MESH:D004298), milrinone (MESH:D020105), alcohol (MESH:D000438), glucose (MESH:D005947), Creatinine (MESH:D003404), FAR (-), SA (MESH:D000077145), dobutamine (MESH:D004280), norepinephrine (MESH:D009638), phenylephrine (MESH:D010656), aldosterone (MESH:D000450), epinephrine (MESH:D004837)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Figures

13 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12965584/full.md

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Source: https://tomesphere.com/paper/PMC12965584