# Prognostic Value of Tryptophanyl-tRNA Synthetase in Sepsis Combined with Kidney Dysfunction or Urinary Tract Infection: A Prospective Observational Study

**Authors:** Uihwan Kim, Sijin Lee, Kap Su Han, Su Jin Kim, Sungwoo Lee, Dae Won Park, Juhyun Song

PMC · DOI: 10.3390/diagnostics15202634 · Diagnostics · 2025-10-19

## TL;DR

This study shows that high levels of tryptophanyl-tRNA synthetase (WRS) in sepsis patients predict higher 30-day mortality, especially in those with kidney issues or urinary tract infections.

## Contribution

The study identifies WRS as a novel prognostic biomarker for sepsis, particularly in patients with kidney dysfunction or urinary tract infections.

## Key findings

- WRS levels were higher in septic shock patients compared to non-shock patients (p = 0.018).
- WRS predicted 30-day mortality with an AUC of 0.648 and a cut-off of 84.15 µg/L.
- WRS was an independent risk factor for 30-day mortality (hazard ratio = 1.003).

## Abstract

Background: Although tryptophanyl-tRNA synthetase (WRS) is a novel biomarker released during bacterial and viral infections, its prognostic value in sepsis has rarely been reported. This study aimed to evaluate the prognostic performance of WRS in patients with sepsis in the emergency department (ED). Methods: This prospective, observational study included 243 patients with sepsis. Blood samples were collected to measure full-length WRS levels. The prognostic value of WRS was evaluated using the area under the receiver operating characteristic curve, Kaplan–Meier survival curve analysis, and the Cox proportional hazards model. Results: The WRS levels were higher in patients with septic shock than in those without shock (p = 0.018). WRS could predict 30-day mortality (area under the curve, 0.648; 95% confidence interval [CI], 0.569–0.726; sensitivity, 56.7%; specificity, 73.3%; cut-off value, 84.15 µg/L; p < 0.001). Patients with WRS levels of ≥84.15 µg/L showed higher 30-day mortality than those with WRS levels of <84.15 µg/L. Among patients with WRS levels of ≥84.15 µg/L, those with positive urine culture results had higher 30-day mortality than those with negative urine culture. Patients with renal Sequential Organ Failure Assessment (SOFA) score of ≥1 had higher 30-day mortality than those with renal SOFA score of 0. WRS was an independent risk factor of 30-day mortality (hazard ratio = 1.003; 95% CI, 1.001–1.005; p = 0.014). Conclusions: WRS effectively predicted clinical outcome in patients with sepsis and could be more useful in those with kidney dysfunction or urinary tract infection.

## Linked entities

- **Genes:** KCNQ1 (potassium voltage-gated channel subfamily Q member 1) [NCBI Gene 3784]
- **Diseases:** urinary tract infection (MONDO:0005247)

## Full-text entities

- **Genes:** WARS1 (tryptophanyl-tRNA synthetase 1) [NCBI Gene 7453] {aka GAMMA-2, HMN9, HMND9, IFI53, IFP53, NEDMSBA}
- **Diseases:** viral infections (MESH:D014777), shock (MESH:D012769), Kidney Dysfunction (MESH:D007674), Urinary Tract Infection (MESH:D014552), septic (MESH:D001170), Sepsis (MESH:D018805), Sequential Organ Failure (MESH:D009102)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC12564849/full.md

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Source: https://tomesphere.com/paper/PMC12564849