Evaluation of the Wnt signaling pathway as a prognostic marker in patients with urosepsis.


Journal

Molecular and cellular biochemistry
ISSN: 1573-4919
Titre abrégé: Mol Cell Biochem
Pays: Netherlands
ID NLM: 0364456

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 28 03 2020
accepted: 18 06 2020
pubmed: 27 6 2020
medline: 29 4 2021
entrez: 27 6 2020
Statut: ppublish

Résumé

The Wnt signaling pathway has critical roles in dysregulated inflammation during sepsis; however, its impacts on clinical outcomes remain uncertain. This prospective observational study investigated the association between the Wnt pathway and clinical outcomes in patients with urosepsis. The study included 38 patients with urosepsis and 20 healthy individuals. Wnt3a and Wnt5a levels were measured at admission. The primary outcome was the occurrence of major adverse kidney events (MAKE), defined as new renal replacement therapy, stage 3 acute kidney injury, or death. Both Wnt3a and Wnt5a levels were higher in the patient group than in the control (P = 0.001 and P < 0.001, respectively). The primary outcome occurred in 13 (34.2%) subjects. The levels of Wnt5a were higher in subjects with MAKE than in those without MAKE (P = 0.015); however, Wnt3a levels showed no significant difference. Moreover, Wnt5a levels could be a marker to predict the possibility of MAKE (area under the curve 0.74 [0.57-0.92]; P = 0.016). Serum creatinine levels on day 0, day 5, and on discharge day were evaluated. The levels of creatinine on discharge day were higher in patients with high Wnt5a levels, compared to those with low Wnt5a levels (P = 0.030); however, no difference in Wnt5a levels was observed on day 0 and 5. Wnt3a and Wnt5a levels increased in patients with urosepsis. Moreover, evaluation of Wnt5a levels might help to predict the occurrence of MAKE and renal recovery in these patients.

Identifiants

pubmed: 32588279
doi: 10.1007/s11010-020-03804-9
pii: 10.1007/s11010-020-03804-9
doi:

Substances chimiques

Biomarkers 0
WNT3A protein, human 0
WNT5A protein, human 0
Wnt-5a Protein 0
Wnt3A Protein 0

Types de publication

Clinical Trial Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

15-23

Auteurs

Jungho Shin (J)

Department of Internal Medicine, Chung-Ang University College of Medicine, Seoul, Korea.

Yoosik Yoon (Y)

Department of Microbiology, Chung-Ang University College of Medicine, Seoul, Korea.

Dong-Jin Oh (DJ)

Department of Internal Medicine, Myongji Hospital, Hanyang University College of Medicine, 5 Hwasu-ro 14, Deogyang-gu, Goyang, 10475, Korea. intmdoh@hanmail.net.

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Classifications MeSH