Clinical significance of peripheral blood DDR1 and CtBP gene methylation detection in patients with acute pancreatitis.


Journal

Epigenetics
ISSN: 1559-2308
Titre abrégé: Epigenetics
Pays: United States
ID NLM: 101265293

Informations de publication

Date de publication:
Dec 2024
Historique:
medline: 1 11 2024
pubmed: 1 11 2024
entrez: 1 11 2024
Statut: ppublish

Résumé

To investigate the clinical value of methylation levels of peripheral blood DDR1 and CtBP genes in evaluating the severity of acute pancreatitis (AP). Collect 90 blood samples from AP patients and healthy volunteers, and test methylation levels of SPINK1, STAT3, KIT, CFTR, DDR1, CtBP1, CtBP2 genes by bisulfite amplicon sequencing (BSAS). The gene methylation and clinical predictors of SAP early prediction were determined by univariate and multifactorial analysis, respectively. (1) The methylation level of CtBP1 gene and MCTSI score were independent predictors of SAP, with AUC values of 0.723 and 0.8895, respectively. (2) The methylation levels of DDR1, CtBP2, CFTR and SPINK1 genes were statistically significant in HC group vs AP group, HC group vs MAP group, and HC group vs SAP group. (3) The combined detection of CtBP1 gene methylation level and MCTSI score predicted the sensitivity, specificity, AUC, and 95%CI of SAP were 0.750, 0.957, 0.902, and 0.816-0.989, respectively. (1) The methylation level of CtBP1 gene in peripheral blood is an independent risk factor for predicting SAP and is a potentially good predictor of SAP, and the combined testing with the MCTSI score does not further significantly improve the early predictive value for SAP. (2) The methylation levels of DDR1, SPINK1, CtBP2, and CFTR genes were potential indicators for recognizing AP.

Identifiants

pubmed: 39485950
doi: 10.1080/15592294.2024.2421631
doi:

Substances chimiques

Alcohol Oxidoreductases EC 1.1.-
C-terminal binding protein EC 1.1.1.-
DNA-Binding Proteins 0
Discoidin Domain Receptor 1 EC 2.7.10.1
DDR1 protein, human EC 2.7.10.1
CTBP2 protein, human EC 1.1.-
Carrier Proteins 0
CFTR protein, human 0
SPINK1 protein, human 0
Trypsin Inhibitor, Kazal Pancreatic 50936-63-5
Cystic Fibrosis Transmembrane Conductance Regulator 126880-72-6
Co-Repressor Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2421631

Auteurs

Zeng-Hui Ma (ZH)

The Second Clinical Medical College, Lanzhou University, Lanzhou, Gansu, China.
Department of Gastroenterology, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Key laboratory of Digestive Diseases, Lanzhou University Second Hospital, Lanzhou, Gansu, China.

Xue-Ni Ma (XN)

The Second Clinical Medical College, Lanzhou University, Lanzhou, Gansu, China.
Department of Gastroenterology, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Key laboratory of Digestive Diseases, Lanzhou University Second Hospital, Lanzhou, Gansu, China.

Hong-Wen Zhu (HW)

The Second Clinical Medical College, Lanzhou University, Lanzhou, Gansu, China.
Department of Gastroenterology, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Key laboratory of Digestive Diseases, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Cuiying Biomedical Research Center, Lanzhou University Second Hospital, Lanzhou, Gansu, China.

Long Cheng (L)

The Second Clinical Medical College, Lanzhou University, Lanzhou, Gansu, China.
Department of Gastroenterology, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Key laboratory of Digestive Diseases, Lanzhou University Second Hospital, Lanzhou, Gansu, China.

Ling-Zhu Gou (LZ)

The Second Clinical Medical College, Lanzhou University, Lanzhou, Gansu, China.
Department of Gastroenterology, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Key laboratory of Digestive Diseases, Lanzhou University Second Hospital, Lanzhou, Gansu, China.

De-Kui Zhang (DK)

Department of Gastroenterology, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Key laboratory of Digestive Diseases, Lanzhou University Second Hospital, Lanzhou, Gansu, China.

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Classifications MeSH