Thrombospondin 1 and Nuclear Factor Kappa B Signaling Pathways in Non-alcoholic Fatty Liver Disease.


Journal

Journal of gastrointestinal and liver diseases : JGLD
ISSN: 1842-1121
Titre abrégé: J Gastrointestin Liver Dis
Pays: Romania
ID NLM: 101272825

Informations de publication

Date de publication:
15 09 2022
Historique:
received: 22 04 2022
accepted: 19 07 2022
entrez: 16 9 2022
pubmed: 17 9 2022
medline: 21 9 2022
Statut: epublish

Résumé

We aimed to evaluate the circulating thrombospondin-1 (TSP-1) and nuclear factor kappa B (NF-κB) in nonalcoholic fatty liver disease (NAFLD) in order to integrate these signaling pathways in the inflammatory and fibrogenic processes of this liver disorder. Ninety-five NAFLD patients were recruited in the study. The study also included 83 age-sex matched healthy controls. The number of patients with metabolic syndrome (MetS) criteria was 57 (60%). TSP-1 level was found to be statistically significantly lower in the NAFLD group compared to the control group (p=0.037). However, NF-κB level was found to be significantly higher in the NAFLD group compared to the control group (p=0.004). There was a significant negative correlation between plasma TSP-1 levels with glucose (r=-0.235, p=0.022), alanine aminotransferase (r=-0.261, p=0.011) and aspartate transaminase (r=-0.328, p=0.001) levels. In addition, a significant negative correlation was found between plasma TSP-1 and NF-κB levels (r=-0.729, p<0.001). Our results suggest a close relationship between increased NF-κB and reduced TSP-1 in NAFLD. TSP-1 and NF-κB signaling pathways might have a role in the inflammatory and fibrogenic processes. Furthermore, they may be used as a noninvasive marker and could assist as a therapeutic target for NAFLD.

Identifiants

pubmed: 36112712
doi: 10.15403/jgld-4390
doi:

Substances chimiques

NF-kappa B 0
Thrombospondin 1 0
Aspartate Aminotransferases EC 2.6.1.1
Alanine Transaminase EC 2.6.1.2
Glucose IY9XDZ35W2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

309-316

Auteurs

Iskender Ekinci (I)

Health Sciences University, Kanuni Sultan Suleyman Training and Research Hospital, Department of Internal Medicine, Istanbul, Turkey. . driskenderekinci@gmail.com.

Seyma Dumur (S)

Istanbul Atlas University, Faculty of Medicine, Department of Medical Biochemistry, Istanbul, Turkey. seyma_dumur@hotmail.com.

Hafize Uzun (H)

Istanbul Atlas University, Faculty of Medicine, Department of Medical Biochemistry, Istanbul, Turkey. huzun59@hotmail.com.

Gulden Anataca (G)

Health Sciences University, Kanuni Sultan Suleyman Training and Research Hospital, Department of Internal Medicine, Istanbul, Turkey. ganataca@yahoo.com.

Isa Yalcinkaya (I)

Health Sciences University, Kanuni Sultan Suleyman Training and Research Hospital, Department of Internal Medicine, Istanbul, Turkey. isayk@hotmail.com.

Mitat Buyukkaba (M)

Health Sciences University, Kanuni Sultan Suleyman Training and Research Hospital, Department of Internal Medicine, Istanbul, Turkey. dr.mitat@hotmail.com.

Ahmet Cinar (A)

Arnavutkoy State Hospital, Department of Internal Medicine, Istanbul, Turkey. drahmetcinar@hotmail.com.

Hanise Ozkan (H)

Health Sciences University, Kanuni Sultan Suleyman Training and Research Hospital, Department of Internal Medicine, Istanbul, Turkey. haniseozkan@hotmail.com.

Irem Kirac Utku (IK)

Health Sciences University, Kanuni Sultan Suleyman Training and Research Hospital, Department of Internal Medicine, Istanbul, Turkey. iremkrac@yahoo.com.

Murat Akarsu (M)

Health Sciences University, Kanuni Sultan Suleyman Training and Research Hospital, Department of Internal Medicine, Istanbul, Turkey. muratakarsu79@gmail.com.

Omur Tabak (O)

Health Sciences University, Kanuni Sultan Suleyman Training and Research Hospital, Department of Internal Medicine, Istanbul, Turkey. omurtabak@gmail.com.

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Classifications MeSH