Ghrelin polymorphism/TRPV1 receptor expression in Egyptian IBS patients. (April 2022)
- Record Type:
- Journal Article
- Title:
- Ghrelin polymorphism/TRPV1 receptor expression in Egyptian IBS patients. (April 2022)
- Main Title:
- Ghrelin polymorphism/TRPV1 receptor expression in Egyptian IBS patients
- Authors:
- Samy, Walaa
El Gebaly, Ahmed
Ahmed, Nabila H.
Talaat, Aliaa - Abstract:
- Abstract: Introduction/objective: Irritable bowel syndrome is a functional gastrointestinal disorder. Ghrelin is a peptide hormone which affects gastrointestinal motility. We have studied the association between ghrelin gene polymorphism, ghrelin expression, and their effect on TRPV1 correlating this with IBS manifestations in the Egyptian patients. Methods: Participants included 60 IBS patients meeting the Rome III criteria and 60 controls similar in age and gender were recruited. Whole blood samples were used for genotyping of Ghrelin polymorphisms rs696217. Colonic biopsies were processed for mRNA expression analysis of ghrelin and TRPV1. Results: The rs696217 GG genotype frequency was higher in patients (78.3%) compared to controls (57%). According to GT\TT genotype there was significant difference between IBS and control group: 21.7%, 43% respectively (p = 0.0126). In allele frequency distribution, G allele in the IBS group was 87.5% while in the control group was 74%.T allele presents in 12.5% of IBS patients and 26% in the control group (p = 0.010). The genotype frequencies did not significantly differ between IBS subtypes. TRPV1 mRNA levels in were significantly increased in IBS patients than in controls (p < 0.05), while GHRL mRNA expression was significantly decreased (p < 0.05). The IBS-C group showed significantly higher levels of TRPV1 and lower levels of GHRL mRNA expression (p < 0.05) Conclusions: we showed that ghrelin rs696217 might have a role in IBS, asAbstract: Introduction/objective: Irritable bowel syndrome is a functional gastrointestinal disorder. Ghrelin is a peptide hormone which affects gastrointestinal motility. We have studied the association between ghrelin gene polymorphism, ghrelin expression, and their effect on TRPV1 correlating this with IBS manifestations in the Egyptian patients. Methods: Participants included 60 IBS patients meeting the Rome III criteria and 60 controls similar in age and gender were recruited. Whole blood samples were used for genotyping of Ghrelin polymorphisms rs696217. Colonic biopsies were processed for mRNA expression analysis of ghrelin and TRPV1. Results: The rs696217 GG genotype frequency was higher in patients (78.3%) compared to controls (57%). According to GT\TT genotype there was significant difference between IBS and control group: 21.7%, 43% respectively (p = 0.0126). In allele frequency distribution, G allele in the IBS group was 87.5% while in the control group was 74%.T allele presents in 12.5% of IBS patients and 26% in the control group (p = 0.010). The genotype frequencies did not significantly differ between IBS subtypes. TRPV1 mRNA levels in were significantly increased in IBS patients than in controls (p < 0.05), while GHRL mRNA expression was significantly decreased (p < 0.05). The IBS-C group showed significantly higher levels of TRPV1 and lower levels of GHRL mRNA expression (p < 0.05) Conclusions: we showed that ghrelin rs696217 might have a role in IBS, as those patients carrying the GG genotype showed a significant decrease in ghrelin mRNA expression, with a subsequent significant increase in TRPV1 gene expression, and could explain some of the IBS manifestations. … (more)
- Is Part Of:
- Cytokine. Volume 152(2022)
- Journal:
- Cytokine
- Issue:
- Volume 152(2022)
- Issue Display:
- Volume 152, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 152
- Issue:
- 2022
- Issue Sort Value:
- 2022-0152-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-04
- Subjects:
- Irritable bowel syndrome -- Constipation -- Diarrhea -- Functional gastrointestinal disorders -- Ghrelin -- TRPV1
TRPV1 Transient receptor potential vanilloid type I -- GHRL Ghrelin -- IBS Irritable bowel syndrome -- SNPs Single nucleotide polymorphisms
Cytokines -- Periodicals
571.844 - Journal URLs:
- http://www.sciencedirect.com/science/journal/10434666 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.cyto.2022.155827 ↗
- Languages:
- English
- ISSNs:
- 1043-4666
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3506.778000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21033.xml