IL-17A, MCP-1, CCR-2, and ABCA1 polymorphisms in children with non-alcoholic fatty liver disease
| dc.authorid | 0000-0001-9987-3351 | |
| dc.authorid | 0000-0002-4815-1591 | |
| dc.authorid | 0000-0001-6226-4712 | |
| dc.authorid | 0000-0001-7388-874X | |
| dc.authorid | 0000-0002-5098-4787 | |
| dc.contributor.author | Akbulut, Ulas Emre | |
| dc.contributor.author | Emeksiz, Hamdi Cihan | |
| dc.contributor.author | Citli, Senol | |
| dc.contributor.author | Cebi, Alper Han | |
| dc.contributor.author | Korkmaz, Hatice Ayca Ata | |
| dc.contributor.author | Baki, Gaye | |
| dc.date.accessioned | 2025-05-10T19:50:24Z | |
| dc.date.issued | 2019 | |
| dc.department | İstanbul Medeniyet Üniversitesi | |
| dc.description.abstract | Objective: The prevalence of non-alcoholic fatty liver disease in children has risen significantly, owing to the worldwide childhood obesity epidemic in the last two decades. Non-alcoholic fatty liver disease is closely linked to sedentary lifestyle, increased body mass index, and visceral adiposity. In addition, individual genetic variations also have a role in the development and progression of non-alcoholic fatty liver disease. The aim of this study was to investigate the gene polymorphisms of MCP-1 (-2518 A/G) (rs1024611), CCR-2 (190 G/A) (rs1799864), ABCA1 (883 G/A) (rs4149313), and IL-17A (-197 G/A) (rs2275913) in obese Turkish children with non-alcoholic fatty liver disease. Methods: The study recruited 186 obese children aged 10-17 years, including 101 children with non-alcoholic fatty liver disease and 85 children without non-alcoholic fatty liver disease. Anthropometric measurements, insulin resistance, a liver panel, a lipid profile, liver ultrasound examination, and genotyping of the four variants were performed. Results: No difference was found between the groups in respect to age and gender, body mass index, waist/hip ratio, or body fat ratio. In addition to the elevated ALT levels, AST and GGT levels were found significantly higher in the non-alcoholic fatty liver disease group compared to the non non-alcoholic fatty liver disease group (p< 0.05). The A-allele of IL-17A (-197 G/A) (rs2275913) was associated with non-alcoholic fatty liver disease (odds ratio [OR] 2.05, 95% confidence interval: 1.12-3.77, p= 0.02). Conclusions: The findings of this study suggest that there may be an association between IL-17A (-197 G/A) (rs2275913) polymorphism and non-alcoholic fatty liver disease development in obese Turkish children. (C) 2018 Sociedade Brasileira de Pediatria. Published by Elsevier Editora Ltda. | |
| dc.description.sponsorship | Kanuni Training and Research Hospital | |
| dc.description.sponsorship | This work was supported by the Kanuni Training and Research Hospital. | |
| dc.identifier.doi | 10.1016/j.jped.2018.03.005 | |
| dc.identifier.endpage | 357 | |
| dc.identifier.issn | 0021-7557 | |
| dc.identifier.issn | 1678-4782 | |
| dc.identifier.issue | 3 | |
| dc.identifier.pmid | 29733805 | |
| dc.identifier.scopus | 2-s2.0-85047092048 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.startpage | 350 | |
| dc.identifier.uri | https://doi.org/10.1016/j.jped.2018.03.005 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14730/12349 | |
| dc.identifier.volume | 95 | |
| dc.identifier.wos | WOS:000473330800014 | |
| dc.identifier.wosquality | Q1 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.indekslendigikaynak | PubMed | |
| dc.language.iso | en | |
| dc.publisher | Soc Brasil Pediatria | |
| dc.relation.ispartof | Jornal De Pediatria | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.snmz | KA_WOS_20250302 | |
| dc.subject | Liver disease | |
| dc.subject | Single-nucleotide polymorphisms | |
| dc.subject | Obesity | |
| dc.subject | Children | |
| dc.subject | Interleukin-17 | |
| dc.title | IL-17A, MCP-1, CCR-2, and ABCA1 polymorphisms in children with non-alcoholic fatty liver disease | |
| dc.type | Article |
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