• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

非酒精性脂肪性肝病与过氧化氢酶 (CAT) 水平降低、CT 基因型和 -262 C/T 多态性的 T 等位基因有关。

Non-Alcoholic Fatty Liver Disease Is Associated with a Decreased Catalase (CAT) Level, CT Genotypes and the T Allele of the -262 C/T Polymorphism.

机构信息

Department of Clinical Pharmacology, Medical University of Lodz, 90-153 Lodz, Poland.

Department of Nucleic Acid Biochemistry, Medical University of Lodz, 92-213 Lodz, Poland.

出版信息

Cells. 2023 Sep 7;12(18):2228. doi: 10.3390/cells12182228.

DOI:10.3390/cells12182228
PMID:37759451
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10527641/
Abstract

BACKGROUND

It is well known that oxidative stress plays an important role in the development of non-alcoholic fatty liver disease (NAFLD). It has been suggested that an insufficient antioxidant defense system composed of antioxidant enzymes, including catalase (CAT) and nonenzymatic molecules, is a key factor triggering oxidative damage in the progression of liver disease. Therefore, the aim of our study was to assess whether the level of CAT and -262 C/T polymorphism in the promoter of (rs1001179) are associated with NAFLD.

METHODS

In total, 281 adults (152/129 female/male, aged 65.61 ± 10.44 years) were included in the study. The patients were assigned to an NAFLD group ( = 139) or a group without NAFLD ( = 142) based on the results of an ultrasound, the Hepatic Steatosis Index, and the Fatty Liver Index (FLI). CAT levels were determined using an ELISA test, and genomic DNA was extracted via the standard phenol/chloroform-based method and genotyped via RFLP-PCR.

RESULTS

The CAT level was decreased in NAFLD patients ( < 0.001), and an ROC analysis revealed that a CAT level lower than 473.55 U/L significantly increases the risk of NAFLD. In turn, genotyping showed that the CT genotype and the T allele of -262 C/T polymorphism elevate the risk of NAFLD. The diminished CAT level in the NAFLD group correlated with increased FLI, waist circumference and female gender.

CONCLUSION

The obtained results support observations that oxidative damage associated with NAFLD may be the result of a decreased CAT level as a part of the antioxidant defense system.

摘要

背景

众所周知,氧化应激在非酒精性脂肪性肝病(NAFLD)的发展中起着重要作用。有人认为,由抗氧化酶(如过氧化氢酶(CAT))和非酶分子组成的抗氧化防御系统不足是触发肝病进展中氧化损伤的关键因素。因此,我们的研究目的是评估 CAT 水平和启动子中 -262 C/T 多态性(rs1001179)是否与 NAFLD 相关。

方法

共纳入 281 名成年人(152/129 名女性/男性,年龄 65.61±10.44 岁)。根据超声、肝脂肪变性指数和脂肪性肝病指数(FLI)的结果,将患者分为 NAFLD 组(n=139)和非 NAFLD 组(n=142)。使用 ELISA 试验测定 CAT 水平,并通过标准酚/氯仿法提取基因组 DNA,通过 RFLP-PCR 进行基因分型。

结果

NAFLD 患者的 CAT 水平降低(<0.001),ROC 分析显示,CAT 水平低于 473.55 U/L 显著增加了 NAFLD 的风险。相反,基因分型显示-262 C/T 多态性的 CT 基因型和 T 等位基因增加了 NAFLD 的风险。NAFLD 组中 CAT 水平降低与 FLI、腰围和女性性别增加相关。

结论

所得结果支持这样的观察结果,即与 NAFLD 相关的氧化损伤可能是抗氧化防御系统中 CAT 水平降低的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab64/10527641/2292a187ceb5/cells-12-02228-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab64/10527641/f4d9c0cd2c7e/cells-12-02228-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab64/10527641/2292a187ceb5/cells-12-02228-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab64/10527641/f4d9c0cd2c7e/cells-12-02228-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab64/10527641/2292a187ceb5/cells-12-02228-g002.jpg

相似文献

1
Non-Alcoholic Fatty Liver Disease Is Associated with a Decreased Catalase (CAT) Level, CT Genotypes and the T Allele of the -262 C/T Polymorphism.非酒精性脂肪性肝病与过氧化氢酶 (CAT) 水平降低、CT 基因型和 -262 C/T 多态性的 T 等位基因有关。
Cells. 2023 Sep 7;12(18):2228. doi: 10.3390/cells12182228.
2
Association of the rs7359397 Gene Polymorphism with Steatosis Severity in Subjects with Obesity and Non-Alcoholic Fatty Liver Disease.rs7359397 基因多态性与肥胖合并非酒精性脂肪性肝病患者肝脂肪变性严重程度的相关性研究。
Nutrients. 2020 Apr 29;12(5):1260. doi: 10.3390/nu12051260.
3
Oxidative stress biomarkers in the serum and plasma of patients with non-alcoholic fatty liver disease (NAFLD). Can plasma AGE be a marker of NAFLD? Oxidative stress biomarkers in NAFLD patients.非酒精性脂肪性肝病 (NAFLD) 患者血清和血浆中的氧化应激生物标志物。血浆 AGE 可以作为 NAFLD 的标志物吗?NAFLD 患者的氧化应激生物标志物。
Free Radic Res. 2019 Aug;53(8):841-850. doi: 10.1080/10715762.2019.1635691. Epub 2019 Jul 8.
4
rs7903146 (C/T) polymorphism of Transcription factor 7 like 2 (TCF7L-2) gene is independently associated with non-alcoholic fatty liver disease in Asian Indians.rs7903146(C/T)多态性转录因子 7 样 2(TCF7L-2)基因与亚洲印第安人非酒精性脂肪性肝病独立相关。
Diabetes Metab Syndr. 2020 May-Jun;14(3):175-180. doi: 10.1016/j.dsx.2020.02.011. Epub 2020 Feb 21.
5
Association of rs5764455 and rs6006473 polymorphisms in PARVB with liver damage of nonalcoholic fatty liver disease in Han Chinese population.汉族人群中PARVB基因rs5764455和rs6006473多态性与非酒精性脂肪性肝病肝损伤的关联
Gene. 2016 Jan 10;575(2 Pt 1):270-5. doi: 10.1016/j.gene.2015.09.007. Epub 2015 Sep 4.
6
Genetic variations of three important antioxidative enzymes SOD2, CAT, and GPX1 in nonalcoholic steatohepatitis.三种重要抗氧化酶 SOD2、CAT 和 GPX1 在非酒精性脂肪性肝炎中的遗传变异。
J Chin Med Assoc. 2021 Jan 1;84(1):14-18. doi: 10.1097/JCMA.0000000000000437.
7
Fatty liver index vs waist circumference for predicting non-alcoholic fatty liver disease.预测非酒精性脂肪性肝病的脂肪肝指数与腰围对比
World J Gastroenterol. 2016 Mar 14;22(10):3023-30. doi: 10.3748/wjg.v22.i10.3023.
8
Association between PNPLA3rs738409 polymorphism decreased kidney function in postmenopausal type 2 diabetic women with or without non-alcoholic fatty liver disease.载脂蛋白 L3(APOL1)基因 rs738409 多态性与绝经后 2 型糖尿病女性非酒精性脂肪性肝病患者或不伴非酒精性脂肪性肝病患者的肾功能下降相关。
Diabetes Metab. 2019 Oct;45(5):480-487. doi: 10.1016/j.diabet.2019.01.011. Epub 2019 Feb 11.
9
TRIB1 rs17321515 gene polymorphism increases the risk of coronary heart disease in general population and non-alcoholic fatty liver disease patients in Chinese Han population.TRIB1 rs17321515 基因多态性增加汉族人群冠心病和非酒精性脂肪性肝病患者的发病风险。
Lipids Health Dis. 2019 Aug 31;18(1):165. doi: 10.1186/s12944-019-1108-2.
10
Association of inflammatory genes in obstructive sleep apnea and non alcoholic fatty liver disease in Asian Indians residing in north India.印度北方居住的印度裔人群中阻塞性睡眠呼吸暂停和非酒精性脂肪性肝病的炎症基因关联。
PLoS One. 2018 Jul 12;13(7):e0199599. doi: 10.1371/journal.pone.0199599. eCollection 2018.

引用本文的文献

1
Physiological and Metabolic Responses of Mongolian Horses to a 20 km Endurance Exercise and Screening for New Oxidative-Imbalance Biomarkers.蒙古马对20公里耐力运动的生理和代谢反应及新氧化失衡生物标志物的筛选
Animals (Basel). 2025 May 7;15(9):1350. doi: 10.3390/ani15091350.
2
Metabolic dysfunction-associated steatotic liver disease-induced changes in the antioxidant system: a review.代谢功能障碍相关脂肪性肝病引起的抗氧化系统变化:综述
Arch Toxicol. 2025 Jan;99(1):1-22. doi: 10.1007/s00204-024-03889-x. Epub 2024 Oct 23.
3
A Systematic Review of Proteomics in Obesity: Unpacking the Molecular Puzzle.

本文引用的文献

1
Non-Alcoholic Fatty Liver Disease or Type 2 Diabetes Mellitus-The Chicken or the Egg Dilemma.非酒精性脂肪性肝病还是2型糖尿病——先有鸡还是先有蛋的困境。
Biomedicines. 2023 Apr 4;11(4):1097. doi: 10.3390/biomedicines11041097.
2
Impact of metabolic risk factors on hepatic and cardiac outcomes in patients with alcohol- and non-alcohol-related fatty liver disease.代谢风险因素对酒精性和非酒精性脂肪性肝病患者肝脏和心脏结局的影响。
JHEP Rep. 2023 Mar 5;5(6):100721. doi: 10.1016/j.jhepr.2023.100721. eCollection 2023 Jun.
3
Non-alcoholic fatty liver disease is associated with an increased risk of type 2 diabetes.
肥胖症蛋白质组学的系统评价:揭开分子谜题。
Curr Obes Rep. 2024 Sep;13(3):403-438. doi: 10.1007/s13679-024-00561-4. Epub 2024 May 4.
4
What are the common downstream molecular events between alcoholic and nonalcoholic fatty liver?酒精性和非酒精性脂肪肝的下游常见分子事件有哪些?
Lipids Health Dis. 2024 Feb 8;23(1):41. doi: 10.1186/s12944-024-02031-1.
非酒精性脂肪性肝病与 2 型糖尿病的风险增加有关。
Eur J Gastroenterol Hepatol. 2023 Jun 1;35(6):662-667. doi: 10.1097/MEG.0000000000002555. Epub 2023 Apr 15.
4
Cellular Red-Ox system in health and disease: The latest update.健康与疾病中的细胞氧化还原系统:最新进展
Biomed Pharmacother. 2023 Jun;162:114606. doi: 10.1016/j.biopha.2023.114606. Epub 2023 Mar 28.
5
Progress in Nonalcoholic Fatty Liver Disease: SIRT Family Regulates Mitochondrial Biogenesis.非酒精性脂肪性肝病的研究进展:SIRT 家族调节线粒体生物发生。
Biomolecules. 2022 Aug 5;12(8):1079. doi: 10.3390/biom12081079.
6
Ethanol Metabolism in the Liver, the Induction of Oxidant Stress, and the Antioxidant Defense System.肝脏中的乙醇代谢、氧化应激的诱导及抗氧化防御系统
Antioxidants (Basel). 2022 Jun 26;11(7):1258. doi: 10.3390/antiox11071258.
7
Association of Polymorphisms in Antioxidant Enzyme-Encoding Genes with Diabetic Nephropathy in a Group of Saudi Arabian Patients with Type II Diabetes Mellitus.一组沙特阿拉伯2型糖尿病患者中抗氧化酶编码基因多态性与糖尿病肾病的关联
Int J Gen Med. 2022 Jul 1;15:5919-5928. doi: 10.2147/IJGM.S367673. eCollection 2022.
8
NAFLD: Mechanisms, Treatments, and Biomarkers.非酒精性脂肪性肝病:发病机制、治疗方法及生物标志物
Biomolecules. 2022 Jun 13;12(6):824. doi: 10.3390/biom12060824.
9
Catalase C262T genetic variation and cancer susceptibility: A comprehensive meta-analysis with meta-regression and trial sequential analysis.过氧化氢酶 C262T 基因变异与癌症易感性:荟萃分析、荟萃回归分析和试验序贯分析。
Int J Biol Markers. 2022 Sep;37(3):227-240. doi: 10.1177/03936155221104128. Epub 2022 May 30.
10
American Association of Clinical Endocrinology Clinical Practice Guideline for the Diagnosis and Management of Nonalcoholic Fatty Liver Disease in Primary Care and Endocrinology Clinical Settings: Co-Sponsored by the American Association for the Study of Liver Diseases (AASLD).美国临床内分泌学会临床实践指南:原发性保健和内分泌学临床环境中非酒精性脂肪性肝病的诊断和管理:由美国肝病研究协会(AASLD)共同赞助。
Endocr Pract. 2022 May;28(5):528-562. doi: 10.1016/j.eprac.2022.03.010.