PNPLA3样磷脂酶结构域3 (PNPLA3)变异rs 738408和rs 738409单核苷酸多态性作为代谢相关脂肪肝疾病及其进展的预测因子

IF 1.2 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL
Benash Altaf, Shireen Jawed, Wan Syaheedah Wan Ghazali, Ahmad Aizat Abdul Aziz, Rana Muhammad Tahir Salam, Abid Rasheed, Mahaneem Mohamed
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引用次数: 0

摘要

目的:确定PNPLA3基因变异作为巴基斯坦人群代谢性脂肪性肝病(MAFLD)及其进展的潜在预测因子。方法:横断面研究,包括158名参与者。本研究采用非概率目的抽样技术从巴基斯坦阿齐兹法蒂玛教学医院放射科和阿齐兹法蒂玛医学和牙科学院纳入研究。研究时间为2021年12月5日至2024年4月4日。抽取血液样本(10mL)进行肝酶、基因分析,最终将PCR产物送去进行桑格测序。数据采用SPSS 26进行分析,p值≤0.05为显著性。结果:158名研究参与者中,43.7%为男性,56.3%为女性。人群中51.3%为mld阳性,对照组为48.7%。结果显示,CT和TT基因型rs738408在MAFLD组中较为常见(p=0.039和0.060),且是发生MAFLD的重要预测因子(OR=2.484, p=0.019和OR=5.167)。结论:738408的CT和TT基因型以及738409的GG基因型与MAFLD相关,且具有较高的疾病进展风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Patatin-like phospholipase domain-containing 3 (PNPLA3) variants rs 738408 and rs 738409 single nucleotide polymorphism as predictor of metabolic associated fatty liver disease and its progression.

Objective: To identify the PNPLA3 genetic variants as the potential predictors for metabolic associated fatty liver disease (MAFLD) and its progression among Pakistani population.

Method: A cross sectional study comprising of 158 participants. They were included in this study with non-probability purposive sampling technique from Radiology Department of Aziz Fatimah Teaching Hospital and Aziz Fatimah Medical and Dental College, Pakistan. The duration of study was December 5, 2021 to April 4, 2024. Blood samples (10mL) were drawn for liver enzymes, gene analysis and ultimately PCR products were sent for Sanger sequencing. Data was analyzed using SPSS version 26 with p-Values ≤0.05 considered significant.

Results: From 158 studied participants, 43.7% were male, and 56.3% were female. Of total population 51.3% were MAFLD positive while 48.7% were control subjects. Present results showed that CT and TT genotypes of rs738408 were frequently found in MAFLD group (p=0.039 and 0.060, respectively) and significant predictor for developing MAFLD (OR=2.484, p=0.019 and OR=5.167, p<0.001, respectively). Concerning progression of the disease CT genotype showed that subject with this genotype progress to moderate grade of fatty liver disease (OR=2.832, p=0.013). Whereas Odd ratio for TT genotype was significant for severe grade fatty liver diseases (OR=15.50, p=0.007). GG genotype of rs738409 was frequently found in MAFLD group (p=0.032). Odds ratio for GG genotype of rs738409 was significant for developing MAFLD (OR=4.565, p=0.025) and responsible to progress to moderate grade of fatty liver disease (OR= 5.083, p=0.022).

Conclusion: CT and TT genotypes of 738408 and GG genotype of 738409 are associated with MAFLD and are at more risk for disease progression.

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来源期刊
Pakistan Journal of Medical Sciences
Pakistan Journal of Medical Sciences 医学-医学:内科
CiteScore
4.10
自引率
9.10%
发文量
363
审稿时长
3-6 weeks
期刊介绍: It is a peer reviewed medical journal published regularly since 1984. It was previously known as quarterly "SPECIALIST" till December 31st 1999. It publishes original research articles, review articles, current practices, short communications & case reports. It attracts manuscripts not only from within Pakistan but also from over fifty countries from abroad. Copies of PJMS are sent to all the import medical libraries all over Pakistan and overseas particularly in South East Asia and Asia Pacific besides WHO EMRO Region countries. Eminent members of the medical profession at home and abroad regularly contribute their write-ups, manuscripts in our publications. We pursue an independent editorial policy, which allows an opportunity to the healthcare professionals to express their views without any fear or favour. That is why many opinion makers among the medical and pharmaceutical profession use this publication to communicate their viewpoint.
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