Department of Hepatobiliary and Pancreatic Surgery, The First Affiliated Hospital of Zhengzhou University, China; Henan Key Laboratory of Digestive Organ Transplantation, China; Zhengzhou Engineering Laboratory of Organ Transplantation Technique and Application, China.
Department of Hepatobiliary and Pancreatic Surgery, The First Affiliated Hospital of Zhengzhou University, China; Henan Key Laboratory of Digestive Organ Transplantation, China; Zhengzhou Engineering Laboratory of Organ Transplantation Technique and Application, China.
Infect Genet Evol. 2022 Jul;101:105289. doi: 10.1016/j.meegid.2022.105289. Epub 2022 Apr 28.
The risk of chronic hepatitis B (CHB) infection is often affected by polyunsaturated fatty acids (PUFAs) metabolism which is strongly influenced by single nucleotide polymorphisms (SNPs) within the PUFA metabolic pathway. Given this, we designed this study to determine the relationship between specific polymorphisms within fatty acid desaturase 2 (FADS2), a key enzyme in PUFA metabolism, and CHB infection. We completed this evaluation using a case-control study comprising 230 CHB patients and 234 unrelated healthy controls in which the genetic relationships between three previously identified SNPs, isolated via mass spectrometry, and CHB infection. Our data revealed that none of these three SNPs (rs174568, rs174601, and rs2727270) were significantly associated with susceptibility to CHB infection when compared to healthy controls. However, when we stratified our cohort by sex, male subjects with the TC genotype for FADS2 exhibited a decreased risk for CHB infection (OR = 0.62, 95%CI = 0.39-0.96; OR = 0.64, 95%CI = 0.41-1.00; OR = 0.57, 95%CI = 0.36-0.90). Furthermore, age stratification revealed that both the T allele and the TC genotypes for each of the three target SNPs were less common in Chinese CHB cases in people younger than 50 years old. Correlation analysis also revealed that there was no statistically significant relationship between these three SNPs and HBV-DNA replication or hepatitis B surface antigen (HBsAg) levels. Thus, our data suggests that rs174568, rs174601, and rs2727270 may affect the CHB outcomes in various age or sex subgroups, suggesting that they may be useful predictive or diagnostic biomarkers of CHB infection in some populations.
乙型慢性肝炎(CHB)感染的风险通常受多不饱和脂肪酸(PUFA)代谢的影响,而 PUFA 代谢途径中的单核苷酸多态性(SNP)对其影响很大。鉴于此,我们设计了这项研究,以确定脂肪酸去饱和酶 2(FADS2)中特定多态性与 CHB 感染之间的关系,FADS2 是 PUFA 代谢中的关键酶。我们使用病例对照研究完成了这项评估,该研究包括 230 名 CHB 患者和 234 名无关的健康对照者,通过质谱法鉴定了三个先前确定的 SNP,并评估了它们与 CHB 感染之间的遗传关系。我们的数据显示,与健康对照组相比,这三个 SNP(rs174568、rs174601 和 rs2727270)均与 CHB 感染易感性无显著相关性。然而,当我们按性别对队列进行分层时,FADS2 的 TC 基因型的男性患者患 CHB 感染的风险降低(OR=0.62,95%CI=0.39-0.96;OR=0.64,95%CI=0.41-1.00;OR=0.57,95%CI=0.36-0.90)。此外,年龄分层显示,在年龄小于 50 岁的中国 CHB 患者中,三个目标 SNP 的 T 等位基因和 TC 基因型均较少。相关性分析还显示,这三个 SNP 与 HBV-DNA 复制或乙型肝炎表面抗原(HBsAg)水平之间没有统计学意义的关系。因此,我们的数据表明,rs174568、rs174601 和 rs2727270 可能会影响不同年龄或性别的亚组的 CHB 结局,这表明它们可能是某些人群中 CHB 感染的有用预测或诊断生物标志物。