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本文引用的文献

1
Natural mutations in IFITM3 modulate post-translational regulation and toggle antiviral specificity.IFITM3中的自然突变调节翻译后调控并改变抗病毒特异性。
EMBO Rep. 2016 Nov;17(11):1657-1671. doi: 10.15252/embr.201642771. Epub 2016 Sep 6.
2
IFITM3 and severe influenza virus infection. No evidence of genetic association.干扰素诱导跨膜蛋白3(IFITM3)与严重流感病毒感染。无基因关联证据。
Eur J Clin Microbiol Infect Dis. 2016 Nov;35(11):1811-1817. doi: 10.1007/s10096-016-2732-7. Epub 2016 Aug 4.
3
Hospitalization Risk Due to Respiratory Illness Associated with Genetic Variation at IFITM3 in Patients with Influenza A(H1N1)pdm09 Infection: A Case-Control Study.甲型H1N1pdm09流感感染患者中与IFITM3基因变异相关的呼吸道疾病导致的住院风险:一项病例对照研究
PLoS One. 2016 Jun 28;11(6):e0158181. doi: 10.1371/journal.pone.0158181. eCollection 2016.
4
Host genetics of severe influenza: from mouse Mx1 to human IRF7.重症流感的宿主遗传学:从小鼠Mx1到人类IRF7
Curr Opin Immunol. 2016 Feb;38:109-20. doi: 10.1016/j.coi.2015.12.002. Epub 2016 Jan 4.
5
Interferon-Inducible Transmembrane Protein 3 Genetic Variant rs12252 and Influenza Susceptibility and Severity: A Meta-Analysis.干扰素诱导跨膜蛋白3基因变体rs12252与流感易感性及严重程度:一项荟萃分析
PLoS One. 2015 May 5;10(5):e0124985. doi: 10.1371/journal.pone.0124985. eCollection 2015.
6
Early hypercytokinemia is associated with interferon-induced transmembrane protein-3 dysfunction and predictive of fatal H7N9 infection.早期细胞因子血症与干扰素诱导跨膜蛋白 3 功能障碍有关,并可预测 H7N9 感染的致命性。
Proc Natl Acad Sci U S A. 2014 Jan 14;111(2):769-74. doi: 10.1073/pnas.1321748111. Epub 2013 Dec 23.
7
IFITM3 and susceptibility to respiratory viral infections in the community.IFITM3 与社区呼吸道病毒感染易感性。
J Infect Dis. 2014 Apr 1;209(7):1028-31. doi: 10.1093/infdis/jit468. Epub 2013 Aug 30.
8
The antiviral effector IFITM3 disrupts intracellular cholesterol homeostasis to block viral entry.抗病毒效应分子 IFITM3 通过破坏细胞内胆固醇稳态来阻止病毒进入。
Cell Host Microbe. 2013 Apr 17;13(4):452-64. doi: 10.1016/j.chom.2013.03.006.
9
Characteristics of IFITM, the newly identified IFN-inducible anti-HIV-1 family proteins.IFITM 蛋白家族的特性,这是新近鉴定出的 IFN 诱导型抗 HIV-1 蛋白家族。
Microbes Infect. 2013 Apr;15(4):280-90. doi: 10.1016/j.micinf.2012.12.003. Epub 2013 Jan 30.
10
Interferon-induced transmembrane protein-3 genetic variant rs12252-C is associated with severe influenza in Chinese individuals.干扰素诱导跨膜蛋白 3 基因变异 rs12252-C 与中国人的严重流感相关。
Nat Commun. 2013;4:1418. doi: 10.1038/ncomms2433.

IFITM3 rs12252 多态性、BMI、糖尿病和高胆固醇血症与伊朗人群轻度流感的关联。

Association of IFITM3 rs12252 polymorphisms, BMI, diabetes, and hypercholesterolemia with mild flu in an Iranian population.

机构信息

Influenza and Other Respiratory Viruses Department, Pasteur Institute of Iran, Tehran, Iran.

Department of Epidemiology and Biostatistics, Research Centre for Emerging and Reemerging Infectious Diseases, Pasteur Institute of Iran, Tehran, Iran.

出版信息

Virol J. 2017 Nov 9;14(1):218. doi: 10.1186/s12985-017-0884-4.

DOI:10.1186/s12985-017-0884-4
PMID:29121968
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5680824/
Abstract

BACKGROUND

IFITM3 has been suggested to be associated with infection in some ethnic groups. Diabetes and hypercholesterolemia are also important clinical conditions that can predispose individuals to infection. The aim of this study was to investigate the association of rs12252 C polymorphism, BMI, diabetes, and hypercholesterolemia with mild flu in an Iranian population.

METHODS

We conducted a case-control study, including 79 mild flu and 125 flu-negative individuals attending primary care centers of three provinces of Iran (i.e, Markazi, Semnan, and Zanjan). Pharyngeal swab specimens were collected from all participants, and were subjected to RNA and DNA extractions for Real-time PCR and PCR tests. All PCR products were then sequenced to find T/C polymorphisms in the rs12252 region. Data on demographic, anthropometric, and clinical variables were collected from participants' medical records available in the primary care centers. The data was analyzed using DNASIS (v. 2.5) and Stata (v.11) software.

RESULTS

All participants were of Fars ethnic background. The allele frequency for rs12252-C was found to be 9.49% among cases and 2.40% among controls. Carriers of the rs12252 C allele (CT + CC genotypes) showed 5.92 folds increase in the risk of mild flu comparing to the T allele homozygotes (P value: 0.007). We also found a significant positive association between rs12252 C allele heterozygote and mild flu (OR: 7.62, P value: 0.008), but not in C allele homozygote group (OR: 2.71, P value: 0.406). Similarly, we did not find a significant association between mild flu and BMI (OR: 1.06, P value: 0.087), diabetes (OR: 0.61, P value: 0.392), and hypercholesterolemia (OR: 0.50, P value: 0.393) in multivariable logistic regression.

CONCLUSIONS

This is the first study evaluating the association between rs12252 polymorphisms, diabetes, hypercholesterolemia, and BMI and susceptibility to mild flu in an Iranian population. Our results suggest a significant positive association between mild flu and rs12252 C allele heterozygous and carriage. Future replication of the strong association observed here between rs12252 C allele carriage and mild flu might candidate this polymorphism as a genetic marker for early screening of susceptibility to mild flu. Lack of significant association between C allele homozygous and mild flu, observed in this study, might be the result of small sample size in this group.

TRIAL REGISTRATION

IR.PII.REC.1395.3.

摘要

背景

IFITM3 已被认为与某些族群的感染有关。糖尿病和高胆固醇血症也是重要的临床状况,可能使个体易感染。本研究的目的是调查伊朗人群中 rs12252 C 多态性、BMI、糖尿病和高胆固醇血症与轻度流感的关联。

方法

我们进行了病例对照研究,包括 79 名轻度流感和 125 名流感阴性个体,他们在伊朗三个省份(即马赞德兰、塞姆南和赞詹)的基层医疗中心就诊。从所有参与者中采集咽拭子标本,进行 RNA 和 DNA 提取,用于实时 PCR 和 PCR 检测。然后对所有 PCR 产物进行测序,以发现 rs12252 区域的 T/C 多态性。从基层医疗中心的参与者病历中收集人口统计学、人体测量学和临床变量的数据。使用 DNASIS(v. 2.5)和 Stata(v.11)软件分析数据。

结果

所有参与者均为法尔斯族裔。病例组的 rs12252-C 等位基因频率为 9.49%,对照组为 2.40%。与 T 等位基因纯合子相比,携带 rs12252 C 等位基因(CT+CC 基因型)的个体患轻度流感的风险增加了 5.92 倍(P 值:0.007)。我们还发现 rs12252 C 等位基因杂合子与轻度流感之间存在显著正相关(OR:7.62,P 值:0.008),但 C 等位基因纯合子组无显著相关(OR:2.71,P 值:0.406)。同样,在多变量逻辑回归中,我们也没有发现 BMI(OR:1.06,P 值:0.087)、糖尿病(OR:0.61,P 值:0.392)和高胆固醇血症(OR:0.50,P 值:0.393)与轻度流感之间存在显著关联。

结论

这是第一项评估伊朗人群中 rs12252 多态性、糖尿病、高胆固醇血症和 BMI 与轻度流感易感性之间关联的研究。我们的结果表明,轻度流感与 rs12252 C 等位基因杂合子和携带之间存在显著正相关。如果未来能够复制观察到的 rs12252 C 等位基因携带与轻度流感之间的强关联,那么该多态性可能成为早期筛查轻度流感易感性的遗传标志物。在本研究中,未观察到 C 等位基因纯合子与轻度流感之间存在显著关联,这可能是由于该组样本量较小所致。

试验注册

IR.PII.REC.1395.3.