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LBA 研究中 C10X 多态性与年轻健康个体中炎症标志物的关联。

Association between C10X polymorphism in the CARD8 gene and inflammatory markers in young healthy individuals in the LBA study.

机构信息

Cardiovascular Research Centre, School of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.

Clinical Epidemiology and Biostatistics, School of Medical Sciences, Örebro University, Örebro, Sweden.

出版信息

BMC Cardiovasc Disord. 2024 Feb 13;24(1):103. doi: 10.1186/s12872-024-03765-7.

Abstract

BACKGROUND

The Caspase activation and recruitment domain 8 (CARD8) protein is a component of innate immunity as a negative regulator of NF- ĸB, and has been associated with regulation of proteins involved in inflammation. Expression of CARD8 mRNA and protein has been identified in human atherosclerotic lesions, and the truncated T30A variant (rs2043211) of CARD8 has been associated with lower C-reactive (CRP) and MCP-1 levels in myocardial infarction patients. The present study examines the role of a genetic variation in the CARD8 gene in relation to a selection of markers of inflammation.

METHODS

In a cross-sectional study of young healthy individuals (18.0-25.9 yrs, n = 744) the association between the rs2043211 variant in the CARD8 gene and protein markers of inflammation was assessed. Genotyping of the CARD8 C10X (rs2043211) polymorphism was performed with TaqMan real time PCR on DNA from blood samples. Protein levels were studied via Olink inflammation panel ( https://olink.com/ ). Using linear models, we analyzed men and two groups of women with and without estrogen containing contraceptives separately, due to previous findings indicating differences between estrogen users and non-estrogen using women. Genotypes were analyzed by additive, recessive and dominant models.

RESULTS

The minor (A) allele of the rs2043211 polymorphism in the CARD8 gene was associated with lower levels of CCL20 and IL-6 in men (CCL20, Additive model: p = 0.023; Dominant model: p = 0.016. IL-6, Additive model: p = 0.042; Dominant model: p = 0.039). The associations remained significant also after adjustment for age and potential intermediate variables.

CONCLUSIONS

Our data indicate that CARD8 may be involved in the regulation of CCL20 and IL-6 in men. No such association was observed in women. These findings strengthen and support previous in vitro data on IL-6 and CCL20 and highlight the importance of CARD8 as a factor in the regulation of inflammatory proteins. The reason to the difference between sexes is however not clear, and the influence of estrogen as a possible factor important for the inflammatory response needs to be further explored.

摘要

背景

Caspase activation and recruitment domain 8(CARD8)蛋白是先天免疫的一个组成部分,作为 NF-κB 的负调节剂,并且与参与炎症的蛋白质的调节有关。CARD8 mRNA 和蛋白的表达已在人类动脉粥样硬化病变中被鉴定出来,并且 CARD8 的截断 T30A 变体(rs2043211)与心肌梗死患者的 CRP 和 MCP-1 水平降低有关。本研究探讨了 CARD8 基因中的遗传变异与一系列炎症标志物之间的关系。

方法

在一项年轻健康个体(18.0-25.9 岁,n=744)的横断面研究中,评估了 CARD8 基因中 rs2043211 变体与炎症蛋白标志物之间的关联。使用 TaqMan 实时 PCR 对来自血液样本的 CARD8 C10X(rs2043211)多态性进行基因分型。通过 Olink 炎症面板(https://olink.com/)研究蛋白水平。使用线性模型,我们分别分析了男性和两组使用和不使用含雌激素避孕药的女性,因为先前的研究结果表明雌激素使用者和非雌激素使用者之间存在差异。通过加性、隐性和显性模型分析基因型。

结果

CARD8 基因 rs2043211 多态性的次要(A)等位基因与男性中 CCL20 和 IL-6 的水平较低相关(CCL20,加性模型:p=0.023;显性模型:p=0.016。IL-6,加性模型:p=0.042;显性模型:p=0.039)。即使在调整年龄和潜在中间变量后,关联仍然显著。

结论

我们的数据表明,CARD8 可能参与调节男性中的 CCL20 和 IL-6。在女性中未观察到这种关联。这些发现加强和支持了先前关于 IL-6 和 CCL20 的体外数据,并突出了 CARD8 作为调节炎症蛋白的一个因素的重要性。然而,性别之间差异的原因尚不清楚,雌激素作为影响炎症反应的一个重要因素的影响需要进一步探讨。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0310/10863129/afd3979956c9/12872_2024_3765_Fig1_HTML.jpg

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