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胱抑素 C 和肌酐肾功能全基因组关联分析在中国女性中的应用。

Genome-wide association analysis of cystatin c and creatinine kidney function in Chinese women.

机构信息

College of Public Health, Southwest Medical University, Luzhou, Sichuan, China.

Department of Epidemiology, College of Preventive Medicine, Third Military Medical University (Army Medical University), Chongqing, China.

出版信息

BMC Med Genomics. 2024 Nov 18;17(1):272. doi: 10.1186/s12920-024-02048-6.

Abstract

BACKGROUND

With increasing incidence and treatment costs, chronic kidney disease (CKD) has become an important public health problem in China, especially in females. However, the genetic determinants are very limited. The estimated glomerular filtration rate (eGFR) based on creatinine is commonly used as a measure of renal function but can be easily affected by other factors. In contrast, eGFR based on both creatinine and cystatin C (eGFRcr-cys) improved the diagnostic accuracy of CKD. To our knowledge, no genome-wide association analysis of eGFRcr-cys has been conducted in the Chinese population.

METHODS

By conducting a Genome-Wide association study(GWAS), a method used to identify associations between genetic regions (genomes) and traits/diseases, we examined the relationship between genetic factors and eGFRcr-cys in Chinese women, with 1983 participants and 3,838,121 variants included in the final analysis.

RESULT

One significant locus (20p11.21) was identified in the Chinese female population, which has been reported to be associated with eGFR based on cystatin C (eGFRcys) in the European population. More importantly, we found two new suggestive loci (1p31.1 and 11q24.2), which have not yet been reported. A total of three single nucleotide polymorphisms were identified as the most important variants in these regions, including rs2405367 (CST3), rs66588571(KRT8P21), and rs626995 (OR8B2).

CONCLUSION

We identified 3 loci 20p11.21, 1p31.1, and 11q24.2 to be significantly associated with eGFRcr-cys. These findings and subsequent functional analysis describe new biological clues related to renal function in Chinese women and provide new ideas for the diagnosis and treatment development of CKD.

摘要

背景

随着发病率和治疗费用的增加,慢性肾脏病(CKD)已成为中国一个重要的公共卫生问题,尤其是在女性中。然而,遗传决定因素非常有限。基于肌酐的估计肾小球滤过率(eGFR)通常用作肾功能的衡量标准,但很容易受到其他因素的影响。相比之下,基于肌酐和胱抑素 C 的 eGFR(eGFRcr-cys)提高了 CKD 的诊断准确性。据我们所知,尚未在中国人群中进行基于胱抑素 C 的 eGFRcr-cys 的全基因组关联分析。

方法

通过进行全基因组关联研究(GWAS),一种用于识别遗传区域(基因组)与特征/疾病之间关联的方法,我们研究了遗传因素与中国女性 eGFRcr-cys 之间的关系,最终分析包括 1983 名参与者和 3838121 个变体。

结果

在中国女性人群中鉴定出一个显著的位点(20p11.21),该位点已在欧洲人群中报告与基于胱抑素 C 的 eGFR(eGFRcys)相关。更重要的是,我们发现了两个新的提示性位点(1p31.1 和 11q24.2),这些位点尚未被报道。这三个区域共鉴定出三个最重要的单核苷酸多态性,包括 rs2405367(CST3)、rs66588571(KRT8P21)和 rs626995(OR8B2)。

结论

我们确定了与 eGFRcr-cys 显著相关的 3 个位点 20p11.21、1p31.1 和 11q24.2。这些发现和随后的功能分析描述了与中国女性肾功能相关的新生物学线索,并为 CKD 的诊断和治疗发展提供了新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab8/11575226/d2f34be54b9c/12920_2024_2048_Fig1_HTML.jpg

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