中国女性胱抑素 c 与肌酐肾功能的全基因组关联分析

IF 2.1 4区 医学 Q3 GENETICS & HEREDITY BMC Medical Genomics Pub Date : 2024-11-18 DOI:10.1186/s12920-024-02048-6
Yang Cai, Hongyao Lv, Meng Yuan, Jiao Wang, Wenhui Wu, Xiaoyu Fang, Changying Chen, Jialing Mu, Fangyuan Liu, Xincheng Gu, Hankun Xie, Yu Liu, Haifeng Xu, Yao Fan, Chong Shen, Xiangyu Ma
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引用次数: 0

摘要

背景:随着慢性肾脏病(CKD)发病率和治疗费用的增加,慢性肾脏病已成为中国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。以血肌酐为基础的肾小球滤过率(eGFR)通常用来衡量肾功能,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 诊断的准确性。据我们所知,在中国人群中还没有进行过 eGFRcr-cys 的全基因组关联分析:通过开展全基因组关联研究(GWAS)--一种用于识别遗传区域(基因组)与性状/疾病之间关联的方法--我们研究了中国女性的遗传因素与 eGFRcr-cys 之间的关系:结果:在中国女性人群中发现了一个重要位点(20p11.21),据报道,该位点与欧洲人群中基于胱抑素 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),这两个位点尚未被报道过。在这些区域中,共有三个单核苷酸多态性被确定为最重要的变异,包括rs2405367(CST3)、rs66588571(KRT8P21)和rs626995(OR8B2):我们发现 20p11.21、1p31.1 和 11q24.2 这三个位点与 eGFRcr-cys 显著相关。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,为 CKD 的诊断和治疗发展提供了新思路。
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Genome-wide association analysis of cystatin c and creatinine kidney function in Chinese women.

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.

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来源期刊
BMC Medical Genomics
BMC Medical Genomics 医学-遗传学
CiteScore
3.90
自引率
0.00%
发文量
243
审稿时长
3.5 months
期刊介绍: BMC Medical Genomics is an open access journal publishing original peer-reviewed research articles in all aspects of functional genomics, genome structure, genome-scale population genetics, epigenomics, proteomics, systems analysis, and pharmacogenomics in relation to human health and disease.
期刊最新文献
Private detection of relatives in forensic genomics using homomorphic encryption. Elevated expression of APOO as a potential prognostic marker in breast cancer: insights from bioinformatic analysis and experimental validation. Genome-wide association analysis of cystatin c and creatinine kidney function in Chinese women. Hearing impairment and vestibular function in patients with a pathogenic splice variant in the LHX3 gene. Association between miR-30 polymorphism and ischemic stroke in Chinese population.
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