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Exp Eye Res. 2024 Aug;245:109978. doi: 10.1016/j.exer.2024.109978. Epub 2024 Jun 21.
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Identification of hub genes and molecular pathways in keratoconus by integrating bioinformatics and literature mining at the RNA level.通过整合 RNA 水平的生物信息学和文献挖掘,鉴定圆锥角膜的枢纽基因和分子途径。
Int Ophthalmol. 2024 Jun 21;44(1):244. doi: 10.1007/s10792-024-03071-3.
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STON2 variations are involved in synaptic dysfunction and schizophrenia-like behaviors by regulating Syt1 trafficking.STON2 变异通过调节 Syt1 转运参与突触功能障碍和类似精神分裂症的行为。
Sci Bull (Beijing). 2024 May 30;69(10):1458-1471. doi: 10.1016/j.scib.2024.02.013. Epub 2024 Feb 13.
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The evolving roles of Wnt signaling in stem cell proliferation and differentiation, the development of human diseases, and therapeutic opportunities.Wnt信号通路在干细胞增殖与分化、人类疾病发展及治疗机会方面不断演变的作用。
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8
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沙特裔圆锥角膜患者中rs2371597多态性的性别特异性关联

Gender-specific association of rs2371597 polymorphism in keratoconus patients of Saudi origin.

作者信息

Kondkar Altaf A, Sultan Tahira, Azad Taif A, Khatlani Tanvir, Lobo Glenn P, Kalantan Hatem, Al-Obeidan Saleh A, Al-Muammar Abdulrahman M

机构信息

Department of Ophthalmology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.

Glaucoma Research Chair in Ophthalmology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.

出版信息

Front Genet. 2024 Dec 9;15:1505629. doi: 10.3389/fgene.2024.1505629. eCollection 2024.

DOI:10.3389/fgene.2024.1505629
PMID:39717479
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11663935/
Abstract

OBJECTIVE

To investigate the association of specific genetic polymorphisms (rs2371597 in , rs11720822 in , rs387907358 in , and rs77542162 in ) in a Saudi cohort of keratoconus (KC) patients compared to controls.

METHODS

A retrospective case-control genetic association study was conducted. The study included 99 KC patients and 193 healthy controls. Genotyping was performed using real-time PCR with TaqMan assays. Associations between genetic polymorphisms and KC were assessed using various genetic models and binary logistic regression analysis.

RESULTS

None of the tested polymorphisms showed an overall association with KC risk. Specifically, the rs2371597 polymorphism in did not demonstrate a significant association with KC risk across different genetic models. However, a gender-specific effect of rs2371597 was noted: in men, the C/G genotype was associated with a higher risk of KC, particularly in the dominant model, while no significant association was observed in women. Age and sex were identified as significant predictors of KC risk, but rs2371597 did not significantly affect KC risk in regression analysis.

CONCLUSION

Preliminary evidence suggests a gender-specific effect of the rs2371597 polymorphism in , with an increased KC risk associated with C/G-C/C genotypes in men which was age-dependent. This result highlights the importance of considering population-specific genetic factors and the potential gender-specific effects on KC susceptibility. However, these findings need further validation with larger age- and sex-matched samples of diverse populations.

摘要

目的

在沙特圆锥角膜(KC)患者队列中,研究特定基因多态性( 中的rs2371597、 中的rs11720822、 中的rs387907358和 中的rs77542162)与对照组相比的关联。

方法

进行了一项回顾性病例对照基因关联研究。该研究纳入了99例KC患者和193名健康对照。使用TaqMan分析法通过实时PCR进行基因分型。使用各种遗传模型和二元逻辑回归分析评估基因多态性与KC之间的关联。

结果

所测试的多态性均未显示与KC风险存在总体关联。具体而言, 中的rs2371597多态性在不同遗传模型中均未显示与KC风险有显著关联。然而,注意到rs2371597存在性别特异性效应:在男性中,C/G基因型与较高的KC风险相关,尤其是在显性模型中,而在女性中未观察到显著关联。年龄和性别被确定为KC风险的显著预测因素,但在回归分析中rs2371597并未显著影响KC风险。

结论

初步证据表明 中rs2371597多态性存在性别特异性效应,男性中C/G - C/C基因型与KC风险增加相关,且与年龄有关。这一结果凸显了考虑人群特异性遗传因素以及对KC易感性潜在性别特异性效应的重要性。然而,这些发现需要在更大规模的、年龄和性别匹配的不同人群样本中进一步验证。