Association between relative telomere length and a genetic variant of SIRT1 gene and age-related macular degeneration

Q4 Medicine
L. Moshetova, O. Dmitrenko, O. I. Abramova, N. Karpova, K. I. Turkina, I. Saburina, M. Pathophysiology
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引用次数: 0

Abstract

One of the most important factors predisposing to the development of age-related macular degeneration (AMD) is aging. Telomeres are important for aging by maintaining genome stability. Aim: to identify the association between relative telomere length of buccal epithelial cells and SIRT1 rs12778366 genetic variation and late AMD. Patients and Methods: 100 patients (200 eyes) were enrolled, i.e., 50 patients with AMD (AREDS category 4) and 50 patients without AMD. Genomic DNA isolated from buccal epithelial cells by phenol-chloroform extraction was used. Genotyping of SIRT1 rs12778366 polymorphic locus was performed by TaqMan® real-time PCR. Telomere length was measured by real-time PCR as described earlier [Cawthon, 2002] using specific primers. Relative telomere length was assessed by the relative telomere to single-copy gene (T/S) ratio. Results: the rate of allele C was 25% in the study group and 14% in the control group (p=0.049). The rate of heterozygotic TC genotype was twice higher in the study group compared to the control group (p=0.045). In heterozygotic carriers of the allele C of the SIRT1 rs12778366 gene, the risk of AMD is 2.048- and 2.425-times higher in сodominant and dominant inheritance pattern, respectively. In patients with late AMD, there are more short telomeres (64% vs. 48% in the control group, р=0.0002). Conclusions: further studies of a polymorphic SIRT1 gene locus in the association with telomere length in a larger sample are required. In the future, these molecular markers can be applied to predict the individual course of AMD and to implement preventive measures. Keywords: age-related macular degeneration, relative telomere length, rs12778366, SIRT1 gene, age-related diseases, buccal epithelium, genetic testing. For citation: Moshetova L.K., Dmitrenko O.P., Abramova O.I. et al. Association between relative telomere length and a genetic variant of SIRT gene and age-related macular degeneration. Russian Journal of Clinical Ophthalmology. 2021;21(3):143–146 (in Russ.). DOI: 10.32364/2311- 7729-2021-21-3-143-146.
相对端粒长度和SIRT1基因的遗传变异与年龄相关性黄斑变性之间的关系
导致老年性黄斑变性(AMD)发生的最重要因素之一是衰老。端粒通过维持基因组的稳定性对衰老起到重要作用。目的:探讨口腔上皮细胞相对端粒长度与SIRT1 rs12778366遗传变异与晚期AMD的关系。患者与方法:纳入100例患者(200只眼),其中AMD (AREDS分类4)患者50例,非AMD患者50例。用苯酚-氯仿萃取法从口腔上皮细胞中分离基因组DNA。采用TaqMan®实时PCR对SIRT1 rs12778366多态性位点进行基因分型。端粒长度由实时PCR测量,如前面所述[Cawthon, 2002],使用特定引物。相对端粒长度用相对端粒与单拷贝基因(T/S)比值测定。结果:研究组C等位基因检出率为25%,对照组为14% (p=0.049)。研究组的TC基因型杂合子率是对照组的2倍(p=0.045)。在SIRT1 rs12778366基因等位基因C的杂合子携带者中,显性遗传模式和显性遗传模式的AMD风险分别高出2.048倍和2.425倍。在晚期AMD患者中,有更多的短端粒(64% vs.对照组的48%,r =0.0002)。结论:需要在更大的样本中进一步研究SIRT1基因多态性位点与端粒长度的关系。在未来,这些分子标记可用于预测AMD的个体病程并实施预防措施。关键词:老年性黄斑变性,相对端粒长度,rs12778366, SIRT1基因,老年性疾病,颊上皮,基因检测引证:Moshetova l.k., Dmitrenko o.p., Abramova O.I.等。相对端粒长度和SIRT基因的遗传变异与年龄相关性黄斑变性之间的关系。俄罗斯临床眼科学杂志。2021;21(3):143-146。Doi: 10.32364/2311- 7729-2021-21-3-143-146。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.60
自引率
0.00%
发文量
21
审稿时长
20 weeks
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