Angiotensin-Converting Enzyme Insertion/Deletion Polymorphism and the Risk of Leukoaraiosis in a South Chinese Han Population: A Case–Control Study

IF 2.1 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Dong-can Mo, Xiao-ju Wu, Xiao-ling Li, Liu-yu Liu, Yi-ying Jiang, Guo-qiu Zhou, Li-jie Chen, Jiao-xing Li, Man Luo
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引用次数: 0

Abstract

Leukoaraiosis (LA) appears as white matter hyperintensities on T2-weighted brain magnetic resonance imaging scans. Age and hypertension are considered the primary risk factors for LA, but its pathogenesis remains uncertain. This study aims to investigate the correlation between the angiotensin-converting enzyme (ACE) insertion/deletion (I/D) polymorphism and LA. A total of 140 patients with LA and 136 neuroimaging alteration-free controls were recruited in a case–control study. ACE I/D polymorphism was determined using the polymerase chain reaction method. The allele and genotype distributions of the ACE I/D polymorphism were significantly different between subjects with and without LA. Significant difference was observed in the genotypic distribution between LA patients and controls for recessive and additive models. A statistically significant association remained apparent after adjusting for potential risk factors (D/D vs. I/D + I/I: adjusted OR 3.251, 95% CI 1.185–8.918; D/D vs. I/I: adjusted OR 3.277, 95% CI 1.187–9.047). Our results indicate that the D/D genotype and D allele are important risk factors for LA. Future studies with larger populations are needed to validate our results.

中国南方汉族人群血管紧张素转换酶插入/缺失多态性与白细胞增多症风险的病例对照研究。
脑白质增多症(LA)在T2加权脑磁共振成像扫描中表现为白质高信号。年龄和高血压被认为是LA的主要危险因素,但其发病机制尚不确定。本研究旨在探讨血管紧张素转换酶(ACE)插入/缺失(I/D)多态性与LA的相关性。在一项病例对照研究中,共招募了140名LA患者和136名无神经影像学改变的对照者。采用聚合酶链式反应方法测定ACE I/D多态性。ACE I/D多态性的等位基因和基因型分布在患有和不患有LA的受试者之间存在显著差异。在隐性和加性模型中,LA患者与对照组之间的基因型分布存在显著差异。在对潜在风险因素进行调整后,统计学上显著的相关性仍然明显(D/D与I/D + I/I:调整OR 3.251,95%CI 1.185-8.918;D/D与I/I:调整OR 3.277,95%CI 1.187-9.047)。我们的结果表明,D/D基因型和D等位基因是LA的重要危险因素。未来需要对更大人群进行研究来验证我们的结果。
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来源期刊
Biochemical Genetics
Biochemical Genetics 生物-生化与分子生物学
CiteScore
3.90
自引率
0.00%
发文量
133
审稿时长
4.8 months
期刊介绍: Biochemical Genetics welcomes original manuscripts that address and test clear scientific hypotheses, are directed to a broad scientific audience, and clearly contribute to the advancement of the field through the use of sound sampling or experimental design, reliable analytical methodologies and robust statistical analyses. Although studies focusing on particular regions and target organisms are welcome, it is not the journal’s goal to publish essentially descriptive studies that provide results with narrow applicability, or are based on very small samples or pseudoreplication. Rather, Biochemical Genetics welcomes review articles that go beyond summarizing previous publications and create added value through the systematic analysis and critique of the current state of knowledge or by conducting meta-analyses. Methodological articles are also within the scope of Biological Genetics, particularly when new laboratory techniques or computational approaches are fully described and thoroughly compared with the existing benchmark methods. Biochemical Genetics welcomes articles on the following topics: Genomics; Proteomics; Population genetics; Phylogenetics; Metagenomics; Microbial genetics; Genetics and evolution of wild and cultivated plants; Animal genetics and evolution; Human genetics and evolution; Genetic disorders; Genetic markers of diseases; Gene technology and therapy; Experimental and analytical methods; Statistical and computational methods.
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