ACE I/D polymorphism in cognitive impairment and depression among North Indian adults: a pilot study

IF 1.2 Q4 GENETICS & HEREDITY
Apoorva Sharma, Vineet Chaudhary, Mamta Kumari Thakur, Naorem Kiranmala Devi, Kallur Nava Saraswathy
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Abstract

Cognitive impairment and depression are two common mental health conditions affecting millions worldwide. CI and depression both have complex etiology and multiple genetic and environmental factors are thought to play a role in their onset and progression. Further, CI and depression often occur as comorbidities, indicating an overlap in their etiologies. The likelihood of developing major depressive illness and CI, the prognosis in response to treatments, and the possibility of adverse reactions to antidepressant medicines are all significantly influenced by genetics. Looking at the limited literature on the role of ACE I/D polymorphism in CI and depression among Indian populations, the present population-based pilot study was conducted with the aim to understand the association of ACE I/D polymorphism with CI and depression among North Indian adults. The present study was conducted among 195 individuals aged 30 years and above. The results of the present study show that the distributions of some of the studied sociodemographic variables, viz., gender, educational status, and employment status, were significantly different between those with and without CI, where a higher percentage of females, nonliterate and unemployed participants were in CI group than in the without CI group (p value < 0.05). For cognitive impairment, none of the models showed a statistically significant association with ACE I/D genotypes or alleles. For depression, two of the models showed a statistically significant association with ACE I/D genotypes or alleles. The ID + DD (D allele) and DD genotypes of ACE I/D polymorphism, with II as a reference, were found to pose a significantly reduced risk for depression (p value < 0.05). In conclusion, the findings of this study suggest that the D allele of ACE I/D gene polymorphism poses a potentially reduced risk of depression among North Indian adults. In the case of cognitive impairment, the findings suggest that gender, educational status, and employment status may be important factors to consider when assessing the risk of cognitive impairment. However, more research is needed to better understand the complex interplay between sociodemographic and genetic factors and cognitive impairment and depression.
北印度成年人认知障碍和抑郁症中的 ACE I/D 多态性:一项试点研究
认知障碍和抑郁症是两种常见的精神疾病,影响着全球数百万人。认知障碍和抑郁症的病因都很复杂,多种遗传和环境因素被认为在其发病和发展过程中起了作用。此外,CI 和抑郁症经常出现合并症,这表明它们的病因存在重叠。患重度抑郁症和 CI 的可能性、对治疗反应的预后以及对抗抑郁药物产生不良反应的可能性都受到遗传学的重大影响。鉴于有关 ACE I/D 多态性在印度人群中对 CI 和抑郁症的作用的文献有限,本研究以人群为基础,旨在了解北印度成年人中 ACE I/D 多态性与 CI 和抑郁症的关系。本研究在 195 名 30 岁及以上的人群中进行。研究结果表明,一些研究的社会人口学变量,即性别、教育状况和就业状况的分布在有 CI 和无 CI 的人群中存在显著差异,其中女性、文盲和失业者在有 CI 组中的比例高于无 CI 组(P 值小于 0.05)。在认知障碍方面,没有一个模型显示与 ACE I/D 基因型或等位基因有统计学意义的关联。在抑郁症方面,有两个模型显示与 ACE I/D 基因型或等位基因有统计学意义的关联。发现 ACE I/D 多态性的 ID + DD(D 等位基因)和 DD 基因型(以 II 为参照)可显著降低患抑郁症的风险(P 值 < 0.05)。总之,本研究结果表明,ACE I/D 基因多态性的 D 等位基因可能会降低北印度成年人患抑郁症的风险。在认知障碍方面,研究结果表明,性别、教育状况和就业状况可能是评估认知障碍风险时需要考虑的重要因素。然而,要更好地理解社会人口和遗传因素与认知障碍和抑郁之间复杂的相互作用,还需要进行更多的研究。
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
Egyptian Journal of Medical Human Genetics
Egyptian Journal of Medical Human Genetics Medicine-Genetics (clinical)
CiteScore
2.20
自引率
7.70%
发文量
150
审稿时长
18 weeks
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