白介素-1β rs16944和rs1143627多态性与发生重度抑郁症的风险:孟加拉国人群的病例对照研究

IF 2.6 3区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
PLoS ONE Pub Date : 2025-01-22 eCollection Date: 2025-01-01 DOI:10.1371/journal.pone.0317665
Faria Mehreen Toma, Khondoker Tashya Kalam, Md Aminul Haque, Sejuti Reza, Raushanara Akter, Mohammad Safiqul Islam, Md Rabiul Islam, Zabun Nahar
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引用次数: 0

摘要

背景:流行病学研究表明,细胞因子水平的改变与病理生理和重度抑郁症(MDD)的发展有关。基于早期的研究,IL-1β rs16944和rs1143627多态性可能会增加抑郁症的风险。在这里,我们的目的是评估这些多态性与孟加拉国人群中MDD易感性之间的相关性。方法:采集100例重度抑郁症患者和70例对照者的血液样本。采用DSM-5标准对研究对象进行评估,采用PCR-RFLP方法进行基因分型。结果:发现il - 1β rs1143627和rs16944多态性与重度抑郁症的风险有显著相关性。rs1143627 CT杂合子基因型(OR = 2.22, 95% CI = 1.08-4.55, p值= 0.029)和CT+TT联合基因型(OR = 2.35, 95% CI = 1.15-4.79, p值= 0.019)与CC普通基因型相比,MDD风险增加密切相关。此外,过度优势模型显示MDD发展风险高出2.15倍(OR = 2.15, 95% CI = 1.05-4.40, p值= 0.036)。另一方面,IL1β rs16944多态性显示,优势模型中TC+CC组合基因型与TT普通纯合子相比,MDD发展风险增加2.06倍(OR = 2.06, 95% CI = 1.06-3.99, p值= 0.032)。结论:研究表明,IL1β rs16944和rs1143627多态性与MDD风险增加有关。这些发现将为我们了解重度抑郁症的病理生理学提供有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Interleukin-1β rs16944 and rs1143627 polymorphisms and risk of developing major depressive disorder: A case-control study among Bangladeshi population.

Interleukin-1β rs16944 and rs1143627 polymorphisms and risk of developing major depressive disorder: A case-control study among Bangladeshi population.

Interleukin-1β rs16944 and rs1143627 polymorphisms and risk of developing major depressive disorder: A case-control study among Bangladeshi population.

Interleukin-1β rs16944 and rs1143627 polymorphisms and risk of developing major depressive disorder: A case-control study among Bangladeshi population.

Background: Epidemiological research suggests that altered levels of cytokine are associated with pathophysiology and the development of major depressive disorder (MDD). Based on earlier study, IL-1β rs16944 and rs1143627 polymorphisms may increase the risk of depression. Here, we aimed to evaluate the correlation between these polymorphisms and MDD susceptibility among the population in Bangladesh.

Methods: Blood samples were collected from 100 MDD patients and 70 matched controls. Study participants were evaluated by DSM-5 criteria and PCR-RFLP method were applied for genotyping.

Results: The IL1β rs1143627 and rs16944 polymorphisms were found to have a significant association with the risk of MDD. In case of rs1143627 CT heterozygous genotype (OR = 2.22, 95% CI = 1.08-4.55, p-value = 0.029) and combined CT+TT (OR = 2.35, 95% CI = 1.15-4.79, p-value = 0.019) genotype was strongly associated with the increased risk of MDD in comparison to CC common genotype. Moreover, the over-dominant model indicated a 2.15-fold higher risk for MDD development (OR = 2.15, 95% CI = 1.05-4.40, p-value = 0.036). On the other hand, the IL1β rs16944 polymorphisms revealed that the TC+CC combined genotype in the dominant model showed a 2.06-fold increased risk for MDD development compared to the TT common homozygote (OR = 2.06, 95% CI = 1.06-3.99, p-value = 0.032).

Conclusion: Studies suggests that IL1β rs16944 and rs1143627 polymorphisms are associated with an increased risk of MDD. These findings will provide us with valuable insights into the pathophysiology of MDD.

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来源期刊
PLoS ONE
PLoS ONE 生物-生物学
CiteScore
6.20
自引率
5.40%
发文量
14242
审稿时长
3.7 months
期刊介绍: PLOS ONE is an international, peer-reviewed, open-access, online publication. PLOS ONE welcomes reports on primary research from any scientific discipline. It provides: * Open-access—freely accessible online, authors retain copyright * Fast publication times * Peer review by expert, practicing researchers * Post-publication tools to indicate quality and impact * Community-based dialogue on articles * Worldwide media coverage
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