Impact of 5-HTTLPR of SLC6A4 on migraine susceptibility: A meta-analysis with trial sequential analysis

IF 0.5 Q4 GENETICS & HEREDITY Human Gene Pub Date : 2024-10-24 DOI:10.1016/j.humgen.2024.201347
Amrit Sudershan , Hardeep Kumar , Sandeepa Bailam , Rakesh K. Panjaliya , Parvinder Kumar
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Abstract

Background

Migraine disorder is a complicated condition for which a large number of genetic variants determine susceptibility. The 5-HTTLPR of the SLC6A4 gene is one of these genetic variations, and it is hypothesized that it plays a role in defining the susceptibility to the disease.

Aim

Therefore, through the utilization of the meta-analysis methodology, the current investigation aimed to determine whether or not there is an association between the 5-HTTLPR and the likelihood of developing migraines.

Method

The present study utilizes the PRISMA guideline to review existing literature from the electronic database to perform pooled analysis, and also includes quality assessment, association analysis, publication bias, and heterogeneity analysis using the NOS tool, OR with 95 % CI, tests of Begg's with Egger's test, and χ2 based on Cochran's Q Test with I2 tests respectively.

Result

Using a systematic literature review, we found 14 studies representing 2972 participants, with 1276 cases diagnosed with migraine and 1696 serving as controls. It was observed that after utilizing multiple genetic models only allele (1.14 [1.01–1.29], p-value = 0.025) and recessive model (1.24 [1.01–152], p-value = 0.03), in contrast to other genetic models were found to be significantly associated with overall migraine but not with MA and MWA.

Discussion & conclusion

In conclusion, according to the allele and recessive model, the current investigation revealed a statistically significant relationship between 5-HTTLPR and the likelihood of developing migraines.

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SLC6A4的5-HTTLPR对偏头痛易感性的影响:带试验序列分析的荟萃分析
背景偏头痛是一种复杂的疾病,由大量基因变异决定易感性。因此,通过使用荟萃分析方法,本研究旨在确定 5-HTTLPR 与患偏头痛的可能性之间是否存在关联。方法本研究利用 PRISMA 指南对电子数据库中的现有文献进行回顾,以进行汇总分析,还包括质量评估、关联分析、发表偏倚和异质性分析,分别使用 NOS 工具、OR 与 95 % CI、Begg's 与 Egger's 检验以及基于 Cochran's Q 检验与 I2 检验的 χ2 进行分析。结果我们发现,与其他遗传模型相比,只有等位基因模型(1.14 [1.01-1.29],p 值 = 0.025)和隐性模型(1.24 [1.01-152],p 值 = 0.03)与总体偏头痛显著相关,但与 MA 和 MWA 无关。
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来源期刊
Human Gene
Human Gene Biochemistry, Genetics and Molecular Biology (General), Genetics
CiteScore
1.60
自引率
0.00%
发文量
0
审稿时长
54 days
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