Impact of Serotonin Pathway Gene Polymorphisms and Serotonin Levels in Suicidal Behavior.

IF 2.9 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Medical Principles and Practice Pub Date : 2023-09-15 DOI:10.1159/000534069
Sneha Sivaramakrishnan, Vettriselvi Venkatesan, Sampath Kumar Paranthaman, R Sathianathan, Swetha Raghavan, Priyadarshee Pradhan
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Abstract

Objective: Suicide is a significant public health issue and a major cause of death in all ages worldwide. Previous studies have shown the involvement of genetics in suicidal behaviour. This study aimed to assess the role of the genetic variants of the serotonin transporter genes (5HTTLPR, SLC6A4 intron 2) and receptor gene (5HTR2AT102C) in individuals who died of suicide. The study compares the serum levels of serotonin between the cases and controls.

Methods: We conducted a case control study with 120 cases and 126 controls. Socio-economic details of the subjects were collected using a semi-structured proforma and psychological autopsy was used to collect details of medical and other clinical conditions. Blood was drawn after taking informed consent and serum levels of serotonin were estimated by ELISA. Genotyping was performed using appropriate primers followed by polymerase chain reaction (PCR) and a restriction fragment length polymorphism (RFLP).

Results: Mean age was 32.59 ± 12.58 for cases and 33.64 ± 9.78 for controls. The risk associated LL genotype of 5HTTLPR was higher among cases. The heterozygous 12/10 genotype of SLC6A4 intron 2 polymorphism was increased among controls. Serum levels of serotonin were lower among cases. Variant genotypes of all the 3 polymorphisms showed significant interaction (OR= 39.26) indicating that this model may increase suicidal tendency.

Conclusion: The findings of this study suggest that low serum levels of serotonin and two variants of the serotonin gene may influence suicide behaviour in a south Indian population.

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5 -羟色胺通路基因多态性和5 -羟色胺水平对自杀行为的影响。
目的:自杀是一个重大的公共卫生问题,也是全世界各年龄段死亡的主要原因。先前的研究表明,基因与自杀行为有关。本研究旨在评估5 -羟色胺转运基因(5HTTLPR, SLC6A4内含子2)和受体基因(5HTR2AT102C)的遗传变异在自杀死亡个体中的作用。该研究比较了病例和对照组的血清血清素水平。方法:采用病例对照研究,120例病例和126例对照。研究人员使用半结构化的形式表格收集受试者的社会经济细节,并使用心理解剖来收集医疗和其他临床状况的细节。接受知情同意书后抽血,ELISA法测定血清血清素水平。使用合适的引物进行基因分型,然后进行聚合酶链反应(PCR)和限制性片段长度多态性(RFLP)分析。结果:患者平均年龄32.59±12.58岁,对照组平均年龄33.64±9.78岁。5HTTLPR相关LL基因型的风险在病例中较高。SLC6A4内含子2多态性的杂合子12/10基因型在对照组中增加。患者血清血清素水平较低。3个多态性的变异基因型均存在显著的交互作用(OR= 39.26),表明该模型可能增加自杀倾向。结论:这项研究的结果表明,血清血清素水平低和血清素基因的两种变体可能影响南印度人群的自杀行为。
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来源期刊
Medical Principles and Practice
Medical Principles and Practice 医学-医学:内科
CiteScore
6.10
自引率
0.00%
发文量
72
审稿时长
6-12 weeks
期刊介绍: ''Medical Principles and Practice'', as the journal of the Health Sciences Centre, Kuwait University, aims to be a publication of international repute that will be a medium for dissemination and exchange of scientific knowledge in the health sciences.
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