Al-Eitan Laith, Abu Kharmah Hana, Alghamdi Mansour
Department of Biotechnology and Genetic Engineering, Jordan University of Science and Technology, Irbid, Jordan.
Department of Anatomy, College of Medicine, King Khalid University, Abha, Saudi Arabia.
Ann Med. 2025 Dec;57(1):2445779. doi: 10.1080/07853890.2024.2445779. Epub 2024 Dec 28.
Substance use disorders are multifaceted conditions influenced by both genetic and environmental factors. Serotonergic pathways are known to be involved in substance use disorder susceptibility, with genetic markers within serotonin receptor genes identified as potential risk factors.
To further explore this relationship, we conducted a study to investigate the association between several polymorphisms in five serotonin receptor genes (, , ) and substance use disorders (SUD) in Jordanian males by sequencing genotypes in 496 SUD patients and 496 healthy controls.
Our findings revealed an allelic association between rs9567735 in the gene and rs17586428 in the gene with SUD. Haplotype analysis also showed that one haplotype of the gene and four haplotypes of the five included genes were significantly associated with SUD risk. Moreover, we found that motives for substance use were correlated with single nucleotide polymorphisms SNPs rs1923882 and rs1150226, with the latter SNP also being associated with smoking.
These findings suggest that genetic variants of human 5-HT receptor genes may affect individual susceptibility to SUD in Jordan. However, further studies with larger sample sizes and additional variants in the same or different genes must confirm these findings.
物质使用障碍是受遗传和环境因素影响的多方面病症。已知血清素能通路参与物质使用障碍易感性,血清素受体基因内的遗传标记被确定为潜在风险因素。
为进一步探究这种关系,我们开展了一项研究,通过对496例物质使用障碍患者和496例健康对照的基因型进行测序,调查约旦男性中五个血清素受体基因(、、)的几种多态性与物质使用障碍(SUD)之间的关联。
我们的研究结果揭示了基因中的rs9567735与基因中的rs17586428与物质使用障碍之间的等位基因关联。单倍型分析还表明,基因的一种单倍型和所纳入的五个基因中的四种单倍型与物质使用障碍风险显著相关。此外,我们发现物质使用动机与单核苷酸多态性SNP rs1923882和rs1150226相关,后一个SNP也与吸烟有关。
这些发现表明,人类5-羟色胺受体基因的遗传变异可能影响约旦人对物质使用障碍的个体易感性。然而,需要更大样本量以及同一或不同基因中的其他变异进行进一步研究来证实这些发现。