Mohammadi Mojgan, Tahmasebi Abdar Hossein, Mollaei Hamid Reza, Hajghani Hossein, Baneshi Mohammad Reza, Hayatbakhsh Mohammad Mahdi
Immunology Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran ; Department of Immunology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Department of Gastroenterology, Afzalipour Hospital, Kerman University of Medical Sciences, Kerman, Iran.
Middle East J Dig Dis. 2017 Jan;9(1):26-32. doi: 10.15171/mejdd.2016.48.
BACKGROUND Irritable bowel syndrome (IBS) is a digestive system disorder with an unknown etiology. Serotonin has a key role in the secretion and motility of the intestine. Polymorphism in serotonin re-uptake transporter (SERT or SLC6A4) gene may have a functional role in the gut of patients with IBS. The aims of the present study were to investigate the association between SLC6A4 gene polymorphism and IBS and to detect the correlation between rectal serotonin levels and IBS sub-types. METHODS SLC6A4 gene polymorphism in 131 patients with IBS and 211 healthy controls were analysed using the quantitative polymerase chain reaction high-resolution melting (qPCR-HRM) curve technique. Serotonin was measured in rectal biopsies of patients with IBS using the enzyme-linked immunosorbent assay (ELISA) method. RESULTS The patients were categorized into three groups: IBS with diarrhoea (IBS-D): 70 patients, IBS with constipation (IBS-C): 18 patients, and IBS with mixed symptoms (IBS-M): 43 patients. The frequency of SLC6A4 s/s and l/s genotypes was significantly higher in IBS-C than IBS-D, IBS-M, and controls (=0.036). Serotonin levels were similar in IBS sub-types. CONCLUSION SLC6A4 polymorphism is a possible candidate gene associated with the pathogenesis of IBS-C. Although serotonin levels did not differ in rectal biopsies of IBS sub-types, further investigation is recommended.
肠易激综合征(IBS)是一种病因不明的消化系统疾病。血清素在肠道分泌和蠕动中起关键作用。血清素再摄取转运体(SERT或SLC6A4)基因多态性可能在IBS患者的肠道中发挥功能作用。本研究的目的是调查SLC6A4基因多态性与IBS之间的关联,并检测直肠血清素水平与IBS亚型之间的相关性。方法:采用定量聚合酶链反应高分辨率熔解曲线(qPCR-HRM)技术分析131例IBS患者和211例健康对照者的SLC6A4基因多态性。采用酶联免疫吸附测定(ELISA)法检测IBS患者直肠活检组织中的血清素。结果:患者分为三组:腹泻型肠易激综合征(IBS-D):70例,便秘型肠易激综合征(IBS-C):18例,混合型肠易激综合征(IBS-M):43例。IBS-C组中SLC6A4 s/s和l/s基因型的频率显著高于IBS-D组、IBS-M组和对照组(=0.036)。IBS各亚型的血清素水平相似。结论:SLC6A4基因多态性可能是与IBS-C发病机制相关的候选基因。尽管IBS各亚型直肠活检组织中的血清素水平无差异,但仍建议进一步研究。