Edgnülü Tuba G, Özge Aynur, Erdal Nurten, Kuru Oktay, Erdal Mehmet E
Muğla School of Health Sciences, Muğla Sıtkı Koçman University, Muğla, Turkey.
Department of Neurology, Faculty of Medicine, Mersin University, Mersin, Turkey.
Adv Clin Exp Med. 2014 Nov-Dec;23(6):901-6. doi: 10.17219/acem/37333.
Monoamine oxidase (MAO) enzymes play an important role in the etiology of many neurological diseases. Tension type headache (TTH) treatments contain inhibitors for selective re-uptake of serotonin and monoamine oxidase inhibitors. MAO (EC 1.4.3.4) has two isoenzymes known as MAOA and MAOB. A promoter polymorphism of a variable number of tandem repeats (VNTR) in the MAOA gene seems to affect MAOA transcriptional activity in vitro. Also, G/A polymorphism in intron 13 (rs1799836) of the MAOB gene have been previously found to be associated with the variability of MAOB enzyme activity.
The aim of our study was to investigate a possible association of monoamine oxidase (MAOA and MAOB) gene polymorphisms in tension type headache.
MAO gene polymorphisms were examined in a group of 120 TTH patients and in another 168 unrelated healthy volunteers (control group). MAOA promoter and MAOB intron 13 polymorphisms were genotyped using PCR-based methods.
An overall comparison between the genotype of MAOA and MAOB genes and allele frequencies of the patients and the control group did not reveal any statistically significant difference between the patients and the control group (p=0.162).
Factors like estrogen dosage, the limited number of male patients and other genes' neurotransmitters involved in the etiology of TTH could be responsible for our non-significant results.
单胺氧化酶(MAO)在多种神经疾病的病因学中发挥重要作用。紧张型头痛(TTH)的治疗包括5-羟色胺选择性再摄取抑制剂和单胺氧化酶抑制剂。MAO(EC 1.4.3.4)有两种同工酶,即MAOA和MAOB。MAOA基因中可变数量串联重复序列(VNTR)的启动子多态性似乎在体外影响MAOA的转录活性。此外,先前已发现MAOB基因第13内含子(rs1799836)中的G/A多态性与MAOB酶活性的变异性相关。
我们研究的目的是调查紧张型头痛中单胺氧化酶(MAOA和MAOB)基因多态性的可能关联。
在一组120例TTH患者和另一组168例无亲缘关系的健康志愿者(对照组)中检测MAO基因多态性。使用基于PCR的方法对MAOA启动子和MAOB第13内含子多态性进行基因分型。
MAOA和MAOB基因的基因型以及患者与对照组的等位基因频率的总体比较未显示患者与对照组之间有任何统计学上的显著差异(p = 0.162)。
雌激素剂量、男性患者数量有限以及TTH病因中涉及的其他基因神经递质等因素可能是我们未得出显著结果的原因。