Su Shan-Yu, Chen Jonathan Jiunn-Horng, Lai Chien-Chen, Chen Chun-Ming, Tsai Fuu-Jen
Department of Chinese Medicine, China Medical University Hospital, Taichung, Taiwan.
Clin Rheumatol. 2007 Jan;26(1):12-6. doi: 10.1007/s10067-006-0213-6. Epub 2006 Mar 18.
Because fibromyalgia (FM) is often comorbid with anxiety, and monoamine oxidase A (MAOA) was reported to be associated with anxiety, we determine if there is MAOA gene polymorphism associated with FM patients. Moreover, interleukin 4 (IL-4) was found to be an important cytokine participating in the immunologic pathway of T-helper 2 (Th-2) cells, in this study, we search if the genetic polymorphism of IL-4 intron3 could be demonstrated in FM patients. The genotype of sixty-two FM patients was compared with that of control subjects. The polymorphism of IL-4 intron3 variable number of tandem repeats (VNTR) was demonstrated by performing the genomic polymerase chain reaction (PCR) and analyzing the length of PCR product. Furthermore, the MAOA 941 G to T polymorphism was also determined by PCR-RFLP (restriction fragment length polymorphism) analysis. The MAOA 941 position genotype polymorphism between FM and control subjects was found neither statistically different in male (p=0.60) or female (p=0.52), nor total allelic frequency (p=0.52). Similarly, the difference of IL-4 intron3 polymorphism between FM and control was neither existing in genotype (p=0.06), nor allele frequency (p=0.07). The result suggests either the genetic linkage between FM and anxiety or that between FM and immunologic diseases are weak. Accordingly, the MAOA 941 position and IL-4 intron3 polymorphisms are not susceptible markers to predict FM.
由于纤维肌痛(FM)常与焦虑症合并存在,且有报道称单胺氧化酶A(MAOA)与焦虑症相关,因此我们确定FM患者是否存在与MAOA基因多态性相关的情况。此外,白细胞介素4(IL-4)被发现是参与辅助性T细胞2(Th-2)细胞免疫途径的一种重要细胞因子,在本研究中,我们探究FM患者中是否能证实IL-4内含子3的基因多态性。将62例FM患者的基因型与对照组受试者的基因型进行比较。通过进行基因组聚合酶链反应(PCR)并分析PCR产物的长度来证实IL-4内含子3可变串联重复序列(VNTR)的多态性。此外,还通过PCR-限制性片段长度多态性(RFLP)分析来确定MAOA 941 G至T多态性。结果发现,FM患者与对照组受试者之间,MAOA 941位点的基因型多态性在男性(p = 0.60)或女性(p = 0.52)中均无统计学差异,在总等位基因频率方面也无差异(p = 0.52)。同样,FM患者与对照组之间IL-4内含子3多态性在基因型(p = 0.06)或等位基因频率(p = 0.07)方面均无差异。该结果表明,FM与焦虑症之间或FM与免疫性疾病之间的遗传联系较弱。因此,MAOA 第941位点和IL-4内含子3多态性并非预测FM的敏感标志物。