Evaluation the relationship between polymorphism of galactose mutarotase gene by creating jaw sound in patients with temporomandibular disorder (TMD)

Shamsolmolouk Najafi, Hassan Roudgari, Nafiseh Sheikh Bahaei, Zahra Tajik, Shadi Asadighalhari
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Abstract

Objective: One of the concerns of dentists is the referral of patients with temporomandibular prob- lems. Temporomandibular joint disorders (TMD) is a complex multifactorial clinical problem that involves masticatory muscles, temporomandibular joint and related structures. This complication is one of the three common chronic pains after headache and low back pain, which can manifest as pain in the temporoman- dibular region and limitation in joint movements, or even as clicking, crepitus, and popping sounds during temporomandibular joint movements. For the first time, the american association for oral pain (AAOP) proposed the role of genetic factors in the development of TMD. It is thought that a complex disorder such as TMD is multidimensional and can be subjected to environmental conditions as well as multiple gene polymorphisms. Identification of single nucleotide polymorphisms in the human genome can play an important role in clinical setting for diagnosis, prognosis and therapeutic interventions in various diseases including TMD. The aim of this study was to evaluate the relationship between polymorphism of galactose mutarotase gene by creating jaw sound in patients with temporomandibular disorder in a population with high similarity to the whole Iranian population and using the results in prevention and targeted treatment of affected patients. Study Design: 101 patients with TMD using DC/TMD criteria among those referred to Tehran University School of Dentistry and 103 healthy subjects for TMD that have age and gender matched were selected to control groupfrom those referring to the Oral and Maxillofacial Diseases and Oral and Maxillo- facial Pain departments. Blood samples were taken in 5cc and DNA extracted from the blood of both groups by applying the technique PCRARMS in terms of polymorphism rs4776783 in Galm gene were Compared. Results: 101 patients with TMD along with 103 healthy individuals without a history of TMD were evaluated to investigate rs4776783 polymorphism in GALM gene. The average age of the patients was 35.92, and 21 were men and 80 were women. According to the questionnaire, 61 people felt the sound in their jaw while moving. On the other hand, according to the TMD/DC criterion, the number of people who have crepitus in the right and left jaws is equal. The average age of the patients was 35.92, and 21 were men and 80 were women. According to the questionnaire, 61 people felt the sound in their jaw while moving. On the other hand, according to the TMD/DC criterion, the number of people who have crepitus in the right and left jaws is equal. The low prevalence of crepitation with p=0.734 has a significant relationship with the genotype of people. Conclusion: This study showed that there is a significant relationship between the rs4776783 poly- morphism in Galm gene and the occurrence of temporomandibular disorder (TMD), jaw sound and pain in many masticatory muscles such as lateral pterygoid and temporal. Therefore, it can be concluded that TMD has a genetic basis.
颞下颌关节紊乱病(TMD)半乳糖变位酶基因多态性与下颌发声的关系
目的:口腔医生关心的问题之一是颞下颌问题患者的转诊。颞下颌关节紊乱病(TMD)是一个复杂的多因素临床问题,涉及咀嚼肌、颞下颌关节及其相关结构。这种并发症是继头痛和腰痛之后的三种常见慢性疼痛之一,表现为颞下颌区疼痛和关节运动受限,甚至表现为颞颌关节运动过程中的咔嗒声、creitus声和爆裂声。美国口腔疼痛协会(AAOP)首次提出遗传因素在TMD发展中的作用。人们认为,像TMD这样的复杂疾病是多方面的,可能受到环境条件以及多基因多态性的影响。人类基因组单核苷酸多态性的鉴定可以在包括TMD在内的各种疾病的诊断、预后和治疗干预的临床环境中发挥重要作用。本研究的目的是通过在与整个伊朗人群高度相似的人群中创造颞下颌关节紊乱病患者的下颌声音,并将其结果用于对受影响患者的预防和靶向治疗,来评估半乳糖变位酶基因多态性之间的关系。研究设计:从德黑兰大学牙科学院转诊的101名采用DC/TMD标准的TMD患者和103名年龄和性别匹配的TMD健康受试者中,选择口腔颌面疾病和口腔颌面疼痛科的受试者作为对照组。应用PCRARMS技术对两组大鼠的Galm基因rs4776783多态性进行检测,并对两组的血液进行DNA提取比较。结果:对101例TMD患者和103例无TMD病史的健康人进行GALM基因rs4776783多态性检测。患者的平均年龄为35.92岁,其中21人为男性,80人为女性。根据调查问卷,61人在移动时能感觉到下巴发出的声音。另一方面,根据TMD/DC标准,患有左右颌骨皱纹的人数相等。患者的平均年龄为35.92岁,其中21人为男性,80人为女性。根据调查问卷,61人在移动时能感觉到下巴发出的声音。另一方面,根据TMD/DC标准,患有左右颌骨皱纹的人数相等。起哄发生率低(p=0.734)与人的基因型有显著关系。结论:Galm基因rs4776783多态性与颞下颌关节紊乱病(TMD)的发生、下颌声音和翼侧、颞侧等咀嚼肌疼痛之间存在显著关系。因此,TMD具有一定的遗传基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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