对MTHFR和SLC19A1变体的药物遗传学见解,用于治疗类风湿性疾病的低剂量甲状腺素治疗
Goitybell Martínez Téllez1, Beatriz Marcheco Teruel1
1National Center of Medical Genetic, University of Medical Science, Playa, La Havana, Cuba.
在MTHFR和SLC19A1基因的遗传变异影响低剂量甲状腺素治疗自身免疫性疾病. 需要进行研究,特别是在拉丁美洲,以澄清对治疗结果的影响,并指导药物基因组学.
科学领域:
- 药物基因组学 药物基因组学
- 自免疫性疾病 自免疫性疾病
- 分子遗传学 分子遗传学
背景情况:
- 低剂量甲状腺素是对类风湿和自身免疫性疾病的首要治疗方法.
- 识别遗传标记可以改善疾病管理,并预测治疗结果.
- 甲基基酸减少酶 (MTHFR) 和溶解物载体家族 19 成员 1 (SLC19A1) 基因是甲基酸途径的关键.
研究的目的:
- 审查与甲状腺素治疗相关的MTHFR和SLC19A1基因中的候选单核酸多态 (SNPs).
- 总结当前关于这些多形态与甲状腺素功效和不良影响的相关性知识.
主要方法:
- 对研究MTHFR (rs1801133,rs1801131) 和SLC19A1 (rs1051266) 多态性的研究进行文献综述.
- 分析报告的关联与甲状腺素治疗结果.
主要成果:
- 已经研究了MTHFR和SLC19A1中的几个功能多态.
- 与副作用的关联比与缓解或积极反应的关联更频繁地报告.
- 这些多形态对甲状腺素治疗的确切影响尚不清楚.
结论:
- 目前的证据表明,在甲铁沙治疗中,MTHFR和SLC19A1多态性是不确定的.
- 在拉丁美洲人口中,研究显著缺乏.
- 进一步的研究对于开发临床药物基因组学指南和个性化医学至关重要.
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