[不同人群中糖代谢障碍的遗传学]
A I Kozlov1,2,3, B A Malyarchuk4
1D. Anuchin Institute and Museum of Anthropology, Lomonosov Moscow State University, 125009, Moscow, Russian Federation.
Voprosy pitaniia
|May 29, 2024
概括
糖酶-异酸酶基因 (SI) 的遗传突变会影响糖糖的新陈代谢,导致糖酶-异酸酶缺乏症 (SID). 在北极群体中观察到SI delAG缺失的高载体率,影响SID流行率和潜在的健康风险.
科学领域:
- 遗传学 是一个遗传学.
- 胃肠病学 胃肠病学
- 人体生理学 人体生理学
背景情况:
- 脱糖类活性对于碳水化合物消化至关重要.
- 糖酶-异酶基因 (SI) 的遗传变异会影响糖糖的新陈代谢.
- 糖糖异酶缺乏症 (SID) 是一种影响糖糖吸收的疾病.
研究的目的:
- 审查和系统化有关SI基因在糖代谢中的作用的数据.
- 调查SI基因突变对SID流行率的贡献.
- 探索SI基因变异与不同种群中的肠道疾病的关联.
主要方法:
- 对同行评审出版物的系统文献审查.
- 在PubMed和eLibrary数据库中进行的搜索.
- 使用gnomAD数据库来获取遗传变异信息.
主要成果:
- 150个已知的SI基因突变中,有37个影响糖酶活性.
- SI delAG删除 (rs781470490) 在北极土著群体中显示出高载体率 (5-21%).
- 在特定的俄罗斯北极地区的同卵性SI delAG载体中增加了SID表现的风险 (0.2-2.3%).
结论:
- SI变体的表现与同时发生的碳水化合物吸收不良和肠道微生物群有关.
- SI 15Phe变体 (rs9290264) 可能与易怒肠综合征的发展有关.
- 医学遗传方法可以提高SID差异诊断的准确性.
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