Kovalenko E V, Vergasova E O, Shoshina O O, Sheludchenko M S, Popov I V, Kim A A, Plotnikov N A, Rakitko A S, Volokh O I
Health & Nutrition, LLC, 143421, Moscow region, Krasnogorsk district, Russian Federation.
Genotek, Ltd., 105120, Moscow, Russian Federation.
Vopr Pitan. 2025;94(2):38-51. doi: 10.33029/0042-8833-2025-94-2-38-51. Epub 2025 Apr 2.
The ability to digest lactose in adulthood is caused by a genetic mutation that emerged following the domestication of cattle approximately 10 000 years ago. However, many adults retain primary lactase deficiency - the ancestral phenotype characterized by a decline in lactase enzyme activity after weaning. While the global prevalence of this condition is well-documented, reliable large-scale population data for Russia have been lacking so far. Microarray genotyping of genetic markers now enables high-quality, up-to-date research covering representative samples from diverse ethnic groups across Russia's regions. of the research was to compare the frequency of GG genotype in rs4988235 (13910 C/T) in the regulatory region (MCM6) of the lactase enzyme gene LCT, which determines the genetic risk of lactase insufficiency manifestation, in populations living in Russia and evaluate the differences between Russian regions. . The largest multi-ethnic genetic study on lactase deficiency in Russia was conducted on a sample of 24,439 individuals in 56 populations. The percentage of an individual belonging to each ethnic group was estimated by calculating the ancestral contribution to an individual's genetic makeup. In addition, we calculated the frequency of the rs4988235 GG genotype in regions of Russia using information on the individual's current location and place of birth. . The prevalence of lactase deficiency by GG genotype rs4988235 in the Russian population was 45.2 and 42.8% (95% confidence interval 42.1-43.4) in the East Slavs group. The study revealed a significant variability (22.8-83.2%) in the regional prevalence of lactase deficiency by GG rs4988235 genotype. The dependence of the regional prevalence of lactase deficiency on the current place of residence is supported by the geographical features of the Russian territory and the history of pastoralism in different regions. . The findings may be useful for developing regional nutrition recommendations and optimising the Russian market for lactose-free and low-lactose products, and justify the importance of genetic testing for diagnosis, highlighting the interdisciplinary relevance of the study.
成年人消化乳糖的能力是由大约一万年前牛被驯化后出现的基因突变导致的。然而,许多成年人仍存在原发性乳糖酶缺乏症——这是一种祖传表型,其特征是断奶后乳糖酶活性下降。虽然这种情况在全球的患病率已有充分记录,但目前俄罗斯仍缺乏可靠的大规模人口数据。对基因标记进行微阵列基因分型,现在能够开展高质量、最新的研究,涵盖俄罗斯各地区不同族群的代表性样本。该研究的目的是比较俄罗斯不同族群中,乳糖酶基因LCT调控区(MCM6)中rs4988235(13910 C/T)位点的GG基因型频率,该位点决定了乳糖酶不足表现的遗传风险,并评估俄罗斯不同地区之间的差异。俄罗斯规模最大的关于乳糖酶缺乏症的多族群基因研究,是对56个族群的24439名个体进行的抽样调查。通过计算各祖先对个体基因构成的贡献,估算出每个个体所属族群的百分比。此外,我们利用个体当前所在地和出生地的信息,计算了俄罗斯各地区rs4988235 GG基因型的频率。俄罗斯人群中,rs4988235 GG基因型导致的乳糖酶缺乏症患病率,在东斯拉夫人组中为45.2%和42.8%(95%置信区间42.1 - 43.4)。研究发现,rs4988235 GG基因型导致的乳糖酶缺乏症在各地区的患病率存在显著差异(22.8% - 83.2%)。俄罗斯领土的地理特征以及不同地区的畜牧历史,支持了乳糖酶缺乏症地区患病率与当前居住地之间的相关性。这些研究结果可能有助于制定区域营养建议,优化俄罗斯无乳糖和低乳糖产品市场,并证明基因检测在诊断中的重要性,凸显了该研究的跨学科相关性。