Genetiс aspects of lactase persistence in different ethnic groups
Abstract
Aim. The aim of this study was evaluation of the genetic aspects of lactase persistence (LP) in persons from different ethnic groups. Methods. Genealogical and medical information was collected about Ukrainian, Indian, Nigerian, Israel, Egypt, Palestine, Turkey, Jordan students (n=361) and their first degree relatives (n=413). Statistical analysis was carried out by Shapiro-Wilk test, χ2, Spearman correlation. Results. The phenotype of LP was found in 69.9 % of Ukrainians, lactose intolerance - in 7.2 %. The highest LP is observed in 95.2 % of Nigerians, the lowest - Palestinians, 51.9 %. Analysis in all ethnic groups showed that the number of LP people is less among parents than among students (r = - 0.529, p <0.05). The LP score is 72.7 - 95.2 % among Nigerian, Israeli, Egyptian, Turkish, Indian students, and 60 - 76.5 % among their parents. The LP phenotypе is 50 – 68.8 % and 53.9 – 70.9 % among Ukrainian, Palestinian Jordanian students and their parents. It is likely that adult-type hypolactasia may appear after 20 years and older, indicating a high degree of heterozygosity. The highest number of persons with first exogamy degree is 82.6-85.5 % among Turks, Palestinians, Egyptians and the lowest value of LP phenotype is observed in these groups - 51.9 - 72.3 %, (r = – 0.786, p<0.05). A positive correlation is determined between the traits of hypolactasia and first degree of parents exogamy (r = 0.905, p<0.05). The changes in metabolic status with age could be a predictor for multifactorial pathology. Conclusions. Adult hypolactasia is an age-dependent trait. Relations between the parameters of LP and the origin were established.
Keywords: lactase persistence, lactose intolerance, exogamy, genotypes.
References
Gallego Romero I., Basu Mallick C., Liebert A., Crivellaro F., Chaubey G., Itan Y., Metspalu M., Eaaswarkhanth M., Pitchappan R., Villems R., Reich D., Singh L., Thangaraj K., Thomas M.G., Swallow D.M., Mirazón Lahr M., Kivisild T. Herders of Indian and European Cattle Share Their Predominant Allele for Lactase Persistence. Molecular Biology and Evolution. 2012. Vol. 29 (1). P. 249–260. doi: 10.1093/molbev/msr190.
Itan Y., Jones B.L., Ingram C.J., Swallow D.M., Thomas M.G. A worldwide correlation of lactase persistence phenotype and genotypes. BMC Evol Biol. 2010. Vol. 10. P. 36. doi: 10.1186/1471-2148-10-36.
Ugidos-Rodríguez S., Matallana-González M.C., Sánchez-Mata M.C. Lactose malabsorption and intolerance: a review. Food Funct. 2018. Vol. 9 (8). P. 4056–4068. doi: 10.1039/c8fo00555a.
Cho E., Smith-Warner S.A., Spiegelman D., Beeson W.L., van den Brandt P.A., Colditz G.A., Folsom A.R., Fraser G.E., Freudenheim J.L., Giovannucci E., Goldbohm R.A., Graham S., Miller A.B., Pietinen P., Potter J.D., Rohan T.E., Terry P., Toniolo P., Virtanen M.J., Willett W.C., Wolk A., Wu K., Yaun S.S., Zeleniuch-Jacquotte A., Hunter D.J. Dairy foods, calcium, and colorectal cancer: a pooled analysis of 10 cohort studies. J Natl Cancer Inst. 2004. Vol. 96 (13). P. 1015–1022. doi: 10.1093/jnci/djh185.
Liebert A., López S., Jones B.L., Montalva N., Gerbault P., Lau W., Thomas M.G., Bradman N., Maniatis N., Swallow D.M. World-wide distributions of lactase persistence alleles and the complex effects of recombination and selection. HumGenet. 2017. Vol. 136 (11–12). P. 1445–1453. doi: 10.1007/s00439-017-1847-y.
Fedota O., Babalian V., Borozenets V., Mazniakov S., Puzik N. Lactose intolerance and its association with the exogamy degree among the population of eastern Ukraine. Factors in Experimental Evolution of Organisms. 2019. No. 24. P. 249–253. [in Ukrainian]
Rasinperä H., Savilahti E., Enattah N.S., Kuokkanen M., Tötterman N., Lindahl H., Järvelä I., Kolho K.L. A genetic test which can be used to diagnose adult-type hypolactasia in children. Gut. 2004. Vol. 53 (11). P. 1571–1576. doi: 10.1136/gut.2004.040048.
Seppo L., Tuure T., Korpela R., Järvelä I., Rasinperä H., SahiT. Can primary hypolactasia manifest itself after the age of 20 years? A two-decade follow-up study. Scand J Gastroenterol. 2008. Vol. 43 (9). P. 1082–1087. doi: 10.1080/00365520802095485.
Bulhões A.C., Goldani H.A., Oliveira F.S., Matte U.S., Mazzuca R.B., Silveira T.R. Correlation between lactose absorp-tion and the C/T-13910 and G/A-22018 mutations of the lactase-phlorizin hydrolase (LCT) gene in adult-type hypolactasia. Braz J Med Biol Res. 2007. Vol. 40 (11). P. 1441–1446. doi: 10.1590/s0100-879x2007001100004.
Fedota O.M., Lysenko N.G., Ruban S.Yu., Kolisnyk O.I., Goraychuk I.V. Effects of Allelic Polymorphisms in GH and GHR Geneson Production and Reproduction Parameters of Cattle (Bostaurus L., 1758) of the Aberdeen-Angus Breed Tsitologiyai Genetika. 2017. Vol. 5 (51). P. 38–49.
Fedota O., Roschenyuk L., Tyzhnenko T., Merenkova I.,Vorontsov V. Pharmacogenetic effects of methotrexate in Ukrain-ian patients depending on the mthfr genotypes (clinical cases). Georgian Medical News. 2018. Vol. 6 (279). P. 111–117.
Fedota O., Babalian V., Borozenets V., Mazniakov S., Lysenko N. Genetic aspects of lactase persistence in the Eastern Ukraine population. 7th Baltic Genetics Congress: abstracts, (Riga October 24–27, 2018). P. 202.
Coelho M., Luiselli D., Bertorelle G., Lopes A.I., Seixas S., Destro-Bisol G., Rocha J. Microsatellite variation and evolution of human lactase persistence. Hum. Genet. 2005. Vol. 117 (4). P. 329–339. doi: 10.1007/s00439-005-1322-z.