Skip to main content
Log in

Medical Genetic Study of Hereditary Diseases in Abazins of the Karachay-Cherkess Republic

  • Human Genetics
  • Published:
Russian Journal of Genetics Aims and scope Submit manuscript

Abstract

This paper estimates the load and nosological spectrum of monogenic hereditary diseases (HDs) in Abazins of the Karachay-Cherkess Republic (KChR), identified in Cherkessk and ten districts, Abazinsky, Ust-Dzhegutinsky, Malokarachaevsky, Karachaevsky, Prikubansky, Khabezsky, Nogaysky, Adyge-Khablsky, Urupsky, and Zelenchuksky. The number of the investigated population was 387231 individuals (including 33264 Abazins). We detected 153 patients from 105 families with 45 nosological forms of HDs: 83 patients from 50 families with 23 AD diseases, 47 patients from 42 families with 15 AR diseases, and 23 patients from 13 families with 7 X-linked diseases. The total load of HDs in Abazins was 1: 218 individuals (in the rural population 1: 162, in the urban population 1: 305). Frequent and rare nosological forms of HDs and the accumulation of certain diseases in Abazins in comparison with the previously surveyed populations of Russia were determined. On the basis of the prevalence of AD and AR hereditary diseases, a principal component analysis was carried out, which determined the genogeographical position of Abazins among nine ethnic groups (13 populations) of Russian Federation: six Russian regions, Bashkirs of the Bashkortostan, Tatars of the Tatarstan, Chuvashes of the Chuvashia, Maris of the Mari El, Udmurts of the Udmurtia, Adygeans of the Adygea, and Circassians and Abazins of the KChR.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Passarge, E., Color Atlas of Genetics, Stuttgart: George Thieme, 2007, 3rd ed.

    Google Scholar 

  2. Dong-Dong Wu and Ya-Ping Zhang, Different level of population differentiation among human genes, BMC Evol. Biol., 2011, vol. 11, no. 16. doi 10.1186/1471-2148-11-16

    Google Scholar 

  3. Online Mendelian Inheritance in Man. http://www. ncbi.nlm.nih.gov/OMIM. Accessed February, 2017.

  4. Zinchenko, R.A. and Ginter, E.K., Medical genetic counseling in different populations and ethnic groups, Med. Genet., 2008, vol. 7, no. 10, pp. 20–29.

    Google Scholar 

  5. Bliznets, E.A., Kirillov, A.G., Ginter, E.K., et al., Molecular-genetic cause of osteopetrosis in Chuvashia, Med. Genet., 2005, vol. 4, no. 7, pp. 315–321.

    Google Scholar 

  6. Zinchenko, R.A., Mordovtseva, V.V., Petrov, A.N., and Ginter, E.K., Hereditary recessive hypotrichosis in the republics of Mari El and Chuvashia, Med. Genet., 2003, vol. 2, no. 6, pp. 267–272.

    Google Scholar 

  7. Makaov, A.Kh., Zinchenko, R.A., Khlebnikova, O.V., et al., Molecular epidemiology of hereditary pathology in ten populations of the Karachay-Cherkess Republic, Med. Genet., 2016, vol. 15, no. 8, pp. 6–9.

    Google Scholar 

  8. Nazarenko, L.P., Nazarenko, S.A., Kirillina, V.I., and Prokop’eva, Yu.N., Genetiko-ekologicheskaya otsenka sostoyaniya zdorov’ya zhitelei Yakutii (Genetic-Ecological Health Assessment of Yakutia Population), Yakutsk: Imidzh, 2001.

    Google Scholar 

  9. Nazarenko, L.P., Epidemiology of hereditary diseases and the medical genetic counseling, Med. Genet., 2004, vol. 3, no. 3, pp. 133–138.

    Google Scholar 

  10. Puzyrev, V.P. and Nazarenko, L.P., Genetiko-epidemiologicheskoe issledovanie nasledstvennoi patologii v Zapadnoi Sibiri (Genetic Epidemiological Study of Hereditary Disorders in Western Siberia), Tomsk: STT, 2000.

    Google Scholar 

  11. El’chinova, G.I., Shakmanov, M.M., Revazova, Yu.A., and Zinchenko, R.A., Population and genetic characteristics of Abazins in Karachay Cherkessia (maritalmigrations and surname frequency distribution), Russ. J. Genet., 2015, vol. 51, no. 10, pp. 1020–1025. doi 10.1134/S1022795415100051

    Article  CAS  Google Scholar 

  12. Ginter, E.K., Mamedova, R.A., El’chinova, G.I., and Brusintseya, O.V., Genetic structure of regulations and characteristics of geographic distribution of autosomal recessive diseases in the Kirov region, Russ. J. Genet., 1994, vol. 30, no. 1, pp. 97–101.

    Google Scholar 

  13. Ginter, E.K. and Zinchenko, R.A., Epidemiology of hereditary diseases in European sector of Russia, in Genomics and Health in the Developing World, Kumar, D., Ed., New York: Oxford University Press, 2012, pp. 1281–1314.

    Google Scholar 

  14. Abazins, Narody Rossii: atlas kul’tur i religii (Peoples of Russia: Atlas of Cultures and Religions), 2nd ed. Zhuravskii, A.V., Kazmina, O.T., and Tishkov, V.A., Eds., Moscow: Dizain. Informatsiya. Kartografiya, 2010.

  15. https://en.wikipedia.org/wiki/Abaziny. Accessed June, 3, 2017.

  16. Tishkov, V.A., Rossiiskii Kavkaz: kniga dlya politikov (The Russian Caucasus: A Book for Politicians), Moscow: Rosinformagrotekh, 2007.

    Google Scholar 

  17. Neel, J.V., History and the Tey-Sachs allele, in Genetic Diseases among Ashkenazi Jews, Goodman, R.M. and Motulsky, A.G., Eds., New York: Raven, 1979, pp. 285–330.

    Google Scholar 

  18. Zhivotovskii, L.A., Populyatsionnaya biometriya (Population Biometry), Moscow: Nauka, 1991.

    Google Scholar 

  19. Zinchenko, R.A., El’chinova, G.I., Galkina, V.A., et al., Genetic differentiation of ethnic groups of Russia on genes of hereditary diseases, Med. Genet., 2007, vol. 6, no. 2, pp. 29–37.

    Google Scholar 

  20. Zinchenko, R.A., El’chinova, G.I., and Ginter, E.K., Factors determining the spread of hereditary diseases among Russian populations, Med. Genet., 2009, vol. 8, no. 12, pp. 7–23.

    Google Scholar 

  21. Puzyrev, V.P., Erdynieva, L.S., Kucher, A.N., and Nazarenko, L.P., Genetiko-epidemiologicheskoe issledovanie naseleniya Tuvy (Genetic Epidemiological Study of the Tuva Population), Tomsk: STT, 1999.

    Google Scholar 

  22. Orphanet Reports Series: diseases listed by decreasing prevalence or number of published cases. http://www.orpha.net/. Accessed February, 2017.

  23. British Columbia: Health Status Registry (HSR). http://www.phac-aspc.gc.ca/ccasn-rcsac/dss/bc-eng.php. Accessed May, 2017.

  24. Ladda, R.L., Zonana, J., Ramer, J.C., et al., Congenital contractures, ectodermal dysplasia, cleft lip/palate, and developmental impairment: a distinct syndrome, Am. J. Med. Genet., 1993, vol. 47, pp. 550–555.

    Article  PubMed  CAS  Google Scholar 

  25. Scriver, C.R., Prevost, L., Hurtubise, M., et al., PAHdb. http://www.pahdb.mcgill.ca/.

  26. Gundorova, P., Stepanova, A.A., Bushueva, T.V., et al., Genotyping of patients with phenylketonuria from different regions of Russia for determining BH4 responsiveness, Russ. J. Genet., 2017, vol. 53, no. 6, pp. 712–718. doi 10.1134/S1022795417060060

    Article  CAS  Google Scholar 

  27. Moradi, K., Alibakhshi, R., Ghadiri, K., et al., Molecular analysis of exons 6 and 7 of phenylalanine hydroxylase gene mutations in phenylketonuria patients in Western Iran, Indian J. Hum. Genet., 2012, vol. 18, no. 3, pp. 290–293. doi 10.4103/0971-6866.107978

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  28. Santana da Silva, L.C., Carvalho, T.S., da Silva, F.B., et al., Molecular characterization of phenylketonuria in South Brazil, Mol. Genet. Metab., 2003, vol. 79, no. 1, pp. 17–24.

    Article  CAS  Google Scholar 

  29. Song, L., Dang, L., Meng, Y., and Fu, B., Mutation spectrum of phenylalanine hydroxylase gene in patients with phenylketonuria in Tianjin and surrounding areas of Northern China, Chin. J. Med. Genet., 2010, vol. 27, no. 1, pp. 7–12. doi 10.3760/cma.j.issn.1003-9406. 2010.01.002

    CAS  Google Scholar 

  30. Rivera, I., Leandro, P., Lichter-Konecki, U., et al., Population genetics of hyperphenylalaninaemia resulting from phenylalanine hydroxylase deficiency in Portugal, J. Med. Genet., 1998, vol. 35, no. 4, pp. 301–304.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  31. Wang, T., Okano, Y., Eisensmith, R.C., et al., Founder effect of a prevalent phenylketonuria mutation in the Oriental population, Proc. Natl. Acad. Sci. U.S.A., 1991, vol. 88, no. 6, pp. 2146–2150.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  32. Daniele, A., Cardillo, G., Pennino, C., et al., Molecular epidemiology of phenylalanine hydroxylase deficiency in Southern Italy: a 96% detection rate with ten novel mutations, Ann. Hum. Genet., 2007, vol. 71, no. 2, pp. 185–193.

    Article  PubMed  CAS  Google Scholar 

  33. Desviat, L.R., Perez, B., Gamez, A., et al., Genetic and phenotypic aspects of phenylalanine hydroxylase deficiency in Spain: molecular survey by regions, Eur. J. Hum. Genet., 1999, vol. 7, pp. 386–392.

    Article  PubMed  CAS  Google Scholar 

  34. Bercovich, D., Elimelech, A., Yardeni, T., et al., A mutation analysis of the phenylalanine hydroxylase (PAH) gene in the Israeli population, Ann. Hum. Genet., 2008, vol. 72, pp. 305–309.

    Article  PubMed  CAS  Google Scholar 

  35. Gundorova, P., Stepanova, A.A., Makaov, A.Kh., et al., Mutation spectrum of the PAH gene in phenylketonuria patients in the Karachay-Cherkess Republic (Russia), Russ. J. Genet., 2016, vol. 52, no. 12, pp. 1327–1335. doi 10.1134/S1022795416110041

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to R. A. Zinchenko.

Additional information

Original Russian Text © R.A. Zinchenko, A.Kh. Makaov, V.V. Kadyshev, V.A. Galkina, E.L. Dadali, M.F. Shurygina, G.I. El’chinova, L.K. Mikhailova, A.V. Marakhonov, T.A. Vasilyeva, N.V. Petrova, P. Gundorova, A.S. Tanas, V.V. Strelnikov, A.V. Polyakov, E.K. Ginter, 2018, published in Genetika, 2018, Vol. 54, No. 6, pp. 677–687.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Zinchenko, R.A., Makaov, A.K., Kadyshev, V.V. et al. Medical Genetic Study of Hereditary Diseases in Abazins of the Karachay-Cherkess Republic. Russ J Genet 54, 703–711 (2018). https://doi.org/10.1134/S1022795418060170

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S1022795418060170

Keywords

Navigation