HLA-DRB1* ASSOCIATIONS WITH SPORADIC SEPTAL CONGENITAL HEART DISEASES WITHOUT CHROMOSOMAL DISEASES

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Abstract

Associations of HLA-DRB1* alleles were determined with sporadic septal congenital heart defects in children. 97 children (44 boys and 53 girls) with an isolated ventricular septal defect (VSD) without chromosomal diseases and anomalies were examined. Surveyed 132 healthy children (control group). The frequency of occurrence of 14 alleles of the HLA-DRB1 gene (01, 04, 07, 08, 09, 10, 11, 12, 13, 14, 15, 16, 17, 18). Mathematical processing was performed using the STATISTICA 8.0 application package (StatSoftInc., USA). It was revealed that in children with sporadic CHD without chromosomal diseases, HLA-DRB1*15 (p = 0.03) was signifi cantly more frequent in the genotype compared with the control group. The formation of sporadic septal congenital heart defects without chromosomal diseases is positively associated with HLA-DRB1*15.

About the authors

A. V. Tsepokina

Federal state budgetary scientific institution “Research Institute of complex problems of cardiovascular diseases”

Author for correspondence.
Email: fake@neicon.ru

junior researcher of the laboratory of genomic medicine,

Moscow

Russian Federation

N. S. Deev

Federal state budgetary scientific institution “Research Institute of complex problems of cardiovascular diseases”;
Federal state budgetary educational institution of higher education “Kemerovo state medical University” of the Ministry of health of the Russian Federation

Email: fake@neicon.ru

laboratory assistant-researcher of the laboratory of cellular technologies,

Moscow

Russian Federation

S. A. Shmulevich

State budgetary institution of health care “Kemerovo regional clinical cardiology clinic named after academician L. S. Barbarash”

Email: fake@neicon.ru

PhD, head of children’s Department,

Moscow

Russian Federation

A. V. Shabaldin

Federal state budgetary scientific institution “Research Institute of complex problems of cardiovascular diseases”;
Federal state budgetary educational institution of higher education “Kemerovo state medical University” of the Ministry of health of the Russian Federation

Email: weit2007@yandex.ru

M.D., leading researcher of laboratory of cell technologies,

Moscow

Russian Federation

A. A. Korostelev

State budgetary institution of health care “Kemerovo regional clinical cardiology clinic named after academician L. S. Barbarash”

Email: fake@neicon.ru

M.D., professor of the Department of microbiology, immunology. virology,

Moscow

Russian Federation

A. V. Ponasenko

Federal state budgetary scientific institution “Research Institute of complex problems of cardiovascular diseases”

Email: fake@neicon.ru

Ph.D., head of the Department of Genomic Medicine,

Moscow

Russian Federation

References

  1. Inada K., Shima T., Nakashima A. Characterization of regulatory T cells in decidua of miscarriage cases with abnormal or normal fetal chromosomal content. J Reprod Immunol. 2013 Mar; 97(1): 104–111. doi: 10.1016/j.jri.2012.12.001;
  2. Mjosberg J., Berg G., Jenmalm M. C., Ernerudh J. FOXP3+ regulatory T cells and T helper 1, T helper 2, and T helper 17 cells in human early pregnancy deciduas. Biol Reprod. 2010. Apr; 82(4): 698–705. doi: 10.1095/biolreprod.109.081208. Epub 2009 Dec 16.

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Copyright (c) 2019 Tsepokina A.V., Deev N.S., Shmulevich S.A., Shabaldin A.V., Korostelev A.A., Ponasenko A.V.

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This work is licensed under a Creative Commons Attribution 4.0 International License.

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