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Association of polymorphisms KCNN2 and NOS1AP with sudden cardiac death. / Orlov, P. S.; Ivanoshchuk, D. E.; Ivanova, A. A. и др.

в: Russian Journal of Cardiology, Том 23, № 10, 01.01.2018, стр. 59-63.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Orlov, PS, Ivanoshchuk, DE, Ivanova, AA, Malyutina, SK, Novosyolov, VP, Voevoda, MI & Maximov, VN 2018, 'Association of polymorphisms KCNN2 and NOS1AP with sudden cardiac death', Russian Journal of Cardiology, Том. 23, № 10, стр. 59-63. https://doi.org/10.15829/1560-4071-2018-10-59-63

APA

Orlov, P. S., Ivanoshchuk, D. E., Ivanova, A. A., Malyutina, S. K., Novosyolov, V. P., Voevoda, M. I., & Maximov, V. N. (2018). Association of polymorphisms KCNN2 and NOS1AP with sudden cardiac death. Russian Journal of Cardiology, 23(10), 59-63. https://doi.org/10.15829/1560-4071-2018-10-59-63

Vancouver

Orlov PS, Ivanoshchuk DE, Ivanova AA, Malyutina SK, Novosyolov VP, Voevoda MI и др. Association of polymorphisms KCNN2 and NOS1AP with sudden cardiac death. Russian Journal of Cardiology. 2018 янв. 1;23(10):59-63. doi: 10.15829/1560-4071-2018-10-59-63

Author

Orlov, P. S. ; Ivanoshchuk, D. E. ; Ivanova, A. A. и др. / Association of polymorphisms KCNN2 and NOS1AP with sudden cardiac death. в: Russian Journal of Cardiology. 2018 ; Том 23, № 10. стр. 59-63.

BibTeX

@article{7cbf2bd627674eb0a4a46b6863a68b4c,
title = "Association of polymorphisms KCNN2 and NOS1AP with sudden cardiac death",
abstract = "Aim. Assessment of the associations of mononucleotide polymorphisms (MNP) of genes: KCNN2 (rs13184658, rs10076582, rs338625) and NOS1AP (rs12567209, rs348624, rs3751284, rs12143842), with sudden cardiac death (SCD), and evaluation of the clutch units. Material and methods. The study designed as a case-control. Group of males, died SCD (n=278) was formed according with the European Cardiology Society criteria. The controls (n=274), matched by age and gender, was collected from DNA of international research projects MONICA and HAPIEE. Genomic sequencing was done with real time PCR. For inequation assessment of the clutch groups within the MNP pairs, the D{\textquoteright} coefficient was in use. Comparison of the groups by the rates of genotypes and alleles was done with a contingency tables and Chi-square by Pearson. Relative SCD risk was calculated as an odds ratio with Fischer criteria and Chi-square. The differences were noted as significant with p<0,05. Results. For the assessed MNPs gene NOS1AP the following significant differences in genotypes frequencies were found: rs12567209 GG vs AA+AG OR =1,76 (CI 1,07-2,9) p=0,026, rs3751284 CC vs CC+TT OR =0,68 (CI 0,47-0,97) p=0,037, rs12143842 CC vs CT+TT OR =0,54 (CI 0,38-0,75) p=0,0004. For alleles of the gene NOS1AP the following significant differences were found: rs12567209 A vs G OR =0,58 (CI 0,36-0,93) p=0,025 and rs12143842 С vs T OR =0,6 (CI 0,46-0,79) p=0,0004. In further assessment it was shown that the loci rs12143842 and rs12567209 are clutched (D{\textquoteright} =1). In evaluation of the clutch block for rs12143842 and rs12567209 the following was found: TG vs CG+CA OR =1,64 (CI 1,25-2,16) p=0,0004. Conclusion. MNPs (rs13184658, rs10076582, rs33862) of the gene KCNN2 and rs348624 gene NOS1AP, probably, does not play role in SCD in Novosibirsk population. rs12143842, rs12567209 and rs3751284 NOS1AP are associated with SCD. Further studies needed to assess rs12143842 and rs3751284 of gene NOS1AP, as the rs12567209 is clutched with rs12143842.",
keywords = "KCNN2, MNP, NOS1AP, rs10076582, rs12143842, rs12567209, rs13184658, rs338625, rs348624, rs3751284, Sudden cardiac death",
author = "Orlov, {P. S.} and Ivanoshchuk, {D. E.} and Ivanova, {A. A.} and Malyutina, {S. K.} and Novosyolov, {V. P.} and Voevoda, {M. I.} and Maximov, {V. N.}",
note = "Publisher Copyright: {\textcopyright} Russian Journal of Cardiology.",
year = "2018",
month = jan,
day = "1",
doi = "10.15829/1560-4071-2018-10-59-63",
language = "English",
volume = "23",
pages = "59--63",
journal = "Российский кардиологический журнал",
issn = "1560-4071",
publisher = "Russian Society of Cardiology",
number = "10",

}

RIS

TY - JOUR

T1 - Association of polymorphisms KCNN2 and NOS1AP with sudden cardiac death

AU - Orlov, P. S.

AU - Ivanoshchuk, D. E.

AU - Ivanova, A. A.

AU - Malyutina, S. K.

AU - Novosyolov, V. P.

AU - Voevoda, M. I.

AU - Maximov, V. N.

N1 - Publisher Copyright: © Russian Journal of Cardiology.

PY - 2018/1/1

Y1 - 2018/1/1

N2 - Aim. Assessment of the associations of mononucleotide polymorphisms (MNP) of genes: KCNN2 (rs13184658, rs10076582, rs338625) and NOS1AP (rs12567209, rs348624, rs3751284, rs12143842), with sudden cardiac death (SCD), and evaluation of the clutch units. Material and methods. The study designed as a case-control. Group of males, died SCD (n=278) was formed according with the European Cardiology Society criteria. The controls (n=274), matched by age and gender, was collected from DNA of international research projects MONICA and HAPIEE. Genomic sequencing was done with real time PCR. For inequation assessment of the clutch groups within the MNP pairs, the D’ coefficient was in use. Comparison of the groups by the rates of genotypes and alleles was done with a contingency tables and Chi-square by Pearson. Relative SCD risk was calculated as an odds ratio with Fischer criteria and Chi-square. The differences were noted as significant with p<0,05. Results. For the assessed MNPs gene NOS1AP the following significant differences in genotypes frequencies were found: rs12567209 GG vs AA+AG OR =1,76 (CI 1,07-2,9) p=0,026, rs3751284 CC vs CC+TT OR =0,68 (CI 0,47-0,97) p=0,037, rs12143842 CC vs CT+TT OR =0,54 (CI 0,38-0,75) p=0,0004. For alleles of the gene NOS1AP the following significant differences were found: rs12567209 A vs G OR =0,58 (CI 0,36-0,93) p=0,025 and rs12143842 С vs T OR =0,6 (CI 0,46-0,79) p=0,0004. In further assessment it was shown that the loci rs12143842 and rs12567209 are clutched (D’ =1). In evaluation of the clutch block for rs12143842 and rs12567209 the following was found: TG vs CG+CA OR =1,64 (CI 1,25-2,16) p=0,0004. Conclusion. MNPs (rs13184658, rs10076582, rs33862) of the gene KCNN2 and rs348624 gene NOS1AP, probably, does not play role in SCD in Novosibirsk population. rs12143842, rs12567209 and rs3751284 NOS1AP are associated with SCD. Further studies needed to assess rs12143842 and rs3751284 of gene NOS1AP, as the rs12567209 is clutched with rs12143842.

AB - Aim. Assessment of the associations of mononucleotide polymorphisms (MNP) of genes: KCNN2 (rs13184658, rs10076582, rs338625) and NOS1AP (rs12567209, rs348624, rs3751284, rs12143842), with sudden cardiac death (SCD), and evaluation of the clutch units. Material and methods. The study designed as a case-control. Group of males, died SCD (n=278) was formed according with the European Cardiology Society criteria. The controls (n=274), matched by age and gender, was collected from DNA of international research projects MONICA and HAPIEE. Genomic sequencing was done with real time PCR. For inequation assessment of the clutch groups within the MNP pairs, the D’ coefficient was in use. Comparison of the groups by the rates of genotypes and alleles was done with a contingency tables and Chi-square by Pearson. Relative SCD risk was calculated as an odds ratio with Fischer criteria and Chi-square. The differences were noted as significant with p<0,05. Results. For the assessed MNPs gene NOS1AP the following significant differences in genotypes frequencies were found: rs12567209 GG vs AA+AG OR =1,76 (CI 1,07-2,9) p=0,026, rs3751284 CC vs CC+TT OR =0,68 (CI 0,47-0,97) p=0,037, rs12143842 CC vs CT+TT OR =0,54 (CI 0,38-0,75) p=0,0004. For alleles of the gene NOS1AP the following significant differences were found: rs12567209 A vs G OR =0,58 (CI 0,36-0,93) p=0,025 and rs12143842 С vs T OR =0,6 (CI 0,46-0,79) p=0,0004. In further assessment it was shown that the loci rs12143842 and rs12567209 are clutched (D’ =1). In evaluation of the clutch block for rs12143842 and rs12567209 the following was found: TG vs CG+CA OR =1,64 (CI 1,25-2,16) p=0,0004. Conclusion. MNPs (rs13184658, rs10076582, rs33862) of the gene KCNN2 and rs348624 gene NOS1AP, probably, does not play role in SCD in Novosibirsk population. rs12143842, rs12567209 and rs3751284 NOS1AP are associated with SCD. Further studies needed to assess rs12143842 and rs3751284 of gene NOS1AP, as the rs12567209 is clutched with rs12143842.

KW - KCNN2

KW - MNP

KW - NOS1AP

KW - rs10076582

KW - rs12143842

KW - rs12567209

KW - rs13184658

KW - rs338625

KW - rs348624

KW - rs3751284

KW - Sudden cardiac death

UR - http://www.scopus.com/inward/record.url?scp=85057263000&partnerID=8YFLogxK

U2 - 10.15829/1560-4071-2018-10-59-63

DO - 10.15829/1560-4071-2018-10-59-63

M3 - Article

AN - SCOPUS:85057263000

VL - 23

SP - 59

EP - 63

JO - Российский кардиологический журнал

JF - Российский кардиологический журнал

SN - 1560-4071

IS - 10

ER -

ID: 17554239