SIRT1 allele frequencies in depressed patients of European descent in Russia

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SIRT1 allele frequencies in depressed patients of European descent in Russia. / Aftanas, Lyubomir I.; Anisimenko, Maksim S.; Berdyugina, Darya A. et al.

In: Frontiers in Genetics, Vol. 10, No. JAN, 686, 2019.

Research output: Contribution to journal › Article › peer-review

Harvard

Aftanas, LI, Anisimenko, MS, Berdyugina, DA, Garanin, AY, Maximov, VN, Voevoda, MI, Vyalova, NM, Bokhan, NA, Ivanova, SA, Danilenko, KV & Kovalenko, SP 2019, 'SIRT1 allele frequencies in depressed patients of European descent in Russia', Frontiers in Genetics, vol. 10, no. JAN, 686. https://doi.org/10.3389/fgene.2018.00686

APA

Aftanas, L. I., Anisimenko, M. S., Berdyugina, D. A., Garanin, A. Y., Maximov, V. N., Voevoda, M. I., Vyalova, N. M., Bokhan, N. A., Ivanova, S. A., Danilenko, K. V., & Kovalenko, S. P. (2019). SIRT1 allele frequencies in depressed patients of European descent in Russia. Frontiers in Genetics, 10(JAN), [686]. https://doi.org/10.3389/fgene.2018.00686

Vancouver

Aftanas LI, Anisimenko MS, Berdyugina DA, Garanin AY, Maximov VN, Voevoda MI et al. SIRT1 allele frequencies in depressed patients of European descent in Russia. Frontiers in Genetics. 2019;10(JAN):686. doi: 10.3389/fgene.2018.00686

Author

Aftanas, Lyubomir I. ; Anisimenko, Maksim S. ; Berdyugina, Darya A. et al. / SIRT1 allele frequencies in depressed patients of European descent in Russia. In: Frontiers in Genetics. 2019 ; Vol. 10, No. JAN.

BibTeX

@article{071e5b72868f4828b6811add007d19b7,

title = "SIRT1 allele frequencies in depressed patients of European descent in Russia",

abstract = "Depressive disorder (DD) is a widespread mental disorder. Although DD is to some extent inherited, the genes contributing to the risk of this disorder and its genetic mechanisms remain poorly understood. A recent large-scale genome-wide association Chinese study revealed a strong association between the SIRT1 gene variants and DD. The aim of this study was to analyze the occurrence of heterozygote carriers and search for rare SNP variants of the SIRT1 gene in a cohort of DD patients as compared with a cohort of randomly selected members of the Russian population. The complete coding sequences of the SIRT1 gene from 1024 DNA samples from the general Russian population and from 244 samples from patients with DD were analyzed using targeted sequencing. Four new genetic variants of the SIRT1 were discovered. While no significant differences in the allele frequencies were found between the DD patients and the general population, differences between the frequencies of homozygote carriers of specific alleles and occurrences of heterozygous were found to be significant for rs2236318 (P < 0.0001), and putatively, rs7896005 (P < 0.05), and rs36107781 (P < 0.05). The study found for the first time that two new SNPs (i.e., 10:69665829 and 10:69665971) along with recently reported ones (rs773025707 and rs34701705), are putatively associated with DD. The revealed DD-associated SIRT1 SNPs might confer susceptibility to this disorder in Russian population of European descent.",

keywords = "Depressive disorders, European descent, Population, SIRT1 gene, SNP",

author = "Aftanas, {Lyubomir I.} and Anisimenko, {Maksim S.} and Berdyugina, {Darya A.} and Garanin, {Aleksandr Yu} and Maximov, {Vladimir N.} and Voevoda, {Mikhail I.} and Vyalova, {Natalya M.} and Bokhan, {Nikolay A.} and Ivanova, {Svetlana A.} and Danilenko, {Konstantin V.} and Kovalenko, {Sergei P.}",

year = "2019",

doi = "10.3389/fgene.2018.00686",

language = "English",

volume = "10",

journal = "Frontiers in Genetics",

issn = "1664-8021",

publisher = "Frontiers Media S.A.",

number = "JAN",

}

RIS

TY - JOUR

T1 - SIRT1 allele frequencies in depressed patients of European descent in Russia

AU - Aftanas, Lyubomir I.

AU - Anisimenko, Maksim S.

AU - Berdyugina, Darya A.

AU - Garanin, Aleksandr Yu

AU - Maximov, Vladimir N.

AU - Voevoda, Mikhail I.

AU - Vyalova, Natalya M.

AU - Bokhan, Nikolay A.

AU - Ivanova, Svetlana A.

AU - Danilenko, Konstantin V.

AU - Kovalenko, Sergei P.

PY - 2019

Y1 - 2019

N2 - Depressive disorder (DD) is a widespread mental disorder. Although DD is to some extent inherited, the genes contributing to the risk of this disorder and its genetic mechanisms remain poorly understood. A recent large-scale genome-wide association Chinese study revealed a strong association between the SIRT1 gene variants and DD. The aim of this study was to analyze the occurrence of heterozygote carriers and search for rare SNP variants of the SIRT1 gene in a cohort of DD patients as compared with a cohort of randomly selected members of the Russian population. The complete coding sequences of the SIRT1 gene from 1024 DNA samples from the general Russian population and from 244 samples from patients with DD were analyzed using targeted sequencing. Four new genetic variants of the SIRT1 were discovered. While no significant differences in the allele frequencies were found between the DD patients and the general population, differences between the frequencies of homozygote carriers of specific alleles and occurrences of heterozygous were found to be significant for rs2236318 (P < 0.0001), and putatively, rs7896005 (P < 0.05), and rs36107781 (P < 0.05). The study found for the first time that two new SNPs (i.e., 10:69665829 and 10:69665971) along with recently reported ones (rs773025707 and rs34701705), are putatively associated with DD. The revealed DD-associated SIRT1 SNPs might confer susceptibility to this disorder in Russian population of European descent.

AB - Depressive disorder (DD) is a widespread mental disorder. Although DD is to some extent inherited, the genes contributing to the risk of this disorder and its genetic mechanisms remain poorly understood. A recent large-scale genome-wide association Chinese study revealed a strong association between the SIRT1 gene variants and DD. The aim of this study was to analyze the occurrence of heterozygote carriers and search for rare SNP variants of the SIRT1 gene in a cohort of DD patients as compared with a cohort of randomly selected members of the Russian population. The complete coding sequences of the SIRT1 gene from 1024 DNA samples from the general Russian population and from 244 samples from patients with DD were analyzed using targeted sequencing. Four new genetic variants of the SIRT1 were discovered. While no significant differences in the allele frequencies were found between the DD patients and the general population, differences between the frequencies of homozygote carriers of specific alleles and occurrences of heterozygous were found to be significant for rs2236318 (P < 0.0001), and putatively, rs7896005 (P < 0.05), and rs36107781 (P < 0.05). The study found for the first time that two new SNPs (i.e., 10:69665829 and 10:69665971) along with recently reported ones (rs773025707 and rs34701705), are putatively associated with DD. The revealed DD-associated SIRT1 SNPs might confer susceptibility to this disorder in Russian population of European descent.

KW - Depressive disorders

KW - European descent

KW - Population

KW - SIRT1 gene

KW - SNP

UR - http://www.scopus.com/inward/record.url?scp=85064139543&partnerID=8YFLogxK

U2 - 10.3389/fgene.2018.00686

DO - 10.3389/fgene.2018.00686

M3 - Article

C2 - 30662452

AN - SCOPUS:85064139543

VL - 10

JO - Frontiers in Genetics

JF - Frontiers in Genetics

SN - 1664-8021

IS - JAN

M1 - 686

ER -

ID: 26147417