SIRT1 allele frequencies in depressed patients of European descent in Russia

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

Research output: Contribution to journalArticle

1 Citation (Scopus)

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.

Original languageEnglish
JournalFrontiers in Genetics
Volume10
Issue numberJAN
DOIs
Publication statusPublished - 1 Jan 2019

Fingerprint

Russia
Depressive Disorder
Gene Frequency
Single Nucleotide Polymorphism
Population
Genes
Inborn Genetic Diseases
Genome-Wide Association Study
Homozygote
Heterozygote
Mental Disorders
Alleles
DNA

Keywords

  • Depressive disorders
  • European descent
  • Population
  • SIRT1 gene
  • SNP

ASJC Scopus subject areas

  • Molecular Medicine
  • Genetics
  • Genetics(clinical)

Cite this

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

SIRT1 allele frequencies in depressed patients of European descent in Russia. / Aftanas, Lyubomir I.; Anisimenko, Maksim S.; Berdyugina, Darya A.; Garanin, Aleksandr Yu; Maximov, Vladimir N.; Voevoda, Mikhail I.; Vyalova, Natalya M.; Bokhan, Nikolay A.; Ivanova, Svetlana A.; Danilenko, Konstantin V.; Kovalenko, Sergei P.

In: Frontiers in Genetics, Vol. 10, No. JAN, 01.01.2019.

Research output: Contribution to journalArticle

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. https://doi.org/10.3389/fgene.2018.00686
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 Jan 1;10(JAN). https://doi.org/10.3389/fgene.2018.00686
Aftanas, Lyubomir I. ; Anisimenko, Maksim S. ; Berdyugina, Darya A. ; Garanin, Aleksandr Yu ; Maximov, Vladimir N. ; Voevoda, Mikhail I. ; Vyalova, Natalya M. ; Bokhan, Nikolay A. ; Ivanova, Svetlana A. ; Danilenko, Konstantin V. ; Kovalenko, Sergei P. / SIRT1 allele frequencies in depressed patients of European descent in Russia. In: Frontiers in Genetics. 2019 ; Vol. 10, No. JAN.
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AU - Ivanova, Svetlana A.

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