TY - JOUR
T1 - Beta 1, Beta 2 and Beta 3 Adrenergic Receptor Gene Polymorphisms in a Southeastern European Population
AU - Katsarou, Martha Spyridoula
AU - Karathanasopoulou, Aikaterini
AU - Andrianopoulou, Angeliki
AU - Desiniotis, Vasileios
AU - Tzinis, Efthymios
AU - Dimitrakis, Efthimios
AU - Lagiou, Maria
AU - Charmandari, Evangelia
AU - Aschner, Michael
AU - Tsatsakis, Aristeidis M.
AU - Chrousos, George P.
AU - Drakoulis, Nikolaos
N1 - Funding Information:
We would like to thank EMK Genomed Group for providing anonymized samples of general population.
Publisher Copyright:
© Copyright © 2018 Katsarou, Karathanasopoulou, Andrianopoulou, Desiniotis, Tzinis, Dimitrakis, Lagiou, Charmandari, Aschner, Tsatsakis, Chrousos and Drakoulis.
PY - 2018/11/28
Y1 - 2018/11/28
N2 - Genetic polymorphisms in β1-, β2- and β3-adrenergic receptors (β-ARs) have been associated with chronic non-communicable disorders, such as cardiovascular diseases, asthma, chronic obstructive pulmonary disease (COPD) and obesity, as well as β-agonists and antagonists response and toxicity. The purpose of this study was to determine the frequency distribution of ADRB1 genetic variants Ser49Gly and Arg389Gly, ADRB2 variants Gly16Arg and Gln27Glu, ADRB3 variant Trp64Arg in a Southeastern European Caucasian (SEC) population sample and to establish a comparison with existing data from other human populations. A sample of 431 men and 590 women volunteered to participate in this genotyping analysis after anonymization and de-identification. Real Time PCR (Melting Curve Analysis) followed DNA extraction from buccal swabs and statistical analysis of the results was performed. The allele frequencies in the SEC population were Ser49 (90.3%), Arg389 (69.49%), Gly16 (61.61%), Gln27 (65.72%), and Trp64 (94.52%), while a Hardy-Weinberg Equilibrium (HWE) was detected in the population studied. Comparisons for the Ser49Gly, Gln27Glu, and Trp64Arg allele distributions demonstrated significant differences between SEC and the European group. European subgroups comparisons showed that allele distributions were similar for four of the five SNPs between SEC and Southwestern European Caucasians (SWC), while they were quite distinct from the Northwestern European Caucasians (NWC). These data underline the importance of interethnic variability of β-ARs genetic polymorphisms.
AB - Genetic polymorphisms in β1-, β2- and β3-adrenergic receptors (β-ARs) have been associated with chronic non-communicable disorders, such as cardiovascular diseases, asthma, chronic obstructive pulmonary disease (COPD) and obesity, as well as β-agonists and antagonists response and toxicity. The purpose of this study was to determine the frequency distribution of ADRB1 genetic variants Ser49Gly and Arg389Gly, ADRB2 variants Gly16Arg and Gln27Glu, ADRB3 variant Trp64Arg in a Southeastern European Caucasian (SEC) population sample and to establish a comparison with existing data from other human populations. A sample of 431 men and 590 women volunteered to participate in this genotyping analysis after anonymization and de-identification. Real Time PCR (Melting Curve Analysis) followed DNA extraction from buccal swabs and statistical analysis of the results was performed. The allele frequencies in the SEC population were Ser49 (90.3%), Arg389 (69.49%), Gly16 (61.61%), Gln27 (65.72%), and Trp64 (94.52%), while a Hardy-Weinberg Equilibrium (HWE) was detected in the population studied. Comparisons for the Ser49Gly, Gln27Glu, and Trp64Arg allele distributions demonstrated significant differences between SEC and the European group. European subgroups comparisons showed that allele distributions were similar for four of the five SNPs between SEC and Southwestern European Caucasians (SWC), while they were quite distinct from the Northwestern European Caucasians (NWC). These data underline the importance of interethnic variability of β-ARs genetic polymorphisms.
KW - Arg389Gly
KW - Gln27Glu
KW - Gly16Arg
KW - Ser49Gly
KW - Trp64Arg
KW - personalized medicine
KW - pharmacogenomics
KW - single nucleotide polymorphisms
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U2 - 10.3389/fgene.2018.00560
DO - 10.3389/fgene.2018.00560
M3 - Article
AN - SCOPUS:85066790656
SN - 1664-8021
VL - 9
JO - Frontiers in Genetics
JF - Frontiers in Genetics
M1 - 560
ER -