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1.
Am J Phys Anthropol ; 147(1): 30-4, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21989907

RESUMO

The rs9939609 SNP located in the first intron of the fat mass and obesity associated gene (FTO) has been found to be associated with common obesity mainly in populations of European descent. The Roma/Gypsy population as an ethnic minority of Asian Indian origin is well known for its adverse health status with a high prevalence of obesity. The main aim of this study was to examine the contribution of the rs9939609 FTO polymorphism to the high prevalence of obesity in the Roma/Gypsy population. Following a number of anthropometric measurements, the FTO rs9939609 polymorphism was genotyped in 312 Roma/Gypsy individuals. We observed significant differences in body mass index (BMI), waist circumference, and waist-to-hip ratio between different genotypes (P = 0.003, P = 0.012, and P = 0.03, respectively). The waist circumference in the subjects with AA genotype was about 7.1 cm larger than in those with TT genotypes (P = 0.005). However, the strongest association of minor allele A of the rs9939609 FTO polymorphism was found with BMI (odds ratio, 1.55; 95% confidence interval, 1.129-2.128; P = 0.007), even after adjusting for age, sex, and smoking status. This study provides the first report of allele and genotype frequencies for the rs9939609 polymorphism and also the first evidence of the association of the FTO variant with obesity in the Roma/Gypsy population.


Assuntos
Obesidade/genética , Proteínas/genética , Roma (Grupo Étnico)/genética , Adulto , Idoso , Dioxigenase FTO Dependente de alfa-Cetoglutarato , Índice de Massa Corporal , Feminino , Predisposição Genética para Doença , Genótipo , Humanos , Masculino , Pessoa de Meia-Idade , Epidemiologia Molecular , Obesidade/epidemiologia , Obesidade/etnologia , Razão de Chances , Polimorfismo de Nucleotídeo Único , Roma (Grupo Étnico)/estatística & dados numéricos , Eslováquia/epidemiologia , Estatísticas não Paramétricas , Circunferência da Cintura , Relação Cintura-Quadril
2.
Forensic Sci Int Genet ; 5(3): e53-62, 2011 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20837407

RESUMO

Haplotype data of 11 Y-STR loci (DYS391, DYS389I, DYS439, DYS389II, DYS438, DYS437, DYS19, DYS392, DYS393, DYS390 and DYS385) was obtained from 629 Slovak Caucasian men living in Eastern Slovakia. A total of 474 haplotypes were identified, of which 395 were unique. The haplotype diversity value was 0.9982. Pairwise haplotype distances showed that the Eastern Slovak Caucasian population is not significantly different from the Slavs populations and is separated from the Balkan nations and the German speaking populations.


Assuntos
Cromossomos Humanos Y , Frequência do Gene , Genética Populacional , Repetições de Microssatélites/genética , Haplótipos , Humanos , Masculino , Eslováquia
3.
Anthropol Anz ; 68(2): 111-27, 2010.
Artigo em Inglês | MEDLINE | ID: mdl-21452677

RESUMO

Eleven Y-chromosomal microsatellite loci included in the Powerplex Y multiplex kit were analyzed in different Slovak population samples: Habans (n = 39), Romanies (n = 100) and Slovak Caucasian (n = 148) individuals, respectively, from different regions of Slovakia. The analysis of molecular variance between populations indicated that 89.27% of the haplotypic variations were found within populations and only 10.72% between populations (Fst = 0.1027; p = 0.0000). The haplotype diversities were ranging from 0.9258 to 0.9978, and indicated a high potential for differentiating between male individuals. The study reports differences in allele frequencies between the Romanies, Habans and Slovak Caucasian men. Selected loci showed that both the Romany and Haban population belonged to endogamous and relatively small founder population groups, which developed in relatively reproductive isolated groups surrounded by the Slovak Caucasian population.


Assuntos
Cromossomos Humanos Y , Repetições de Microssatélites , Grupos Raciais/genética , Análise de Variância , Loci Gênicos , Haplótipos , Humanos , Masculino , Epidemiologia Molecular , Polimorfismo de Nucleotídeo Único , Eslováquia
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