Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0085580 (
essential hypertension
)
14,686
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Objective:
Genetic factors are involved in the occurrence, development, and progression of
essential hypertension
(EH). To study the association between single nucleotide polymorphisms (SNPs) of the rs6435156 and rs1048829 loci of the bone morphogenetic protein receptor type 2 (BMPR2) gene, the rs121909287 and rs121909284 loci of the activin receptor-like kinase 1 (ACVRL1) gene, and the rs397514716 and rs121918359 loci of the mothers against decapentaplegic homolog 9 (
SMAD9
) gene with the risk of EH in the Chinese Han population.
Materials and methods
:
A total of 460 EH patients and 460 healthy controls were recruited for the study. Genomic DNA of white blood cells was extracted, and the genotypes were analyzed by Sanger sequencing after polymerase chain reaction amplification. Multi-factor dimensionality reduction (MDR) was used to analyze the effect of gene-environment interactions on EH risk.
Results:
The risk of EH increased in the
BMPR2
gene rs6435156 locus dominant model (adjusted odds ratio [OR] = 1.572, 95% confidence interval [CI]: 1.385-1.765,
P
<0.001) and recessive model (adjusted OR = 1.926, 95% CI: 1.693-2.067,
P
<0.001). The risk of EH increased in the rs1048829 recessive model (adjusted OR = 1.444, 95% CI: 1.142-1.696,
P
=0.003). The risk of EH increased in the recessive model of the
ACVRL1
gene rs121909287 locus (adjusted OR = 1.403, 95% CI: 1.101-1.660,
P
=0.008). The risk of EH increased in the
SMAD9
gene rs397514716 locus dominant model (adjusted OR = 1.370, 95% CI: 1.183-1.559,
P
<0.001) and recessive model (adjusted OR = 1.803, 95% CI: 1.470-1.983,
P
<0.001). The CG haplotype of the rs6435156 and rs1048829 loci of the
BMPR2
gene, the CC haplotype of the
ACVRL1
gene rs121909287 and rs121909284 loci, and the CC haplotype of the rs397514716 and rs121918359 loci of the
SMAD9
gene were factors that protect against EH, whereas the TT haplotype of the rs6435156 and rs1048829 loci in the
BMPR2
gene was a risk factor for EH. MDR analysis showed that the
BMPR2
gene rs6435156 locus TT genotype carriers, the
SMAD9
gene rs397514716 locus TT genotype carriers, and alcohol drinkers had the highest EH risk (OR = 4.523, 95% CI: 2.235-6.871,
P
<0.001).
Conclusion:
The SNPs of the rs6435156 and rs1048829 locus in the
BMPR2
gene, the rs121909287 loci in the
ACVRL1
gene, and the rs397514716 locus in the
SMAD9
gene were associated with a risk of EH in Han Chinese.
...
PMID:Association of the gene polymorphisms of
BMPR2, ACVRL1, SMAD9
and their interactions with the risk of essential hypertension in the Chinese Han population. 3061 53