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:C0038454 (
stroke
)
147,016
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Sequence variations in genes involved in inflammation system are known to contribute to the risk of cardiovascular diseases (CVD) including
stroke
. In this study, we performed a genetic association study on the single nucleotide polymorphisms (SNPs) present in the genes CD14 (-159 C/T), TNFalpha (-308 G/A), IL-1alpha (-889 C/T), IL-6 (-174 G/C),
PSMA6
(-8 C/G), and PDE4D (SNP83 T/C, respectively) in order to discern their possible role in the susceptibility to
stroke
in a North Indian population. These SNPs were previously found to be associated with CVD through their contribution to inflammation. A case-control design was used to examine 176
stroke
patients (112 ischemic and 64 hemorrhagic
stroke
patients) and 212 unrelated healthy control individuals. After adjustment for the confounding risk factors, the IL-1alpha -889 T allele carriers (TT+CT) were found to be strongly associated with both forms of
stroke
(OR=2.56; 95% CI=1.53-4.29; P=0.0004). The CC genotype of PDE4D was found to be associated only with ischemic
stroke
(OR=2.02; 95% CI=1.08-3.76; P=0.03). None of the variants tested for the CD14, TNFalpha, IL-6, and
PSMA6
genes found to confer risk for
stroke
in the study population. In conclusion, the -889 C/T and SNP83 T/C SNPs of the IL-1alpha and PDE4D genes, respectively, appear to be genetic risk factors for
stroke
in our study population.
...
PMID:Inflammatory system gene polymorphism and the risk of stroke: a case-control study in an Indian population. 1815 10
Frequency of allelic variants of proteasome subunits genes LMP2 (Arg60 --> His) and
PSMA6
were determined in patients with ischemic
stroke
using real-time PCR. Allelic variants of
PSMA6
were disposed in the next manner: C/C - 80.2%, C/G - 19.8%, G/G--were not (in control) and C/C - 75.5%, C/G - 21.4%, G/G - 3.1% (P = 0.22) in patients with IS. It was shown that distribution of LMP2 allelic variants was the following: Arg/Arg - 53.3%, Arg/His - 43.5%, His/His - 6.7% in control and Arg/Arg - 55.9%, Arg/His - 34.3%, His/His - 9.8% in IS group (P > 0.05). The data show that LMP2 and
PSMA6
gene polymorphism is not a risk factor of ischemic
stroke
in Ukrainian population.
...
PMID:[Frequency of allele polymorphism of immune proteasome catalytic subunits in patients with ischemic stroke]. 2480 74