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Updated: Jul 13, 2026

A Method to Study the C924T Polymorphism of the Thromboxane A2 Receptor Gene
Published on: April 1, 2019
Angiotensinogen gene polymorphism as a risk factor for ischemic stroke.
Taizen Nakase1, Toshiki Mizuno, Sanae Harada
1Department of Neurology, Research Institute for Brain and Blood Vessels, 6-10 Senshu Kubota Machi, Akita, Japan 010-0874. nakase@akita-noken.go.jp
The angiotensinogen (AGT) M allele may increase the risk of lacunar infarction, a type of ischemic stroke, in Japanese men. This genetic risk appears independent of hypertension and other clinical factors.
Area of Science:
- Genetics
- Neurology
- Cardiovascular Science
Background:
- Gene polymorphism for angiotensinogen (AGT) is linked to blood pressure regulation and salt sensitivity.
- The association between AGT gene polymorphism and ischemic stroke risk is debated.
- AGT M235T polymorphism is a specific variant under investigation.
Purpose of the Study:
- To investigate the hypothesis that AGT gene polymorphism is a risk factor for ischemic stroke.
- To examine the relationship between AGT M235T polymorphism and different stroke subtypes.
- To assess potential synergistic effects between AGT polymorphism and clinical risk factors.
Main Methods:
- Case-control study involving 147 stroke patients and 133 healthy controls.
- Analysis of the AGT gene M235T polymorphism in all participants.
- Categorization of stroke patients into four types and two vascular groups.
Main Results:
- The AGT M allele was significantly associated with an increased risk of single lacunar, multiple lacunar, and small arterial lesions in male patients.
- Statistical significance was observed for these associations (p=0.029, 0.031, and 0.026, respectively).
- No synergistic effects were found between AGT gene polymorphism and major clinical risk factors.
Conclusions:
- The AGT M allele may represent an independent risk factor for lacunar infarctions in Japanese men.
- This genetic predisposition to lacunar stroke is not influenced by hypertension.
- Further research may elucidate the precise mechanisms linking AGT polymorphism to specific stroke types.
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