Key result
The CYP2C9 rs2860905 AA genotype did not significantly increase the risk of non-responsiveness to losartan compared to the GG genotype (OR 1.99, p=0.48).
Why the study?
Genetic variations in CYP2C9 affect losartan metabolism and response, prompting an evaluation of the effect of the CYP2C9 rs2860905 G>A polymorphism on losartan efficacy.
Does the CYP2C9 rs2860905 G>A polymorphism affect the blood pressure lowering efficacy of losartan in hypertensive patients?
Observational (n=48)
Yes
Does the CYP2C9 rs2860905 G>A polymorphism affect the blood pressure lowering efficacy of losartan in hypertensive patients?
Odds Ratio: 1.99 (95% CI 0.3–13.1)
p-value: p=0.48
The CYP2C9 rs2860905 G>A polymorphism does not significantly affect the blood pressure lowering efficacy of losartan in Pakistani hypertensive patients, though a non-significant trend towards better response was seen with the GG genotype.
May inform personalized losartan dosing via genetic variants; leaves open clinical utility pending validation trials.
Hypertension is a multifactorial disease characterized by high blood pressure in blood vessels. It is caused by the dysregulation of renin angiotensin aldosterone system (RAAS). It is a major risk factor for other metabolic diseases including cardiovascular diseases, diabetes, and others. Various RAAS targeting drugs such as losartan are prescribed as the first line therapy to treat hypertension. However, their efficacy varies among individuals owing to genetic variations in drug binding substrates or drug metabolizing enzymes, which convert the prodrug to active drug. CYP2C9 gene encodes for an enzyme which metabolizes losartan. Various studies have concluded that genetic variations in CYP2C9 affect the response of losartan due to the variation in its metabolism. Thus, the current study aimed to check the effect of CYP2C9 rs2860905 G>A polymorphism on the efficacy of losartan. For this purpose, a total of 48 subjects were selected and genotyped for rs2860905 polymorphism using in-house developed tetra-ARMS-PCR. The subjects were divided into responding (n=34) and non-responding (n=14) groups on the basis of their blood pressure after treatment with losartan. Statistical analysis demonstrated that rs2860905 GG genotype was more prevalent in the responding group as compared to the non-responding group (50% vs. 36%). Multinomial regression analysis showed that the carriers of GA or AA genotype did not respond to losartan treatment efficiently as compared to those of GG genotype. However, these results could not achieve statistical significance. To conclude, CYP2C9 rs2860905 G>A polymorphism does not affect the efficacy of losartan in Pakistani hypertensive subjects.
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Haider et al. (2023) conducted an observational in Hypertension (n=48). CYP2C9 rs2860905 AA genotype vs. CYP2C9 rs2860905 GG genotype was evaluated on Non-responsiveness to losartan therapy (OR 1.99, 95% CI 0.30-13.1, p=0.48). The CYP2C9 rs2860905 AA genotype did not significantly increase the risk of non-responsiveness to losartan compared to the GG genotype (OR 1.99, p=0.48).
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