Key result
Pharmacogenomics-guided therapy linked to ~14.6-fold higher odds of blood pressure control on CCBs.
Why the study?
The association of rs776746 with short-term blood pressure outcomes among Chinese patients with hypertension receiving CCB-containing regimens was not well characterized.
Does a pharmacogenomics-guided treatment strategy improve short-term blood pressure control in Chinese patients with hypertension receiving CCB-containing regimens?
Observational (n=5,026)
Open-label (Hunan) and Single-blind (Fujian) in parent cohorts
Yes
Does a pharmacogenomics-guided treatment strategy improve short-term blood pressure control in Chinese patients with hypertension receiving CCB-containing regimens?
Odds Ratio: 14.56 (95% CI 12.49–16.96)
Absolute Event Rate: 81.83% vs 25.07%
Absolute Risk Reduction: 56.76%
p-value: p=<0.001
A pharmacogenomics-guided strategy targeting calcium channel blocker metabolism and response pathways may significantly improve short-term blood pressure control compared to conventional empirical therapy.
Supports genotype-guided BP control in Chinese CCB users; leaves open need for RCT confirmation before practice change.
Introduction: rs776746 with short-term blood pressure (BP) outcomes among Chinese patients with hypertension receiving CCB-containing regimens. Methods: This secondary exploratory analysis included patients receiving CCB-containing regimens from two previously completed multicenter randomized cohorts conducted in Hunan and Fujian provinces, China. The Hunan cohort assessed a 4-week PGx-guided strategy combined with structured management, while the Fujian cohort evaluated genotype-guided treatment during 4-8 weeks after an initial standardized management phase. The primary endpoint was BP control at the last follow-up; secondary endpoints included changes in systolic BP (SBP) and diastolic BP (DBP), medication use, and short-term safety outcomes. Multivariable regression models were used to adjust for prespecified clinical covariates. Results: A total of 4608 patients in Hunan and 418 patients in Fujian were included. In the Hunan cohort, the genotype-guided group had higher 4‑week BP control (81.83% vs 25.07%; adjusted OR = 14.56, P < 0.001) and greater SBP/DBP decreases. In the Fujian cohort, genotype-guided therapy was associated with higher 8‑week BP control (81.74% vs 77.39%; adjusted OR = 2.43, P = 0.003) and greater DBP decrease. Associations were stronger among patients whose BP remained uncontrolled after standardized management. No short-term safety concerns were identified. Conclusion: rs776746, was associated with improved short-term BP control among Chinese patients with hypertension receiving CCB-containing regimens, without an apparent short-term safety disadvantage. However, these findings should be interpreted as exploratory associations rather than proof of causal benefit. Further prospective randomized studies are needed to confirm these findings.
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Deng et al. (2026) conducted an observational in Hypertension (n=5,026). Pharmacogenomics-guided antihypertensive strategy (integrating CACNA1C rs2238032 and CYP3A5 rs776746) vs. Standard empirical antihypertensive therapy was evaluated on Blood pressure control (SBP <140 mmHg and DBP <90 mmHg) at the 4-week follow-up (Hunan cohort) (adjusted OR 14.56, 95% CI 12.49-16.96, p=<0.001). A pharmacogenomics-guided antihypertensive strategy significantly improved short-term blood pressure control compared to standard care in Chinese patients on calcium channel blockers (adjusted OR 14.56).
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