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Association Between β1-Selective Beta-Blocker Use and P-Wave Terminal Force in Lead V1 in Hypertensive Patients With
Erkan Alpaslan1, Sedat Taş1, Ümmü Taş1
1Department of Cardiology Faculty of Medicine İzmir Demokrasi University İzmir Türkiye.
Background:
P-wave terminal force in lead V1 (PTFV1) is an electrocardiographic marker of atrial electrical abnormality. We investigated whether β1-selective beta-blocker use was associated with PTFV1 in hypertensive patients with echocardiographically confirmed left ventricular hypertrophy (LVH).
Methods:
This retrospective study included 182 eligible patients with essential hypertension and LVH selected from 1372 screened patients. Patients were classified as β1-selective beta-blocker users (n = 82) or nonusers (n = 100). Abnormal PTFV1 was defined as ≥ 0.04 mm s. Multivariable regression and sensitivity analyses were performed.
Results:
PTFV1 was lower in beta-blocker users than in nonusers (0.024 [0.015-0.036] vs. 0.030 [0.020-0.048] mm s, p = 0.005). In the primary adjusted model, beta-blocker use was associated with lower PTFV1 (B = -0.008, standardized β = -0.202, 95% CI -0.014 to -0.002, p = 0.009), although model explanatory capacity was limited (R 2 = 0.064; adjusted R 2 = 0.021; overall p = 0.168). In an extended sensitivity analysis additionally adjusting for diabetes, renal function, and concomitant antihypertensive therapies, beta-blocker group status remained associated with lnPTFV1 (standardized β = 0.294, p < 0.001; R 2 = 0.147; adjusted R 2 = 0.081; overall p = 0.011). Beta-blocker use was also associated with lower odds of abnormal PTFV1 (OR = 0.43, 95% CI 0.22-0.84, p = 0.013).
Conclusion:
β1-Selective beta-blocker use was associated with lower PTFV1 and a lower likelihood of abnormal PTFV1. These findings suggest a more favorable atrial electrical profile but should be considered hypothesis-generating given the retrospective design and modest model explanatory capacity.
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