Research Article: Tea consumption and major adverse cardiovascular events in coronary heart disease: a non-linear dose–response analysis with joint effect modification by lipoprotein(a) and systemic inflammation — a UK Biobank study
Abstract:
Tea consumption is inversely associated with cardiovascular risk in general populations, but evidence from patients with established coronary heart disease (CHD) is limited. Whether lipoprotein(a) [Lp(a)] and C-reactive protein (CRP) modify this association has not been examined.
From the UK Biobank, 25,306 participants with established CHD were identified (3,773 MACE events over a mean follow-up of 13.9?years). Cox regression with progressive adjustment was performed on 22,012 participants with complete covariate data. Restricted cubic splines (RCS), causal mediation analysis for Lp(a), and three-way interaction tests (tea × Lp(a)?×?CRP) were performed. A four-quadrant stratification by Lp(a) (cut-off 50?nmol/L) and CRP (cut-off 3?mg/L) was constructed.
RCS analysis identified a non-linear dose–response relationship ( p <?0.0001), with the lowest MACE risk at approximately 3 cups/day (HR 0.828, 95% CI 0.790–0.867, relative to 0 cups/day). Fully adjusted heavy tea consumption (?4 cups/day) was associated with reduced risk (HR 0.895, p =?0.037). Lp(a) did not mediate the association (ACME p >?0.05). A three-way interaction was suggested at the boundary of conventional significance ( p =?0.050): the low-Lp(a)/high-CRP subgroup showed the strongest benefit (HR 0.670, p <?0.001), while the high-Lp(a)/high-CRP subgroup showed none (HR 0.992, p =?0.960).
In CHD patients, tea consumption of approximately 3 cups/day is associated with the lowest MACE risk. This association is jointly modified by the Lp(a)–CRP profile, with the greatest benefit in patients whose residual risk is predominantly inflammation-driven.
Introduction:
Tea consumption is inversely associated with cardiovascular risk in general populations, but evidence from patients with established coronary heart disease (CHD) is limited. Whether lipoprotein(a) [Lp(a)] and C-reactive protein (CRP) modify this association has not been examined.
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