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. 2026 Feb 6;17:1747121. doi: 10.3389/fphar.2026.1747121

TABLE 6.

Multivariate Cox regression analysis of MACE risk in patients with different CYP2C19 metabolizers.

Metabolic type Variable HR 95%CI P值
EM type Tica. (vs. Clop.) 1.05 0.36–3.02 0.931
Age (for each additional year) 1.02 0.96–1.09 0.512
Gender (M vs. F) 1.21 0.41–3.59 0.731
Hypertension (yes vs. no) 1.35 0.45–4.08 0.592
Diabetes (yes vs. no) 1.58 0.52–4.76 0.416
Smoking (yes vs. no) 1.12 0.38–3.31 0.836
IM type Tica. (vs. Clop.) 0.52 0.28–0.98 0.043
Age (for each additional year) 1.03 0.99–1.07 0.105
Gender (M vs. F) 1.18 0.64–2.18 0.601
Hypertension (yes vs. no) 1.29 0.69–2.41 0.426
Diabetes (yes vs. no) 1.45 0.78–2.70 0.241
Smoking (yes vs. no) 1.09 0.59–2.01 0.782
PM type Tica. (vs. Clop.) 0.32 0.11–0.89 0.029
Age (for each additional year) 1.04 0.97–1.12 0.279
Gender (M vs. F) 1.41 0.55–3.62 0.473
Hypertension (yes vs. no) 1.62 0.63–4.17 0.318
Diabetes (yes vs. no) 1.78 0.69–4.55 0.230
Smoking (yes vs. no) 0.85 0.33–2.17 0.730

MACE, major adverse cardiovascular event;HR, hazard ratio; CI, confidence interval. Analysis was based on propensity score-matched cohort and adjusted for covariates listed in table.