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. 2021 Apr 23;116(1):29. doi: 10.1007/s00395-021-00864-w

Table 2.

Effect of the homozygous Q222R DNase 1 SNP on cardiovascular and all-cause mortality of STEMI patients at long-term follow-up

Factor Cardiovascular mortality All-cause mortality
Adjusted HR 95% CI p-value Adjusted HR 95% CI p-value
Age 1.09 1.06–1.12  < 0.0001 1.07 1.05–1.09  < 0.0001
Male sex 0.99 0.56–1.77 0.975 1.29 0.84–1.99 0.246
BMI 1.02 0.97–1.08 0.440 0.99 0.94–1.03 0.531
Hyperlipidemia 0.73 0.43–1.25 0.248 0.68 0.46–1.02 0.061
Arterial hypertension 0.72 0.34–1.37 0.322 0.55 0.35–0.87 0.010
Diabetes mellitus 2.57 1.50–4.41 0.001 2.28 1.50–3.47  < 0.0001
Ever smoker 0.66 0.38–1.13 0.127 0.85 0.57–1.29 0.450
Creatinine on admission 2.63 1.83–3.78  < 0.0001 2.84 2.15–3.76  < 0.0001
DNase 1 SNP 2.02 1.01–4.01 0.046 2.01 1.91–3.39 0.009

Multivariable Cox regression was used to assess the influence of a homozygous SNP in the Q222R DNase 1 gene on cardiovascular and all-cause mortality, after a median follow-up of 60.0 [IQR 30.3, 91.5] months

BMI body mass index, CI confidence interval, DNase deoxyribonuclease, HR hazard ratio, IQR interquartile range, SNP single nucleotide polymorphism, STEMI ST-segment elevation myocardial infarction