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. 2022 Jul 13:9:930755.
doi: 10.3389/fcvm.2022.930755. eCollection 2022.

Association Between Pulse Pressure With All-Cause and Cardiac Mortality in Acute Coronary Syndrome: An Observational Cohort Study

Affiliations

Association Between Pulse Pressure With All-Cause and Cardiac Mortality in Acute Coronary Syndrome: An Observational Cohort Study

Man Wang et al. Front Cardiovasc Med. .

Abstract

Background: Pulse pressure (PP) is a surrogate of aortic stiffness, and reflects cardiac performance and stroke volume. Previous studies have indicated that PP was a robust predictor of cardiovascular outcomes and mortality. However, results have been mixed, and very few studies have focused on the association of PP with mortality in acute coronary syndrome (ACS). Thus, we aimed to investigate the relationship between admission PP and the prognosis of patients with ACS.

Methods: This cohort study included 10,824 patients diagnosed with ACS from the Cardiovascular Center Beijing Friendship Hospital Database Bank (CBDBANK) from January 2013 to October 2018. Patients with cardiogenic shock, malignancy, severe trauma and, no PP at admission were excluded. Restricted cubic spline and Cox proportional hazards regression were used to evaluate the association between PP and 1-year all-cause and cardiac mortality.

Results: In the whole cohort, a total of 237 (2.19%) all-cause deaths were reported at 1-year follow-up. Restricted cubic spline analysis suggested a J-shaped relationship between PP and mortality. Among patients with ACS, both lower and higher PP levels were related to an increased risk of mortality (P non-linear < 0.001); with a PP level of 30 or 80 mmHg, as compared with 50 mmHg, the adjusted hazard ratios for 1-year all-cause mortality were 2.02 (95% CI, 1.27-3.22) and 1.62 (95% CI, 1.13-2.33), respectively, after adjustments for potential confounders. Similar results were observed for cardiac deaths. The J-shaped relationship between PP and mortality remained in a series of subgroup analyses.

Conclusion: Our results suggested that both low and high PP were associated with an increased risk of mortality in patients with ACS.

Keywords: acute coronary syndrome; all-cause mortality; cardiac mortality; cohort study; pulse pressure.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
Flowchart of study population selection.
FIGURE 2
FIGURE 2
Restricted cubic spline analysis for association of PP and 1-year all-cause mortality. Adjusted model included age, gender, BMI, previous diabetes mellitus, previous hypertension, previous MI, current smoking, atrial fibrillation, previous DAPT, heart rate, LVEF < 50%, HbA1c, LDL-C, eGFR, peak value of cTnI, angiography findings (LM lesion, multi-vessel lesion, chronic total occlusion lesion), and in-hospital treatments (PCI, DAPT, ACEI/ARB, statins).
FIGURE 3
FIGURE 3
Restricted cubic spline analysis for association of PP and 1-year cardiac mortality. Adjusted model included age, gender, BMI, previous diabetes mellitus, previous hypertension, previous MI, current smoking, atrial fibrillation, previous DAPT, heart rate, LVEF < 50%, HbA1c, LDL-C, eGFR, peak value of cTnI, angiography findings (LM lesion, multi-vessel lesion, chronic total occlusion lesion), and in-hospital treatments (PCI, DAPT, ACEI/ARB, statins).
FIGURE 4
FIGURE 4
Adjusted survival curves for 1-year all-cause and cardiac mortality according to different PP levels. Adjusted model included age, gender, BMI, previous diabetes mellitus, previous hypertension, previous MI, current smoking, atrial fibrillation, previous DAPT, heart rate, LVEF < 50%, HbA1c, LDL-C, eGFR, peak value of cTnI, angiography findings (LM lesion, multi-vessel lesion, chronic total occlusion lesion), and in-hospital treatments (PCI, DAPT, ACEI/ARB, statins).
FIGURE 5
FIGURE 5
Restricted cubic spline analysis for association of PP and 1-year all-cause and cardiac mortality according to different subgroups. Adjusted model included age, gender, BMI, previous diabetes mellitus, previous hypertension, previous MI, current smoking, atrial fibrillation, previous DAPT, heart rate, LVEF < 50%, HbA1c, LDL-C, eGFR, peak value of cTnI, angiography findings (LM lesion, multi-vessel lesion, chronic total occlusion lesion), and in-hospital treatments (PCI, DAPT, ACEI/ARB, statins).

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References

    1. Dzau VJ. Atherosclerosis and hypertension: mechanisms and Interrelationships. J Cardiovasc Pharmacol. (1990) 15(Suppl. 5):S59–64. - PubMed
    1. Lewington S, Clarke R, Qizilbash N, Peto R, Collins R. Age-specific relevance of usual blood pressure to vascular mortality: a meta-analysis of individual data for one million adults in 61 prospective studies. Lancet. (2002) 360:1903–13. 10.1016/s0140-6736(02)11911-8 - DOI - PubMed
    1. Staessen JA, Gasowski J, Wang JG, Thijs L, Den Hond E, Boissel JP, et al. Risks of untreated and treated isolated systolic hypertension in the elderly: meta-analysis of outcome trials. Lancet. (2000) 355:865–72. 10.1016/s0140-6736(99)07330-4 - DOI - PubMed
    1. Wright JT, Jr, Williamson JD, Whelton PK, Snyder JK, Sink KM, Rocco MV, et al. A randomized trial of intensive versus standard blood-pressure control. N Engl J Med. (2015) 373:2103–16. 10.1056/NEJMoa1511939 - DOI - PMC - PubMed
    1. Millar JA, Lever AF, Burke V. Pulse pressure as a risk factor for cardiovascular events in the MRC mild hypertension trial. J Hypertens. (1999) 17:1065–72. 10.1097/00004872-199917080-00004 - DOI - PubMed