Key result
Every standard deviation decrease in rate-pressure product reactivity to mental stress was associated with an increased risk of cardiovascular death or nonfatal MI (HR 1.30 in MIPS, HR 1.41 in MIMS2).
Why the study?
The clinical significance of hemodynamic reactivity to mental stress in patients with coronary artery disease was unclear.
Does blunted hemodynamic reactivity to mental stress increase the risk of adverse cardiovascular events in patients with stable CAD?
Cohort (n=938)
Yes
Does blunted hemodynamic reactivity to mental stress increase the risk of adverse cardiovascular events in patients with stable CAD?
Answers are grounded in this paper and cite their sources.
Blunted cardiovascular reactivity to mental stress is associated with an increased risk of adverse cardiovascular events in patients with stable CAD.
Importance: The clinical significance of hemodynamic reactivity to mental stress in the population with coronary artery disease (CAD) is unclear. Objective: To investigate the association between hemodynamic reactivity to mental stress and the risk of adverse cardiovascular events in patients with stable CAD. Design, Setting, and Participants: This cohort study included individuals with stable CAD from 2 prospective studies from a university-based hospital network: the Mental Stress Ischemia Prognosis Study (MIPS) and the Myocardial Infarction and Mental Stress Study 2 (MIMS2). Participants were enrolled between June 2011 and March 2016 and followed up for a median of 6.0 (IQR, 5.6-6.0) years in MIPS and 4.6 (IQR, 3.8-5.3) years in MIMS2. Data were analyzed from December 1, 2022, to February 15, 2023. Exposures: The rate-pressure product (RPP) was calculated as the mean systolic blood pressure times the mean heart rate at rest. Rate-pressure product reactivity was calculated as the maximum RPP during a standardized mental stress test minus the RPP at rest. Main Outcomes and Measures: The primary outcome was a composite of cardiovascular death or nonfatal myocardial infarction. The secondary end point additionally included hospitalizations for heart failure. Results: From the total of 938 individuals from the pooled cohort (mean [SD] age, 60.2 [10.1] years; 611 [65.1%] men), 631 participated in MIPS and 307 in MIMS2. A total of 373 individuals (39.8%) were Black, 519 (55.3%) were White, and 46 (4.9%) were of unknown race or ethnicity. The RPP increased by a mean (SD) of 77.1% (23.1%) during mental stress (mean [SD] absolute change, 5651 [2878]). For every SD decrease in RPP reactivity with mental stress, the adjusted hazard ratios for the primary and secondary end points were 1.30 (95% CI, 1.04-1.72) and 1.30 (95% CI, 1.06-1.56), respectively, in MIPS and 1.41 (95% CI, 1.06-1.97) and 1.21 (95% CI, 1.02-1.60), respectively, in MIMS2. In the pooled sample, when RPP reactivity to mental stress was added to a model including traditional clinical risk characteristics, model discrimination for adverse events improved (increase in C statistic of 5% for the primary end point; P = .009). Conclusions and Relevance: In this cohort study of individuals with stable CAD, a blunted cardiovascular reactivity to mental stress was associated with adverse outcomes. Future studies are needed to assess the clinical utility of mental stress reactivity testing in this population.
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Moazzami et al. (2023) conducted a cohort in stable coronary artery disease (n=938). Hemodynamic reactivity to mental stress was evaluated on Composite of cardiovascular death or nonfatal myocardial infarction (HR 1.30, 95% CI 1.04-1.72). Every standard deviation decrease in rate-pressure product reactivity to mental stress was associated with an increased risk of cardiovascular death or nonfatal MI (HR 1.30 in MIPS, HR 1.41 in MIMS2).
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