4.6 Article

Association Between Change in Circulating Progenitor Cells During Exercise Stress and Risk of Adverse Cardiovascular Events in Patients With Coronary Artery Disease

期刊

JAMA CARDIOLOGY
卷 5, 期 2, 页码 147-155

出版社

AMER MEDICAL ASSOC
DOI: 10.1001/jamacardio.2019.4528

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资金

  1. National Institutes of Health [P01 HL101398, R01 HL109413, R01HL109413-02S1, R01HL125246, K24HL077506, K24 MH076955, UL1TR000454, KL2TR000455, K23HL127251, T32HL130025, 1R61HL138657-02, 1P30DK111024-03S1, 5R01HL095479-08, 3RF1AG051633-01S2, 5R01AG042127-06, 2P01HL086773-08]
  2. American Heart Association [15SFCRN23910003]
  3. [U54AG062334-01]
  4. [1R01HL141205-01]
  5. [5P01HL101398-02]
  6. [1P20HL113451-01]
  7. [5P01HL086773-09 1RF1AG051633-01]
  8. [R01 NS064162-01]
  9. [R01 HL89650-01]
  10. [HL095479-01]
  11. [1DP3DK094346-01]
  12. [2P01HL086773]

向作者/读者索取更多资源

Key PointsQuestionAre changes in circulating progenitor cells during exercise associated with future cardiovascular events in individuals with coronary artery disease? FindingsIn this cohort study of 454 patients with coronary artery disease, for every 50% reduction in circulating progenitor cell counts during exercise stress, the adverse event risk more than doubled. Stress-induced ischemia was no longer associated with outcomes after stress-induced changes in circulating progenitor cell counts were included in the analysis. MeaningAmong patients with coronary artery disease, a decrease in circulating progenitor cell counts during exercise is associated with a worse prognosis and is a stronger factor in outcomes than the presence of stress-induced myocardial ischemia. ImportanceStem and progenitor cells mobilize from the bone marrow in response to myocardial ischemia. However, the association between the change in circulating progenitor cell (CPC) counts and disease prognosis among patients with ischemia is unknown. ObjectiveTo investigate the association between the change in CPC counts during stress testing and the risk of adverse cardiovascular events in patients with stable coronary artery disease (CAD). Design, Setting, and ParticipantsThis prospective cohort study included a population-based sample of 454 patients with stable CAD who were recruited between June 1, 2011, and August 15, 2014, at Emory University-affiliated hospitals and followed up for 3 years. Data were analyzed from September 15, 2018, to October 15, 2018. ExposuresMyocardial perfusion imaging with technetium Tc 99m sestamibi at rest and 30 to 60 minutes after conventional stress testing. Main Outcomes and MeasuresCirculating progenitor cells were enumerated with flow cytometry as CD34-expressing mononuclear cells (CD45(med)/CD34(+)), with additional quantification of subsets coexpressing the chemokine (C-X-C motif) receptor 4 (CD34(+)/CXCR4(+)). Changes in CPC counts were calculated as poststress minus resting CPC counts. Cox proportional hazards regression models were used to identify factors associated with the combined end point of cardiovascular death and myocardial infarction after adjusting for clinical covariates, including age, sex, race, smoking history, body mass index, and history of heart failure, hypertension, dyslipidemia, and diabetes. ResultsOf the 454 patients (mean [SD] age, 63 [9] years; 76% men) with stable CAD enrolled in the study, 142 (31.3%) had stress-induced ischemia and 312 (68.7%) did not, as measured by single-photon emission computed tomography. During stress testing, patients with stress-induced ischemia had a mean decrease of 20.2% (interquartile range [IQR], -45.3 to 5.5; P<.001) in their CD34(+)/CXCR4(+) counts, and patients without stress-induced ischemia had a mean increase of 3.2% (IQR, -20.6 to 35.1; P<.001) in their CD34(+)/CXCR4(+) counts. Twenty-four patients (5.2%) experienced adverse events. After adjustment, baseline CPC counts were associated with worse adverse outcomes, but this association was not present after stress-induced ischemia was included in the model. However, the change in CPC counts during exercise remained significantly associated with adverse events (hazard ratio, 2.59; 95% CI, 1.15-5.32, per 50% CD34(+)/CXCR4(+) count decrease), even after adjustment for clinical variables and the presence of ischemia. The discrimination of risk factors associated with incident adverse events improved (increase in C statistic from 0.72 to 0.77; P=.003) with the addition of the change in CD34(+)/CXCR4(+) counts to a model that included clinical characteristics, baseline CPC count, and ischemia. Conclusions and RelevanceIn this study of patients with CAD, a decrease in CPC counts during exercise is associated with a worse disease prognosis compared with the presence of stress-induced myocardial ischemia. Further studies are needed to evaluate whether strategies to improve CPC responses during exercise stress will be associated with improvements in the prognosis of patients with CAD. This cohort study of 454 patients with stable coronary artery disease investigates the association between the change in circulating progenitor cell counts during exercise and the risk of adverse cardiovascular events among patients with and without stress-induced myocardial ischemia. (c) 2019 American Medical Association. All rights reserved.

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