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No prognostic significance of chronic infection with Chlamydia pneumoniae in acute coronary syndromes: insights from the Global Utilization of Strategies to Open Occluded Arteries IV Acute Coronary Syndromes trial.

Publication ,  Journal Article
Westerhout, CM; Gnarpe, J; Chang, W-C; FitzPatrick, S; Barnathan, ES; Boersma, E; Califf, RM; Wallentin, L; Simoons, ML; Armstrong, PW ...
Published in: Am Heart J
August 2007

BACKGROUND: Although relationships between chronic Chlamydia pneumoniae (Cpn) infection and the risk of coronary events in stable coronary artery disease patients have been reported, a similar link in acute coronary syndrome (ACS) patients has not been consistently observed. METHODS: In a nested case-control substudy of the Global Utilization of Strategies to Open Occluded Arteries IV Acute Coronary Syndromes trial, 295 cases (30-day death/myocardial infarction [MI]) were matched by age, sex, baseline creatine kinase-myocardial kinase, and smoking status with 295 control subjects. To test the hypothesis on 1-year mortality, another subset (n = 276) was drawn from the 590-patient cohort; 138 patients who died at 1 year plus the matching controls who survived at 1 year. We measured Cpn IgG and IgA antibody titers in baseline serum with microimmunofluorescence. Conditional logistic regression was used to quantify the prognostic relevance seropositivity (IgG > or = 1:32; IgA > or = 1:16) and elevated titer levels. RESULTS: The prevalence of Cpn IgG and IgA was similar between cases and controls (30-day death/MI: IgG, 80% vs 85%, P = .126; IgA, 45% vs 37%, P = .079), and were not statistically significant predictors of 30-day death/MI after baseline adjustment. Likewise, the 1-year death cohort had comparable proportions of Cpn IgG and IgA among cases and controls (86% vs 91% [P = .265] and 49% vs 43% [P = .334], respectively), and did not add prognostic value. CONCLUSIONS: These findings are in concert with study results suggesting that chronic Cpn infection is not associated with 30-day death/MI or 1-year mortality in non-ST elevation ACS.

Duke Scholars

Published In

Am Heart J

DOI

EISSN

1097-6744

Publication Date

August 2007

Volume

154

Issue

2

Start / End Page

306 / 312

Location

United States

Related Subject Headings

  • Prognosis
  • Prevalence
  • Myocardial Infarction
  • Middle Aged
  • Male
  • Immunoglobulin G
  • Immunoglobulin A
  • Humans
  • Female
  • Chronic Disease
 

Citation

APA
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ICMJE
MLA
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Westerhout, C. M., Gnarpe, J., Chang, W.-C., FitzPatrick, S., Barnathan, E. S., Boersma, E., … GUSTO IV ACS Investigators, . (2007). No prognostic significance of chronic infection with Chlamydia pneumoniae in acute coronary syndromes: insights from the Global Utilization of Strategies to Open Occluded Arteries IV Acute Coronary Syndromes trial. Am Heart J, 154(2), 306–312. https://doi.org/10.1016/j.ahj.2007.04.010
Westerhout, Cynthia M., Judy Gnarpe, Wei-Ching Chang, Susan FitzPatrick, Elliot S. Barnathan, Eric Boersma, Robert M. Califf, et al. “No prognostic significance of chronic infection with Chlamydia pneumoniae in acute coronary syndromes: insights from the Global Utilization of Strategies to Open Occluded Arteries IV Acute Coronary Syndromes trial.Am Heart J 154, no. 2 (August 2007): 306–12. https://doi.org/10.1016/j.ahj.2007.04.010.
Westerhout CM, Gnarpe J, Chang W-C, FitzPatrick S, Barnathan ES, Boersma E, Califf RM, Wallentin L, Simoons ML, Armstrong PW, GUSTO IV ACS Investigators. No prognostic significance of chronic infection with Chlamydia pneumoniae in acute coronary syndromes: insights from the Global Utilization of Strategies to Open Occluded Arteries IV Acute Coronary Syndromes trial. Am Heart J. 2007 Aug;154(2):306–312.
Journal cover image

Published In

Am Heart J

DOI

EISSN

1097-6744

Publication Date

August 2007

Volume

154

Issue

2

Start / End Page

306 / 312

Location

United States

Related Subject Headings

  • Prognosis
  • Prevalence
  • Myocardial Infarction
  • Middle Aged
  • Male
  • Immunoglobulin G
  • Immunoglobulin A
  • Humans
  • Female
  • Chronic Disease