Abstract

Coronary artery calcium score (CACS) is a strong predictor of adverse cardiovascular events in the general population. Recent data confirm the prognostic utility of single-photon emission computed tomographic (SPECT) imaging in end-stage renal disease, but whether performing CACS as part of hybrid imaging improves risk prediction in this population is unclear. Consecutive patients (n = 284) were identified after referral to a university hospital for cardiovascular risk stratification in assessment for renal transplantation. Participants underwent technetium-99m SPECT imaging after exercise or standard adenosine stress in those unable to achieve 85% maximal heart rate; multislice CACS was also performed (Siemens Symbia T16, Siemens, Erlangen, Germany). Subjects with known coronary artery disease (n = 88) and those who underwent early revascularization (n = 2) were excluded. The primary outcome was a composite of death or first myocardial infarction. An abnormal SPECT perfusion result was seen in 22% (43 of 194) of subjects, whereas 45% (87 of 194) had at least moderate CACS (>100 U). The frequency of abnormal perfusion (summed stress score ≥4) increased with increasing CACS severity (p = 0.049). There were a total of 15 events (8 deaths, and 7 myocardial infarctions) after a median duration of 18 months (maximum follow-up 3.4 years). Univariate analysis showed diabetes mellitus (Hazard ratio [HR] 3.30, 95% CI 1.14 to 9.54; p = 0.028), abnormal perfusion on SPECT (HR 5.32, 95% CI 1.84 to 15.35; p = 0.002), and moderate-to-severe CACS (HR 3.55, 95% CI 1.11 to 11.35; p = 0.032) were all associated with the primary outcome. In a multivariate model, abnormal perfusion on SPECT (HR 4.18, 95% CI 1.43 to 12.27; p = 0.009), but not moderate-to-severe CACS (HR 2.50, 95% CI 0.76 to 8.20; p = 0.130), independently predicted all-cause death or myocardial infarction. The prognostic value of CACS was not incremental to clinical and SPECT perfusion data (global chi-square change = 2.52, p = 0.112). In conclusion, a perfusion defect on SPECT is an independent predictor of adverse outcome in potential renal transplant candidates regardless of the CACS. The use of CACS as an adjunct to SPECT perfusion data does not provide incremental prognostic utility for the prediction of mortality and nonfatal myocardial infarction in end-stage renal disease.

Highlights

  • We hypothesize that calcium score (CACS) will provide an incremental benefit for the prediction of death and first myocardial infarction (MI) in patients with ESRD beyond that provided by perfusion defect scores on myocardial perfusion imaging

  • This study suggests that quantification of CACS alongside single-photon emission computed tomographic (SPECT) imaging does not provide incremental prognostic utility for prediction of mortality and nonfatal MI in potential renal transplant candidates

  • A CACS >100 U was associated with a worse outcome, the presence of moderateto-severe CAC did not independently predict outcome after adjusting for clinical data and the SPECT perfusion result

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Summary

Renal Disease

The use of CACS as an adjunct to SPECT perfusion data does not provide incremental prognostic utility for the prediction of mortality and nonfatal myocardial infarction in end-stage renal disease. Many transplant centers continue to use stress myocardial perfusion scintigraphy because of longstanding data supporting its prognostic utility in ESRD.4e7 Despite this, myocardial perfusion scintigraphy has poor positive predictive value for identifying coronary artery stenosis on invasive angiography.[5,8] it is not able to detect subclinical atherosclerosis, potentially www.ajconline.org. The predictive role of CACS in subjects with ESRD, is less certain.[10,11] Despite the very high burden of coronary calcification in this population, there is only a modest association between CACS and perfusion defects.[12,13] In the present study, we hypothesize that CACS will provide an incremental benefit for the prediction of death and first myocardial infarction (MI) in patients with ESRD beyond that provided by perfusion defect scores on myocardial perfusion imaging

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