Prognostic Utility of Calcium Scoring as an Adjunct to Stress Myocardial Perfusion Scintigraphy in End-Stage Renal Disease
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 i...
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Published in | The American journal of cardiology Vol. 117; no. 9; pp. 1387 - 1396 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.05.2016
Elsevier Limited Excerpta Medica |
Subjects | |
Online Access | Get full text |
ISSN | 0002-9149 1879-1913 |
DOI | 10.1016/j.amjcard.2016.02.003 |
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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. |
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AbstractList | 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. 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. 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 greater than or equal to 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. 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. |
Author | McNulty, David Berman, Daniel S. Ferro, Charles J. Townend, Jonathan N. Edwards, Nicola C. Lin, Erica L.S. Stoodley, Matthew Steeds, Richard P. Thomson, Louise E. Holloway, Benjamin Moody, William E. |
AuthorAffiliation | b Department of Cardiac Imaging and Nuclear Cardiology, S. Mark Taper Foundation Imaging Center Los Angeles, California a Birmingham Cardio-Renal Group, Department of Cardiology, Institute of Cardiovascular Sciences, Nuffield House, Queen Elizabeth Hospital Birmingham, Edgbaston |
AuthorAffiliation_xml | – name: a Birmingham Cardio-Renal Group, Department of Cardiology, Institute of Cardiovascular Sciences, Nuffield House, Queen Elizabeth Hospital Birmingham, Edgbaston – name: b Department of Cardiac Imaging and Nuclear Cardiology, S. Mark Taper Foundation Imaging Center Los Angeles, California |
Author_xml | – sequence: 1 givenname: William E. orcidid: 0000-0002-2592-618X surname: Moody fullname: Moody, William E. email: william.moody@nhs.net organization: Birmingham Cardio-Renal Group, Department of Cardiology, Institute of Cardiovascular Sciences, Nuffield House, Queen Elizabeth Hospital Birmingham, Edgbaston – sequence: 2 givenname: Erica L.S. surname: Lin fullname: Lin, Erica L.S. organization: Birmingham Cardio-Renal Group, Department of Cardiology, Institute of Cardiovascular Sciences, Nuffield House, Queen Elizabeth Hospital Birmingham, Edgbaston – sequence: 3 givenname: Matthew surname: Stoodley fullname: Stoodley, Matthew organization: Birmingham Cardio-Renal Group, Department of Cardiology, Institute of Cardiovascular Sciences, Nuffield House, Queen Elizabeth Hospital Birmingham, Edgbaston – sequence: 4 givenname: David surname: McNulty fullname: McNulty, David organization: Birmingham Cardio-Renal Group, Department of Cardiology, Institute of Cardiovascular Sciences, Nuffield House, Queen Elizabeth Hospital Birmingham, Edgbaston – sequence: 5 givenname: Louise E. surname: Thomson fullname: Thomson, Louise E. organization: Department of Cardiac Imaging and Nuclear Cardiology, S. Mark Taper Foundation Imaging Center Los Angeles, California – sequence: 6 givenname: Daniel S. surname: Berman fullname: Berman, Daniel S. organization: Department of Cardiac Imaging and Nuclear Cardiology, S. Mark Taper Foundation Imaging Center Los Angeles, California – sequence: 7 givenname: Nicola C. surname: Edwards fullname: Edwards, Nicola C. organization: Birmingham Cardio-Renal Group, Department of Cardiology, Institute of Cardiovascular Sciences, Nuffield House, Queen Elizabeth Hospital Birmingham, Edgbaston – sequence: 8 givenname: Benjamin surname: Holloway fullname: Holloway, Benjamin organization: Birmingham Cardio-Renal Group, Department of Cardiology, Institute of Cardiovascular Sciences, Nuffield House, Queen Elizabeth Hospital Birmingham, Edgbaston – sequence: 9 givenname: Charles J. surname: Ferro fullname: Ferro, Charles J. organization: Birmingham Cardio-Renal Group, Department of Cardiology, Institute of Cardiovascular Sciences, Nuffield House, Queen Elizabeth Hospital Birmingham, Edgbaston – sequence: 10 givenname: Jonathan N. surname: Townend fullname: Townend, Jonathan N. organization: Birmingham Cardio-Renal Group, Department of Cardiology, Institute of Cardiovascular Sciences, Nuffield House, Queen Elizabeth Hospital Birmingham, Edgbaston – sequence: 11 givenname: Richard P. surname: Steeds fullname: Steeds, Richard P. organization: Birmingham Cardio-Renal Group, Department of Cardiology, Institute of Cardiovascular Sciences, Nuffield House, Queen Elizabeth Hospital Birmingham, Edgbaston |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26996769$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1161_JAHA_116_003648 crossref_primary_10_1007_s11883_017_0643_4 crossref_primary_10_1016_j_jcmg_2017_07_012 crossref_primary_10_1007_s12350_018_1412_7 crossref_primary_10_12688_f1000research_16627_1 crossref_primary_10_5301_heartint_5000233 crossref_primary_10_1016_j_amjcard_2017_11_038 crossref_primary_10_1177_1089253216688538 crossref_primary_10_1007_s12350_020_02449_x crossref_primary_10_1007_s12350_017_0944_6 crossref_primary_10_1007_s12350_020_02080_w crossref_primary_10_1093_ckj_sfab103 crossref_primary_10_35366_93332 crossref_primary_10_1007_s11886_019_1147_3 crossref_primary_10_1007_s11897_017_0354_8 |
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SubjectTerms | Adult Age Aged Calcification Calcium Cardiology Cardiovascular Cardiovascular disease Coronary Artery Disease Coronary Artery Disease - diagnosis Coronary Artery Disease - mortality Coronary vessels Defects Diabetes Female Heart attacks Humans Hypertension Ischemia Kidney diseases Kidney Failure, Chronic - complications Kidney Failure, Chronic - diagnostic imaging Kidney Transplantation Male Medical imaging Middle Aged Mortality Multimodal Imaging Multivariate analysis Myocardial Infarction - epidemiology Myocardial Perfusion Imaging Patients Predictive Value of Tests Prognosis Proportional Hazards Models Radiography Risk Assessment Risk factors Severity of Illness Index Tomography, Emission-Computed, Single-Photon Transplants & implants Vascular Calcification - diagnosis Vascular Calcification - mortality |
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