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Diabetologia

, Volume 62, Issue 2, pp 259–268 | Cite as

The role of coronary artery calcification testing in incident coronary artery disease risk prediction in type 1 diabetes

  • Jingchuan Guo
  • Sebhat A. Erqou
  • Rachel G. Miller
  • Daniel Edmundowicz
  • Trevor J. OrchardEmail author
  • Tina Costacou
Article

Abstract

Aims/hypothesis

We sought to assess the role of coronary artery calcification (CAC) and its progression in predicting incident coronary artery disease (CAD) in individuals with type 1 diabetes using data from the Pittsburgh Epidemiology of Diabetes Complications (EDC) Study.

Methods

The present study examined 292 participants who had at least one CAC measure and were free from CAD at baseline; 181 (62%) had repeat CAC assessments 4–8 years later and did not develop CAD between the two CAC measures. The HRs of incident CAD events were estimated using Cox models in categorised or in appropriately transformed CAC scores. C statistics and net reclassification improvement (NRI) were used to assess the added predictive value of CAC for incident CAD.

Results

At baseline, the mean age of participants was 39.4 years and the mean diabetes duration was 29.5 years. There were 76 participants who experienced a first incident CAD event over an average follow-up of 10.7 years. At baseline, compared with those without CAC (Agatston score = 0), the adjusted HR (95% CI) in groups of 1–99, 100–399 and ≥400 was 3.1 (1.6, 6.1), 4.4 (2.0, 9.5) and 4.8 (1.9, 12.0), respectively. CAC density was inversely associated with incident CAD in those with CAC volume ≥100 (HR 0.3 [95% CI 0.1, 0.9]) after adjusting for volume score. Among participants with repeated CAC measures, annual CAC progression was positively associated with incident CAD after controlling for baseline CAC. The HR (95% CI) for above vs below the median annual CAC volume progression was 3.2 (1.2, 8.5). When compared with a model that only included established risk factors, the addition of CAC improved the predictive ability for incident CAD events in the whole group.

Conclusions/interpretation

CAC is strongly associated with incident CAD events in individuals with type 1 diabetes; its inclusion in CAD risk models may lead to improvement in prediction over established risk factors.

Keywords

Coronary artery calcification Coronary artery disease risk prediction Type 1 diabetes 

Abbreviations

AER

Albumin excretion rate

CAC

Coronary artery calcification

CAD

Coronary artery disease

EDC

Epidemiology of Diabetes Complications study

MESA

Multi-Ethnic Study of Atherosclerosis

NRI

Net reclassification improvement

Notes

Acknowledgements

The authors thank the staff and the participants of the EDC study for their contributions.

Data availability

The datasets generated and/or analysed during the current study are available from the corresponding author on reasonable request.

Funding

Research reported in this study was supported by the National Institute of Diabetes and Digestive and Kidney Diseases at the National Institutes of Health (grant R01-DK-034818) and the Rossi Memorial Fund.

Contribution statement

JG conceived and designed the study, acquired, analysed and interpreted the data and drafted the manuscript. SAE conceived and designed the study, interpreted the data, drafted the manuscript and edited and critically reviewed the manuscript for important intellectual content. RGM and DE conceived and designed the study, acquired and interpreted the data and edited and critically reviewed the manuscript for important intellectual content. TJO and TC conceived and designed the study, acquired and interpreted the data, edited and critically reviewed the manuscript for important intellectual content and provided administrative and material support. All authors gave final approval of the version of the manuscript to be published. TJO is the guarantor of this work and, as such, had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.

Duality of interest

The authors declare that there is no duality of interest associated with this manuscript.

Supplementary material

125_2018_4764_MOESM1_ESM.pdf (200 kb)
ESM (PDF 200 kb)

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Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2018

Authors and Affiliations

  1. 1.Department of EpidemiologyUniversity of PittsburghPittsburghUSA
  2. 2.Department of MedicineAlpert Medical School of Brown UniversityProvidenceUSA
  3. 3.Department of MedicineProvidence VA Medical CenterProvidenceUSA
  4. 4.Section of CardiologyTemple University HospitalPhiladelphiaUSA

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