Saving time by replacing the standardised two-hour oral glucose tolerance test with a one-hour test : validation of a new screening algorithm in patients with coronary artery disease from the ESC-EORP EUROASPIRE V registry
- Author
- Giulia Ferrannini, Dirk De Bacquer (UGent) , Viveca Gyberg, Gui De Backer (UGent) , Kornelia Kotseva, Linda G Mellbin, Rebecca Risebrink, Jaakko Tuomilehto, David Wood and Lars Rydén
- Organization
- Abstract
- Aims: An oral glucose tolerance test (OGTT) combining fasting (FPG) and 2-hour plasma glucose (2hPG) is the most sensitive method for detecting type 2 diabetes (T2DM). Since it is considered time-consuming, we aim at validating a previously proposed screening algorithm based on a 1-hour plasma glucose (1hPG) with a 12 mmol/L threshold. Methods: Nine-hundred-eighteen patients with coronary artery disease (CAD) without known T2DM from the EUROASPIRE V cross-sectional survey underwent an OGTT. The reference for T2DM was 2hPG > 11.1 mmol/L. T2DM diagnosis by HbA1c > 6.5%(48 mmol/mol), FPG > 7.0 mmol/L, and 1hPG > 12 mmol/L were compared with the outcome of 2hPG. Results: Mean FPG, HbA1c and 2hPG were 6.1 mmol/L, 5.6%(38 mmol/mol) and 7.8 mmol/L respectively. Ninety-six patients (10%) were diagnosed with T2DM according to 2hPG. Using this definition, in the group with FPG < 6.5 mmol/L and 1hPG < 12 only 5 (1%) were misdiagnosed as false negatives. All patients with a FPG > 8.0 mmol/L and 1hPG > 15.0 mmol/L were identified as having T2DM. According to the algorithm, in 79% of patients T2DM could be excluded by combining FPG < 6.5 mmol/L and 1hPG < 12 mmol/L. Conclusions: T2DM Screening by means of an algorithm combining FPG and 1hPG limits the demand of a 2hOGTT in 79% of CAD patients without known T2DM. HbA1c did not add to the information derived from this algorithm. (c) 2021 Published by Elsevier B.V.
- Keywords
- Endocrinology, General Medicine, Endocrinology, Diabetes and Metabolism, Internal Medicine, Screening, Diagnosis, OGTT, Coronary Artery Disease, Ischemic Heart Disease, Survey, Prevention, ACUTE MYOCARDIAL-INFARCTION, POSTLOAD PLASMA-GLUCOSE, EUROPEAN-SOCIETY, CARDIOVASCULAR-DISEASE, INSULIN-RESISTANCE, DIABETES-MELLITUS, RISK, MORTALITY, MANAGEMENT, HEART
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Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-8732382
- MLA
- Ferrannini, Giulia, et al. “Saving Time by Replacing the Standardised Two-Hour Oral Glucose Tolerance Test with a One-Hour Test : Validation of a New Screening Algorithm in Patients with Coronary Artery Disease from the ESC-EORP EUROASPIRE V Registry.” DIABETES RESEARCH AND CLINICAL PRACTICE, vol. 183, 2021, doi:10.1016/j.diabres.2021.109156.
- APA
- Ferrannini, G., De Bacquer, D., Gyberg, V., De Backer, G., Kotseva, K., Mellbin, L. G., … Rydén, L. (2021). Saving time by replacing the standardised two-hour oral glucose tolerance test with a one-hour test : validation of a new screening algorithm in patients with coronary artery disease from the ESC-EORP EUROASPIRE V registry. DIABETES RESEARCH AND CLINICAL PRACTICE, 183. https://doi.org/10.1016/j.diabres.2021.109156
- Chicago author-date
- Ferrannini, Giulia, Dirk De Bacquer, Viveca Gyberg, Gui De Backer, Kornelia Kotseva, Linda G Mellbin, Rebecca Risebrink, Jaakko Tuomilehto, David Wood, and Lars Rydén. 2021. “Saving Time by Replacing the Standardised Two-Hour Oral Glucose Tolerance Test with a One-Hour Test : Validation of a New Screening Algorithm in Patients with Coronary Artery Disease from the ESC-EORP EUROASPIRE V Registry.” DIABETES RESEARCH AND CLINICAL PRACTICE 183. https://doi.org/10.1016/j.diabres.2021.109156.
- Chicago author-date (all authors)
- Ferrannini, Giulia, Dirk De Bacquer, Viveca Gyberg, Gui De Backer, Kornelia Kotseva, Linda G Mellbin, Rebecca Risebrink, Jaakko Tuomilehto, David Wood, and Lars Rydén. 2021. “Saving Time by Replacing the Standardised Two-Hour Oral Glucose Tolerance Test with a One-Hour Test : Validation of a New Screening Algorithm in Patients with Coronary Artery Disease from the ESC-EORP EUROASPIRE V Registry.” DIABETES RESEARCH AND CLINICAL PRACTICE 183. doi:10.1016/j.diabres.2021.109156.
- Vancouver
- 1.Ferrannini G, De Bacquer D, Gyberg V, De Backer G, Kotseva K, Mellbin LG, et al. Saving time by replacing the standardised two-hour oral glucose tolerance test with a one-hour test : validation of a new screening algorithm in patients with coronary artery disease from the ESC-EORP EUROASPIRE V registry. DIABETES RESEARCH AND CLINICAL PRACTICE. 2021;183.
- IEEE
- [1]G. Ferrannini et al., “Saving time by replacing the standardised two-hour oral glucose tolerance test with a one-hour test : validation of a new screening algorithm in patients with coronary artery disease from the ESC-EORP EUROASPIRE V registry,” DIABETES RESEARCH AND CLINICAL PRACTICE, vol. 183, 2021.
@article{8732382, abstract = {{Aims: An oral glucose tolerance test (OGTT) combining fasting (FPG) and 2-hour plasma glucose (2hPG) is the most sensitive method for detecting type 2 diabetes (T2DM). Since it is considered time-consuming, we aim at validating a previously proposed screening algorithm based on a 1-hour plasma glucose (1hPG) with a 12 mmol/L threshold. Methods: Nine-hundred-eighteen patients with coronary artery disease (CAD) without known T2DM from the EUROASPIRE V cross-sectional survey underwent an OGTT. The reference for T2DM was 2hPG > 11.1 mmol/L. T2DM diagnosis by HbA1c > 6.5%(48 mmol/mol), FPG > 7.0 mmol/L, and 1hPG > 12 mmol/L were compared with the outcome of 2hPG. Results: Mean FPG, HbA1c and 2hPG were 6.1 mmol/L, 5.6%(38 mmol/mol) and 7.8 mmol/L respectively. Ninety-six patients (10%) were diagnosed with T2DM according to 2hPG. Using this definition, in the group with FPG < 6.5 mmol/L and 1hPG < 12 only 5 (1%) were misdiagnosed as false negatives. All patients with a FPG > 8.0 mmol/L and 1hPG > 15.0 mmol/L were identified as having T2DM. According to the algorithm, in 79% of patients T2DM could be excluded by combining FPG < 6.5 mmol/L and 1hPG < 12 mmol/L. Conclusions: T2DM Screening by means of an algorithm combining FPG and 1hPG limits the demand of a 2hOGTT in 79% of CAD patients without known T2DM. HbA1c did not add to the information derived from this algorithm. (c) 2021 Published by Elsevier B.V.}}, articleno = {{109156}}, author = {{Ferrannini, Giulia and De Bacquer, Dirk and Gyberg, Viveca and De Backer, Gui and Kotseva, Kornelia and Mellbin, Linda G and Risebrink, Rebecca and Tuomilehto, Jaakko and Wood, David and Rydén, Lars}}, issn = {{0168-8227}}, journal = {{DIABETES RESEARCH AND CLINICAL PRACTICE}}, keywords = {{Endocrinology,General Medicine,Endocrinology,Diabetes and Metabolism,Internal Medicine,Screening,Diagnosis,OGTT,Coronary Artery Disease,Ischemic Heart Disease,Survey,Prevention,ACUTE MYOCARDIAL-INFARCTION,POSTLOAD PLASMA-GLUCOSE,EUROPEAN-SOCIETY,CARDIOVASCULAR-DISEASE,INSULIN-RESISTANCE,DIABETES-MELLITUS,RISK,MORTALITY,MANAGEMENT,HEART}}, language = {{eng}}, pages = {{8}}, title = {{Saving time by replacing the standardised two-hour oral glucose tolerance test with a one-hour test : validation of a new screening algorithm in patients with coronary artery disease from the ESC-EORP EUROASPIRE V registry}}, url = {{http://doi.org/10.1016/j.diabres.2021.109156}}, volume = {{183}}, year = {{2021}}, }
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