Temporal change in glucose tolerance in non-ST-elevation myocardial infarction
We assessed the prevalence and 3-month change in glucose tolerance status in consecutive non-ST-elevation myocardial infarction (NSTEMI; European Society of Cardiology 2007 definition) patients ( N = 49; mean (S.D.) age 65 (11) years) admitted to a coronary care unit, without known diabetes. These p...
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Published in | Diabetes research and clinical practice Vol. 82; no. 3; pp. 310 - 316 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Ireland
Elsevier Ireland Ltd
01.12.2008
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Subjects | |
Online Access | Get full text |
ISSN | 0168-8227 1872-8227 1872-8227 |
DOI | 10.1016/j.diabres.2008.08.016 |
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Abstract | We assessed the prevalence and 3-month change in glucose tolerance status in consecutive non-ST-elevation myocardial infarction (NSTEMI; European Society of Cardiology 2007 definition) patients (
N
=
49; mean (S.D.) age 65 (11) years) admitted to a coronary care unit, without known diabetes. These patients underwent an oral glucose tolerance test (OGTT) 36-hour (median, IQR: 18–72) after admission and at 3 months. Undiagnosed abnormal glucose tolerance (AGT: impaired fasting glucose (IFG), impaired glucose tolerance (IGT) or new diabetes) was common (61% at admission and 41% at 3 months,
p
<
0.05) and the majority (∼3/4) had IGT. Glucose tolerance status improved in a higher proportion of patients than it worsened (31% vs. 8%,
p
=
0.04). At 3 months, fasting glucose was unchanged but 2-hour OGTT glucose was lower (mean (S.D.): 8.5 (2.7)
mmol/L vs. 7.7 (2.7)
mmol/L,
p
=
0.004). ‘Stress hyperglycaemia’ could explain higher admission glucose levels and this raises the question about the optimal timing of OGTT in relation to myocardial infarction. Newly diagnosed diabetes was present in ∼10% of patients and this was not reliably detected by fasting plasma glucose. In NSTEMI patients OGTT is the only reliable strategy to identify subjects with IGT and diabetes. |
---|---|
AbstractList | We assessed the prevalence and 3-month change in glucose tolerance status in consecutive non-ST-elevation myocardial infarction (NSTEMI; European Society of Cardiology 2007 definition) patients (
N
=
49; mean (S.D.) age 65 (11) years) admitted to a coronary care unit, without known diabetes. These patients underwent an oral glucose tolerance test (OGTT) 36-hour (median, IQR: 18–72) after admission and at 3 months. Undiagnosed abnormal glucose tolerance (AGT: impaired fasting glucose (IFG), impaired glucose tolerance (IGT) or new diabetes) was common (61% at admission and 41% at 3 months,
p
<
0.05) and the majority (∼3/4) had IGT. Glucose tolerance status improved in a higher proportion of patients than it worsened (31% vs. 8%,
p
=
0.04). At 3 months, fasting glucose was unchanged but 2-hour OGTT glucose was lower (mean (S.D.): 8.5 (2.7)
mmol/L vs. 7.7 (2.7)
mmol/L,
p
=
0.004). ‘Stress hyperglycaemia’ could explain higher admission glucose levels and this raises the question about the optimal timing of OGTT in relation to myocardial infarction. Newly diagnosed diabetes was present in ∼10% of patients and this was not reliably detected by fasting plasma glucose. In NSTEMI patients OGTT is the only reliable strategy to identify subjects with IGT and diabetes. We assessed the prevalence and 3-month change in glucose tolerance status in consecutive non-ST-elevation myocardial infarction (NSTEMI; European Society of Cardiology 2007 definition) patients (N=49; mean (S.D.) age 65 (11) years) admitted to a coronary care unit, without known diabetes. These patients underwent an oral glucose tolerance test (OGTT) 36-hour (median, IQR: 18-72) after admission and at 3 months. Undiagnosed abnormal glucose tolerance (AGT: impaired fasting glucose (IFG), impaired glucose tolerance (IGT) or new diabetes) was common (61% at admission and 41% at 3 months, p<0.05) and the majority (approximately 3/4) had IGT. Glucose tolerance status improved in a higher proportion of patients than it worsened (31% vs. 8%, p=0.04). At 3 months, fasting glucose was unchanged but 2-hour OGTT glucose was lower (mean (S.D.): 8.5 (2.7) mmol/L vs. 7.7 (2.7) mmol/L, p=0.004). 'Stress hyperglycaemia' could explain higher admission glucose levels and this raises the question about the optimal timing of OGTT in relation to myocardial infarction. Newly diagnosed diabetes was present in approximately 10% of patients and this was not reliably detected by fasting plasma glucose. In NSTEMI patients OGTT is the only reliable strategy to identify subjects with IGT and diabetes. We assessed the prevalence and 3-month change in glucose tolerance status in consecutive non-ST-elevation myocardial infarction (NSTEMI; European Society of Cardiology 2007 definition) patients (N=49; mean (S.D.) age 65 (11) years) admitted to a coronary care unit, without known diabetes. These patients underwent an oral glucose tolerance test (OGTT) 36-hour (median, IQR: 18-72) after admission and at 3 months. Undiagnosed abnormal glucose tolerance (AGT: impaired fasting glucose (IFG), impaired glucose tolerance (IGT) or new diabetes) was common (61% at admission and 41% at 3 months, p<0.05) and the majority (approximately 3/4) had IGT. Glucose tolerance status improved in a higher proportion of patients than it worsened (31% vs. 8%, p=0.04). At 3 months, fasting glucose was unchanged but 2-hour OGTT glucose was lower (mean (S.D.): 8.5 (2.7) mmol/L vs. 7.7 (2.7) mmol/L, p=0.004). 'Stress hyperglycaemia' could explain higher admission glucose levels and this raises the question about the optimal timing of OGTT in relation to myocardial infarction. Newly diagnosed diabetes was present in approximately 10% of patients and this was not reliably detected by fasting plasma glucose. In NSTEMI patients OGTT is the only reliable strategy to identify subjects with IGT and diabetes.We assessed the prevalence and 3-month change in glucose tolerance status in consecutive non-ST-elevation myocardial infarction (NSTEMI; European Society of Cardiology 2007 definition) patients (N=49; mean (S.D.) age 65 (11) years) admitted to a coronary care unit, without known diabetes. These patients underwent an oral glucose tolerance test (OGTT) 36-hour (median, IQR: 18-72) after admission and at 3 months. Undiagnosed abnormal glucose tolerance (AGT: impaired fasting glucose (IFG), impaired glucose tolerance (IGT) or new diabetes) was common (61% at admission and 41% at 3 months, p<0.05) and the majority (approximately 3/4) had IGT. Glucose tolerance status improved in a higher proportion of patients than it worsened (31% vs. 8%, p=0.04). At 3 months, fasting glucose was unchanged but 2-hour OGTT glucose was lower (mean (S.D.): 8.5 (2.7) mmol/L vs. 7.7 (2.7) mmol/L, p=0.004). 'Stress hyperglycaemia' could explain higher admission glucose levels and this raises the question about the optimal timing of OGTT in relation to myocardial infarction. Newly diagnosed diabetes was present in approximately 10% of patients and this was not reliably detected by fasting plasma glucose. In NSTEMI patients OGTT is the only reliable strategy to identify subjects with IGT and diabetes. Abstract We assessed the prevalence and 3-month change in glucose tolerance status in consecutive non-ST-elevation myocardial infarction (NSTEMI; European Society of Cardiology 2007 definition) patients ( N = 49; mean (S.D.) age 65 (11) years) admitted to a coronary care unit, without known diabetes. These patients underwent an oral glucose tolerance test (OGTT) 36-hour (median, IQR: 18–72) after admission and at 3 months. Undiagnosed abnormal glucose tolerance (AGT: impaired fasting glucose (IFG), impaired glucose tolerance (IGT) or new diabetes) was common (61% at admission and 41% at 3 months, p < 0.05) and the majority (∼3/4) had IGT. Glucose tolerance status improved in a higher proportion of patients than it worsened (31% vs. 8%, p = 0.04). At 3 months, fasting glucose was unchanged but 2-hour OGTT glucose was lower (mean (S.D.): 8.5 (2.7) mmol/L vs. 7.7 (2.7) mmol/L, p = 0.004). ‘Stress hyperglycaemia’ could explain higher admission glucose levels and this raises the question about the optimal timing of OGTT in relation to myocardial infarction. Newly diagnosed diabetes was present in ∼10% of patients and this was not reliably detected by fasting plasma glucose. In NSTEMI patients OGTT is the only reliable strategy to identify subjects with IGT and diabetes. |
Author | Delduca, A.-M. Somauroo, J.D. Jordan, T.S. Srinivas-Shankar, U. Bowles, S.A. Rutter, M.K. |
Author_xml | – sequence: 1 givenname: U. surname: Srinivas-Shankar fullname: Srinivas-Shankar, U. email: usrinivas@manchester.ac.uk organization: The Department of Diabetes and Endocrinology, Countess of Chester NHS Hospital Trust, Liverpool Road, Chester CH2 1UL, UK – sequence: 2 givenname: J.D. surname: Somauroo fullname: Somauroo, J.D. organization: The Cardiology Unit, Countess of Chester NHS Hospital Trust, Liverpool Road, Chester CH2 1UL, UK – sequence: 3 givenname: A.-M. surname: Delduca fullname: Delduca, A.-M. organization: The Department of Chemical Pathology, Countess of Chester NHS Hospital Trust, Liverpool Road, Chester CH2 1UL, UK – sequence: 4 givenname: T.S. surname: Jordan fullname: Jordan, T.S. organization: The Department of Diabetes and Endocrinology, Countess of Chester NHS Hospital Trust, Liverpool Road, Chester CH2 1UL, UK – sequence: 5 givenname: S.A. surname: Bowles fullname: Bowles, S.A. organization: The Department of Chemical Pathology, Countess of Chester NHS Hospital Trust, Liverpool Road, Chester CH2 1UL, UK – sequence: 6 givenname: M.K. surname: Rutter fullname: Rutter, M.K. email: Martin.Rutter@cmmc.nhs.uk organization: The Department of Diabetes and Endocrinology, Countess of Chester NHS Hospital Trust, Liverpool Road, Chester CH2 1UL, UK |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/18842319$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1002_dmrr_993 crossref_primary_10_2298_SARH1008430S crossref_primary_10_1016_j_clinbiochem_2012_05_020 crossref_primary_10_1007_s11892_016_0721_y crossref_primary_10_1002_pdi_1647 crossref_primary_10_1016_j_ghir_2015_07_009 crossref_primary_10_1186_1475_2840_11_155 crossref_primary_10_1186_s12871_024_02592_9 |
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Keywords | NSTEMI CRP 2hrPG NSTE-ACS DM IFG UA AGT Risk factors Glucose tolerance ACS HbA 1c IGT STEMI Non-ST-elevation myocardial infarction TnT Diabetes FPG OGTT Acute coronary syndrome BMI high sensitivity C-reactive protein ST-elevation myocardial infarction oral glucose tolerance test impaired glucose tolerance 2-h plasma glucose glycosylated haemoglobin non-ST-elevation myocardial infarction troponin T acute coronary syndrome impaired fasting glucose abnormal glucose tolerance body mass index non-ST-elevation acute coronary syndrome unstable angina fasting plasma glucose diabetes |
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Snippet | We assessed the prevalence and 3-month change in glucose tolerance status in consecutive non-ST-elevation myocardial infarction (NSTEMI; European Society of... Abstract We assessed the prevalence and 3-month change in glucose tolerance status in consecutive non-ST-elevation myocardial infarction (NSTEMI; European... |
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SubjectTerms | Acute coronary syndrome Aged Blood Glucose - analysis Diabetes Endocrinology & Metabolism Glucose Intolerance - etiology Glucose tolerance Glucose Tolerance Test Humans Hyperglycemia - etiology Middle Aged Myocardial Infarction - complications Non-ST-elevation myocardial infarction Prevalence Risk factors Time Factors |
Title | Temporal change in glucose tolerance in non-ST-elevation myocardial infarction |
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