HbA1c Identifies Subjects With Prediabetes and Subclinical Left Ventricular Diastolic Dysfunction
ContextPrediabetes is associated with subclinical cardiac changes associated with heart failure development.ObjectiveWe investigated diastolic function and its association with markers of glycation and inflammation related to cardiovascular disease in patients with prediabetes. We focused on individ...
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Published in | The journal of clinical endocrinology and metabolism Vol. 102; no. 10; pp. 3756 - 3764 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Washington, DC
Endocrine Society
01.10.2017
Copyright Oxford University Press Oxford University Press |
Subjects | |
Online Access | Get full text |
ISSN | 0021-972X 1945-7197 1945-7197 |
DOI | 10.1210/jc.2017-00954 |
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Abstract | ContextPrediabetes is associated with subclinical cardiac changes associated with heart failure development.ObjectiveWe investigated diastolic function and its association with markers of glycation and inflammation related to cardiovascular disease in patients with prediabetes. We focused on individuals with prediabetes identified only by glycated hemoglobin A1c [HbA1c; 5.7% to 6.4% and normal fasting glucose (NFG) and normal glucose tolerance (NGT) after an oral glucose tolerance test (OGTT)].DesignCross-sectional study.SettingDepartments of Clinical and Experimental Medicine and Cardiology, University of Catania, Catania, Italy.Main Outcome MeasuresHbA1c, OGTT, Doppler echocardiography, soluble receptor for advanced glycation end products (sRAGEs), and endogenous secretory RAGE (esRAGE) were evaluated.PatientsWe recruited 167 subjects with NFG/NGT who were stratified according to HbA1c level: controls (HbA1c <5.7%) and HbA1c prediabetes (HbA1c 5.7% to 6.4%).ResultsPatients with HbA1c prediabetes (n = 106) showed a lower peak mitral inflow in early diastole (E wave) to late diastolic atrial filling velocity (A wave) ratio (E/A ratio) than controls (n = 61) (1.10 ± 0.24 vs 1.18 ± 0.23; P < 0.05). They showed a higher left atrium volume (LAV) (28.4 ± 5 vs 22.1 ± 3; P < 0.05) and sphericity index (SI) (0.6 ± 0.06 vs 0.5 ± 0.05; P < 0.05). After multiple regression analyses, HbA1c, sRAGE, and esRAGE were the major determinants of E/A ratio, LAV, and SI.ConclusionsSubjects with HbA1c prediabetes exhibited subclinical cardiac alterations associated with sRAGE, esRAGE, and HbA1c. These subjects would not have been classified as having prediabetes on the basis of fasting glycemia or post-OGTT values.This study demonstrated the ability of HbA1c to identify subjects with prediabetes and subclinical alterations of diastolic function that would not have been detected using fasting glucose or OGTT. |
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AbstractList | ContextPrediabetes is associated with subclinical cardiac changes associated with heart failure development.ObjectiveWe investigated diastolic function and its association with markers of glycation and inflammation related to cardiovascular disease in patients with prediabetes. We focused on individuals with prediabetes identified only by glycated hemoglobin A1c [HbA1c; 5.7% to 6.4% and normal fasting glucose (NFG) and normal glucose tolerance (NGT) after an oral glucose tolerance test (OGTT)].DesignCross-sectional study.SettingDepartments of Clinical and Experimental Medicine and Cardiology, University of Catania, Catania, Italy.Main Outcome MeasuresHbA1c, OGTT, Doppler echocardiography, soluble receptor for advanced glycation end products (sRAGEs), and endogenous secretory RAGE (esRAGE) were evaluated.PatientsWe recruited 167 subjects with NFG/NGT who were stratified according to HbA1c level: controls (HbA1c <5.7%) and HbA1c prediabetes (HbA1c 5.7% to 6.4%).ResultsPatients with HbA1c prediabetes (n = 106) showed a lower peak mitral inflow in early diastole (E wave) to late diastolic atrial filling velocity (A wave) ratio (E/A ratio) than controls (n = 61) (1.10 ± 0.24 vs 1.18 ± 0.23; P < 0.05). They showed a higher left atrium volume (LAV) (28.4 ± 5 vs 22.1 ± 3; P < 0.05) and sphericity index (SI) (0.6 ± 0.06 vs 0.5 ± 0.05; P < 0.05). After multiple regression analyses, HbA1c, sRAGE, and esRAGE were the major determinants of E/A ratio, LAV, and SI.ConclusionsSubjects with HbA1c prediabetes exhibited subclinical cardiac alterations associated with sRAGE, esRAGE, and HbA1c. These subjects would not have been classified as having prediabetes on the basis of fasting glycemia or post-OGTT values. Prediabetes is associated with subclinical cardiac changes associated with heart failure development. We investigated diastolic function and its association with markers of glycation and inflammation related to cardiovascular disease in patients with prediabetes. We focused on individuals with prediabetes identified only by glycated hemoglobin A1c [HbA1c; 5.7% to 6.4% and normal fasting glucose (NFG) and normal glucose tolerance (NGT) after an oral glucose tolerance test (OGTT)]. Cross-sectional study. Departments of Clinical and Experimental Medicine and Cardiology, University of Catania, Catania, Italy. HbA1c, OGTT, Doppler echocardiography, soluble receptor for advanced glycation end products (sRAGEs), and endogenous secretory RAGE (esRAGE) were evaluated. We recruited 167 subjects with NFG/NGT who were stratified according to HbA1c level: controls (HbA1c <5.7%) and HbA1c prediabetes (HbA1c 5.7% to 6.4%). Patients with HbA1c prediabetes (n = 106) showed a lower peak mitral inflow in early diastole (E wave) to late diastolic atrial filling velocity (A wave) ratio (E/A ratio) than controls (n = 61) (1.10 ± 0.24 vs 1.18 ± 0.23; P < 0.05). They showed a higher left atrium volume (LAV) (28.4 ± 5 vs 22.1 ± 3; P < 0.05) and sphericity index (SI) (0.6 ± 0.06 vs 0.5 ± 0.05; P < 0.05). After multiple regression analyses, HbA1c, sRAGE, and esRAGE were the major determinants of E/A ratio, LAV, and SI. Subjects with HbA1c prediabetes exhibited subclinical cardiac alterations associated with sRAGE, esRAGE, and HbA1c. These subjects would not have been classified as having prediabetes on the basis of fasting glycemia or post-OGTT values. Abstract Prediabetes is associated with subclinical cardiac changes associated with heart failure development. We investigated diastolic function and its association with markers of glycation and inflammation related to cardiovascular disease in patients with prediabetes. We focused on individuals with prediabetes identified only by glycated hemoglobin A1c [HbA1c ; 5.7% to 6.4% and normal fasting glucose (NFG) and normal glucose tolerance (NGT) after an oral glucose tolerance test (OGTT)]. Cross-sectional study. Departments of Clinical and Experimental Medicine and Cardiology, University of Catania, Catania, Italy. HbA1c , OGTT, Doppler echocardiography, soluble receptor for advanced glycation end products (sRAGEs), and endogenous secretory RAGE (esRAGE) were evaluated. We recruited 167 subjects with NFG/NGT who were stratified according to HbA1c level: controls (HbA1c <5.7%) and HbA1c prediabetes (HbA1c 5.7% to 6.4%). Patients with HbA1c prediabetes (n = 106) showed a lower peak mitral inflow in early diastole (E wave) to late diastolic atrial filling velocity (A wave) ratio (E/A ratio) than controls (n = 61) (1.10 ± 0.24 vs 1.18 ± 0.23; P < 0.05). They showed a higher left atrium volume (LAV) (28.4 ± 5 vs 22.1 ± 3; P < 0.05) and sphericity index (SI) (0.6 ± 0.06 vs 0.5 ± 0.05; P < 0.05). After multiple regression analyses, HbA1c , sRAGE, and esRAGE were the major determinants of E/A ratio, LAV, and SI. Subjects with HbA1c prediabetes exhibited subclinical cardiac alterations associated with sRAGE, esRAGE, and HbA1c . These subjects would not have been classified as having prediabetes on the basis of fasting glycemia or post-OGTT values. This study demonstrated the ability of HbA1c to identify subjects with prediabetes and subclinical alterations of diastolic function that would not have been detected using fasting glucose or OGTT. Prediabetes is associated with subclinical cardiac changes associated with heart failure development.ContextPrediabetes is associated with subclinical cardiac changes associated with heart failure development.We investigated diastolic function and its association with markers of glycation and inflammation related to cardiovascular disease in patients with prediabetes. We focused on individuals with prediabetes identified only by glycated hemoglobin A1c [HbA1c; 5.7% to 6.4% and normal fasting glucose (NFG) and normal glucose tolerance (NGT) after an oral glucose tolerance test (OGTT)].ObjectiveWe investigated diastolic function and its association with markers of glycation and inflammation related to cardiovascular disease in patients with prediabetes. We focused on individuals with prediabetes identified only by glycated hemoglobin A1c [HbA1c; 5.7% to 6.4% and normal fasting glucose (NFG) and normal glucose tolerance (NGT) after an oral glucose tolerance test (OGTT)].Cross-sectional study.DesignCross-sectional study.Departments of Clinical and Experimental Medicine and Cardiology, University of Catania, Catania, Italy.SettingDepartments of Clinical and Experimental Medicine and Cardiology, University of Catania, Catania, Italy.HbA1c, OGTT, Doppler echocardiography, soluble receptor for advanced glycation end products (sRAGEs), and endogenous secretory RAGE (esRAGE) were evaluated.Main Outcome MeasuresHbA1c, OGTT, Doppler echocardiography, soluble receptor for advanced glycation end products (sRAGEs), and endogenous secretory RAGE (esRAGE) were evaluated.We recruited 167 subjects with NFG/NGT who were stratified according to HbA1c level: controls (HbA1c <5.7%) and HbA1c prediabetes (HbA1c 5.7% to 6.4%).PatientsWe recruited 167 subjects with NFG/NGT who were stratified according to HbA1c level: controls (HbA1c <5.7%) and HbA1c prediabetes (HbA1c 5.7% to 6.4%).Patients with HbA1c prediabetes (n = 106) showed a lower peak mitral inflow in early diastole (E wave) to late diastolic atrial filling velocity (A wave) ratio (E/A ratio) than controls (n = 61) (1.10 ± 0.24 vs 1.18 ± 0.23; P < 0.05). They showed a higher left atrium volume (LAV) (28.4 ± 5 vs 22.1 ± 3; P < 0.05) and sphericity index (SI) (0.6 ± 0.06 vs 0.5 ± 0.05; P < 0.05). After multiple regression analyses, HbA1c, sRAGE, and esRAGE were the major determinants of E/A ratio, LAV, and SI.ResultsPatients with HbA1c prediabetes (n = 106) showed a lower peak mitral inflow in early diastole (E wave) to late diastolic atrial filling velocity (A wave) ratio (E/A ratio) than controls (n = 61) (1.10 ± 0.24 vs 1.18 ± 0.23; P < 0.05). They showed a higher left atrium volume (LAV) (28.4 ± 5 vs 22.1 ± 3; P < 0.05) and sphericity index (SI) (0.6 ± 0.06 vs 0.5 ± 0.05; P < 0.05). After multiple regression analyses, HbA1c, sRAGE, and esRAGE were the major determinants of E/A ratio, LAV, and SI.Subjects with HbA1c prediabetes exhibited subclinical cardiac alterations associated with sRAGE, esRAGE, and HbA1c. These subjects would not have been classified as having prediabetes on the basis of fasting glycemia or post-OGTT values.ConclusionsSubjects with HbA1c prediabetes exhibited subclinical cardiac alterations associated with sRAGE, esRAGE, and HbA1c. These subjects would not have been classified as having prediabetes on the basis of fasting glycemia or post-OGTT values. ContextPrediabetes is associated with subclinical cardiac changes associated with heart failure development.ObjectiveWe investigated diastolic function and its association with markers of glycation and inflammation related to cardiovascular disease in patients with prediabetes. We focused on individuals with prediabetes identified only by glycated hemoglobin A1c [HbA1c; 5.7% to 6.4% and normal fasting glucose (NFG) and normal glucose tolerance (NGT) after an oral glucose tolerance test (OGTT)].DesignCross-sectional study.SettingDepartments of Clinical and Experimental Medicine and Cardiology, University of Catania, Catania, Italy.Main Outcome MeasuresHbA1c, OGTT, Doppler echocardiography, soluble receptor for advanced glycation end products (sRAGEs), and endogenous secretory RAGE (esRAGE) were evaluated.PatientsWe recruited 167 subjects with NFG/NGT who were stratified according to HbA1c level: controls (HbA1c <5.7%) and HbA1c prediabetes (HbA1c 5.7% to 6.4%).ResultsPatients with HbA1c prediabetes (n = 106) showed a lower peak mitral inflow in early diastole (E wave) to late diastolic atrial filling velocity (A wave) ratio (E/A ratio) than controls (n = 61) (1.10 ± 0.24 vs 1.18 ± 0.23; P < 0.05). They showed a higher left atrium volume (LAV) (28.4 ± 5 vs 22.1 ± 3; P < 0.05) and sphericity index (SI) (0.6 ± 0.06 vs 0.5 ± 0.05; P < 0.05). After multiple regression analyses, HbA1c, sRAGE, and esRAGE were the major determinants of E/A ratio, LAV, and SI.ConclusionsSubjects with HbA1c prediabetes exhibited subclinical cardiac alterations associated with sRAGE, esRAGE, and HbA1c. These subjects would not have been classified as having prediabetes on the basis of fasting glycemia or post-OGTT values.This study demonstrated the ability of HbA1c to identify subjects with prediabetes and subclinical alterations of diastolic function that would not have been detected using fasting glucose or OGTT. |
Author | Scandura, Salvatore Purrello, Francesco Mangiafico, Sarah Urbano, Francesca Tamburino, Corrado Di Pino, Antonino Rabuazzo, Agata Maria D’Agate, Veronica Piro, Salvatore Scicali, Roberto |
AuthorAffiliation | 1Department of Clinical and Experimental Medicine, Garibaldi Hospital, University of Catania, 95122 Catania, Italy 2Division of Cardiology, Ferrarotto Hospital, University of Catania, 95100 Catania, Italy |
AuthorAffiliation_xml | – name: 1Department of Clinical and Experimental Medicine, Garibaldi Hospital, University of Catania, 95122 Catania, Italy 2Division of Cardiology, Ferrarotto Hospital, University of Catania, 95100 Catania, Italy – name: 1Department of Clinical and Experimental Medicine, Garibaldi Hospital, University of Catania, Italy 2 Division of Cardiology, Ferrarotto Hospital, University of Catania, Italy |
Author_xml | – sequence: 1 givenname: Antonino surname: Di Pino fullname: Di Pino, Antonino organization: 1Department of Clinical and Experimental Medicine, Garibaldi Hospital, University of Catania, 95122 Catania, Italy – sequence: 2 givenname: Sarah surname: Mangiafico fullname: Mangiafico, Sarah organization: 2Division of Cardiology, Ferrarotto Hospital, University of Catania, 95100 Catania, Italy – sequence: 3 givenname: Francesca surname: Urbano fullname: Urbano, Francesca organization: 1Department of Clinical and Experimental Medicine, Garibaldi Hospital, University of Catania, 95122 Catania, Italy – sequence: 4 givenname: Roberto surname: Scicali fullname: Scicali, Roberto organization: 1Department of Clinical and Experimental Medicine, Garibaldi Hospital, University of Catania, 95122 Catania, Italy – sequence: 5 givenname: Salvatore surname: Scandura fullname: Scandura, Salvatore organization: 2Division of Cardiology, Ferrarotto Hospital, University of Catania, 95100 Catania, Italy – sequence: 6 givenname: Veronica surname: D’Agate fullname: D’Agate, Veronica organization: 2Division of Cardiology, Ferrarotto Hospital, University of Catania, 95100 Catania, Italy – sequence: 7 givenname: Salvatore surname: Piro fullname: Piro, Salvatore organization: 1Department of Clinical and Experimental Medicine, Garibaldi Hospital, University of Catania, 95122 Catania, Italy – sequence: 8 givenname: Corrado surname: Tamburino fullname: Tamburino, Corrado organization: 2Division of Cardiology, Ferrarotto Hospital, University of Catania, 95100 Catania, Italy – sequence: 9 givenname: Francesco surname: Purrello fullname: Purrello, Francesco email: fpurrell@unict.it organization: 1Department of Clinical and Experimental Medicine, Garibaldi Hospital, University of Catania, 95122 Catania, Italy – sequence: 10 givenname: Agata Maria surname: Rabuazzo fullname: Rabuazzo, Agata Maria organization: 1Department of Clinical and Experimental Medicine, Garibaldi Hospital, University of Catania, 95122 Catania, Italy |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28973588$$D View this record in MEDLINE/PubMed |
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PublicationDecade | 2010 |
PublicationPlace | Washington, DC |
PublicationPlace_xml | – name: Washington, DC – name: United States – name: Washington |
PublicationTitle | The journal of clinical endocrinology and metabolism |
PublicationTitleAlternate | J Clin Endocrinol Metab |
PublicationYear | 2017 |
Publisher | Endocrine Society Copyright Oxford University Press Oxford University Press |
Publisher_xml | – name: Endocrine Society – name: Copyright Oxford University Press – name: Oxford University Press |
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Snippet | ContextPrediabetes is associated with subclinical cardiac changes associated with heart failure development.ObjectiveWe investigated diastolic function and its... Prediabetes is associated with subclinical cardiac changes associated with heart failure development. We investigated diastolic function and its association... Abstract Prediabetes is associated with subclinical cardiac changes associated with heart failure development. We investigated diastolic function and its... Prediabetes is associated with subclinical cardiac changes associated with heart failure development.ContextPrediabetes is associated with subclinical cardiac... |
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SubjectTerms | Adolescent Adult Advanced glycosylation end products Aged Asymptomatic Diseases Atrium Blood glucose Blood Glucose - analysis Cardiovascular diseases Congestive heart failure Coronary artery disease Cross-Sectional Studies Diastole Doppler effect Echocardiography Fasting Female Glucose Glucose tolerance Glucose Tolerance Test Glycated Hemoglobin A - analysis Glycosylation Heart diseases Hemoglobin Humans Laboratory testing Male Middle Aged Prediabetic State - blood Prediabetic State - classification Prediabetic State - complications Prediabetic State - diagnosis Ventricle Ventricular Dysfunction, Left - blood Ventricular Dysfunction, Left - complications Ventricular Dysfunction, Left - diagnosis Young Adult |
Title | HbA1c Identifies Subjects With Prediabetes and Subclinical Left Ventricular Diastolic Dysfunction |
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