Usefulness of Growth Differentiation Factor-15 Levels to Predict Diabetic Cardiomyopathy in Asymptomatic Patients With Type 2 Diabetes Mellitus

Growth differentiation factor-15 (GDF-15) is a stress-responsive cytokine that increased in patients with established type 2 diabetes mellitus (DM). Diabetic cardiomyopathy (DC), defined as left ventricular diastolic dysfunction (LVDD) in patients with type 2 DM in the absence of arterial hypertensi...

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Veröffentlicht in:The American journal of cardiology 2014-09, Vol.114 (6), p.890-894
Hauptverfasser: Dominguez-Rodriguez, Alberto, MD, PhD, Abreu-Gonzalez, Pedro, PhD, Avanzas, Pablo, MD, PhD
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creator Dominguez-Rodriguez, Alberto, MD, PhD
Abreu-Gonzalez, Pedro, PhD
Avanzas, Pablo, MD, PhD
description Growth differentiation factor-15 (GDF-15) is a stress-responsive cytokine that increased in patients with established type 2 diabetes mellitus (DM). Diabetic cardiomyopathy (DC), defined as left ventricular diastolic dysfunction (LVDD) in patients with type 2 DM in the absence of arterial hypertension, heart disease, or other heart disease, was assessed by GDF-15 levels in type 2 DM patients with and without DC. A total of 213 DM outpatients had blood samples drawn and on the same day (basal) underwent echocardiography and treadmill exercise testing. Plasma GDF-15 concentrations were measured by an enzyme-linked immunosorbent assay (ELISA) at baseline. DC was diagnosed in the presence of LVDD, defined when early mitral valve flow velocity (E) and early diastolic lengthening velocity (E′) ratio was E/E′ ≥15. The prevalence of DC was 21.13%. GDF-15 levels were higher in patients with DC compared with those without DC (5,273 [8,708.4] vs 2,812.66 [7,662.1] pg/ml, respectively, p
doi_str_mv 10.1016/j.amjcard.2014.06.020
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Diabetic cardiomyopathy (DC), defined as left ventricular diastolic dysfunction (LVDD) in patients with type 2 DM in the absence of arterial hypertension, heart disease, or other heart disease, was assessed by GDF-15 levels in type 2 DM patients with and without DC. A total of 213 DM outpatients had blood samples drawn and on the same day (basal) underwent echocardiography and treadmill exercise testing. Plasma GDF-15 concentrations were measured by an enzyme-linked immunosorbent assay (ELISA) at baseline. DC was diagnosed in the presence of LVDD, defined when early mitral valve flow velocity (E) and early diastolic lengthening velocity (E′) ratio was E/E′ ≥15. The prevalence of DC was 21.13%. GDF-15 levels were higher in patients with DC compared with those without DC (5,273 [8,708.4] vs 2,812.66 [7,662.1] pg/ml, respectively, p &lt;0.001). We assessed predictors of DC using multivariate regression analysis. GDF-15 (odds ratio 9.9; 95% confidence interval [3.9 to 24.5], p &lt;0.001) was the unique independent predictor of DC. The results of receiver operating characteristic curve show that the cut-off point of 3,812 pg/ml of GDF-15 was indicative for DC (AUC = 0.83, sensitivity = 82.2% and specificity = 70.2%, p &lt;0.0001). In conclusion, GDF-15 represents a useful and novel tool to screen DC in patients with type 2 DM.</description><identifier>ISSN: 0002-9149</identifier><identifier>EISSN: 1879-1913</identifier><identifier>DOI: 10.1016/j.amjcard.2014.06.020</identifier><identifier>PMID: 25073564</identifier><identifier>CODEN: AJCDAG</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Biomarkers - blood ; Body mass index ; Cardiomyopathy ; Cardiovascular ; Cardiovascular disease ; Confidence intervals ; Cytokines ; Diabetes ; Diabetes Mellitus, Type 2 - blood ; Diabetes Mellitus, Type 2 - complications ; Diabetic Cardiomyopathies - blood ; Diabetic Cardiomyopathies - epidemiology ; Diabetic Cardiomyopathies - etiology ; Echocardiography ; Electrocardiography ; Enzyme-Linked Immunosorbent Assay ; Enzymes ; Exercise Test ; Female ; Fitness equipment ; Flow velocity ; Gender ; Growth Differentiation Factor 15 - blood ; Heart attacks ; Heart failure ; Heart Ventricles - diagnostic imaging ; Heart Ventricles - physiopathology ; Humans ; Hypertension ; Logistics ; Male ; Middle Aged ; Normal distribution ; Oxidative Stress ; Prevalence ; Prognosis ; Regression analysis ; ROC Curve ; Spain - epidemiology ; Statins ; Stroke Volume ; Variables</subject><ispartof>The American journal of cardiology, 2014-09, Vol.114 (6), p.890-894</ispartof><rights>Elsevier Inc.</rights><rights>2014 Elsevier Inc.</rights><rights>Copyright © 2014 Elsevier Inc. 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Diabetic cardiomyopathy (DC), defined as left ventricular diastolic dysfunction (LVDD) in patients with type 2 DM in the absence of arterial hypertension, heart disease, or other heart disease, was assessed by GDF-15 levels in type 2 DM patients with and without DC. A total of 213 DM outpatients had blood samples drawn and on the same day (basal) underwent echocardiography and treadmill exercise testing. Plasma GDF-15 concentrations were measured by an enzyme-linked immunosorbent assay (ELISA) at baseline. DC was diagnosed in the presence of LVDD, defined when early mitral valve flow velocity (E) and early diastolic lengthening velocity (E′) ratio was E/E′ ≥15. The prevalence of DC was 21.13%. GDF-15 levels were higher in patients with DC compared with those without DC (5,273 [8,708.4] vs 2,812.66 [7,662.1] pg/ml, respectively, p &lt;0.001). We assessed predictors of DC using multivariate regression analysis. GDF-15 (odds ratio 9.9; 95% confidence interval [3.9 to 24.5], p &lt;0.001) was the unique independent predictor of DC. The results of receiver operating characteristic curve show that the cut-off point of 3,812 pg/ml of GDF-15 was indicative for DC (AUC = 0.83, sensitivity = 82.2% and specificity = 70.2%, p &lt;0.0001). In conclusion, GDF-15 represents a useful and novel tool to screen DC in patients with type 2 DM.</description><subject>Biomarkers - blood</subject><subject>Body mass index</subject><subject>Cardiomyopathy</subject><subject>Cardiovascular</subject><subject>Cardiovascular disease</subject><subject>Confidence intervals</subject><subject>Cytokines</subject><subject>Diabetes</subject><subject>Diabetes Mellitus, Type 2 - blood</subject><subject>Diabetes Mellitus, Type 2 - complications</subject><subject>Diabetic Cardiomyopathies - blood</subject><subject>Diabetic Cardiomyopathies - epidemiology</subject><subject>Diabetic Cardiomyopathies - etiology</subject><subject>Echocardiography</subject><subject>Electrocardiography</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Enzymes</subject><subject>Exercise Test</subject><subject>Female</subject><subject>Fitness equipment</subject><subject>Flow velocity</subject><subject>Gender</subject><subject>Growth Differentiation Factor 15 - blood</subject><subject>Heart attacks</subject><subject>Heart failure</subject><subject>Heart Ventricles - diagnostic imaging</subject><subject>Heart Ventricles - physiopathology</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Logistics</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Normal distribution</subject><subject>Oxidative Stress</subject><subject>Prevalence</subject><subject>Prognosis</subject><subject>Regression analysis</subject><subject>ROC Curve</subject><subject>Spain - epidemiology</subject><subject>Statins</subject><subject>Stroke Volume</subject><subject>Variables</subject><issn>0002-9149</issn><issn>1879-1913</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFUsFu1DAQjRCIbgufALLEhUvCTBw7mwuoWmhBWkQlWnG0vM5E9ZLEW9spylf0l_FqF5B64WLLmjdvnt-bLHuFUCCgfLct9LA12rdFCVgVIAso4Um2wGXd5Nggf5otAKDMG6yak-w0hG16Igr5PDspBdRcyGqRPdwE6qZ-pBCY69ild7_iLftou448jdHqaN3ILrSJzuco2JruqQ8sOnblqbUmJqzeULSGrZIY64bZ7XS8nZkd2XmYh110g96Xr9KZGAP7YdOE63lHrDw2U2Bfqe9tnMKL7Fmn-0Avj_dZdnPx6Xr1OV9_u_yyOl_nRgiMedtsaFMiyM5ICaarAbQ2HETHK1k1nNeiQhClrIkv26pGCdBCVTeCUqFs-Vn29sC78-5uohDVYINJIvRIbgoq-YSNbJYgE_TNI-jWTX5M6hRK5EuUJYeEEgeU8S4ET53aeTtoPysEtU9MbdUxMbVPTIFUKbHU9_rIPm0Gav92_YkoAT4cAMl3urfkVTDJSJPc92Siap3974j3jxhMb0drdP-TZgr_fqNCqUB936_NfmuwAuSyXvLfvW-99A</recordid><startdate>20140915</startdate><enddate>20140915</enddate><creator>Dominguez-Rodriguez, Alberto, MD, PhD</creator><creator>Abreu-Gonzalez, Pedro, PhD</creator><creator>Avanzas, Pablo, MD, PhD</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7Z</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20140915</creationdate><title>Usefulness of Growth Differentiation Factor-15 Levels to Predict Diabetic Cardiomyopathy in Asymptomatic Patients With Type 2 Diabetes Mellitus</title><author>Dominguez-Rodriguez, Alberto, MD, PhD ; 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Diabetic cardiomyopathy (DC), defined as left ventricular diastolic dysfunction (LVDD) in patients with type 2 DM in the absence of arterial hypertension, heart disease, or other heart disease, was assessed by GDF-15 levels in type 2 DM patients with and without DC. A total of 213 DM outpatients had blood samples drawn and on the same day (basal) underwent echocardiography and treadmill exercise testing. Plasma GDF-15 concentrations were measured by an enzyme-linked immunosorbent assay (ELISA) at baseline. DC was diagnosed in the presence of LVDD, defined when early mitral valve flow velocity (E) and early diastolic lengthening velocity (E′) ratio was E/E′ ≥15. The prevalence of DC was 21.13%. GDF-15 levels were higher in patients with DC compared with those without DC (5,273 [8,708.4] vs 2,812.66 [7,662.1] pg/ml, respectively, p &lt;0.001). We assessed predictors of DC using multivariate regression analysis. GDF-15 (odds ratio 9.9; 95% confidence interval [3.9 to 24.5], p &lt;0.001) was the unique independent predictor of DC. The results of receiver operating characteristic curve show that the cut-off point of 3,812 pg/ml of GDF-15 was indicative for DC (AUC = 0.83, sensitivity = 82.2% and specificity = 70.2%, p &lt;0.0001). In conclusion, GDF-15 represents a useful and novel tool to screen DC in patients with type 2 DM.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25073564</pmid><doi>10.1016/j.amjcard.2014.06.020</doi><tpages>5</tpages></addata></record>
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subjects Biomarkers - blood
Body mass index
Cardiomyopathy
Cardiovascular
Cardiovascular disease
Confidence intervals
Cytokines
Diabetes
Diabetes Mellitus, Type 2 - blood
Diabetes Mellitus, Type 2 - complications
Diabetic Cardiomyopathies - blood
Diabetic Cardiomyopathies - epidemiology
Diabetic Cardiomyopathies - etiology
Echocardiography
Electrocardiography
Enzyme-Linked Immunosorbent Assay
Enzymes
Exercise Test
Female
Fitness equipment
Flow velocity
Gender
Growth Differentiation Factor 15 - blood
Heart attacks
Heart failure
Heart Ventricles - diagnostic imaging
Heart Ventricles - physiopathology
Humans
Hypertension
Logistics
Male
Middle Aged
Normal distribution
Oxidative Stress
Prevalence
Prognosis
Regression analysis
ROC Curve
Spain - epidemiology
Statins
Stroke Volume
Variables
title Usefulness of Growth Differentiation Factor-15 Levels to Predict Diabetic Cardiomyopathy in Asymptomatic Patients With Type 2 Diabetes Mellitus
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