Association of Elevated Arterial Stiffness With Cardiac Target Organ Damage and Cardiac Autonomic Neuropathy in Young Adults With Diabetes: The SEARCH for Diabetes in Youth Study

Author:

Urbina Elaine M.1ORCID,Isom Scott2,Dabelea Dana3,D’Agostino Ralph2,Daniels Stephen R.4,Dolan Lawrence M.1,Imperatore Giuseppina5,Lustigova Eva6,Marcovina Santica7,Mottl Amy8,Pihoker Catherine9,Shah Amy S.1

Affiliation:

1. 1Department of Pediatrics, Cincinnati Children’s Hospital Medical Center and University of Cincinnati, Cincinnati, OH

2. 2Department of Biostatistics and Data Science, Wake Forest School of Medicine, Winston-Salem, NC

3. 3Lifecourse Epidemiology of Adiposity and Diabetes (LEAD) Center, University of Colorado Anschutz Medical Campus (CU-Anschutz), Aurora, CO

4. 4Department of Pediatrics, University of Colorado Anschutz Medical Campus (CU-Anschutz), Aurora, CO

5. 5Division of Diabetes Translation, Centers for Disease Control and Prevention, Atlanta, GA

6. 6Department of Research & Evaluation, Kaiser Permanente Southern California, Pasadena, CA

7. 7Department of Medicine, University of Washington, Seattle, WA

8. 8Division of Nephrology and Hypertension, University of North Carolina School of Medicine, Chapel Hill, NC

9. 9Department of Pediatrics, University of Washington, Seattle, WA

Abstract

OBJECTIVEAdults with diabetes are at risk for cardiovascular (CV) events, possibly due to increased arterial stiffness (AS) and cardiac autonomic neuropathy (CAN). We sought to determine whether 1) AS is associated with cardiac target organ damage in young adults with youth-onset diabetes, 2) whether CAN is associated with AS, as one possible etiology for increased AS in this cohort, and 3) whether these relationships differ by type of diabetes.RESEARCH DESIGN AND METHODSParticipants from the SEARCH for Diabetes in Youth Study (type 1 diabetes [T1D], n = 222; type 2 diabetes [T2D], n = 177; mean age 23 years) had clinical, echocardiographic, AS, and CAN assessed. Linear regression was performed to determine whether AS was associated with cardiac changes and CAN and whether relationships differed by diabetes type.RESULTSAS was significantly associated with cardiac structure (left ventricular mass index, P < 0.0001), systolic function (ejection fraction, P = 0.03) and diastolic function (transmitral peak early [E]/atrial [A] wave velocities ratio, P = 0.008; early [e′]/atrial [a′] waves, P = 0.02) after adjustments for CV risk factors. The association between AS and CAN was not significant when other important covariates were added. These relationships were mostly similar in both T1D and T2D.CONCLUSIONSAS is associated with cardiac changes in young adults with diabetes. CAN-induced AS does not appear to be an etiology for cardiac abnormalities in this cohort.

Funder

Barbara Davis Center at the University of Colorado at Denver

University of Colorado Pediatric Clinical and Translational Research Center, NIH/NCATS

Clinical & Translational Research Institute

Southern California Permanente Medical Group

Seattle Children’s Hospital

the Medical University of South Carolina, NIH/National Center for Advancing Translational Sciences

the University of Cincinnati, NIH/NCATS

NIH

Kaiser Foundation Health Plan

Clinical Research Center

Centers for Disease Control and Prevention

National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases

Kaiser Permanente Southern California

National Institute of Diabetes and Digestive and Kidney Diseases

NIH/NCATS

University of Washington

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

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