Obesity dominates early effects on cardiac structure and arterial stiffness in people with type 2 diabetes

Layla A. Abushamat*, Daniel Enge, Takashi Fujiwara, Michal Schäfer, Ethan W. Clark, Erin K. Englund, Rebecca L. Scalzo, Aspen Johnston, Deirdre Rafferty, Irene E. Schauer, Mary O. Whipple, Kendall Hunter, Amy G. Huebschmann, Kristen J. Nadeau, Kelly Jarvis, Alex J. Barker, Judith G. Regensteiner, Jane E.B. Reusch

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Objective:Type 2 diabetes (T2D) and obesity are global epidemics leading to excess cardiovascular disease (CVD). This study investigates standard and novel cardiac MRI parameters to detect subclinical cardiac and central vascular dysfunction in inactive people with and without T2D.Methods:Physically inactive age and BMI-similar premenopausal women and men with (n = 22) and without [n = 34, controls with overweight/obesity (CWO)] uncomplicated T2D were compared to an age-similar and sex-similar reference control cohort (n = 20). Left ventricular (LV) structure, function, and aortic stiffness were assessed by MRI. Global arterial pulse wave velocity (PWV) was assessed using carotid-to-femoral applanation tonometry. Regional PWV was measured via 2D phase-contrast MRI and 4D flow MRI.Results:Global arterial PWV did not differ between CWO and T2D. 2D PC-MRI PWV in the ascending aorta was higher in people with T2D compared with CWOs (P < 0.01). 4D flow PWV in the thoracic aorta was higher in CWO (P < 0.01), and T2D (P < 0.001) compared with RC. End-diastolic volume, end-systolic volume, stroke volume, and cardiac output were lower in CWO and T2D groups compared with reference control.Conclusion:Subclinical changes in arterial stiffening and cardiac remodeling in inactive CWO and T2D compared with reference control support obesity and/or physical inactivity as determinants of incipient CVD complications in uncomplicated T2D. Future studies should determine the mechanistic causes of the CVD complications in greater detail in order to create therapeutic targets.Clinical Trial Registration:Cardiovascular Mechanisms of Exercise Intolerance in Diabetes and the Role of Sex (NCT03419195).

Original languageEnglish (US)
Pages (from-to)1775-1784
Number of pages10
JournalJournal of hypertension
Volume41
Issue number11
DOIs
StatePublished - Nov 1 2023

Funding

Research reported in this publication was supported, in part, by the National Institutes of Health's National Institute on Aging, Grant Number P30AG059988 and K01AG080070. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. Other funding includes the VA Clinical Merit CX001532 (J.E.B.R.), VA Merit BX002046, NIH-5T32HL007171, VA CDA2 BX004533 (R.L.S.), NIH-NCATS, UL1TR001082 (J.E.B.R., J.G.R., R.L.S.), Ludeman Family Center for Women's Health Research (R.L.S., J.G.R., J.E.B.R., D.E.), ADA Cardiovascular Metabolism Fellowship Award 1-21-CMF-003 (L.A.). NIH predoctoral support T32DK120520 (D.E.), P30 DK116073 (J.E.B.R.), NIH/NCATS Colorado CTSA Grant Number KL2 TR002534 (E.K.E.), AHA853697 (E.K.E.) and ADA Junior Faculty Award 7-11-JF-42 (I.E.S.).

Keywords

  • aortic stiffness
  • cardiac MRI
  • heart failure
  • obesity
  • physical inactivity
  • pulse wave velocity
  • type 2 diabetes

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Physiology
  • Internal Medicine

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