Journal of Diabetes and Metabolic Disorders

Volume 2017; Issue 01
12 Aug 2017

Getting to the Heart of Diabetes: Translational Science to Interventional Cardiology

Anh Pham1, Son Pham2, Robert JChilton2

1Director of Interventional Cardiology, VA hospital
2Department of Medicine, University of Texas Health Science Center, San Antonio, Texas

*Corresponding author: Robert J Chilton,Department of Medicine, University of Texas Health Science Center

San Antonio, Texas, Tel: 210 617-5100; Email:

Received Date:9February, 2017; Accepted Date: 9March, 2017; Published Date: 16 March, 2017





Suggested Citation



For the first time since 1993, data from the Centers for Disease Control and Prevention (CDC) show a decrease in life expectancy and an increase in deaths particularly among people younger than 65. Life expectancy decreased by 0.1 year from 78.9 to 78.8 and the age-adjusted death rate increased 1.2% from 724.6/100,000 standard population to 733.1 for the total U.S. population from 2014 to 2015. (figure 1)[1]. This raises significant concerns over the increasing obesity and diabetes pandemic.


Using animal models in translational research, we were able to understand some of the mechanisms by which diabetes increases Cardiovascular (CV) risks in patients.


Starting as early as the postnatal period, overfeeding in small animals was found to be associated with an increase in metabolic CV risk. In an elegant small animal study, Li et al found overweight animals have an increased production of reactive oxygen species in the heart as well as an increase in left ventricular dimension associated with a reduction in left ventricular ejection fraction[2]. With caloric reduction, there was improvement in left ventricular dimension and ejection fraction. Additionally, overfeeding causes early changes in cardiovascular gene expression resulting in an abnormal increase in the production of endothelin [1], Matrix Metalloproteinase (MMP) [2], and collagen density along with a decrease in the production and function of the antioxidant enzyme SOD superoxide dismutase[3].  These studies from animal research support previous human long term cardiovascular health outcomes[4,5].


The delivery of micronutrients to cardiac and skeletal muscle depends on adequate perfusion. We have known for years that insulin increases nitric oxide production and dilates arterioles in normal subjects[6]   However, in the insulin resistant state, nitric oxide production is decreased due to endothelial cell dysfunction[7]. Recent studies evaluating the effects of overfeeding found that overfeeding reduces nitric oxide production and stimulates endothelin 1 function (vasoconstriction) in skeletal muscle[8].(Figure 2) Additionally, prior studies found that insulin increases the sympathetic drive leading to an increased release of noradrenalin from postganglionic fibers[9]. Patients with type 2 diabetes were frequently noted to have hypertension as noted in the SAVOR, EXAMINE, TECOS and EMPA-REG trials[10].


In summary, translational changes seen in diabetes makes one consider the close inter-relationship of metabolic disease to cardiovascular disease. The increased incidence of obesity and diabetes and the decreased life expectancy require more than drug treatment to lower glucose level, blood pressure, and biomarkers. Lifestyle modifications remain the best option but at present, seem to be difficult to achieve by many people. The absolute risk reduction with medications remains suboptimal (figure 3).



  1. Jiaquan Xu, Sherry L Murphy, Kenneth D Kochanek (2015) Mortality in the United States, DHHS: CS272651.
  2. Li N, Guenancia C, Rigal E, Hachet O, Chollet P (2016) Short-term moderate diet restriction in adulthood can reverse oxidative, cardiovascular and metabolic alterations induced by postnatal overfeeding in mice. Sci Rep6:30817.
  3. Ahmed Habbout, Charles Guenancia, Julie Lorin, Eve Rigal (2013) Postnatal Overfeeding Causes Early Shifts in Gene Expression in the Heart and Long-Term Alterations in Cardiometabolic and Oxidative Parameters. PLoS One 8: e56981.
  4. Singhal A, Cole TJ, Fewtrell M, Kennedy K, Stephenson T, et al. (2007) Promotion of faster weight gain in infants born small for gestational age: Is there an adverse effect on later blood pressure? Circulation115:213-220.
  5. Elisa Fabbri, Chee W Chia, Richard G Spencer, Kenneth W Fishbein,David A Reiter (2017) Insulin Resistance Is Associated with Reduced Mitochondrial Oxidative Capacity Measured by 31P-MagneticResonance Spectroscopy in Participants Without Diabetes from the Baltimore Longitudinal Study of Aging Diabetes. Lancet 363: 1571-1578.
  6. Coggins M, Lindner J, Rattigan S, Jahn L, Fasy E, et al. (2001) Physiologic hyperinsulinemia enhances human skeletal muscle perfusion by capillary recruitment. Diabetes. 50:2682-2690.
  7. Wallis MG, Wheatley CM, Rattigan S, Barrett EJ, Clark AD, et al. (2002) Insulin-mediated hemodynamic changes are impaired in muscle of Zucker obese rats. Diabetes 51:3492-3498.
  8. Anna L Emanuel, Rick I. Meijer, Marcel HA Muskiet, Daniel H van Raalte (2017) Role of Insulin-Stimulated Adipose Tissue Perfusion in the Development of Whole-Body Insulin Resistance. ArteriosclerThrombVascBiol37: 411-418.
  9. Kleinridders A, Ferris HA, Cai W, Kahn CR (2014) Insulin action in brain regulates systemic metabolism and brain function. Diabetes 63:2232-2243.
  10. Michael EFarkouh, Michael Domanski, Lynn A Sleeper, Flora SSiami (2012) Strategies for Multivessel Revascularization in Patients with Diabetes. N Engl J Med 367:2375-2384.


Figure 1: Diabetes continues to have increasing deaths, etiologies and exact causes are complex but obesity and diabetes with CV disease are major risk factors. The drop in overall life expectancy was seen for the first time since 1993, particularly among people younger than 65.

Figure 2: The importance of the FREEDOM trial has many important facts, but one that is frequently overlooked is the continued high CV event rate in the best know revascularization procedure for ischemic heart disease in diabetes.

Figure3: This shows the important inter-relationship of diabetes and CV disease at a basic level.

Suggested Citation


Citation: Pham A, Pham S, ChiltonRJ (2017) Getting to the Heart of Diabetes: Translational Science to Interventional Cardiology. J Diabetes Treat 2017: J112.

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