4.7 Article

Relationship Between Left Ventricular Structural and Metabolic Remodeling in Type 2 Diabetes

期刊

DIABETES
卷 65, 期 1, 页码 44-52

出版社

AMER DIABETES ASSOC
DOI: 10.2337/db15-0627

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资金

  1. Oxford Partnership Comprehensive Biomedical Research Centre
  2. Department of Health's National Institute for Health Research Biomedical Research Centers
  3. British Heart Foundation (BHF) Centre of Research Excellence, Oxford
  4. Sir Henry Dale Fellowship - Wellcome Trust [098436/Z/12/Z]
  5. Sir Henry Dale Fellowship - Royal Society [098436/Z/12/Z]
  6. Oxford National Institute for Health Research Biomedical Research Centre
  7. British Heart Foundation [FS/11/50/29038, FS/12/32/29559] Funding Source: researchfish
  8. Medical Research Council [1239347] Funding Source: researchfish
  9. National Institute for Health Research [CL-2015-11-001, NF-SI-0512-10005] Funding Source: researchfish

向作者/读者索取更多资源

Concentric left ventricular (LV) remodeling is associated with adverse cardiovascular events and is frequently observed in patients with type 2 diabetes mellitus (T2DM). Despite this, the cause of concentric remodeling in diabetes per se is unclear, but it may be related to cardiac steatosis and impaired myocardial energetics. Thus, we investigated the relationship between myocardial metabolic changes and LV remodeling in T2DM. Forty-six nonhypertensive patients with T2DM and 20 matched control subjects underwent cardiovascular magnetic resonance to assess LV remodeling (LV mass-to-LV end diastolic volume ratio), function, tissue characterization before and after contrast using T1 mapping, and H-1 and P-31 magnetic resonance spectroscopy for myocardial triglyceride content (MTG) and phosphocreatine-to-ATP ratio, respectively. When compared with BMI- and blood pressure-matched control subjects, subjects with diabetes were associated with concentric LV remodeling, higher MTG, impaired myocardial energetics, and impaired systolic strain indicating a subtle contractile dysfunction. Importantly, cardiac steatosis independently predicted concentric remodeling and systolic strain. Extracellular volume fraction was unchanged, indicating the absence of fibrosis. In conclusion, cardiac steatosis may contribute to concentric remodeling and contractile dysfunction of the LV in diabetes. Because cardiac steatosis is modifiable, strategies aimed at reducing MTG may be beneficial in reversing concentric remodeling and improving contractile function in the hearts of patients with diabetes.

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