Key result
A 6-hour combined hyperglycemic and hyperinsulinemic clamp increased myocardial lipid content by 34.4% (from 0.20% to 0.26%; P=0.0009) in healthy subjects.
Why the study?
Does acute combined hyperglycemia and hyperinsulinemia increase myocardial lipid content and alter myocardial function in healthy subjects?
Does acute combined hyperglycemia and hyperinsulinemia increase myocardial lipid content and alter myocardial function in healthy subjects?
Effect estimate: 34.4% increase
Absolute Event Rate: 0.26% vs 0.2%
p-value: p=0.0009
Acute combined hyperglycemia and hyperinsulinemia induce short-term myocardial lipid accumulation and functional alterations in healthy subjects, suggesting a mechanism for cardiac steatosis in metabolic diseases.
Acute hyperglycemia may promote myocardial steatosis; leaves open its role in diabetic cardiomyopathy.
Increased myocardial lipid content (MYCL) recently has been linked to the development of cardiomyopathy in diabetes. In contrast to steatosis in skeletal muscle and liver, previous investigations could not confirm a link between MYCL and insulin resistance. Thus, we hypothesized that cardiac steatosis might develop against the background of the metabolic environment typical for prediabetes and early type 2 diabetes: combined hyperglycemia and hyperinsulinemia. Therefore, we aimed to prove the principle that acute hyperglycemia (during a 6-h clamp) affects MYCL and function (assessed by (1)H magnetic resonance spectroscopy and imaging) in healthy subjects (female subjects: n = 8, male subjects: n = 10; aged 28 ± 5 years; BMI 22.4 ± 2.6 kg/m(2)). Combined hyperglycemia (202.0 ± 10.6 mg/dL) and hyperinsulinemia (110.6 ± 59.0 μU/mL) were, despite insulin-mediated suppression of free fatty acids, associated with a 34.4% increase in MYCL (baseline: 0.20 ± 0.17%, clamp: 0.26 ± 0.22% of water signal; P = 0.0009), which was positively correlated with the area under the curve of insulin (R = 0.59, P = 0.009) and C-peptide (R = 0.81, P < 0.0001) during the clamp. Furthermore, an increase in ejection fraction (P < 0.0001) and a decrease in end-systolic volume (P = 0.0002) were observed, which also were correlated with hyperinsulinemia. Based on our findings, we conclude that combined hyperglycemia and hyperinsulinemia induce short-term myocardial lipid accumulation and alterations in myocardial function in normal subjects, indicating that these alterations might be directly responsible for cardiac steatosis in metabolic diseases.
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Winhofer et al. (2012) studied Healthy subjects (n=18). Combined hyperglycemia and hyperinsulinemia clamp vs. Baseline was evaluated on Myocardial lipid content (MYCL) (34.4% increase, p=0.0009). A 6-hour combined hyperglycemic and hyperinsulinemic clamp increased myocardial lipid content by 34.4% (from 0.20% to 0.26%; P=0.0009) in healthy subjects.
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