4.7 Article

Insulin Pulse Characteristics and Insulin Action in Non-diabetic Humans

Journal

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
Volume 106, Issue 6, Pages 1702-1709

Publisher

ENDOCRINE SOC
DOI: 10.1210/clinem/dgab100

Keywords

insulin pulses; C-peptide kinetics; insulin action; endogenous glucose production; gluconeogenesis; glucose disappearance

Funding

  1. US National Institutes of Health [DK78646, DK116231]
  2. MIUR (Italian Minister for Education) under the initiative Departments of Excellence
  3. Mayo Clinic General Clinical Research Center [UL1 TR000135]

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The study showed that characteristics of pulsatile insulin secretion do not correlate with hepatic and peripheral insulin sensitivity in nondiabetic humans, even when considered independently of other factors.
Objective: Pulsatile insulin secretion is impaired in diseases such as type 2 diabetes that are characterized by insulin resistance. This has led to the suggestion that changes in insulin pulsatility directly impair insulin signaling. We sought to examine the effects of pulse characteristics on insulin action in humans, hypothesizing that a decrease in pulse amplitude or frequency is associated with impaired hepatic insulin action. Methods: We studied 29 nondiabetic subjects on two occasions. On 1 occasion, hepatic and peripheral insulin action was measured using a euglycemic clamp. The deuterated water method was used to estimate the contribution of gluconeogenesis to endogenous glucose production. On a separate study day, we utilized nonparametric stochastic deconvolution of frequently sampled peripheral C-peptide concentrations during fasting to reconstruct portal insulin secretion. In addition to measuring basal and pulsatile insulin secretion, we used approximate entropy to measure orderliness and Fourier transform to measure the average, and the dispersion of, insulin pulse frequencies. Results: In univariate analysis, basal insulin secretion (R-2 = 0.16) and insulin pulse amplitude (R-2 = 0.09) correlated weakly with insulin-induced suppression of gluconeogenesis. However, after adjustment for age, sex, and weight, these associations were no longer significant. The other pulse characteristics also did not correlate with the ability of insulin to suppress endogenous glucose production (and gluconeogenesis) or to stimulate glucose disappearance. Conclusions: Overall, our data demonstrate that insulin pulse characteristics, considered independently of other factors, do not correlate with measures of hepatic and peripheral insulin sensitivity in nondiabetic humans.

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