Cited by 76Diabetes, Cardiovascular Risks, and LipoproteinsDiabetes Treatment and ManagementPhosphodiesterase function and regulation

Treatment with Sildenafil Improves Insulin Sensitivity in Prediabetes: A Randomized, Controlled Trial

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Ramirez, Claudia E., Nian, Hui, Yu, Chang, Gamboa, Jorge L., Luther, James M., Brown, Nancy J., Shibao, Cyndya A.·2015·The Journal of Clinical Endocrinology & Metabolism

Abstract

CONTEXT: Sildenafil increases insulin sensitivity in mice. In humans, phosphodiesterase 5 inhibition improves disposition index, but the mechanism of this effect has not been elucidated and may depend on duration. In addition, increasing cyclic GMP without increasing nitric oxide could have beneficial effects on fibrinolytic balance. OBJECTIVE: The objective was to test the hypothesis that chronic phosphodiesterase 5 inhibition with sildenafil improves insulin sensitivity and secretion without diminishing fibrinolytic function. DESIGN: This was a randomized, double-blind, placebo-controlled study. SETTING: This trial was conducted at Vanderbilt Clinical Research Center. PARTICIPANTS: Participants included overweight individuals with prediabetes. INTERVENTIONS: Subjects were randomized to treatment with sildenafil 25 mg three times a day or matching placebo for 3 months. Subjects underwent a hyperglycemic clamp prior to and at the end of treatment. MAIN OUTCOME MEASURES: The primary outcomes of the study were insulin sensitivity and glucose-stimulated insulin secretion. RESULT: Twenty-one subjects completed each treatment arm. After 3 months, the insulin sensitivity index was significantly greater in the sildenafil group compared to the placebo group by 1.84 mg/kg/min per μU/mL*100 (95% confidence interval, 0.01 to 3.67 mg/kg/min per μU/mL*100; P = .049), after adjusting for baseline insulin sensitivity index and body mass index. In contrast, there was no effect of 3-month treatment with sildenafil on acute- or late-phase glucose-stimulated insulin secretion (P > .30). Sildenafil decreased plasminogen activator inhibitor-1 (P = .01), without altering tissue-plasminogen activator. In contrast to placebo, sildenafil also decreased the urine albumin-to-creatinine ratio from 12.67 ± 14.67 to 6.84 ± 4.86 μg/mg Cr. This effect persisted 3 months after sildenafil discontinuation. CONCLUSIONS: Three-month phosphodiesterase 5 inhibition enhances insulin sensitivity and improves markers of endothelial function.

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Crossref · 10.1210/jc.2015-3415

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  • Sildenafil treatment improved fibrinolytic balance, decreasing PAI-1 concentrations without altering t-PA concentrations.

    “Sildenafil treatment also improved fibrinolytic balance, decreasing PAI-1 concentrations without altering t-PA concentrations.”

    From The Vasculature in Prediabetes (2018) · cites this paper as [234]

  • Ramirez et al reported that three-month treatment with sildenafil did not affect early or late insulin secretion in individuals with prediabetes.

    “Ramirez et al reported that three-month treatment with sildenafil increased the insulin sensitivity index calculated from hyperglycemic clamps in individuals with prediabetes without affecting early or late insulin secretion.234”

    From The Vasculature in Prediabetes (2018) · cites this paper as [234]

  • Ramirez et al reported that three-month treatment with sildenafil increased the insulin sensitivity index calculated from hyperglycemic clamps in individuals with prediabetes.

    “Ramirez et al reported that three-month treatment with sildenafil increased the insulin sensitivity index calculated from hyperglycemic clamps in individuals with prediabetes without affecting early or late insulin secretion.234”

    From The Vasculature in Prediabetes (2018) · cites this paper as [234]

  • Sildenafil reduced urine microalbuminuria, a marker of endothelial function that predicts adverse cardiovascular outcomes.

    “Sildenafil reduced urine microalbuminuria, a marker of endothelial function that predicts adverse cardiovascular outcomes.”

    From The Vasculature in Prediabetes (2018) · cites this paper as [234]

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References 41 · Cited by 76

Authors
Ramirez, C. E., Nian, H., Yu, C., Gamboa, J. L., Luther, J. M., Brown, N. J., & Shibao, C. A.
Affiliations
  • Departments of Medicine (C.E.R., J.L.G., J.M.L., N.J.B., C.A.S.), Nashville, Tennessee 37232
  • Vanderbilt University (US)
Corresponding author
Brown, Nancy J.
Venue
The Journal of Clinical Endocrinology & Metabolism
Published
2015-12-01
Volume
100
Issue
12
Pages
4533-4540
ISSN
  • 0021-972X (ISSN-L)
  • 1945-7197
OpenAlex
W2173886858
Cited by
76
References
41
Citations by year
2025: 5 · 2024: 7 · 2023: 4 · 2022: 6 · 2021: 6 · 2020: 12 · 2019: 9 · 2018: 6 · 2017: 10 · 2016: 9 · 2015: 1 · 2013: 1
FWCI
7.51
Type
journal article
Language
en
Open access
Locations
  • The Journal of Clinical Endocrinology & Metabolism (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Heart, Lung, and Blood Institute (R01HL060906, K23HL103976, HL060906)
  • National Institute of Diabetes and Digestive and Kidney Diseases (K23DK100533, U24DK059637, DK 059637, R01DK096994, 1DK020593, P30DK020593)
  • National Center for Research Resources (UL1RR024975)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Phosphodiesterase function and regulation
Keywords
sildenafil, phosphodiesterase-5 inhibition, insulin sensitivity, prediabetes, glucose-stimulated insulin secretion, plasminogen activator inhibitor-1, fibrinolysis, endothelial function, albuminuria, cyclic GMP, nitric oxide, hyperglycemic clamp
MeSH terms
Sildenafil Citrate, Adult, Albuminuria, Double-Blind Method, Endothelium, Vascular, Female, Fibrinolysis, Glucose, Glucose Tolerance Test, Hemodynamics, Humans, Insulin, Insulin Resistance, Male, Middle Aged, Prediabetic State, Glucose Clamp Technique, Plasminogen Activator Inhibitor 1, Overweight, Phosphodiesterase 5 Inhibitors

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