Cited by 108Hormonal and reproductive studiesDiabetes, Cardiovascular Risks, and LipoproteinsAdipokines, Inflammation, and Metabolic Diseases

Testosterone and type 2 diabetes

Grossmann, Mathis, Gianatti, Emily J, Zajac, Jeffrey D·2010·Current Opinion in Endocrinology, Diabetes & Obesity

Abstract

Purpose of review To describe the relationship between testosterone levels and type 2 diabetes (T2D). Recent findings Multiple epidemiological studies have shown that low testosterone levels are associated with and predict the future development of T2D and the metabolic syndrome. Although this relationship is confounded by the association of total testosterone with sex hormone-binding globulin, free testosterone remains associated with measures of insulin resistance and T2D in some, but not all studies. Although the link between low testosterone levels and insulin resistance is not solely a consequence of adiposity, current studies suggest that a substantial component is mediated through its association with body fat, in particular abdominal visceral adipose tissue. This testosterone-fat relationship is bi-directional, as both weight loss and testosterone therapy increase testosterone levels, reduce fat mass, and decrease insulin resistance. Summary Low testosterone levels are very commonly found in men with T2D and are associated with aging and obesity. Whether testosterone treatment in men with T2D decreases insulin resistance above that attributable to its fat-reducing effect is currently unknown. Future studies should compare testosterone treatment with lifestyle changes (exercise and weight loss measures), and other insulin-sensitizing agents. Until further evidence is available, testosterone therapy outside clinical trials should be reserved for diabetic men with unequi…

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Crossref · 10.1097/med.0b013e32833919cf

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  • Increased visceral fat releases increased amounts of pro-inflammatory cytokines, insulin and leptin; all of which may inhibit the activity of the HPT axis at multiple levels.

    “In addition to E2, increased visceral fat also releases increased amounts of pro-inflammatory cytokines, insulin and leptin; all of which may inhibit the activity of the HPT axis at multiple levels.30”

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References 73 · Cited by 108

Authors
Grossmann, M., Gianatti, E. J., & Zajac, J. D.
Affiliations
The University of Melbourne (AU)
Corresponding author
Grossmann, Mathis
Venue
Current Opinion in Endocrinology, Diabetes & Obesity
Published
2010-06
Volume
17
Issue
3
Pages
247-256
ISSN
1752-296X (ISSN-L)
OpenAlex
W2094440311
Cited by
108
References
73
Citations by year
2025: 5 · 2024: 1 · 2023: 5 · 2022: 5 · 2021: 1 · 2020: 4 · 2019: 7 · 2018: 9 · 2017: 3 · 2016: 7 · 2015: 6 · 2014: 14 · 2013: 7 · 2012: 16
FWCI
1.85
Type
journal article
Language
en
Open access
closed
Locations
  • Current Opinion in Endocrinology Diabetes and Obesity (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
  • Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
Keywords
testosterone, type 2 diabetes, insulin resistance, metabolic syndrome, sex hormone-binding globulin, free testosterone, visceral adipose tissue, obesity, aging, testosterone replacement therapy, hypogonadism, weight loss
MeSH terms
Aging, Diabetes Mellitus, Type 2, Humans, Insulin Resistance, Male, Sex Hormone-Binding Globulin, Testosterone, Metabolic Syndrome, Adiposity

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