Association of Serum Leptin With Visceral Adiposity and Insulin Resistance in Adults With Obesity

Authors

  • Dr. Emma Richardson Author
  • Dr. Luca Ferraro Author
  • Dr. Nadia Moreau Author
  • Dr. Daniel K. Mensah Author

DOI:

https://doi.org/10.61336/jdme.0602.04

Keywords:

Leptin, obesity, visceral adiposity, insulin resistance, adipose tissue, metabolic risk

Abstract

Leptin is an adipose-derived hormone involved in energy regulation and metabolic homeostasis. Circulating leptin concentrations increase with adiposity, but the relationship between leptin, visceral fat accumulation, and insulin resistance may vary among individuals with obesity. This study evaluated the association between serum leptin, visceral adiposity, and insulin resistance in adults with obesity. A cross-sectional observational study included 156 adults aged 30–65 years with BMI ≥30 kg/m². Anthropometric measurements, serum leptin, fasting glucose, fasting insulin, lipid profile, and inflammatory markers were assessed. Visceral adiposity was estimated using waist circumference and waist-to-height ratio, while HOMA-IR was used as a surrogate measure of insulin resistance. Participants with greater visceral adiposity had significantly higher serum leptin and HOMA-IR concentrations. Serum leptin demonstrated positive correlations with waist circumference, BMI, fasting insulin, and HOMA-IR. After adjustment for age, sex, BMI, and physical activity, leptin remained independently associated with HOMA-IR. These findings suggest that elevated circulating leptin is associated with visceral adiposity and insulin resistance among adults with obesity.

Author Biographies

  • Dr. Emma Richardson

    Department of Endocrinology and Metabolic Medicine

  • Dr. Luca Ferraro

    Department of Internal Medicine

  • Dr. Nadia Moreau

    Department of Endocrinology

  • Dr. Daniel K. Mensah

    Department of Medicine 

References

1. Zhang Y, Proenca R, Maffei M, Barone M, Leopold L, Friedman JM. Positional cloning of the mouse obese gene and its human homologue. Nature. 1994;372(6505):425–432.

2. Friedman JM, Halaas JL. Leptin and the regulation of body weight in mammals. Nature. 1998;395(6704):763–770.

3. Considine RV, Sinha MK, Heiman ML, Kriauciunas A, Stephens TW, Nyce MR, et al. Serum immunoreactive-leptin concentrations in normal-weight and obese humans. N Engl J Med. 1996;334(5):292–295.

4. Myers MG Jr, Leibel RL, Seeley RJ, Schwartz MW. Obesity and leptin resistance: distinguishing cause from effect. Trends Endocrinol Metab. 2010;21(11):643–651.

5. Mantzoros CS. The role of leptin in human obesity and disease: a review of current evidence. Ann Intern Med. 1999;130(8):671–680.

6. Ahima RS, Flier JS. Leptin. Annu Rev Physiol. 2000;62:413–437.

7. Park HK, Ahima RS. Leptin signaling. F1000Prime Rep. 2014;6:73.

8. Friedman JM. Leptin and the regulation of body weight. Keio J Med. 2011;60(1):1–9.

9. Després JP, Lemieux I. Abdominal obesity and metabolic syndrome. Nature. 2006;444(7121):881–887.

10. Neeland IJ, Ross R, Després JP, Matsuzawa Y, Yamashita S, Shai I, et al. Visceral and ectopic fat, atherosclerosis, and cardiometabolic disease. Lancet Diabetes Endocrinol. 2019;7(9):715–725.

11. Kahn SE, Hull RL, Utzschneider KM. Mechanisms linking obesity to insulin resistance and type 2 diabetes. Nature. 2006;444(7121):840–846.

12. Samuel VT, Shulman GI. The pathogenesis of insulin resistance: integrating signaling pathways and substrate flux. J Clin Invest. 2016;126(1):12–22.

13. Hotamisligil GS. Inflammation and metabolic disorders. Nature. 2006;444(7121):860–867.

14. Ouchi N, Parker JL, Lugus JJ, Walsh K. Adipokines in inflammation and metabolic disease. Nat Rev Immunol. 2011;11(2):85–97.

15. Kershaw EE, Flier JS. Adipose tissue as an endocrine organ. J Clin Endocrinol Metab. 2004;89(6):2548–2556.

Published

2026-08-27

Most read articles by the same author(s)

Similar Articles

1-10 of 42

You may also start an advanced similarity search for this article.