Abstract

Purpose De novo lipogenesis has been inversely associated with serum sex hormone-binding globulin (SHBG) levels. However, the directionality of this association has remained uncertain. We, therefore, studied individuals with glycogen storage disease type 1a (GSD1a), who are characterized by a genetic defect in glucose-6-phosphatase resulting in increased rates of de novo lipogenesis, to assess the downstream effect on serum SHBG levels. Methods A case-control study comparing serum SHBG levels in patients with GSD1a (n = 10) and controls matched for age, sex, and BMI (n = 10). Intrahepatic lipid content and saturated fatty acid fraction were quantified by proton magnetic resonance spectroscopy. Results Serum SHBG levels were statistically significantly lower in patients with GSD1a compared to the controls (p = 0.041), while intrahepatic lipid content and intrahepatic saturated fatty acid fraction-a marker of de novo lipogenesis-were significantly higher in patients with GSD1a (p = 0.001 and p = 0.019, respectively). In addition, there was a statistically significant, inverse association of intrahepatic lipid content and saturated fatty acid fraction with serum SHBG levels in patients and controls combined (beta: - 0.28, 95% CI: - 0.47;- 0.09 and beta: - 0.02, 95% CI: - 0.04;- 0.01, respectively). Conclusion Patients with GSD1a, who are characterized by genetically determined higher rates of de novo lipogenesis, have lower serum SHBG levels than controls.
Original languageEnglish
Pages (from-to)1227-1234
Number of pages8
JournalJournal of Endocrinological Investigation
Volume45
Issue number6
Early online date7 Feb 2022
DOIs
Publication statusPublished - Jun 2022

Keywords

  • Glycogen storage disease type 1a
  • De novo lipogenesis
  • Intrahepatic lipid content
  • Sex hormone-binding globulin
  • DE-NOVO LIPOGENESIS
  • LIVER-DISEASE
  • P446L VARIANT
  • TESTOSTERONE
  • GCKR
  • WOMEN
  • CONTRACEPTION
  • MODULATION

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