Aldo-Keto Reductase 1C1 ( AKR1C1) as the First Mutated Gene in a Family with Nonsyndromic Primary Lipedema

Int J Mol Sci. 2020 Aug 29;21(17):6264. doi: 10.3390/ijms21176264.

Abstract

Lipedema is an often underdiagnosed chronic disorder that affects subcutaneous adipose tissue almost exclusively in women, which leads to disproportionate fat accumulation in the lower and upper body extremities. Common comorbidities include anxiety, depression, and pain. The correlation between mood disorder and subcutaneous fat deposition suggests the involvement of steroids metabolism and neurohormones signaling, however no clear association has been established so far. In this study, we report on a family with three patients affected by sex-limited autosomal dominant nonsyndromic lipedema. They had been screened by whole exome sequencing (WES) which led to the discovery of a missense variant p.(Leu213Gln) in AKR1C1, the gene encoding for an aldo-keto reductase catalyzing the reduction of progesterone to its inactive form, 20-α-hydroxyprogesterone. Comparative molecular dynamics simulations of the wild-type vs. variant enzyme, corroborated by a thorough structural and functional bioinformatic analysis, suggest a partial loss-of-function of the variant. This would result in a slower and less efficient reduction of progesterone to hydroxyprogesterone and an increased subcutaneous fat deposition in variant carriers. Overall, our results suggest that AKR1C1 is the first candidate gene associated with nonsyndromic lipedema.

Keywords: AKR1C1; aldo-keto reductase activity; lipedema; molecular modelling; steroid hormone metabolism; subcutaneous fat; whole exome sequencing.

MeSH terms

  • 20-Hydroxysteroid Dehydrogenases / chemistry
  • 20-Hydroxysteroid Dehydrogenases / genetics*
  • 20-Hydroxysteroid Dehydrogenases / metabolism
  • 20-alpha-Dihydroprogesterone / metabolism
  • Adult
  • Aged
  • Female
  • Humans
  • Lipedema / genetics*
  • Lipedema / metabolism
  • Loss of Function Mutation
  • Middle Aged
  • Models, Molecular
  • Molecular Dynamics Simulation
  • Mutation, Missense*
  • Pedigree
  • Progesterone / metabolism
  • Protein Conformation
  • Whole Exome Sequencing / methods*

Substances

  • 20-alpha-Dihydroprogesterone
  • Progesterone
  • 20-Hydroxysteroid Dehydrogenases
  • 3 alpha-beta, 20 beta-hydroxysteroid dehydrogenase