SMIM1 absence is associated with reduced energy expenditure and excess weight

Luca Stefanucci, Camous Moslemi, Ana R. Tomé, Samuel Virtue, Guillaume Bidault, Nicholas S. Gleadall, Laura P.E. Watson, Jing E. Kwa, Frances Burden, Samantha Farrow, , Ji Chen, MAGIC, Urmo Võsa, Keith Burling, Lindsay Walker, John Ord, Peter Baker, James Warner, Amy FraryMattia Frontini (Lead / Corresponding author)

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Abstract

Background: Obesity rates have nearly tripled in the past 50 years, and by 2030 more than 1 billion individuals worldwide are projected to be obese. This creates a significant economic strain due to the associated non-communicable diseases. The root cause is an energy expenditure imbalance, owing to an interplay of lifestyle, environmental, and genetic factors. Obesity has a polygenic genetic architecture; however, single genetic variants with large effect size are etiological in a minority of cases. These variants allowed the discovery of novel genes and biology relevant to weight regulation and ultimately led to the development of novel specific treatments. Methods: We used a case-control approach to determine metabolic differences between individuals homozygous for a loss-of-function genetic variant in the small integral membrane protein 1 (SMIM1) and the general population, leveraging data from five cohorts. Metabolic characterization of SMIM1−/− individuals was performed using plasma biochemistry, calorimetric chamber, and DXA scan. Findings: We found that individuals homozygous for a loss-of-function genetic variant in SMIM1 gene, underlying the blood group Vel, display excess body weight, dyslipidemia, altered leptin to adiponectin ratio, increased liver enzymes, and lower thyroid hormone levels. This was accompanied by a reduction in resting energy expenditure. Conclusion: This research identified a novel genetic predisposition to being overweight or obese. It highlights the need to investigate the genetic causes of obesity to select the most appropriate treatment given the large cost disparity between them. Funding: This work was funded by the National Institute of Health Research, British Heart Foundation, and NHS Blood and Transplant.

Original languageEnglish
Pages (from-to)1-13
Number of pages13
JournalMed
Volume5
Early online date20 Jun 2024
DOIs
Publication statusPublished - 13 Sept 2024

Keywords

  • blood groups
  • BMI
  • dyslipidemia
  • metabolism
  • obesity
  • population genetics
  • SMIM1
  • Translation to patients
  • Vel
  • weight

ASJC Scopus subject areas

  • General Medicine

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