Contribution of circulating Mfge8 to human T2DM and cardiovascular disease

Madhusmita Rout1, Megan W Malone-Perez2, Gilseung Park2

  • 1Department of Pediatrics, Section of Genetics, College of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.

Gene
|June 20, 2024
PubMed

Insights

Milk fat globule-EGF factor 8 (MFGE8) protein is linked to type 2 diabetes mellitus (T2DM) and cardiovascular disease risk. Elevated MFGE8 levels, particularly with a specific genetic variant, may predict T2DM and heart disease in humans.

Area of Science:

  • Genetics and human physiology
  • Cardiovascular research
  • Metabolic disease research

Background:

  • Milk fat globule-EGF factor 8 (MFGE8) is implicated in inflammation and atherosclerosis in animal models of type 2 diabetes mellitus (T2DM).
  • Its role in human obesity, T2DM, and cardiovascular disease, especially concerning a specific Asian Indian population variant (rs371227978; Arg148His), requires further investigation.

Purpose of the Study:

  • To investigate the association between MFGE8, a specific genetic variant, and T2DM risk in diverse human populations.
  • To explore the impact of MFGE8-enriched extracellular vesicles (EVs) on cardiometabolic health using a zebrafish model.

Main Methods:

  • Genetic association study in Asian Indians (n=4897) and multiethnic cohorts from UK Biobank (n=455,808) and the US (n=1150).
  • Analysis of circulating MFGE8 levels and their correlation with glucose in variant carriers and non-carriers.
  • Exposure of zebrafish larvae to MFGE8-enriched human EVs, with and without high-fat diet (HFD), to assess cardiometabolic effects.

Main Results:

  • The Arg148His variant in MFGE8 was associated with higher circulating MFGE8 and a positive correlation with glucose in Asian Indians.
  • This variant was absent in non-South Asian ethnicities, yet serum MFGE8 correlated significantly with blood glucose across these groups.
  • Zebrafish exposed to MFGE8-enriched EVs rapidly developed fatty liver and heart hypertrophy, effects exacerbated by HFD, while controls only showed these after HFD.

Conclusions:

  • Circulating MFGE8 levels, influenced by genetics and potentially EVs, show a significant association with glucose levels and T2DM risk.
  • MFGE8-enriched EVs can induce rapid cardiometabolic changes in zebrafish, supporting its role in disease pathogenesis.
  • MFGE8 may serve as a potential predictive biomarker for T2DM and cardiovascular disease risk in humans.

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