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Updated: Jun 23, 2025

Modeling and Evaluation of Murine Diabetic Cardiomyopathy Model
Published on: November 29, 2024
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.
Abstract:
MFGE8 is a major exosome (EV) protein known to mediate inflammation and atherosclerosis in type 2 diabetes mellitus (T2DM) in animal studies. The pathophysiological role of this protein in obesity, T2DM, and cardiovascular disease is less investigated in humans. Earlier we reported a rare Asian Indian population-specific missense variant (rs371227978; Arg148His) in the MFGE8 gene associated with increased circulating Mfge8 and T2DM. We have further investigated the role of Mfge8 with T2DM risk in additional Asian Indians (n = 4897) and Europeans and other multiethnic cohorts from UK Biobank (UKBB) (n = 455,808) and the US (n = 1150). We also evaluated the exposure of Mfge8-enriched human EVs in zebrafish (ZF) for their impact on cardiometabolic organ system. Most individual carriers of Arg148His variant not only had high circulating Mfge8 but also revealed a positive significant correlation with glucose (r = 0.42; p = 4.9 × 10-04), while the non-carriers showed a negative correlation of Mfge8 with glucose (r = -0.38; p = 0.001) in Asian Indians. The same variant was monomorphic in non-South Asian ethnicities. Even without the variant, serum Mfge8 correlated significantly with blood glucose in other non-South Asian ethnicities (r = 0.47; p = 2.2 × 10-13). Since Mfge8 is an EV marker, we tested the exposure of Mfge8-enriched human EVs to ZF larvae as an exploratory study. The ZF larvae showed rapid effects on insulin-sensitive organs, developing fatty liver disease, heart hypertrophy and exhibiting redundant growth with poor muscular architecture with and without the high-fat diet (HFD). In contrast, the control group fishes developed fatty liver disease and heart hypertrophy only after the HFD feeding. Backed with strong support from animal studies on the role of Mfge8 in obesity, insulin resistance, and atherosclerosis, the current research suggests that circulating Mfge8 may become a potential marker for predicting the risk of T2DM and cardiovascular disease in humans.
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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