Key result
Among non-Hispanic White participants with type 2 diabetes, ANGPTL4 K40 carriers had fasting triglyceride levels 0.33 mmol/L lower than E40 homozygotes (p=0.001).
Why the study?
Are ANGPTL4 variants E40K and T266M associated with lower fasting triglyceride levels in overweight/obese individuals with type 2 diabetes?
Observational (n=2,601)
Yes
Are ANGPTL4 variants E40K and T266M associated with lower fasting triglyceride levels in overweight/obese individuals with type 2 diabetes?
Mean Difference: -0.33
Absolute Event Rate: 1.61% vs 1.94%
p-value: p=0.001
ANGPTL4 E40K and T266M variants are associated with lower fasting triglyceride levels in individuals with type 2 diabetes, independent of lifestyle intervention.
ANGPTL4 E40K variant was associated with lower triglycerides in type 2 diabetes; leaves open whether this supports therapeutic targeting or cardiovascular benefit.
BACKGROUND: Elevated triglyceride levels are a risk factor for cardiovascular disease. Angiopoietin-like protein 4 (Angptl4) is a metabolic factor that raises plasma triglyceride levels by inhibiting lipoprotein lipase (LPL). In non-diabetic individuals, the ANGPTL4 coding variant E40K has been associated with lower plasma triglyceride levels while the T266M variant has been associated with more modest effects on triglyceride metabolism. The objective of this study was to determine whether ANGPTL4 E40K and T266M are associated with triglyceride levels in the setting of obesity and T2D, and whether modification of triglyceride levels by these genetic variants is altered by a lifestyle intervention designed to treat T2D. METHODS: The association of ANGPTL4 E40K and T266M with fasting triglyceride levels was investigated in 2,601 participants from the Look AHEAD Clinical Trial, all of whom had T2D and were at least overweight. Further, we tested for an interaction between genotype and treatment effects on triglyceride levels. RESULTS: Among non-Hispanic White Look AHEAD participants, ANGPTL4 K40 carriers had mean triglyceride levels of 1.61 ± 0.62 mmol/L, 0.33 mmol/L lower than E40 homozygotes (p = 0.001). Individuals homozygous for the minor M266 allele (MAF 30%) had triglyceride levels of 1.75 ± 0.58 mmol/L, 0.24 mmol/L lower than T266 homozygotes (p = 0.002). The association of the M266 with triglycerides remained significant even after removing K40 carriers from the analysis (p = 0.002). There was no interaction between the weight loss intervention and genotype on triglyceride levels. CONCLUSIONS: This is the first study to demonstrate that the ANGPTL4 E40K and T266M variants are associated with lower triglyceride levels in the setting of T2D. In addition, our findings demonstrate that ANGPTL4 genotype status does not alter triglyceride response to a lifestyle intervention in the Look AHEAD study.
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Smart et al. (2011) conducted an observational in Type 2 diabetes and overweight/obesity (n=2,601). ANGPTL4 E40K variant vs. E40 homozygotes (non-carriers) was evaluated on Fasting triglyceride levels (MD -0.33 mmol/L, p=0.001). Among non-Hispanic White participants with type 2 diabetes, ANGPTL4 K40 carriers had fasting triglyceride levels 0.33 mmol/L lower than E40 homozygotes (p=0.001).
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