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Elevated Circulating Glutamate Is Associated With Subclinical Atherosclerosis Independently of Established Risk
Angela Lehn-Stefan1,2, Andreas Peter1,2,3, Jürgen Machann1,2,4
1Institute of Diabetes Research and Metabolic Diseases (IDM) of the Helmholtz Centre Munich, Tübingen, Germany.
Insights
Elevated plasma glutamate levels are linked to increased cardiovascular disease risk. This association may be partly explained by subclinical inflammation indicated by interleukin-6 (IL-6).
Area of Science:
- Metabolic research
- Cardiovascular research
- Inflammation research
Background:
- Elevated plasma glutamate is associated with cardiovascular disease (CVD) risk factors including visceral adiposity, nonalcoholic fatty liver disease, insulin resistance, and high branched-chain amino acid (BCAA) levels.
- The independent contribution of circulating glutamate to atherosclerosis risk remains unclear.
Purpose of the Study:
- To investigate whether elevated plasma glutamate is an independent marker of atherosclerosis risk.
- To explore the relationship between plasma glutamate, metabolic factors, and subclinical inflammation.
Main Methods:
- Plasma glutamate and BCAA levels were measured in 102 individuals.
- Phenotyping included body fat mass and distribution (MR tomography), liver fat content (1H-MR spectroscopy), insulin sensitivity (OGTT and clamp), and carotid intima-media thickness (cIMT).
- Statistical analyses adjusted for age, sex, body fat mass, visceral fat mass, liver fat content, insulin sensitivity, BCAAs, and interleukin-6 (IL-6) levels.
Main Results:
- Plasma glutamate levels positively correlated with liver fat content and cIMT, and negatively with insulin sensitivity, even after adjustments.
- Glutamate levels were associated with cIMT independently of liver fat, insulin sensitivity, and BCAAs.
- An independent positive association was observed between glutamate and IL-6 levels.
- IL-6 most strongly attenuated the relationship between glutamate and cIMT.
Conclusions:
- Elevated plasma glutamate is associated with increased cIMT, independent of established CVD risk factors.
- This association may be partially explained by IL-6-mediated subclinical inflammation.
Objective:
Elevated plasma glutamate levels are associated with an increased risk of cardiovascular disease (CVD). Because plasma glutamate levels are also strongly associated with visceral adiposity, nonalcoholic fatty liver disease, insulin resistance, and high circulating levels of branched-chain amino acids (BCAAs), it is unknown to what extent elevated circulating glutamate is an independent marker of an increased risk of atherosclerosis.
Methods:
Plasma levels of glutamate and BCAAs were measured in 102 individuals who were precisely phenotyped for body fat mass and distribution (magnetic resonance [MR] tomography), liver fat content (1H-MR spectroscopy), insulin sensitivity (oral glucose tolerance test and hyperinsulinemic, euglycemic clamp [N = 57]), and carotid intima media thickness (cIMT).
Results:
Plasma glutamate levels, adjusted for age, sex, body fat mass, and visceral fat mass, correlated positively with liver fat content and cIMT (all std β ≥ .22, all P ≤ .023) and negatively with insulin sensitivity (std β ≤ -.31, P ≤ .002). Glutamate levels also were associated with cIMT, independently of additional adjustment for liver fat content, insulin sensitivity and BCAAs levels (std β ≥ .24, P ≤ .02). Furthermore, an independent positive association of glutamate and interleukin-6 (IL-6) levels was observed (N = 50; std β = .39, P = .03). Although glutamate, adjusted for age, sex, body fat mass, and visceral fat mass, also correlated positively with cIMT in this subgroup (std β = .31, P = .02), after additional adjustment for the parameters liver fat content, insulin sensitivity, BCAAs, or IL-6 levels, adjustment for IL-6 most strongly attenuated this relationship (std β = .28, P = .05).
Conclusions:
Elevated plasma glutamate levels are associated with increased cIMT, independently of established CVD risk factors, and this relationship may in part be explained by IL-6-associated subclinical inflammation.
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