Association of Endotoxemia with Low-Grade Inflammation, Metabolic Syndrome and Distinct Response to Lipopolysaccharide in Type 1 Diabetes.
Aleksejs FedulovsLeonora PahirkoKaspars JekabsonsLiga KunradeJānis ValeinisUna RiekstiņaValdis PīrāgsJelizaveta SokolovskaPublished in: Biomedicines (2023)
The association of endotoxemia with metabolic syndrome (MS) and low-grade inflammation in type 1 diabetes (T1D) is little-studied. We investigated the levels of lipopolysaccharide (LPS), lipopolysaccharide-binding protein (LBP), endogenous anti-endotoxin core antibodies (EndoCAb IgG and IgM) and high-sensitivity C-reactive protein (hsCRP) in 74 T1D patients with different MS statuses and 33 control subjects. Within the T1D group, 31 patients had MS. These subjects had higher levels of LPS compared to patients without MS (MS 0.42 (0.35-0.56) or no MS 0.34 (0.3-0.4), p = 0.009). MS was associated with LPS/HDL (OR = 6.5 (2.1; 20.0), p = 0.036) and EndoCAb IgM (OR = 0.32 (0.11; 0.93), p = 0.036) in patients with T1D. LBP (β = 0.30 (0.09; 0.51), p = 0.005), EndoCAb IgG (β = 0.29 (0.07; 0.51), p = 0.008) and the LPS/HDL ratio (β = 0.19 (0.03; 0.41, p = 0.084) were significantly associated with log-transformed hsCRP in T1D. Higher levels of hsCRP and EndoCAb IgG were observed in T1D compared to the control ( p = 0.002 and p = 0.091, respectively). In contrast to the situation in the control group, LPS did not correlate with LBP, EndoCAb, leukocytes or HDL in T1D. To conclude, endotoxemia is associated with low-grade inflammation, MS and a distinct response to LPS in T1D.
Keyphrases
- low grade
- ms ms
- inflammatory response
- mass spectrometry
- high grade
- lps induced
- type diabetes
- metabolic syndrome
- multiple sclerosis
- end stage renal disease
- anti inflammatory
- ejection fraction
- chronic kidney disease
- toll like receptor
- newly diagnosed
- peritoneal dialysis
- prognostic factors
- cardiovascular disease
- insulin resistance
- binding protein
- liquid chromatography tandem mass spectrometry
- weight loss
- skeletal muscle
- computed tomography