ABCA1 and ABCG1 genes encode the cholesterol transporter proteins that play a key role in cholesterol and phospholipids homeostasis. This study was aimed at evaluating and comparing ABCA1 and ABCG1 genes expression in metabolic syndrome patients and healthy individuals. This case-control study was performed on 36 patients with metabolic syndrome and the same number of healthy individuals in Hamadan (west of Iran) during 2013-2014. Total RNA was extracted from mononuclear cells and purified using RNeasy Mini Kit column. The expression of ABCA1 and ABCG1 genes was performed by qRT-PCR. Lipid profile and fasting blood glucose were measured using colorimetric procedures. ABCG1 expression in metabolic syndrome patients was significantly lower (about 75%) compared to that of control group, while for ABCA1 expression, there was no significant difference between the two studied groups. Comparison of other parameters such as HDL-C, FBS, BMI, waist circumference, and systolic and diastolic blood pressure between metabolic syndrome patients and healthy individuals showed significant differences (P < 0.05). Decrease in ABCG1 expression in metabolic syndrome patients compared to healthy individuals suggests that hyperglycemia, related metabolites, and hyperlipidemia over the transporter capacity resulted in decreased expression of ABCG1. Absence of a significant change in ABCA1 gene expression between two groups can indicate a different regulation mechanism for ABCA1 expression.
Keyphrases
- metabolic syndrome
- poor prognosis
- gene expression
- end stage renal disease
- blood pressure
- ejection fraction
- newly diagnosed
- body mass index
- chronic kidney disease
- insulin resistance
- heart failure
- peritoneal dialysis
- type diabetes
- dna methylation
- prognostic factors
- genome wide
- binding protein
- uric acid
- cardiovascular disease
- left ventricular
- ms ms
- physical activity
- long non coding rna
- gold nanoparticles
- transcription factor
- heart rate
- adipose tissue
- patient reported
- patient reported outcomes
- peripheral blood
- induced apoptosis
- endoplasmic reticulum stress
- drug induced
- weight gain
- solid phase extraction