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Association Between ABCB1 Gene Polymorphism and Renal Function in Patients with Hypertension: A Case-Control Study
Xiaofang Chen1, Tao Zhou2, Deguang Yang2
1Department of Nursing, The Third Affiliated Hospital of Southern Medical University, Guangzhou, Guangdong, China (mainland).
Insights
The ABCB1 gene, specifically the rs1045642-T allele, may increase the risk of kidney damage in patients with hypertension. This genetic factor is linked to renal function injury in hypertensive individuals.
Area of Science:
- Genetics
- Nephrology
- Cardiology
Background:
- Hypertension is a significant risk factor for target organ damage.
- Genetic factors are implicated in hypertension-related organ damage.
- The role of the ABCB1 gene in hypertension-induced renal injury requires further investigation.
Purpose of the Study:
- To investigate the association between ABCB1 gene polymorphisms and renal function injury in hypertensive patients.
- To identify potential genetic markers for predicting renal complications in hypertension.
Main Methods:
- A case-control study design was employed.
- Patients with hypertension were recruited, and their clinical data and ABCB1 gene polymorphisms (rs1045642, rs10808072, rs1922242) were analyzed using restriction fragment length polymorphism.
- Statistical analyses, including multivariable logistic regression, were used to determine associations.
Main Results:
- Hypertensive patients exhibited higher BMI, systolic blood pressure, total cholesterol, blood urea nitrogen, creatinine, uric acid, estimated glomerular filtration rate, and platelet levels compared to controls.
- A statistically significant difference in genotype frequency distribution was observed for the ABCB1 rs1045642 polymorphism (p<0.001).
- The TT genotype of rs1045642 was associated with a higher risk of renal function injury in hypertensive patients (OR=3.47, 95% CI: 1.19-10.07).
Conclusions:
- The rs1045642-T allele of the ABCB1 gene is potentially associated with an increased risk of renal function injury in hypertensive patients.
- ABCB1 gene polymorphisms may serve as a genetic marker for renal complications in hypertension.
- Further research is warranted to elucidate the precise mechanisms linking ABCB1 and hypertensive kidney disease.
Abstract:
BACKGROUND A previous study found that target organ damage in patients with hypertension was related to genetic factors. The aim of our study aim was to explore the association between the ABCB1 gene and renal function injury induced by hypertension. MATERIAL AND METHODS We used a case-control study design. Patients with hypertension were enrolled from our hospital between July 2015 and December 2015. Questionnaire data included personal information, life habits and behavior. Clinical data included blood routine examination and liver and renal function. We used restriction fragment length polymorphism methods for ABCB1 gene polymorphism detection. RESULTS There were 306 patients with hypertension included in the final analyses: 170 cases of hypertension and 136 controls. Compared to controls, the cases group had higher: drinking ratio (65.3% versus 52.9%, p=0.029), body mass index (p=0.032), systolic blood pressure (p<0.001), total cholesterol (p=0.004), blood urea nitrogen (p=0.029), creatinine (p=0.024), uric acid (p=0.011), estimated glomerular filtration rate level (p<0.001), and platelet level (p=0.003). There were no significant differences for others parameters. Genotype frequency distributions of rs1045642 were statistically significant between the two groups (χ²=24.966, p<0.001). No differences were observed for the frequency distribution of rs10808072 and rs1922242 (χ²=1.293, p=0.524; χ²=0.065, p=0.968). The multivariable logistics results found that patients with TT genotype had a higher risk for renal function injury for hypertensive patients compared to those with CC genotype (OR=3.47, 95% CI: 1.19-10.07). CONCLUSIONS Our results suggested that the rs1045642-T allele of the ABCB1 gene may be associated with increased risk for renal function injury in hypertensive patients.
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