Publication
Urate Transporter Gene SLC22A12 Polymorphisms Associated with Obesity and Metabolic Syndrome in Caucasians with Hypertension
Downloadable Content
- Persistent URL
- Last modified
- 05/15/2025
- Type of Material
- Authors
- Language
- English
- Date
- 2012-06-08
- Publisher
- Karger Publishers Open Access
- Publication Version
- Copyright Statement
- © 2012 S. Karger AG, Basel.
- Final Published Version (URL)
- Title of Journal or Parent Work
- ISSN
- 1420-4096
- Volume
- 35
- Issue
- 6
- Start Page
- 477
- End Page
- 482
- Grant/Funding Information
- The PEAR study, and this research, is supported by a grant from the National Institutes of Health (Bethesda, Md., USA), grant U01 GM074492, funded as part of the Pharmacogenetics Research Network.
- The study was also supported by PEAR CTSA grants UL1-RR092890 (University of Florida), UL1-RR025008 (Emory University), and UL1-RR024150 (Mayo Clinic), and funds from the Mayo Foundation, NIH HL-68607 and an Amgen fellowship grant to Dr. Shafiu.
- Abstract
- Background/Aims: Hyperuricemia is associated with obesity and the metabolic syndrome. URAT1 is a urate transporter, and we tested the association of URAT1 transporter gene (SLC22A12) polymorphisms with obesity and the metabolic syndrome in hypertensive subjects. Methods: Patients with essential hypertension (n = 414) from a randomized controlled study were genotyped for SLC22A12 SNPs rs11602903, rs505802 and rs11231825. Results: In Caucasians, SLC22A12 SNPs were associated with the body mass index (BMI). rs11602903 was associated with BMI (p < 0.0001), waist circumference (p = 0.003), HDL cholesterol (p = 0.018) and the metabolic syndrome (p = 0.033), and accounted for 7% of the variation of BMI in Caucasians. In African Americans, SLC22A12 SNP rs11602903 was not associated with BMI, waist circumference, HDL cholesterol or triglycerides. Conclusion: The URAT1 gene SLC22A12 polymorphism may play a role in obesity and the metabolic syndrome in Caucasian hypertensive subjects.
- Author Notes
- Keywords
- ALLOPURINOL
- Metabolic syndrome
- SLC22A12 polymorphisms
- Obesity
- Physiology
- EXCRETION
- CELLS
- FRUCTOSE
- SLC2A9
- SERUM URIC-ACID
- Peripheral Vascular Disease
- CARDIOVASCULAR-DISEASE
- Uric acid
- HYPERURICEMIA
- RISK-FACTORS
- Urology & Nephrology
- Cardiovascular System & Cardiology
- Life Sciences & Biomedicine
- Hypertension
- URAT1
- BLOOD-PRESSURE
- Science & Technology
- Research Categories
- Health Sciences, Pharmacology
- Health Sciences, Pharmacy
- Biology, Genetics
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