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(Hypertension. 2006;47:532.)
© 2006 American Heart Association, Inc.

Part 2 Original Articles

Sodium Bicarbonate Cotransporter Polymorphisms Are Associated With Baseline and 10-Year Follow-Up Blood Pressures

Steven C. Hunt; Yuanpei Xin; Lily L. Wu; Richard M. Cawthon; Hilary Coon; Sandra J. Hasstedt; Paul N. Hopkins

From the Cardiovascular Genetics Division and Departments of Human Genetics and Psychiatry, University of Utah School of Medicine, Salt Lake City.

Correspondence to Steven C. Hunt, Cardiovascular Genetics, University of Utah, 410 Chipeta Way, Rm 167, Salt Lake City, Utah 84108. E-mail steve{at}ucvg.med.utah.edu

The NaHCO₃ cotransporter gene (SLC4A5) on chromosome 2 encodes a protein that transports sodium and bicarbonate across the cell membrane and regulates cellular pH. The National Heart, Lung, and Blood Institute Family Blood Pressure Program found linkage of blood pressure–related traits to the chromosomal region containing SLC4A5 and phenotype associations with single nucleotide polymorphisms (SNPs) in this gene. However, the results were inconsistent over various phenotypes and SNPs. Nevertheless, the evidence was strong enough to propose this gene as a blood pressure–related gene. To extend these findings, SLC4A5 SNPs were genotyped in an independent set of 96 Utah pedigrees of 1040 adult subjects at baseline, 760 of whom were followed longitudinally for 10 years. After adjusting for age, gender, body mass index, and polygenic correlations within pedigrees, SNP hcv1137534 was significantly associated with both systolic blood pressure and diastolic blood pressure (DBP) at baseline (unadjusted P=0.009 and P=0.043; respectively) and at 10-year follow-up (P=0.008 and P=0.007; respectively). In secondary tests of association of baseline-stressed blood pressure, hcv1137534 was borderline or significantly associated with DBP change during an isometric handgrip test (P=0.054), DBP change from supine to standing (P=0.020), and DBP change after a 50° tilt (P=0.034). There was no evidence for compensation of abnormal SLC4A5 sodium transport by genotype-specific differences in sodium–lithium countertransport, lithium–potassium cotransport, altered plasma sodium, chloride, or CO₂ levels. Therefore, in these Utah pedigrees, the SLC4A5 gene was significantly associated with blood pressure and persisted after 10 years of follow-up. These results additionally confirm the involvement of SLC4A5 with blood pressure control, although the mechanism is still unclear.

Key Words: blood pressure • genetics • polymorphism • ion transport

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