Key result
A higher burden of risk alleles across 8 novel loci was associated with an increased risk of developing hypertension over 7.5 years (OR 1.84; 95% CI 1.29-2.62 for highest vs lowest quartile).
Why the study?
What genetic variants influence blood pressure responses to dietary sodium/potassium interventions and cold pressor tests in Han Chinese individuals?
Observational (n=2,579)
What genetic variants influence blood pressure responses to dietary sodium/potassium interventions and cold pressor tests in Han Chinese individuals?
Odds Ratio: 1.84 (95% CI 1.29–2.62)
p-value: p=0.0003 for trend
Identified 8 novel genetic loci associated with blood pressure responses to sodium/potassium interventions that also predict the long-term risk of developing hypertension.
May support polygenic hypertension risk prediction; leaves open whether loci guide dietary interventions.
BACKGROUND: Blood pressure (BP) responses to dietary sodium and potassium intervention and cold pressor test vary considerably among individuals. We aimed to identify novel genetic variants influencing individuals' BP responses to dietary intervention and cold pressor test. METHODS AND RESULTS: We conducted a genome-wide association study of BP responses in 1881 Han Chinese and de novo genotyped top findings in 698 Han Chinese. Diet-feeding study included a 7-day low-sodium (51.3 mmol/d), a 7-day high-sodium (307.8 mmol/d), and a 7-day high-sodium plus potassium supplementation (60 mmol/d). Nine BP measurements were obtained during baseline observation and each intervention period. The meta-analyses identified 8 novel loci for BP phenotypes, which physically mapped in or near PRMT6 (P=7.29 × 10(-9)), CDCA7 (P=3.57 × 10(-8)), PIBF1 (P=1.78 × 10(-9)), ARL4C (P=1.86 × 10(-8)), IRAK1BP1 (P=1.44 × 10(-10)), SALL1 (P=7.01 × 10(-13)), TRPM8 (P=2.68 × 10(-8)), and FBXL13 (P=3.74 × 10(-9)). There was a strong dose-response relationship between the number of risk alleles of these independent single-nucleotide polymorphisms and the risk of developing hypertension during the 7.5-year follow-up in the study participants. Compared with those in the lowest quartile of risk alleles, odds ratios (95% confidence intervals) for those in the second, third, and fourth quartiles were 1.39 (0.97, 1.99), 1.72 (1.19, 2.47), and 1.84 (1.29, 2.62), respectively (P=0.0003 for trend). CONCLUSIONS: Our study identified 8 novel loci for BP responses to dietary sodium and potassium intervention and cold pressor test. The effect size of these novel loci on BP phenotypes is much larger than those reported by the previously published studies. Furthermore, these variants predict the risk of developing hypertension among individuals with normal BP at baseline.
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He et al. (2013) conducted an observational in Blood pressure responses and hypertension (n=2,579). Genetic risk alleles at 8 novel loci vs. Lowest quartile of risk alleles was evaluated on Risk of developing hypertension (OR 1.84, 95% CI 1.29-2.62, p=0.0003 for trend). A higher burden of risk alleles across 8 novel loci was associated with an increased risk of developing hypertension over 7.5 years (OR 1.84; 95% CI 1.29-2.62 for highest vs lowest quartile).