Association of MYH9 Polymorphisms with Hypertension in Patients with Chronic Kidney Disease in China

Kidney Blood Press Res. 2016;41(6):956-965. doi: 10.1159/000452597. Epub 2016 Dec 8.

Abstract

Background/aims: This study explored the correlation between hypertension and non-muscle myosin heavy chain 9 (MYH9) gene polymorphisms in Chinese chronic kidney disease (CKD) patients.

Methods: This case-control study included 301 patients with CKD and 293 healthy controls. The E1 haplotype single nucleotide polymorphisms (SNPs) rs3752462 and rs4821480 were genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis. The association between MYH9 polymorphisms and high systolic blood pressure (SBP ≥ 140 mmHg) susceptibility in CKD patients was analysed.

Results: The cases and controls had similar genotype and allele distributions at rs3752462 and rs4821480. No GG genotype at rs4821480 was observed. Patients with SBP < 140 mmHg were more likely to have the CC genotype (17.1%) than patients with SBP ≥ 140 mmHg (4.3%) (P = 0.001). Creatinine clearance (OR = 0.99, 95% CI = 0.98-0.10, P = 0.01) was associated with SBP in patients with CKD. The risk of SBP ≥ 140 mmHg was 0.24-fold greater among patients with the CC genotype than among patients with the TT genotype (P = 0.002).

Conclusion: The rs3752462 polymorphism of MYH9 is associated with SBP in patients with CKD. The T allele in the dominant model was associated with an elevated risk for high SBP.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Asian People / genetics
  • Case-Control Studies
  • Child
  • Female
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Hypertension / genetics*
  • Male
  • Middle Aged
  • Molecular Motor Proteins / genetics*
  • Myosin Heavy Chains / genetics*
  • Polymorphism, Single Nucleotide*
  • Renal Insufficiency, Chronic / genetics*
  • Young Adult

Substances

  • MYH9 protein, human
  • Molecular Motor Proteins
  • Myosin Heavy Chains