Unexpected role of the human cytomegalovirus contribute to essential hypertension in the Kazakh Chinese population of Xinjiang

Biosci Rep. 2018 Jun 27;38(3):BSR20171522. doi: 10.1042/BSR20171522. Print 2018 Jun 29.

Abstract

Human cytomegalovirus (HCMV) infection, chronic inflammation and oxidative stress, the renin-angiotensin system (RAS), endothelial function, and DNA methylation play roles in the pathogenesis of essential hypertension (EH); however, the mechanism by which HCMV predisposes patients to hypertension remain unclear. Our group previously demonstrated an association between EH and HCMV infection in Kazakh Chinese. Here, we investigated the relationship between HCMV infection and other clinicopathological features in 720 Kazakh individuals with or without hypertension (n=360 each; age: 18-80). Multiple linear and logistic regression analyses were used to determine the associations between HCMV infection, clinical characteristics, and EH. Notably, patients with EH, particularly those with HCMV infection, exhibited a marked increase in tumor necrosis factor-α (TNF-α) and 8-hydroxy-2-deoxyguanosine (8-OHDG) levels, but a decrease in endothelial nitric oxide synthase (eNOS) and renin levels. Similarly, elevated TNF-α and 8-OHDG levels were independent predictors of increased HCMV antibody titers, whereas eNOS and renin were negatively correlated with the latter. Moreover, serum angiotensin-converting enzyme (sACE, ACE) methylation was increased, whereas 11-β hydroxysteroid dehydrogenase 2 (HSD11β2; HSD3B2) methylation was decreased in patients with EH who were also infected with HCMV. A positive correlation between HSD3B2 methylation and HCMV IgG titer and blood pressure was additionally observed, whereas angiotensin-converting enzyme (ACE) methylation was inversely correlated with blood pressure. Collectively, these data indicate that HCMV may contribute to EH development in the Kazakh Chinese by increasing TNF-α and 8-OHDG levels, suppressing eNOS and renin, and manipulating HSD3B2 and ACE methylation.

Keywords: Essential hypertension; Human cytomegalovirus; Inflammatory response; Methylation; Oxidative stress; Renin-angiotensin system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 8-Hydroxy-2'-Deoxyguanosine
  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Antibodies, Viral / blood
  • Blood Pressure
  • Case-Control Studies
  • China
  • Cytomegalovirus / genetics
  • Cytomegalovirus / isolation & purification
  • Cytomegalovirus Infections / complications
  • Cytomegalovirus Infections / ethnology
  • Cytomegalovirus Infections / immunology
  • Cytomegalovirus Infections / virology*
  • Deoxyguanosine / analogs & derivatives*
  • Deoxyguanosine / blood
  • Deoxyguanosine / immunology
  • Essential Hypertension / complications
  • Essential Hypertension / ethnology
  • Essential Hypertension / immunology
  • Essential Hypertension / virology*
  • Ethnicity
  • Female
  • Humans
  • Male
  • Methylation
  • Middle Aged
  • Nitric Oxide Synthase Type III / blood
  • Nitric Oxide Synthase Type III / immunology*
  • Peptidyl-Dipeptidase A / blood
  • Peptidyl-Dipeptidase A / immunology
  • Progesterone Reductase / blood
  • Progesterone Reductase / immunology
  • Renin / blood
  • Renin / immunology*
  • Tumor Necrosis Factor-alpha / blood
  • Tumor Necrosis Factor-alpha / immunology*

Substances

  • Antibodies, Viral
  • Tumor Necrosis Factor-alpha
  • 8-Hydroxy-2'-Deoxyguanosine
  • 3 beta-hydroxysteroid dehydrogenase type II
  • Progesterone Reductase
  • NOS3 protein, human
  • Nitric Oxide Synthase Type III
  • ACE protein, human
  • Peptidyl-Dipeptidase A
  • Renin
  • Deoxyguanosine