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Interactions between CYP11B2 Promoter Methylation and Smoking Increase Risk of Essential Hypertension.
Gu, Tianlun; Mao, Shuqi; Fan, Rui; Zhong, Fade; Zhu, Fubao; Hao, Lingmei; Zhang, Lina; Yin, Fengying.
Afiliação
  • Gu T; Department of Preventative Medicine, Zhejiang Provincial Key Laboratory of Pathological and Physiological Technology, Medicine School of Ningbo University, 818 Fenghua Road, Ningbo, Zhejiang Province 315211, China.
  • Mao S; Department of Preventative Medicine, Zhejiang Provincial Key Laboratory of Pathological and Physiological Technology, Medicine School of Ningbo University, 818 Fenghua Road, Ningbo, Zhejiang Province 315211, China.
  • Fan R; Department of Medical Quality, Ningbo Medical Center Lihuili Eastern Hospital, Ningbo, Zhejiang 315211, China.
  • Zhong F; Ningbo Central Blood Station, Ningbo, Zhejiang 315211, China.
  • Zhu F; Health and Family Planning Bureau of Zhenhai District, Ningbo, Zhejiang, China.
  • Hao L; Clinical Laboratory, The Seventh Hospital of Ningbo, Ningbo, Zhejiang 315211, China.
  • Zhang L; Department of Preventative Medicine, Zhejiang Provincial Key Laboratory of Pathological and Physiological Technology, Medicine School of Ningbo University, 818 Fenghua Road, Ningbo, Zhejiang Province 315211, China.
  • Yin F; Clinical Laboratory, The First Hospital of Ningbo, Zhejiang, China.
Biomed Res Int ; 2016: 1454186, 2016.
Article em En | MEDLINE | ID: mdl-28078278
Aldosterone synthase (CYP11B2) is closely linked to essential hypertension (EH). However, it remains unclear whether the methylation of the CYP11B2 promoter is involved in the development of EH in humans. Our study is aimed at evaluating the contribution of CYP11B2 promoter methylation to the risk of EH. Methylation levels were measured using pyrosequencing technology in 192 participants in a hospital-based case-control study. Logistic regression and multiple linear regression analyses were utilized to adjust for confounding factors and the GMDR method was applied to investigate high-order gene-environment interactions. Although no significant result was observed linking the four analyzed CpG sites to EH, GMDR detected significant interactions among CpG1, CpG3, CpG4, and smoking correlated with an increased risk of EH (OR = 4.62, adjusted P = 0.011). In addition, CpG2 (adjusted P = 0.013) and CpG3 (adjusted P = 0.039) methylation was significantly lower in healthy males than in healthy females. Likewise, after adjusting for confounding factors, CpG2 methylation (adjusted P = 0.007) still showed significant gender-specific differences among the participants of the study. CpG1 (P = 0.009) site was significantly positively correlated with age, and CpG3 (P = 0.007) and CpG4 (P = 0.006) were both inversely linked to smoking. Our findings suggest that gene-environment interactions are associated with the pathogenesis and progression of EH.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fumar / Citocromo P-450 CYP11B2 / Metilação de DNA / Hipertensão Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fumar / Citocromo P-450 CYP11B2 / Metilação de DNA / Hipertensão Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article