1. Academic Validation
  2. BMPR2 promoter methylation and its expression in valvular heart disease complicated with pulmonary artery hypertension

BMPR2 promoter methylation and its expression in valvular heart disease complicated with pulmonary artery hypertension

  • Aging (Albany NY). 2021 Nov 18;13(22):24580-24604. doi: 10.18632/aging.203690.
Ni Li 1 2 Linwen Zhu 1 Caimin Zhu 1 Hua Zhou 1 Dawei Zheng 1 Guodong Xu 1 Huoshun Shi 1 Jianqing Gao 2 Albert Jiarui Li 3 Zhaoyang Wang 1 Lebo Sun 1 Xiajun Li 4 Guofeng Shao 1
Affiliations

Affiliations

  • 1 Department of Cardiothoracic Surgery, Lihuili Hospital Affiliated to Ningbo University, Ningbo City, Zhejiang 315041, China.
  • 2 Institute of Pharmaceutics, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China.
  • 3 Edgemont High School, Scarsdale, NY 10583, USA.
  • 4 School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.
Abstract

Valvular heart disease (VHD) is a common heart disease that affects blood flow. It usually requires heart surgery. Valvular heart disease complicated with pulmonary artery hypertension (VHD-PAH) may be lethal due to heart failure that results from increased heart burden. It is important for these patients to seek early treatment in order to minimize the heart damage. However, there is no reliable diagnosis method in VHD. In this study, we found DNA methylation was increased at the promoter of BMPR2 gene in the VHD patients compared with the healthy controls. This finding was confirmed by an independent cohort study of VHD patients and healthy controls. In addition, BMPR2 mRNA levels were reduced in the plasma of the VHD patients. There is strong correlation between BMPR2 promoter DNA methylation and the severity of VHD. Indeed, we found that both BMPR2 promoter DNA methylation and BMPR2 mRNA levels in the plasma are good biomarkers of VHD by themselves, with the respective AUC value of 0.879 and 0.725, respectively. When they were used in combination, the diagnostic value was even better, with the AUC value of 0.93. Consistent with the results in the VHD patients, we observed decreased BMPR2 and increased fibrosis in the lung of a PAH model mouse. BMPR2 was also decreased in the hearts of the PAH mice, whereas BMP4 was increased. Furthermore, BMPR2 was reduced in the heart valve tissue samples of human VHD patients after valve replacement with moderate/severe PAH compared with those with mild PAH. There was also increased Apoptosis in the hearts of the PAH mice. BMPR2 promoter DNA methylation and its expression appear to be good biomarkers for VHD. Our results also suggest that DNA methylation may cause PAH through deregulation of BMP signaling and increased Apoptosis.

Keywords

BMPR2; DNA methylation; apoptosis; biomarker; pulmonary artery hypertension (PAH); valvular heart disease (VHD).

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