TY - JOUR
T1 - NEDD4L基因多态性与血压钠钾反应性的相关性分析
AU - Niu, Zejiaxin
AU - Du, Mingfei
AU - Hu, Guilin
AU - Zhang, Xi
AU - Wang, Dan
AU - Wang, Lan
AU - Luo, Wenjing
AU - Chang, Mingke
AU - Zou, Ting
AU - Zhang, Xiaoyu
AU - Yan, Yu
AU - Chu, Chao
AU - Liao, Yueyuan
AU - Ma, Qiong
AU - Wang, Keke
AU - Jia, Hao
AU - Chen, Chen
AU - Sun, Yue
AU - Guo, Tongshuai
AU - Zhang, Jie
AU - Gao, Weihua
AU - Man, Ziyue
AU - Gao, Ke
AU - Mu, Jianjun
AU - Wang, Yang
N1 - Publisher Copyright:
© 2023, Editorial Board of Journal of Xi'an Jiaotong University (Medical Sciences). All right reserved.
PY - 2023/1/5
Y1 - 2023/1/5
N2 - Objective: 4-like protein with down-regulated expression and development in neural precursor cells (NEDD4L) plays an important role in blood pressure (BP) regulation and sodium homeostasis by regulating epithelial sodium channel protein. In this study, we aimed to explore the relationship of NEDD4L gene polymorphisms with BP responses to sodium and potassium intake. Methods: In 2004, 514 subjects from 124 families in Meixian County, Shaanxi Province, were recruited to establish a salt-sensitive hypertension study cohort. All the subjects received a 3-day baseline survey, a 7-day low-salt diet, a 7-day high-salt diet, and finally a 7-day high-salt and potassium supplementation. Their BP was measured and peripheral blood samples were collected at different intervention periods. The 14 gene polymorphisms of NEDD4L gene were genotyped and analyzed by MassARRAY platform. Results: BP decreased on a low-salt diet, and significantly increased on a high-salt diet, and decreased again after potassium supplementation. NEDD4L SNPs rs74408486 were significantly associated with systolic BP, diastolic BP and mean arterial pressure responses to the low-salt diet. SNPs rs292449 and rs2288775 were significantly associated with pulse pressure response to the high-salt diet. In addition, SNPs rs563283 and rs292449 were significantly associated with diastolic BP, mean arterial pressure, and pulse pressure responses to high-salt and potassium supplementation diet. Conclusion: NEDD4L gene polymorphisms were significantly associated with BP responses to sodium and potassium intake, suggesting that NEDD4L gene may be involved in the development of salt sensitivity and potassium sensitivity.
AB - Objective: 4-like protein with down-regulated expression and development in neural precursor cells (NEDD4L) plays an important role in blood pressure (BP) regulation and sodium homeostasis by regulating epithelial sodium channel protein. In this study, we aimed to explore the relationship of NEDD4L gene polymorphisms with BP responses to sodium and potassium intake. Methods: In 2004, 514 subjects from 124 families in Meixian County, Shaanxi Province, were recruited to establish a salt-sensitive hypertension study cohort. All the subjects received a 3-day baseline survey, a 7-day low-salt diet, a 7-day high-salt diet, and finally a 7-day high-salt and potassium supplementation. Their BP was measured and peripheral blood samples were collected at different intervention periods. The 14 gene polymorphisms of NEDD4L gene were genotyped and analyzed by MassARRAY platform. Results: BP decreased on a low-salt diet, and significantly increased on a high-salt diet, and decreased again after potassium supplementation. NEDD4L SNPs rs74408486 were significantly associated with systolic BP, diastolic BP and mean arterial pressure responses to the low-salt diet. SNPs rs292449 and rs2288775 were significantly associated with pulse pressure response to the high-salt diet. In addition, SNPs rs563283 and rs292449 were significantly associated with diastolic BP, mean arterial pressure, and pulse pressure responses to high-salt and potassium supplementation diet. Conclusion: NEDD4L gene polymorphisms were significantly associated with BP responses to sodium and potassium intake, suggesting that NEDD4L gene may be involved in the development of salt sensitivity and potassium sensitivity.
KW - Blood pressure
KW - Genetic polymorphism
KW - NEDD4L
KW - Potassium
KW - Salt sensitivity
UR - https://www.scopus.com/pages/publications/85145837397
U2 - 10.7652/jdyxb202301005
DO - 10.7652/jdyxb202301005
M3 - 文章
AN - SCOPUS:85145837397
SN - 1671-8259
VL - 44
SP - 30
EP - 37
JO - Journal of Xi'an Jiaotong University (Medical Sciences)
JF - Journal of Xi'an Jiaotong University (Medical Sciences)
IS - 1
ER -