The association of gene polymorphisms in SREBP and its interaction with nutritional status on blood pressure phenotypes among children: a cross-sectional study

作者：Yuan Zeng, Zehui Fan, Yulian Zhu, Huichuan Tian, Mingxia Chen, Yue Gong, Bin Mao, Wanyun Xiang, Xiuqin Hong, Yide Yang · 发表于：BMC Cardiovascular Disorders · 年份：2025 · DOI：10.1186/s12872-025-05038-3 · 被引用次数：1 · 研究领域：Cholesterol and Lipid Metabolism、Peroxisome Proliferator-Activated Receptors、Fatty Acid Research and Health

Previous studies have confirmed that the SREBP polymorphisms are associated with dyslipidemia. However, no researchers investigated the association between SREBP polymorphisms and blood pressure phenotypes in children. A convenient cluster sampling method was adopted to conduct field survey in three middle schools. A total of 872 children were included in this cross-sectional study final analysis. Matrix-supported laser release/ionization time-of-flight mass spectrometry was used for genotyping of SREBP polymorphism. The association between SREBP polymorphisms and blood pressure phenotypes was analyzed by multivariable linear regression and Logistic regression analysis. A Bonferroni-corrected threshold of P < 0.025 ( SREBP1 ) or P < 0.0125 ( SREBP2 ) was considered significant. After adjusting for age, sex, age squared and BMI, individuals with GA/AA genotype of SREBP1 /rs11868035 had higher systolic blood pressure (SBP) ( β = 7.34, P = 0.004) than GG genotype, and SREBP1 /rs2297508 C allele carriers were positively associated with SBP (β = 7.19, P = 0.008). A significant interaction between SREBP2 /rs2228314 and gender on the risk of High Blood Pressure (HBP) ( P interaction = 0.034) was found. In boys, HBP risk increased by 101% for each additional G allele ( OR = 2.01, 95% CI 1.15–3.53, P = 0.015), but not in girls. Besides, we also identified an interaction between SREBP2 /rs2267439 and nutritional status on the risk of HBP ( P interaction =0.023). The risk of HBP in SREB...