Evidence map›Paper›PMID 39578479›Full record

ArticleScientific reports2024

Interplay analysis of lead exposure with key cardiovascular gene polymorphisms on blood pressure in a cross-sectional study of occupational workers.

Xiaoyan Ou, Chen Xiao, Jun Jiang, Xinxia Liu, Lili Liu, Yao Lu, Weipeng Zhang, Yun He, Zhiqiang Zhao

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Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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9 authors.

Xiaoyan Ou *Department of Toxicology, School of Public Health, Sun Yat-sen University, Guangzhou, Guangdong, China.
Chen Xiao *Department of Toxicology, School of Public Health, Sun Yat-sen University, Guangzhou, Guangdong, China.
Jun Jiang *Department of Toxicology, School of Public Health, Sun Yat-sen University, Guangzhou, Guangdong, China.
Xinxia LiuZhongshan Third People's Hospital, Guangdong, Zhongshan, China.
Lili LiuDepartment of Toxicology, Guangdong Province Hospital for Occupational Disease Prevention and Treatment, Guangzhou, Guangdong, China.
Yao LuDepartment of Toxicology, School of Public Health, Sun Yat-sen University, Guangzhou, Guangdong, China.
Weipeng ZhangDepartment of Toxicology, Guangdong Province Hospital for Occupational Disease Prevention and Treatment, Guangzhou, Guangdong, China.
Yun HeDepartment of Toxicology, School of Public Health, Sun Yat-sen University, Guangzhou, Guangdong, China. heyun7@mail.sysu.edu.cn.
Zhiqiang ZhaoDepartment of Toxicology, School of Public Health, Sun Yat-sen University, Guangzhou, Guangdong, China. zhaozq68@163.com.

Funding

Anhui Provincial Department of Education Natural Science Research Key Project KJ2018A0805Guangdong Provincial Medical Research Fund Project A2021421National Natural Science Foundation of China 81273097
6 · The paper itself

Abstract

An increasing number of studies have shown that lead is an important cardiovascular risk factor, but the impact of cardiovascular related gene polymorphisms on lead induced cardiovascular diseases is still unclear. To assess the interaction of lead exposure and related key cardiovascular regulating gene polymorphisms on blood pressure traits, three single-nucleotide polymorphisms including NOTCH1 rs3124591, Cerebral cavernous malformations 3 (CCM3) rs3804610 and Vascular endothelial growth factor receptor type 2 (VEGFR2) rs2305948 were selected and genotyped using improved multiplex ligase detection reaction method in 568 lead exposure workers in South China. General characteristics, blood lead and biochemical parameters including glucose, lipid profile and creatinine were also collected according to standard protocols. Regression analysis was used to evaluate the association of blood pressure with lead exposure, polymorphisms and their interaction. This study displayed that CCM3 rs3804610 had a positive interaction with lead and VEGFR2 rs2305948 had a negative interaction with lead. Specifcally, compared with the wild-type population, the blood lead of the genotype population carrying the risk allele increased by 1 µg/dL, systolic blood pressure increased by 0.53 mmHg (p < 0.01) and diastolic blood pressure increased by 0.34 mmHg (p < 0.05) for CCM3 rs3804610, and systolic blood pressure decreased by 0.28 mmHg (p < 0.05) and diastolic blood pressure decreased by 0.22 mmHg (p < 0.05) for VEGFR2 rs2305948. Thus our findings showed that the interaction between CCM3 rs3804610 and VEGFR2 rs2305948 and lead exposure were associated with blood pressure and may provide guidance for future research on hypertension prevention and personalized clinical treatment in lead exposed populations.

Indexed as

Blood PressureLeadOccupational ExposurePolymorphism, Single NucleotideAdultCardiovascular DiseasesChinaCross-Sectional StudiesFemaleGenetic Predisposition to DiseaseGenotypeHumansMaleMiddle AgedVascular Endothelial Growth Factor Receptor-2KDR protein, humanLeadVascular Endothelial Growth Factor Receptor-2blood pressureCardiovascular regulating geneGene-environment interactionLead exposureSingle-nucleotide polymorphism

Identifiers

PMID39578479
PMCPMC11584784

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