Association of circadian genes with diurnal blood pressure changes and non-dipper essential hypertension: a genetic association with young-onset hypertension

Recent studies have suggested that circadian genes have important roles in maintaining the circadian rhythm of the cardiovascular system. However, the associations between diurnal BP changes and circadian genes remain undetermined. We conducted a genetic association study of young-onset hypertension...

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Veröffentlicht in:Hypertension research 2015-02, Vol.38 (2), p.155-162
Hauptverfasser: Leu, Hsin-Bang, Chung, Chia-Min, Lin, Shing-Jong, Chiang, Kuang-Mao, Yang, Hsin-Chou, Ho, Hung-Yun, Ting, Chih-Tai, Lin, Tsung-Hsien, Sheu, Sheng-Hsiung, Tsai, Wei-Chuan, Chen, Jyh-Hong, Yin, Wei-Hsian, Chiu, Ting-Yu, Chen, Chin-Iuan, Fann, Cathy Sj, Chen, Yuan-Tsong, Pan, Wen-Harn, Chen, Jaw-Wen
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Sprache:eng
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Zusammenfassung:Recent studies have suggested that circadian genes have important roles in maintaining the circadian rhythm of the cardiovascular system. However, the associations between diurnal BP changes and circadian genes remain undetermined. We conducted a genetic association study of young-onset hypertension, in which 24-h ambulatory blood pressure (BP) monitoring was performed. A total of 23 tag single-nucleotide polymorphisms (SNPs) on 11 genes involved in circadian rhythms were genotyped for correlations with diurnal BP variation phenotypes. A permutation test was used to correct for multiple testing. Five tag SNPs within five loci, including rs3888170 in NPAS2, rs6431590 in PER2, rs1410225 in RORββ, rs3816358 in BMAL1 and rs10519096 in RORα, were significantly associated with the non-dipper phenotype in 372 young hypertensive patients. A genetic risk score was generated by counting the risk alleles and effects for each individual. Genotyping was performed in an additional independent set of 619 young-onset hypertensive subjects. Altogether, non-dippers had a higher weighted genetic risk score than dippers (1.67±0.56 vs. 1.54±0.55, P
ISSN:0916-9636
1348-4214
DOI:10.1038/hr.2014.152