Evidence map›Paper›PMID 25410879›Full record

ArticleHypertension research : official journal of the Japanese Society of Hypertension2015

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

Hsin-Bang Leu, Chia-Min Chung, Shing-Jong Lin, Kuang-Mao Chiang, Hsin-Chou Yang, Hung-Yun Ho, Chih-Tai Ting, Tsung-Hsien Lin, Sheng-Hsiung Sheu, Wei-Chuan Tsai and 8 more

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Article in Hypertension research : official journal of the Japanese Society of Hypertension, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.0field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 50 citations in OpenAlex.

  1. Trial
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  3. Association ofGenes · 2026
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  4. Review
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  6. Rare variants inProceedings of the National Academy of Sciences of the United States of America · 2025
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  9. Determination of the Relationship Between DNA Methylation Status ofBalkan journal of medical genetics : BJMG · 2023
    Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Sex Differences in Circadian Clock Genes and Myocardial Infarction Susceptibility.Journal of cardiovascular development and disease · 2021
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 8 institutions in 1 country.

Hsin-Bang Leu1] Institute of Clinical Medicine and Cardiovascular Research Center, National Yang-Ming University, Taipei, Taiwan [2] Heath Care and Management Center, Taipei Veterans General Hospital, Taipei, Taiwan [3] Divison of Cardiology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Chia-Min Chung1] Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan [2] Environment-Omics-Disease Research Center, China Medical University Hospital, Taichung, Taiwan [3] Graduate Institute of Clinical Medical Science, China Medical University, Taichung, Taiwan.
Shing-Jong Lin1] Institute of Clinical Medicine and Cardiovascular Research Center, National Yang-Ming University, Taipei, Taiwan [2] Divison of Cardiology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Kuang-Mao ChiangInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Hsin-Chou YangInstitute of Statistical Science, Academia Sinica, Taipei, Taiwan.
Hung-Yun HoTaichung Veterans General Hospital, Taichung, Taiwan.
Chih-Tai TingTaichung Veterans General Hospital, Taichung, Taiwan.
Tsung-Hsien LinKaohsiung Medical University Chung-Ho Memorial Hospital, Kaohsiung, Taiwan.
Sheng-Hsiung SheuKaohsiung Medical University Chung-Ho Memorial Hospital, Kaohsiung, Taiwan.
Wei-Chuan TsaiNational Cheng Kung University Hospital, Tainan, Taiwan.
Jyh-Hong ChenNational Cheng Kung University Hospital, Tainan, Taiwan.
Wei-Hsian YinCheng Hsin Rehabilitation Medical Center, Taipei, Taiwan.
Ting-Yu ChiuMin Sheng General Hospital, Taoyuan, Taiwan.
Chin-Iuan ChenMin Sheng General Hospital, Taoyuan, Taiwan.
Cathy Sj FannInstitute of Statistical Science, Academia Sinica, Taipei, Taiwan.
Yuan-Tsong ChenInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Wen-Harn PanInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Jaw-Wen Chen1] Institute of Clinical Medicine and Cardiovascular Research Center, National Yang-Ming University, Taipei, Taiwan [2] Divison of Cardiology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan [3] Institute of Pharmacology, National Yang-Ming University, Taipei, Taiwan.
Institute of Biomedical Sciences, Academia Sinica · TWNational Cheng Kung University Hospital · TWInstitute of Statistical Science, Academia Sinica · TWKaohsiung Medical University Chung-Ho Memorial Hospital · TWMin Sheng General Hospital · TWNational Yang Ming Chiao Tung University · TWTaichung Veterans General Hospital · TWCheng Hsin General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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<0.001), and the additive genetic risk score also indicated a graded association with decreased diurnal BP changes (P=0.006), as well as a non-dipper phenotype (P=0.031). After multivariable logistic analysis, only the circadian genetic risk score (odds ratio (OR), 1550; 95% confidence interval (CI), 1.225-1.961, P<0.001) and the use of β-blockers (OR, 1.519; 95% CI, 1.164-1.982, P=0.003) were independently associated with the presence of non-dippers among subjects with young-onset hypertension. Genetic variants in circadian genes were associated with the diurnal phenotype of hypertension, suggesting a genetic association with diurnal BP changes in essential hypertension.

Indexed as

AdultAge of OnsetAllelesBlood PressureBlood Pressure Monitoring, AmbulatoryCircadian RhythmCircadian Rhythm Signaling Peptides and ProteinsFemaleGene FrequencyGenetic Association StudiesGenotypeHumansHypertensionMaleMiddle AgedYoung AdultCircadian Rhythm Signaling Peptides and Proteins

Identifiers

PMID25410879
OpenAlexW2015232755

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.