Evidence map›Paper›PMID 26962801›Full record

Observational studyMedicine2016

Genetic Variation in the Human SORBS1 Gene is Associated With Blood Pressure Regulation and Age at Onset of Hypertension: A SAPPHIRe Cohort Study.

Tien-Jyun Chang, Wen-Chang Wang, Chao A Hsiung, Chih-Tsueng He, Ming-Wei Lin, Wayne Huey-Herng Sheu, Yi-Cheng Chang, Tom Quertermous, Ida Chen, Jerome Rotter and 2 more

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Polymorphisms ofAnimals : an open access journal from MDPI · 2021
    Article
  7. Article
  8. Article
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  10. Article
  11. Review
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

12 authors at 2 institutions in 2 countries.

Tien-Jyun ChangFrom the Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan (T-JC, Y-CC, L-MC); The Ph.D. Program for Translational Medicine, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan (W-CW); Division of Biostatistics and Bioinformatics, Institute of Population Health Sciences, National Health Research Institutes, Zhunan, Taiwan (W-CW, C-AH); Department of Endocrinology and Metabolism, Tri-Service General Hospital, Taipei, Taiwan (C-TH); Institute of Public Health, National Yang-Ming University, Taipei, Taiwan (M-WL); Department of Medical Research & Education, Taipei Veterans General Hospital, Taipei, Taiwan (M-WL); Department of Endocrinology and Metabolism, Taichung Veterans General Hospital, Taichung, Taiwan (WH-HS); Graduate Institute of Medical Genomics and Proteomics, National Taiwan University Medical College, Taipei, Taiwan (Y-CC); Division of Cardiovascular Medicine, Falk CVRC, Stanford University School of Medicine, Stanford, CA (TQ); Los Angles Biomedical Research Institute, Los Angeles, CA (IC, JR); Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan (L-MC).
Wen-Chang Wang
Chao A Hsiung
Chih-Tsueng He
Ming-Wei Lin
Wayne Huey-Herng Sheu
Yi-Cheng Chang
Tom Quertermous
Ida Chen
Jerome Rotter
Lee-Ming Chuang
and the SAPPHIRe Study Group
Mitsubishi Corporation (Japan) · JPNational Yang Ming Chiao Tung University · TW

Funding

Transgenic & Knock-out MouseP30DK063491 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Andrea L Hevener · 2003 to 2026
$40.4M
Mechanism of the Coronary Heart Disease Association at Chromosome 6q23.2R01HL109512 · NHLBI · STANFORD UNIVERSITY · PI QUERTERMOUS, THOMAS · 2011 to 2019
$6.1M
GENETIC DETERMINANTS OF HYPERTENSIONU01HL054527 · NHLBI · STANFORD UNIVERSITY · PI QUERTERMOUS, THOMAS NONE · 1995 to 2004
$4.6M
NHLBI NIH HHS R01 HL109512NHLBI NIH HHS U01 HL054527NIDDK NIH HHS P30 DK063491
6 · The paper itself

Abstract

Essential hypertension is a complex disease involving multiple genetic and environmental factors. A human gene containing a sorbin homology domain and 3 SH3 domains in the C-terminal region, termed SORBS1, plays a significant role in insulin signaling. We previously found a significant association between the T228A polymorphism and insulin resistance, obesity, and type 2 diabetes. It has been hypothesized that a set of genes responsible for insulin resistance may be closely linked with genes susceptible to the development of hypertension. Identification of insulin resistance-related genetic factors may, therefore, enhance our understanding of essential hypertension. This study aimed to examine whether common SORBS1 genetic variations are associated with blood pressure and age at onset of hypertension in an ethnic Chinese cohort.We genotyped 9 common tagged single nucleotide polymorphisms of the SORBS1 gene in 1136 subjects of Chinese origin from the Stanford Asia-Pacific Program for Hypertension and Insulin Resistance family study. Blood pressure was measured upon enrolment. The associations of the SORBS1 single nucleotide polymorphisms with blood pressure and the presence of hypertension were analyzed with a generalized estimating equation model. We used the false-discovery rate measure Q value with a cutoff <0.1 to adjust for multiple comparisons. In the Cox regression analysis for hypertension-free survival, a robust sandwich variance estimator was used to deal with the within-family correlations with age at onset of hypertension. Gender, body mass index, and antihypertension medication were adjustment covariates in the Cox regression analysis.In this study, genetic variants of rs2281939 and rs2274490 were significantly associated with both systolic and diastolic blood pressure. A genetic variant of rs2274490 was also significantly associated with the presence of hypertension. Furthermore, genetic variants of rs2281939 and rs2274490 were associated with age at onset of hypertension after adjustment for gender, body mass index, and antihypertension medication.In conclusion, we provide evidence for an association between common SORBS1 genetic variations and blood pressure, presence of hypertension, and age at onset of hypertension. The biological mechanism of genetic variation associated with blood pressure regulation needs further investigation.

Indexed as

AdultAge of OnsetBlood PressureCohort StudiesDiastoleFemaleGenotypeHumansHypertensionMaleMicrofilament ProteinsMiddle AgedPolymorphism, Single NucleotidePrevalenceSystoleTaiwanMicrofilament ProteinsSORBS1 protein, human

Identifiers

PMID26962801
PMCPMC4998882
OpenAlexW2294776129

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.