Evidence map›Paper›PMID 22161147›Full record

ReviewCurrent hypertension reports2012

Between candidate genes and whole genomes: time for alternative approaches in blood pressure genetics.

Jacob Basson, Jeannette Simino, D C Rao

Open access · greenAbstract readReview
In one paragraph

Review in Current hypertension reports, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 6% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Pathway-based analyses.BMC genetics · 2016
    Article
  11. Regulation of blood pressure, oxidative stress and AT1R by high salt diet in mutant human dopamine D5 receptor transgenic mice.Hypertension research : official journal of the Japanese Society of Hypertension · 2015
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
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  18. An overview of the genomics of metabolic syndrome.Journal of nursing scholarship : an official publication of Sigma Theta Tau International Honor Society of Nursing · 2013
    Review
  19. An approach to the etiology of metabolic syndrome.Colombia medica (Cali, Colombia) · 2013
    Review
  20. 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

3 authors at 1 institution in 1 country.

Jacob BassonDivision of Biostatistics, Washington University School of Medicine, St. Louis, MO 63110-1093, USA.
Jeannette Simino
D C Rao
Washington University in St. Louis · US

Funding

Genome-Wide Association Analysis in Essential Hypertension (FEHGAS study)R01HL086694 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ARAVINDA CHAKRAVARTI · 2007 to 2026
$21.2M
HYPERGEN: GENETICS OF LEFT VENTRICULAR HYPERTROPHYR01HL055673 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI ARNETT, DONNA K · 1996 to 2016
$18.1M
Genetic Epidemiology of Blood Pressure InterventionU01HL072507 · NHLBI · TULANE UNIVERSITY OF LOUISIANA · PI HE, JIANG · 2002 to 2008
$7.6M
The Family Blood Pressure Program (Program Data Center)U01HL054473 · NHLBI · WASHINGTON UNIVERSITY · PI RAO, DABEERU C · 2000 to 2008
$5.8M
Post-Doctoral Research Training in Genetic EpidemiologyT32HL091823 · NHLBI · WASHINGTON UNIVERSITY · PI RAO, DABEERU C · 2008 to 2017
$2.1M
Pre-doctoral Research Training in Human Genetic EpidemiologyT32HL083822 · NHLBI · WASHINGTON UNIVERSITY · PI PROVINCE, MICHAEL A. · 2008 to 2012
$1.2M
NHLBI NIH HHS R01 HL055673NHLBI NIH HHS R01 HL086694NHLBI NIH HHS R01 HL55673NHLBI NIH HHS T32 HL083822NHLBI NIH HHS U01 HL054473NHLBI NIH HHS U01 HL072507NHLBI NIH HHS U01 HL72507
6 · The paper itself

Abstract

Blood pressure has a significant genetic component, but less than 3% of the observed variance has been attributed to genetic variants identified to date. Candidate gene studies of rare, monogenic hypertensive syndromes have conclusively implicated several genes altering renal sodium balance, and studies of essential hypertension have inconsistently implicated over 50 genes in pathways affecting renal sodium balance and other functions. Genome-wide linkage scans have replicated numerous quantitative trait loci throughout the genome, and over 50 single nucleotide polymorphisms (SNPs) have been replicated in multiple genome-wide association studies. These studies provide considerable evidence that epistasis and other interactions play a role in the genetic architecture of blood pressure regulation, but candidate gene studies have limited scope to test for epistasis, and genome-wide studies have low power for both main effects and interactions. This review summarizes the genetic findings to date for blood pressure, and it proposes focused, pathway-based approaches involving epistasis, gene-environment interactions, and next-generation sequencing to further the genetic dissection of blood pressure and hypertension.

Indexed as

GenomeBlood PressureBlood Pressure DeterminationEpistasis, GeneticForecastingGene-Environment InteractionGenetic LinkageGenome-Wide Association StudyHumansHypertensionMultifactorial InheritancePolymorphism, Single NucleotideSequence Analysis

Identifiers

PMID22161147
PMCPMC7774509
OpenAlexW1990864313

What OpenQuestion holds

Textmetadata
LicenceTDM
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.