Evidence map›Paper›PMID 21167003›Full record

ArticleClinical and translational science2010

Variants in genes involved in functional pathways associated with hypertension in African Americans.

Maria P Martinez Cantarin, Adam Ertel, Stephanie Deloach, Paolo Fortina, Kathryn Scott, Trudy L Burns, Bonita Falkner

Abstract read
In one paragraph

Article in Clinical and translational science, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 3 pooled it
1.5field-weighted citation impact, top 16% 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

20 citing papers in PubMed, 3 syntheses or guidelines pooled it, 26 citations in OpenAlex.

  1. Association BetweenInternational journal of environmental research and public health · 2026
    Pooled it
  2. Pooled it
  3. Pooled it
  4. Cardiorespiratory function associated with dietary nitrate supplementation.Applied physiology, nutrition, and metabolism = Physiologie appliquee, nutrition et metabolisme · 2014
    Trial
  5. G protein-coupled receptor kinases in hypertension: physiology, pathogenesis, and therapeutic targets.Hypertension research : official journal of the Japanese Society of Hypertension · 2024
    Review
  6. Dopamine Receptor DThe Yale journal of biology and medicine · 2023
    Review
  7. Review
  8. Review
  9. Gastrorenal Axis.Hypertension (Dallas, Tex. : 1979) · 2016
    Review
  10. Article
  11. Article
  12. G protein-coupled receptor kinase 4: role in hypertension.Hypertension (Dallas, Tex. : 1979) · 2015
    Review
  13. Review
  14. Article
  15. Article
  16. Dopamine, the kidney, and hypertension.Current hypertension reports · 2012
    Review
  17. Review
  18. Abnormalities in renal dopamine signaling and hypertension: the role of GRK4.Current opinion in nephrology and hypertension · 2012
    Review
  19. Article
  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

7 authors at 2 institutions in 1 country.

Maria P Martinez CantarinDepartment of Medicine, Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Adam Ertel
Stephanie Deloach
Paolo Fortina
Kathryn Scott
Trudy L Burns
Bonita Falkner
Thomas Jefferson University · USUniversity of Iowa · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Essential hypertension (HBP) is a complex trait with a substantial heritable component. The purpose of this study was to determine if variants in the G-protein coupled receptor Kinase-4 (GRK4), nitric oxide synthase-3 (NOS3), or angiotensin converting enzyme (ACE) genes are associated singly or through complex interactions, with HBP in African Americans aged 18-49 years. TaqMan Assays were used for genotyping the GRK4 and NOS3 variants. The ACE I/D variant was obtained by polymerase chain reaction and electrophoresis. Allelic association tests were performed for the five markers using PLINK. Logistic regression models were fitted to investigate associations between HBP status and the genetic markers. Multilocus analyses were also conducted. The study included 173 hypertensives and 239 normotensives, with stratification into obese and nonobese groups. The GRK4 A486V variant was negatively associated with HBP in the nonobese group (p = 0.048). The TT/CT genotype of GRK4 A486V was associated with decreased risk for HBP relative to the CC genotype after adjusting for age, sex, and body mass index (p = 0.028). Individuals having at least one NOS3 A allele and GRK4 R65L genotype GG had odds of HBP of 2.97 relative to GG homozygotes for NOS3 and GRK4 R65L. These results show very modest effects and do not fully replicate previous studies.

Indexed as

Genetic Predisposition to DiseaseAdolescentAdultBlack or African AmericanBlood PressureBody SizeFemaleGene FrequencyGenetic LociG-Protein-Coupled Receptor Kinase 4HumansHypertensionINDEL MutationIntronsLogistic ModelsMaleG-Protein-Coupled Receptor Kinase 4Nitric Oxide Synthase Type IIINOS3 protein, humanPeptidyl-Dipeptidase A

Identifiers

PMID21167003
PMCPMC5439635
OpenAlexW2027559090

What OpenQuestion holds

Textmetadata
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.