Evidence map›Paper›PMID 31805646›Full record

SynthesisInternational journal of environmental research and public health2019

DNA Methylation of Candidate Genes (ACE II, IFN-γ, AGTR 1, CKG, ADD1, SCNN1B and TLR2) in Essential Hypertension: A Systematic Review and Quantitative Evidence Synthesis.

Laurens Holmes, Andrew Lim, Camillia R Comeaux, Kirk W Dabney, Osatohamwen Okundaye

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis in International journal of environmental research and public health, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

28 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Epigenetic Mechanisms in Heart Diseases.Reviews in cardiovascular medicine · 2025
    Review
  7. Review
  8. Article
  9. Article
  10. Epigenetic Signatures in Hypertension.Journal of personalized medicine · 2023
    Article
  11. Article
  12. Involvement of epigenetics in affecting host immunity during SARS-CoV-2 infection.Biochimica et biophysica acta. Molecular basis of disease · 2023
    Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Health of the Newborn and Breastfeeding during the COVID-19 Pandemic: A Literature Review.Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia · 2022
    Review
  18. Article
  19. Review
  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

5 authors at 1 institution in 1 country.

Laurens HolmesNemours/A.I. DuPont Children's Hospital, Nemours Office of Health Equity & Inclusion, 2200 Concord Pike, 7th Floor, Wilmington, DE 19803, USA.
Andrew LimNemours/A.I. DuPont Children's Hospital, Nemours Office of Health Equity & Inclusion, 2200 Concord Pike, 7th Floor, Wilmington, DE 19803, USA.ORCID 0000-0003-1154-1796
Camillia R ComeauxNemours/A.I. DuPont Children's Hospital, Nemours Office of Health Equity & Inclusion, 2200 Concord Pike, 7th Floor, Wilmington, DE 19803, USA.
Kirk W DabneyNemours/A.I. DuPont Children's Hospital, Nemours Office of Health Equity & Inclusion, 2200 Concord Pike, 7th Floor, Wilmington, DE 19803, USA.
Osatohamwen OkundayeNemours/A.I. DuPont Children's Hospital, Nemours Office of Health Equity & Inclusion, 2200 Concord Pike, 7th Floor, Wilmington, DE 19803, USA.
DuPont (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Physical, chemical, and social environments adversely affect the molecular process and results in cell signal transduction and the subsequent transcription factor dysregulation, leading to impaired gene expression and abnormal protein synthesis. Stressful environments such as social adversity, isolation, sustained social threats, physical inactivity, and highly methylated diets predispose individuals to molecular level alterations such as aberrant epigenomic modulations that affect homeostasis and hemodynamics. With cardiovascular disease as the leading cause of mortality in the US and blacks/African Americans being disproportionately affected by hypertension (HTN) which contributes substantially to these deaths, reflecting the excess mortality and survival disadvantage of this sub-population relative to whites, understanding the molecular events, including epigenomic and socio-epigenomic modulations, is relevant to narrowing the black-white mortality risk differences. We aimed to synthesize epigenomic findings in HTN namely (a) angiotensin-converting enzyme 2 (ACE II) gene, (b) Toll-like receptor 2 (TLR2) gene, (c) interferon γ (IFN-γ) gene, and (d) Capping Actin Protein, Gelosin-Like (

Indexed as

DNA MethylationEssential HypertensionFemaleGenotypeHumansDNA methylation and hypertensionepigenomicsessential hypertensionhypertension candidate genessocio-epigenomics

Identifiers

PMID31805646
PMCPMC6926644
OpenAlexW2990878859

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.