Evidence map›Paper›PMID 38545780›Full record

ReviewHypertension (Dallas, Tex. : 1979)2024

Genetic and Epigenetic Mechanisms Regulating Blood Pressure and Kidney Dysfunction.

Kailash N Pandey

Open access · greenAbstract readReview
In one paragraph

Review in Hypertension (Dallas, Tex. : 1979), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
20.0field-weighted citation impact, top 1% 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

19 citing papers in PubMed, 18 citations in OpenAlex.

  1. Renal Tubule Cell-SpecificHypertension (Dallas, Tex. : 1979) · 2026
    Article
  2. Article
  3. The role of IPPflugers Archiv : European journal of physiology · 2026
    Review
  4. Hypertension Prevalence and Associated Risk Factors in a South African Population.International journal of environmental research and public health · 2026
    Observational
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Different Polymorphisms of the Renin-Angiotensin-Aldosterone System Genes are Associated with Poorer Blood Pressure Control in Hypertensive Older Adults.High blood pressure & cardiovascular prevention : the official journal of the Italian Society of Hypertension · 2025
    Article
  11. Review
  12. Review
  13. Article
  14. Nature or nurture? That is the question.Hypertension research : official journal of the Japanese Society of Hypertension · 2025
    Article
  15. Epigenomics and transcriptomics association study of blood pressure and incident diagnosis of hypertension in twins.Hypertension research : official journal of the Japanese Society of Hypertension · 2025
    Article
  16. Review
  17. Review
  18. Podocyte cell-specificPhysiological genomics · 2024
    Article
  19. Epigenetic mechanisms differentially regulate blood pressure and renal dysfunction in male and female Npr1 haplotype mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    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

1 author at 1 institution in 1 country.

Kailash N PandeyDepartment of Physiology, Tulane University Health Sciences Center, School of Medicine, New Orleans, LA.ORCID 0000-0002-5430-1672
Tulane University · US

Funding

Study of ANP Receptor:Gene Targeting and ExpressionR01HL062147 · NHLBI · TULANE UNIVERSITY OF LOUISIANA · PI PANDEY, KAILASH N · 1998 to 2020
$5.0M
ANP Receptor: Genetic and Epigenetic Mechanisms Regulating Blood Pressure and Kidney Injury and DysfunctionR01DK133833 · NIDDK · TULANE UNIVERSITY OF LOUISIANA · PI PANDEY, KAILASH N · 2022 to 2025
$1.8M
NHLBI NIH HHS R01 HL062147NIDDK NIH HHS R01 DK133833
6 · The paper itself

Abstract

The pioneering work of Dr Lewis K. Dahl established a relationship between kidney, salt, and high blood pressure (BP), which led to the major genetic-based experimental model of hypertension. BP, a heritable quantitative trait affected by numerous biological and environmental stimuli, is a major cause of morbidity and mortality worldwide and is considered to be a primary modifiable factor in renal, cardiovascular, and cerebrovascular diseases. Genome-wide association studies have identified monogenic and polygenic variants affecting BP in humans. Single nucleotide polymorphisms identified in genome-wide association studies have quantified the heritability of BP and the effect of genetics on hypertensive phenotype. Changes in the transcriptional program of genes may represent consequential determinants of BP, so understanding the mechanisms of the disease process has become a priority in the field. At the molecular level, the onset of hypertension is associated with reprogramming of gene expression influenced by epigenomics. This review highlights the specific genetic variants, mutations, and epigenetic factors associated with high BP and how these mechanisms affect the regulation of hypertension and kidney dysfunction.

Indexed as

Blood PressureEpigenesis, GeneticHypertensionAnimalsGenome-Wide Association StudyHumansKidneyKidney DiseasesPolymorphism, Single Nucleotideblood pressureDNA methylationhistone codehypertensionpolymorphisms, genetic

Identifiers

PMID38545780
PMCPMC11168895
OpenAlexW4393277370

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.