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Natriuretic Peptides

Drugs and Chemicals · NLM MeSH · updated 2026-10-31 · version 1

Citations verified against PubMedNot yet clinician-reviewed9 referencesApproximately 3 min read

Peptides that regulate the water-electrolyte balance in the body, also known as natriuretic peptide hormones.

Table of Contents

1. Definition2. Research landscape3. Reading the evidence4. Open-access studies5. Key reviews6. References7. About this article

Definition and research guide

This page combines a MeSH definition, publication statistics and selected research abstracts. It is a starting point for reading the literature, not a medical textbook or a systematic evidence review.

Content available: 3 complete abstracts (611 words), 9 references. Full article text is not stored or reproduced here; follow the PMID, DOI or PMC links to read the original sources and their access terms.

Definition

Peptides that regulate the water-electrolyte balance in the body, also known as natriuretic peptide hormones. Several have been sequenced (atrial natriuretic factor; brain natriuretic peptide; c-type natriuretic peptide).

Definition: NLM Medical Subject Headings (MeSH) scope note (Public domain (U.S. National Library of Medicine); attribution requested). View the MeSH record.

Also known as: Peptides, Natriuretic; Natriuretic Peptide; Peptide, Natriuretic; Natriuretic Peptide Hormones; Peptide Hormones, Natriuretic.

Where it fits in the MeSH classification

Broader topics
Peptide Hormones
Narrower topics
Atrial Natriuretic Factor; Natriuretic Peptide, Brain; Natriuretic Peptide, C-Type

Related concepts

  • Water-Electrolyte Balance
  • Atrial Natriuretic Factor
  • Brain Natriuretic Peptide
  • C-Type Natriuretic Peptide

Research landscape

PubMed indexes 34,413 records tagged with the MeSH heading “Natriuretic Peptides” (counts retrieved 2026-10-31). 5,231 of them (15.2%) were published from 2020 onward, and the busiest period so far is 2010-2019 with 10,323 records.

Reviews account for 3,631 records (10.6%) and meta-analyses for 330. Randomized controlled trials number 2,118 (6.2%) as a share of all records on the topic.

PubMed records by publication periodthrough 1999: 10,322 records; 2000-2009: 8,537 records; 2010-2019: 10,323 records; 2020 onward: 5,231 records10,322through 19998,5372000-200910,3232010-20195,2312020 onward
Records in PubMed indexed with this heading, by publication period. Real counts from NCBI E-utilities; the final period covers only part of the current year. Volume reflects how much has been published, not how strong the evidence is.
Show the data
PeriodRecords
through 199910,322
2000-20098,537
2010-201910,323
2020 onward5,231
Share of records by publication typeReviews: 10.6 percent; Meta-analyses: 1.0 percent; Randomized controlled trials: 6.2 percentReviews10.6% (3,631)Meta-analyses1.0% (330)Randomized controlled trials6.2% (2,118)
Share of all PubMed records on this heading that carry each publication type. Types overlap with other records, so the shares do not sum to 100%.
Publication-type chart data
Publication types among 34,413 PubMed records
TypeRecordsShare
Reviews3,63110.6%
Meta-analyses3301.0%
Randomized controlled trials2,1186.2%

Method: PubMed query "Natriuretic Peptides"[MeSH Terms] with publication-type and date filters, retrieved 2026-10-31.

Reading the evidence in drugs and chemicals

Studies of a chemical or drug can answer very different questions: what it is and how it behaves in cells and animals, how the body handles it, and whether it changes outcomes in people. Laboratory and animal findings often do not carry over to patients, and observational studies of exposures are confounded by who uses a substance and why. Nothing on this page is a recommendation to use, avoid, start or stop any substance or medicine; talk to a qualified clinician or pharmacist about your own situation. Check the dose, the species, the comparison group and whether a patient-relevant outcome was measured.

Evidence from open-access studies

These open-access studies come from PubMed’s best-match results for this heading (papers whose main topic it is), ranked here by citation count, with one recent addition. Each abstract is reproduced in full under its recorded open licence so that you can read the authors’ own words. They illustrate the literature; they are not a systematic summary of it. Citation counts measure attention, not reliability or clinical benefit.

Study comparison — selected abstracts, not a systematic review
Study / authorsYearSource label / designEurope PMC citationsLicence / source
The Impact of Natriuretic Peptides on Heart Development, Homeostasis, and Disease
Giovou AE, Gladka MM, Christoffels VM
2024Review article
Design not recorded in structured metadata
23cc by
PMID 38891063 · DOI · PMC11172276
In-hospital initiation of angiotensin receptor-neprilysin inhibition in acute heart failure: the PREMIER trial
Tanaka A, Kida K, Matsue Y, Imai T, Suwa S, Taguchi I, et al.
2024Randomized controlled trial
Design not recorded in structured metadata
19cc by
PMID 39215531 · DOI · PMC11544311
Single intramuscular injection of self-amplifying RNA of Nppa to treat myocardial infarction
Zhang K, Tao H, Zhu D, Yue Z, Hu S, Wu Y, et al.
2026Research article
Design not recorded in structured metadata
14cc by
PMID 41785353 · DOI · PMC13124201

The Impact of Natriuretic Peptides on Heart Development, Homeostasis, and Disease [1]

Review article Giovou AE, Gladka MM, Christoffels VM · · 2024 · cited 23 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
During mammalian heart development, the clustered genes encoding peptide hormones, Natriuretic Peptide A (NPPA; ANP) and B (NPPB; BNP), are transcriptionally co-regulated and co-expressed predominately in the atrial and ventricular trabecular cardiomyocytes.
Closing excerpt
Here, we review recent insights into the regulation of expression and intracardiac functions of NPPA and NPPB during heart development, homeostasis, and disease.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (218 words)

During mammalian heart development, the clustered genes encoding peptide hormones, Natriuretic Peptide A (NPPA; ANP) and B (NPPB; BNP), are transcriptionally co-regulated and co-expressed predominately in the atrial and ventricular trabecular cardiomyocytes. After birth, expression of NPPA and a natural antisense transcript NPPA-AS1 becomes restricted to the atrial cardiomyocytes. Both NPPA and NPPB are induced by cardiac stress and serve as markers for cardiovascular dysfunction or injury. NPPB gene products are extensively used as diagnostic and prognostic biomarkers for various cardiovascular disorders. Membrane-localized guanylyl cyclase receptors on many cell types throughout the body mediate the signaling of the natriuretic peptide ligands through the generation of intracellular cGMP, which interacts with and modulates the activity of cGMP-activated kinase and other enzymes and ion channels. The natriuretic peptide system plays a fundamental role in cardio-renal homeostasis, and its potent diuretic and vasodilatory effects provide compensatory mechanisms in cardiac pathophysiological conditions and heart failure. In addition, both peptides, but also CNP, have important intracardiac actions during heart development and homeostasis independent of the systemic functions. Exploration of the intracardiac functions may provide new leads for the therapeutic utility of natriuretic peptide-mediated signaling in heart diseases and rhythm disorders. Here, we review recent insights into the regulation of expression and intracardiac functions of NPPA and NPPB during heart development, homeostasis, and disease.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 38891063 · DOI · PMC11172276

In-hospital initiation of angiotensin receptor-neprilysin inhibition in acute heart failure: the PREMIER trial [2]

Randomized controlled trial Tanaka A, Kida K, Matsue Y, Imai T, Suwa S, Taguchi I, et al. · · 2024 · cited 19 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Background and aimsThe efficacy and safety of early sacubitril/valsartan (Sac/Val) initiation after acute heart failure (AHF) has not been demonstrated outside North America.
Closing excerpt
gov (NCT05164653) and Japan Registry of Clinical Trials (jRCTs021210046).
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (262 words)

Background and aimsThe efficacy and safety of early sacubitril/valsartan (Sac/Val) initiation after acute heart failure (AHF) has not been demonstrated outside North America. The present study aimed to evaluate the effect of in-hospital Sac/Val therapy initiation after an AHF episode on N-terminal pro-B-type natriuretic peptide (NT-proBNP) level in Japanese patients.MethodsThis was an investigator-initiated, multicentre, prospective, randomized, open-label, blinded-endpoint pragmatic trial. After haemodynamic stabilization within 7 days after hospitalization, eligible inpatients were allocated to switch from angiotensin-converting enzyme inhibitor or angiotensin receptor blocker to Sac/Val (Sac/Val group) or to continue angiotensin-converting enzyme inhibitor or angiotensin receptor blocker (control group). The primary efficacy endpoint was the 8-week proportional change in geometric means of NT-proBNP levels.ResultsA total of 400 patients were equally randomized, and 376 (median age 75 years, 31.9% women, de novo heart failure rate 55.6%, and median left ventricular ejection fraction 37%) were analysed. The per cent changes in NT-proBNP level geometric means at Weeks 4/8 were -35%/-45% (Sac/Val group) and -18%/-32% (control group), and their group ratio (Sac/Val vs. control) was 0.80 (95% confidence interval 0.68-0.94; P = .008) at Week 4 and 0.81 (95% confidence interval 0.68-0.95; P = .012) at Week 8, respectively. In the pre-specified subgroup analyses, the effects of Sac/Val were confined to patients with a left ventricular ejection fraction ConclusionsIn-hospital Sac/Val therapy initiation in addition to contemporary recommended therapy triggered a greater NT-proBNP level reduction in Japanese patients hospitalized for AHF. These findings may expand the evidence on Sac/Val therapy in this clinical situation outside North America.Clinical trial registrationClinicalTrial.gov (NCT05164653) and Japan Registry of Clinical Trials (jRCTs021210046).

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 39215531 · DOI · PMC11544311

Single intramuscular injection of self-amplifying RNA of Nppa to treat myocardial infarction [3]

Research article Zhang K, Tao H, Zhu D, Yue Z, Hu S, Wu Y, et al. · · 2026 · cited 14 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Self-amplifying RNA (saRNA) enables sustained protein expression from a single administration.
Closing excerpt
Together, these results demonstrate that one-shot saNppa-LNP therapy offers durable cardioprotection, supporting the broader potential of saRNA-LNP-based approaches for cardiac therapy.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (131 words)

Self-amplifying RNA (saRNA) enables sustained protein expression from a single administration. In this study, we developed an intramuscular saRNA-lipid nanoparticle (saNppa-LNP) therapy encoding natriuretic peptide type A (Nppa) for cardioprotection. A single injection induced sustained pro-atrial natriuretic peptide (pro-ANP) secretion for 4 weeks; pro-ANP was subsequently cleaved by the cardiac protease corin into active ANP, producing robust cardioprotection in mouse and swine myocardial infarction models. At equivalent doses, saNppa achieved greater efficacy than conventional mRNA. Single-nucleus transcriptomics identified natriuretic peptide receptor 1-positive (Npr1+) endothelial and epicardial cells as primary effectors, with saNppa-LNPs reshaping their paracrine profile to promote cardiomyocyte regeneration and suppress fibrosis. Longitudinal biosafety assessments revealed no systemic toxicity. Together, these results demonstrate that one-shot saNppa-LNP therapy offers durable cardioprotection, supporting the broader potential of saRNA-LNP-based approaches for cardiac therapy.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 41785353 · DOI · PMC13124201

Key reviews and meta-analyses

The most cited review-type papers among PubMed’s best-match results for this heading, listed with bibliographic details only. Follow the links for the full text and access terms.

  • Research article Heart Failure Association of the European Society of Cardiology practical guidance on the use of natriuretic peptide concentrations [4]
    Mueller C, McDonald K, de Boer RA, Maisel A, Cleland JGF, Kozhuharov N, et al. · Eur J Heart Fail · 2019 · cited 590 times (Europe PMC)
  • Research article Cardiac natriuretic peptides [5]
    Goetze JP, Bruneau BG, Ramos HR, Ogawa T, de Bold MK, de Bold AJ · Nat Rev Cardiol · 2020 · cited 445 times (Europe PMC)
  • Research article B-type natriuretic peptides and cardiovascular risk: systematic review and meta-analysis of 40 prospective studies [6]
    Di Angelantonio E, Chowdhury R, Sarwar N, Ray KK, Gobin R, Saleheen D, et al. · Circulation · 2009 · cited 300 times (Europe PMC)
  • Research article BNP and NT-proBNP as Diagnostic Biomarkers for Cardiac Dysfunction in Both Clinical and Forensic Medicine [7]
    Cao Z, Jia Y, Zhu B · Int J Mol Sci · 2019 · cited 267 times (Europe PMC)
  • Research article The diagnostic accuracy of the natriuretic peptides in heart failure: systematic review and diagnostic meta-analysis in the acute care setting [8]
    Roberts E, Ludman AJ, Dworzynski K, Al-Mohammad A, Cowie MR, McMurray JJ, et al. · BMJ · 2015 · cited 260 times (Europe PMC)
  • Research article The prognostic value of pre-operative and post-operative B-type natriuretic peptides in patients undergoing noncardiac surgery: B-type natriuretic peptide and N-terminal fragment of pro-B-type natriuretic peptide: a systematic review and individual patient data meta-analysis [9]
    Rodseth RN, Biccard BM, Le Manach Y, Sessler DI, Lurati Buse GA, Thabane L, et al. · J Am Coll Cardiol · 2014 · cited 220 times (Europe PMC)

References

  1. Giovou AE, Gladka MM, Christoffels VM. The Impact of Natriuretic Peptides on Heart Development, Homeostasis, and Disease. . 2024. PMID 38891063 · DOI · PMC11172276
  2. Tanaka A, Kida K, Matsue Y, Imai T, Suwa S, Taguchi I, et al.. In-hospital initiation of angiotensin receptor-neprilysin inhibition in acute heart failure: the PREMIER trial. . 2024. PMID 39215531 · DOI · PMC11544311
  3. Zhang K, Tao H, Zhu D, Yue Z, Hu S, Wu Y, et al.. Single intramuscular injection of self-amplifying RNA of Nppa to treat myocardial infarction. . 2026. PMID 41785353 · DOI · PMC13124201
  4. Mueller C, McDonald K, de Boer RA, Maisel A, Cleland JGF, Kozhuharov N, et al.. Heart Failure Association of the European Society of Cardiology practical guidance on the use of natriuretic peptide concentrations. Eur J Heart Fail. 2019. PMID 31222929 · DOI
  5. Goetze JP, Bruneau BG, Ramos HR, Ogawa T, de Bold MK, de Bold AJ. Cardiac natriuretic peptides. Nat Rev Cardiol. 2020. PMID 32444692 · DOI
  6. Di Angelantonio E, Chowdhury R, Sarwar N, Ray KK, Gobin R, Saleheen D, et al.. B-type natriuretic peptides and cardiovascular risk: systematic review and meta-analysis of 40 prospective studies. Circulation. 2009. PMID 19917883 · DOI
  7. Cao Z, Jia Y, Zhu B. BNP and NT-proBNP as Diagnostic Biomarkers for Cardiac Dysfunction in Both Clinical and Forensic Medicine. Int J Mol Sci. 2019. PMID 31013779 · DOI · PMC6515513
  8. Roberts E, Ludman AJ, Dworzynski K, Al-Mohammad A, Cowie MR, McMurray JJ, et al.. The diagnostic accuracy of the natriuretic peptides in heart failure: systematic review and diagnostic meta-analysis in the acute care setting. BMJ. 2015. PMID 25740799 · DOI · PMC4353288
  9. Rodseth RN, Biccard BM, Le Manach Y, Sessler DI, Lurati Buse GA, Thabane L, et al.. The prognostic value of pre-operative and post-operative B-type natriuretic peptides in patients undergoing noncardiac surgery: B-type natriuretic peptide and N-terminal fragment of pro-B-type natriuretic peptide: a systematic review and individual patient data meta-analysis. J Am Coll Cardiol. 2014. PMID 24076282 · DOI

About this article

Sources
NLM Medical Subject Headings (definition, synonyms); NCBI PubMed (counts, identifiers); Europe PMC (open-access abstracts and citation counts).
Verification
Every reference was resolved against PubMed on 2026-10-31; title, year and DOI matched.
Review state
automated source verified; no human expert review has been recorded yet.
Version
1, last updated 2026-10-31.

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At a glance

34,413
PubMed records on this heading
15%
published since 2020
3,631
review articles
2,118
randomized trials
9
verified references below

Counts come from PubMed on 2026-10-31; they show how much has been written, not how strong the evidence is.

Related topics See all →

  • Atrial Natriuretic FactorDrugs and Chemicals
  • Peptide HormonesDrugs and Chemicals
  • Peptide YYDrugs and Chemicals
  • Parathyroid Hormone-Related ProteinDrugs and Chemicals
  • GlucagonDrugs and Chemicals

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