Evidence map›Paper›PMID 40705694›Full record

ArticlePain2025

Upregulated natriuretic peptide B expression as a hallmark of chronic itch.

Pang-Yen Tseng, Huey Ling Liew, Matthias Ringkamp, Keisuke Nagao, Mark A Hoon

Abstract read
In one paragraph

Article in Pain, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

5 authors.

Pang-Yen TsengMolecular Genetics Section, National Institute of Dental and Craniofacial Research, National Institute of Health, Bethesda, MD, United States.ORCID 0000-0003-2039-0002
Huey Ling LiewDepartment of Neurosurgery, Neurosurgery Pain Research Institute, Johns Hopkins University, Baltimore, MD, United States.
Matthias RingkampDepartment of Neurosurgery, Neurosurgery Pain Research Institute, Johns Hopkins University, Baltimore, MD, United States.
Keisuke NagaoCutaneous Leukocyte Biology Section, Dermatology Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, United States.
Mark A HoonMolecular Genetics Section, National Institute of Dental and Craniofacial Research, National Institute of Health, Bethesda, MD, United States.ORCID 0000-0002-8794-1684

Funding

Molecular Genetic Studies of SomatosensationZIADE000721 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI HOON, MARK · 2009 to 2025
$26.6M
Peripheral Neuronal Mechanisms of ItchR01AR070875 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI LA MOTTE, ROBERT H, RINGKAMP, MATTHIAS · 2016 to 2020
$3.4M
Intramural NIH HHS ZIA DE000721Marlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland PHPA-3014NIAMS NIH HHS R01 AR070875NIAMS NIH HHS R01AR070875NIDCR NIH HHS ZIADE000721
6 · The paper itself

Abstract

abstractChronic itch can arise from a variety of etiologies, ranging from dermatological conditions like eczema and psoriasis to systemic diseases such as liver disease and kidney failure. However, it remains unclear whether there are common molecular features associated with chronic itch, and whether these features are selective for chronic itch compared to chronic pain. To identify potential genes or molecular characteristics that are specifically associated with chronic itch, we examined transcriptomic data from sensory neurons collected from 3 mouse models of chronic itch and a monkey model of contact dermatitis. We compared these data to transcriptomic data from 3 mouse models of pain and clinical data from patients with neuropathic pain. Our analyses revealed that the upregulation of Nppb expression in sensory neurons is consistently associated with models of itch, but not with models of pain. Further, our cellular characterization showed that the increased expression of Nppb arises from increased cell-autonomous expression rather than the recruitment of Nppb expression in other classes of sensory neurons. Given that Nppb is a well-established itch neurotransmitter, our findings suggest that the increased expression of Nppb in sensory neurons may contribute to chronic itch. In addition, based on our results, we propose that Nppb could serve as a conserved biomarker for chronic itch.

Indexed as

PruritusSensory Receptor CellsUp-RegulationAnimalsChronic DiseaseDisease Models, AnimalFemaleGanglia, SpinalHumansMacaca fascicularisMaleMiceMice, Inbred C57BLNeuralgiaBNPBrain natriuretic peptideChronic itchItchNatriuretic peptide BNPPBPainPruritus

Identifiers

PMID40705694
PMCPMC12313139

What Socratic 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 Socratic graph.