Evidence map›Paper›PMID 40192001›Full record

ArticleThe Laryngoscope2025

Sensory and Autonomic Fibers in Anterior Ethmoid, Posterior Nasal, Posterolateral Nasal Nerves.

John R Craig, William Mason, Geoffroy Laumet, Wamidh Alkhoory, Mark D Hensley, Desiree Holleman, Noor Hason

Abstract read
In one paragraph

Article in The Laryngoscope, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Trial
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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.

John R CraigDepartment of Otolaryngology-Head and Neck Surgery, Henry Ford Health, Detroit, Michigan, USA.ORCID 0000-0002-7377-4782
William MasonDepartment of Otolaryngology-Head and Neck Surgery, Henry Ford Health, Detroit, Michigan, USA.ORCID 0009-0009-5877-634X
Geoffroy LaumetCollege of Human Medicine, Michigan State University, East Lansing, Michigan, USA.
Wamidh AlkhooryDepartment of Pathology, Henry Ford Health, Detroit, Michigan, USA.
Mark D HensleyHensely Biostats, Washington, USA.
Desiree HollemanAerin Medical Inc., Mountain View, California, USA.
Noor HasonAerin Medical Inc., Mountain View, California, USA.

Funding

Aerin Medical IncHenry Ford Health System Dept of Otolaryngology internal funding
6 · The paper itself

Abstract

backgroundSensory and autonomic nerves supply the sinonasal mucosa and contribute to the pathophysiology of certain forms of chronic rhinitis, rhinosinusitis, and craniofacial pain. The compositions of these intranasal nerves have been incompletely studied. The purpose of this cadaveric study was to investigate the relative areas of sensory, parasympathetic, and sympathetic nerve fibers within different nasal nerves.

methodsTen fresh cadaver heads were dissected, and anterior ethmoid (AEN), posterior nasal (PNN), and posterolateral (PLNN) sections were harvested unilaterally via endonasal and transorbital approaches. Specimens were formalin-fixed, sectioned, and stained with hematoxylin and eosin, as well as for neuropeptides (substance-P, calcitonin gene-related peptide [CGRP], neurokinins-A and B [NKA, NKB], vasointestinal peptide [VIP], neuropeptide Y [NPY]), and enzymes (choline acetyltransferase [ChAT] and tyrosine hydroxylase [TH]). Enzyme and neuropeptide nerve marker percent areas were calculated using brightfield analysis. Sensory and autonomic nerve marker percent areas were then compared within and between AENs, PNNs, and PLNNs.

resultsIn total, 10 PNNs and AENs and 8 PLNNs were available for analyses. Sensory, parasympathetic, and sympathetic nerve markers were identified in every PNN, PLNN, and AEN, and were mostly equivalent between nerves. Only neurokinin-A demonstrated a significantly greater percent area than other markers across different nasal nerves.

conclusionSensory and autonomic nerve markers were present in all AENs, PNNs, and PLNNs, and were largely equivalent between nerves. NKA presented the greatest percent area consistently across each of the nerve types. Future studies should explore the relative contributions of sensory versus autonomic dysfunction in chronic rhinitis, rhinosinusitis, and craniofacial pain. LEVEL OF EVIDENCE: Level 4.

Indexed as

Ethmoid SinusNasal MucosaNoseSensory Receptor CellsCadaverHumansMalechronic rhinitisendoscopic sinus surgeryneurectomynonallergic rhinitissphenopalatine artery ligation

Identifiers

PMID40192001
PMCPMC12255380

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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.