Evidence map›Paper›PMID 41788551›Full record

ArticleFrontiers in neuroscience2026

Human vagus nerve fascicular anatomy and its implications for targeted cardiac stimulation: a microCT segmentation and histological pilot anatomical study.

Nicole Thompson, Svetlana Mastitskaya, Francesco Iacoviello, Felicia Turhani, Paul R Shearing, Kirill Aristovich, David Holder

Abstract read
In one paragraph

Article in Frontiers in neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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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

4 citing papers in PubMed.

  1. Article
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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.

Nicole ThompsonDepartment of Medical Physics and Biomedical Engineering, University College London, London, United Kingdom.
Svetlana MastitskayaDepartment of Medical Physics and Biomedical Engineering, University College London, London, United Kingdom.
Francesco IacovielloElectrochemical Innovations Lab, Department of Chemical Engineering, University College London, London, United Kingdom.
Felicia TurhaniDepartment of Medical Physics and Biomedical Engineering, University College London, London, United Kingdom.
Paul R ShearingElectrochemical Innovations Lab, Department of Chemical Engineering, University College London, London, United Kingdom.
Kirill AristovichDepartment of Medical Physics and Biomedical Engineering, University College London, London, United Kingdom.
David HolderDepartment of Medical Physics and Biomedical Engineering, University College London, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The functional anatomy of autonomic nerve fascicles has remained poorly understood. Building on prior evidence of organotopic organization in the pig cervical vagus nerve, this study examined the thoracic branches of the human vagus nerve using microcomputed tomography (microCT) and histological validation. Methods: Left and right vagus nerves ( Results: Cardiac, pulmonary, and recurrent laryngeal fascicles preserved partial organization near their entry points but merged further along the nerve. In left nerves, cardiac and pulmonary fascicles merged while recurrent laryngeal fascicles remained separate; in right nerves, cardiac fascicles merged with both pulmonary and recurrent laryngeal fascicles. Right nerves had a larger diameter and contained more fascicles, with counts varying along their length, indicative of the observed anastomoses. Discussion: Notably, the superior cardiac branch on both sides remained distinct near the typical vagus nerve stimulation cuff site, highlighting potential for targeted cardiac neuromodulation potentially relevant to conditions including myocardial infarction, heart failure, and atrial fibrillation. These findings advance understanding of human vagus nerve organization and support the design of selective stimulation strategies for precise autonomic regulation.

Indexed as

fasciclesfascicular anatomyhistologyhuman vagus nervemicroCTneuroanatomyneurophysiologyorganotopic organization

Identifiers

PMID41788551
PMCPMC12956647

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