Evidence map›Paper›PMID 35074504›Full record

ArticleNeuroImage2022

Functional connectome of brainstem nuclei involved in autonomic, limbic, pain and sensory processing in living humans from 7 Tesla resting state fMRI.

Simone Cauzzo, Kavita Singh, Matthew Stauder, María Guadalupe García-Gomar, Nicola Vanello, Claudio Passino, Jeffrey Staab, Iole Indovina, Marta Bianciardi

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in NeuroImage, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06603168 (Autonomic Recalibration Approach to Myofascial Pain Elimination), which is not on this map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
6.5field-weighted citation impact, top 2% 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.

NCT06603168 nacompletednot on this mapstarted 2023, after this paper: background citation

Autonomic Recalibration Approach to Myofascial Pain Elimination

TypeinterventionalSponsorEdward Via Virginia College of Osteopathic MedicineRan2023 to 2024Enrolled20ConditionsChronic Pain (Back / Neck), Autonomic DysregulationArmsAutonomic Recalibration Treatment
3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

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  4. Structure-function coupling in the human brainstem.bioRxiv : the preprint server for biology · 2026
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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

9 authors at 7 institutions in 3 countries.

Simone CauzzoBrainstem Imaging Laboratory, Department of Radiology, Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA; Life Sciences Institute, Sant'Anna School of Advanced Studies, Pisa, Italy; Research Center E. Piaggio, University of Pisa, Pisa, Italy. Electronic address: simone.cauzzo@santannapisa.it.
Kavita SinghBrainstem Imaging Laboratory, Department of Radiology, Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Matthew StauderBrainstem Imaging Laboratory, Department of Radiology, Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
María Guadalupe García-GomarBrainstem Imaging Laboratory, Department of Radiology, Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA; Escuela Nacional de Estudios Superiores, Juriquilla, Universidad Nacional Autónoma de México, Querétaro, México.
Nicola VanelloDipartimento di Ingegneria dell'Informazione, University of Pisa, Pisa, Italy.
Claudio PassinoLife Sciences Institute, Sant'Anna School of Advanced Studies, Pisa, Italy; Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
Jeffrey StaabDepartment of Psychiatry and Psychology, Mayo Clinic, Rochester, MN, USA; Department of Otorhinolaryngology - Head and Neck Surgery, Mayo Clinic, Rochester, MN, USA.
Iole IndovinaDepartment of Biomedical and Dental Sciences and Morphofunctional Imaging, University of Messina, Italy; Laboratory of Neuromotor Physiology, IRCCS Santa Lucia Foundation, Rome, Italy.
Marta BianciardiBrainstem Imaging Laboratory, Department of Radiology, Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA; Division of Sleep Medicine, Harvard University, Boston, MA USA. Electronic address: martab@mgh.harvard.edu.
Athinoula A. Martinos Center for Biomedical Imaging · USMassachusetts General Hospital · USFondazione Santa Lucia · ITMayo Clinic · USPiaggio (Italy) · ITScuola Superiore Sant'Anna · ITUniversity of Pisa · IT

Funding

Brainstem-based imaging biomarkers of premanifest synucleinopathyR01AG063982 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI BIANCIARDI, MARTA · 2020 to 2024
$3.6M
In vivo atlas of the ascending arousal system in health and traumatic comaK01EB019474 · NIBIB · MASSACHUSETTS GENERAL HOSPITAL · PI BIANCIARDI, MARTA · 2016 to 2019
$691k
In vivo mapping of human brainstem vestibular and autonomic pathwaysR21DC015888 · NIDCD · MASSACHUSETTS GENERAL HOSPITAL · PI BIANCIARDI, MARTA · 2017 to 2018
$470k
NIA NIH HHS R01 AG063982NIBIB NIH HHS K01 EB019474NIDCD NIH HHS R21 DC015888
6 · The paper itself

Abstract

Despite remarkable advances in mapping the functional connectivity of the cortex, the functional connectivity of subcortical regions is understudied in living humans. This is the case for brainstem nuclei that control vital processes, such as autonomic, limbic, nociceptive and sensory functions. This is because of the lack of precise brainstem nuclei localization, of adequate sensitivity and resolution in the deepest brain regions, as well as of optimized processing for the brainstem. To close the gap between the cortex and the brainstem, on 20 healthy subjects, we computed a correlation-based functional connectome of 15 brainstem nuclei involved in autonomic, limbic, nociceptive, and sensory function (superior and inferior colliculi, ventral tegmental area-parabrachial pigmented nucleus complex, microcellular tegmental nucleus-prabigeminal nucleus complex, lateral and medial parabrachial nuclei, vestibular and superior olivary complex, superior and inferior medullary reticular formation, viscerosensory motor nucleus, raphe magnus, pallidus, and obscurus, and parvicellular reticular nucleus - alpha part) with the rest of the brain. Specifically, we exploited 1.1mm isotropic resolution 7 Tesla resting-state fMRI, ad-hoc coregistration and physiological noise correction strategies, and a recently developed probabilistic template of brainstem nuclei. Further, we used 2.5mm isotropic resolution resting-state fMRI data acquired on a 3 Tesla scanner to assess the translatability of our results to conventional datasets. We report highly consistent correlation coefficients across subjects, confirming available literature on autonomic, limbic, nociceptive and sensory pathways, as well as high interconnectivity within the central autonomic network and the vestibular network. Interestingly, our results showed evidence of vestibulo-autonomic interactions in line with previous work. Comparison of 7 Tesla and 3 Tesla findings showed high translatability of results to conventional settings for brainstem-cortical connectivity and good yet weaker translatability for brainstem-brainstem connectivity. The brainstem functional connectome might bring new insight in the understanding of autonomic, limbic, nociceptive and sensory function in health and disease.

Indexed as

AdultAutonomic Nervous SystemBrain StemConnectomeFemaleHealthy VolunteersHumansImage Processing, Computer-AssistedMagnetic Resonance ImagingMaleNeural Pathways7 TeslaBrainstemCentral autonomic networkHuman functional connectomeVestibular network

Identifiers

PMID35074504
PMCPMC8885980
OpenAlexW4221127040

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Registered trials

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.