Evidence map›Paper›PMID 35997391›Full record

ReviewPathophysiology : the official journal of the International Society for Pathophysiology2022

Pathophysiology of Nociception and Rare Genetic Disorders with Increased Pain Threshold or Pain Insensitivity.

Marco Cascella, Maria Rosaria Muzio, Federica Monaco, Davide Nocerino, Alessandro Ottaiano, Francesco Perri, Massimo Antonio Innamorato

Open access · goldAbstract readReview
In one paragraph

Review in Pathophysiology : the official journal of the International Society for Pathophysiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.1field-weighted citation impact, top 7% 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.

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

8 citing papers in PubMed, 31 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Marco CascellaDivision of Anesthesia, Istituto Nazionale Tumori IRCCS-Fondazione G. Pascale, 80131 Naples, Italy.ORCID 0000-0002-5236-3132
Maria Rosaria MuzioDivision of Infantile Neuropsychiatry, UOMI-Maternal and Infant Health, ASL NA3/Sud, 80059 Naples, Italy.
Federica MonacoDivision of Anesthesia, Istituto Nazionale Tumori IRCCS-Fondazione G. Pascale, 80131 Naples, Italy.ORCID 0000-0002-5986-3594
Davide NocerinoDivision of Anesthesia, Istituto Nazionale Tumori IRCCS-Fondazione G. Pascale, 80131 Naples, Italy.ORCID 0000-0002-9981-5431
Alessandro OttaianoSSD Innovative Therapies for Abdominal Metastases, Istituto Nazionale Tumori IRCCS-Fondazione G. Pascale, 80130 Naples, Italy.ORCID 0000-0002-2901-3855
Francesco PerriMedical and Experimental Head and Neck Oncology Unit, Istituto Nazionale Tumori IRCCS-Fondazione G. Pascale, 80131 Naples, Italy.ORCID 0000-0001-8158-7509
Massimo Antonio InnamoratoDepartment of Neuroscience, Pain Unit, Santa Maria delle Croci Hospital, AUSL Romagna, Viale Vincenzo Randi 5, 48121 Ravenna, Italy.
Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITOspedale "Santa Maria delle Croci" di Ravenna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pain and nociception are different phenomena. Nociception is the result of complex activity in sensory pathways. On the other hand, pain is the effect of interactions between nociceptive processes, and cognition, emotions, as well as the social context of the individual. Alterations in the nociceptive route can have different genesis and affect the entire sensorial process. Genetic problems in nociception, clinically characterized by reduced or absent pain sensitivity, compose an important chapter within pain medicine. This chapter encompasses a wide range of very rare diseases. Several genes have been identified. These genes encode the Nav channels 1.7 and 1.9 (

Indexed as

Angelman syndromecancerChromosome 15q duplication syndromeChromosome 4 interstitial deletionhereditary sensory and autonomic neuropathiesnociceptionnociceptorspain insensitivityPrader Willy syndrome

Identifiers

PMID35997391
PMCPMC9397076
OpenAlexW4289519157

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.