Evidence map›Paper›PMID 41931163›Full record

ArticleJournal of neural transmission (Vienna, Austria : 1996)2026

Baseline blink reflex R2 changes correlate with affective and interoceptive domains in functional movement disorders.

Claudia Vinciguerra, Marialuisa Gandolfi, Angela Sandri, Michela Russo, Carlo Ricciardi, Maria Romano, Ilaria Antonella Di Vico, Giovanna Maddalena Squintani, Giuseppe Piscosquito, Giuseppe De Biasi and 21 more

Abstract read
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In one paragraph

Article in Journal of neural transmission (Vienna, Austria : 1996), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Observational
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

31 authors.

Claudia Vinciguerra *Neurology Unit, University Hospital "San Giovanni di Dio e Ruggi d'Aragona", 84131, Salerno, Italy. claudia.vinciguerra@sangiovannieruggi.it.
Marialuisa Gandolfi *University of Verona, Verona, Italy.
Angela SandriAzienda Ospedaliera Universitaria Integrata Verona, Verona, Italy.
Michela RussoDepartment of Electrical Engineering and Information Technology, University of Naples Federico II, Naples, Italy.
Carlo RicciardiDepartment of Electrical Engineering and Information Technology, University of Naples Federico II, Naples, Italy.
Maria RomanoDepartment of Electrical Engineering and Information Technology, University of Naples Federico II, Naples, Italy.
Ilaria Antonella Di VicoAzienda Ospedaliera Universitaria Integrata Verona, Verona, Italy.
Giovanna Maddalena SquintaniAzienda Ospedaliera Universitaria Integrata Verona, Verona, Italy.
Giuseppe PiscosquitoNeurology Unit, University Hospital "San Giovanni di Dio e Ruggi d'Aragona", 84131, Salerno, Italy.
Giuseppe De BiasiDepartment of Medicine, Surgery and Dentistry, "Scuola Medica Salernitana,", University of Salerno, Baronissi, Italy.
Immacolata CarotenutoDepartment of Medicine, Surgery and Dentistry, "Scuola Medica Salernitana,", University of Salerno, Baronissi, Italy.
Sofia CuocoDepartment of Medicine, Surgery and Dentistry, "Scuola Medica Salernitana,", University of Salerno, Baronissi, Italy.
Marika FamigliettiNeurology Unit, University Hospital "San Giovanni di Dio e Ruggi d'Aragona", 84131, Salerno, Italy.
Simone PrincipeNeurology Unit, University Hospital "San Giovanni di Dio e Ruggi d'Aragona", 84131, Salerno, Italy.
Rocco MazzeoNeurology Unit, University Hospital "San Giovanni di Dio e Ruggi d'Aragona", 84131, Salerno, Italy.
Matteo Francesco LauriolaAzienda Ospedaliera Universitaria Integrata Verona, Verona, Italy.
Maria Chiara TozziAzienda Ospedaliera Universitaria Integrata Verona, Verona, Italy.
Francesca RuscianoAzienda Ospedaliera Universitaria Integrata Verona, Verona, Italy.
Marianna AmboniNeurology Unit, University Hospital "San Giovanni di Dio e Ruggi d'Aragona", 84131, Salerno, Italy.
Roberto ErroNeurology Unit, University Hospital "San Giovanni di Dio e Ruggi d'Aragona", 84131, Salerno, Italy.
Paolo BaroneNeurology Unit, University Hospital "San Giovanni di Dio e Ruggi d'Aragona", 84131, Salerno, Italy.
Andrea GardoniNeuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Silvia BasaiaNeuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Elisa CanuNeuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Daniele Giuseppe RomanoUnit of Diagnostic and Interventional Neuroradiology, University Hospital "San Giovanni di Dio e Ruggi d'Aragona, Salerno, Italy.
Elisa SibillaNeuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Elisabetta SarassoNeuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Federica AgostaNeuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Massimo FilippiNeuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Michele Tinazzi *University of Verona, Verona, Italy.
Maria Teresa Pellecchia *Neurology Unit, University Hospital "San Giovanni di Dio e Ruggi d'Aragona", 84131, Salerno, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Functional motor disorders (FMD) are a common yet often misunderstood group of neurological conditions characterized by abnormal movements, including limb weakness, tremor, dystonia, and gait disturbances. These disorders involve disrupted sensory processing mechanism. Previous studies have shown abnormal prepulse inhibition of the blink reflex (BR) in FMD, but the baseline R2-area, reflecting brainstem excitability and cortical modulation, has not been characterized. This study investigated baseline BR R2-area in patients with FMD compared with healthy controls (HC), its associations with affective and interoceptive factors, and its diagnostic potential when combined with laser-evoked potentials (LEPs). BR responses were recorded in clinically definite patients with FMD (n = 75) and matched HC (n = 75). The R2-component was elicited by supraorbital stimulation and quantified as the area under the curve across ipsilateral, contralateral, and average responses. Associations with with behavioural and interoceptive measures were investigated. LEPs were incorporated into multivariate logistic regression models to assess diagnostic potential. Compared with HC, FMD-patients exhibited a consistent reduction in baseline R2 area. Worst depressive symptoms were associated with larger R2 areas, whereas reduced body awareness was associated with smaller responses, indicating affective and interoceptive influences on brainstem excitability. Baseline R2-metrics, particularly the ipsilateral area, contributed substantially to group discrimination, achieving 71.1% accuracy. Reduced baseline BR R2 area in FMD suggests altered brainstem excitability and possibly enhanced descending inhibition. While LEPs provided complementary information, baseline BR measures provided the strongest signal, highlighting the R2 area as a physiological signature to be integrated into multimodal diagnostic frameworks.

Indexed as

BlinkingBrain StemMovement DisordersAdultElectromyographyFemaleHumansLaser-Evoked PotentialsMaleMiddle AgedPrepulse InhibitionBlink ReflexBrainstem excitabilityFunctional-motor-disordersTrait marker

Identifiers

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Registered trials

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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.