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      Enhanced reactive inhibition in adolescents with non‐suicidal self‐injury disorder

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          Abstract

          Aim

          To investigate whether the core of the pathophysiology underlying non‐suicidal self‐injury (NSSI) relates to poor impulse control due to impaired motor inhibition (i.e. the ability to inhibit a preplanned motor response).

          Method

          We conducted a case–control study to compare the proficiency of two domains of motor inhibition, that is, reactive and proactive inhibition, by giving the reaching arm version of the stop‐signal task and a go‐only task to 28 drug‐naive adolescents with NSSI disorder (NSSID) (mean age [SD] 15 years 8 months [1 year 4 months]; three males and 25 females) and 28 typically developing adolescents (mean age 15 years 8 months [1 year 5 months]; three males and 25 females).

          Results

          Reactive inhibition, as determined by the duration of the stop‐signal reaction time, was enhanced in adolescents with NSSID compared to typically developing controls (194.2 [22.5 ms] vs 217.5 [17.3 ms], p < 0.001). By contrast, proactive inhibition was similar in both groups. Lastly, the level of impulsivity, assessed using the Barratt Impulsiveness Scale Version 11, did not differ between typically developing adolescents and adolescents with NSSID. However, adolescents with NSSID were more impulsive than controls in a subscale of the UPPS‐P Impulsive Behavior Scale.

          Interpretation

          NSSID is not driven by heightened motor impulsivity. Instead, adolescents with NSSID exhibited greater proficiency in reactive inhibition, a proxy for motor impulsivity. We suggest that the enhancement of reactive inhibition strengthens action control, allowing adolescents to suppress their self‐protection instinct and perform NSSI behaviours.

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          Most cited references42

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          The PRISMA 2020 statement: an updated guideline for reporting systematic reviews

          The Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) statement, published in 2009, was designed to help systematic reviewers transparently report why the review was done, what the authors did, and what they found. Over the past decade, advances in systematic review methodology and terminology have necessitated an update to the guideline. The PRISMA 2020 statement replaces the 2009 statement and includes new reporting guidance that reflects advances in methods to identify, select, appraise, and synthesise studies. The structure and presentation of the items have been modified to facilitate implementation. In this article, we present the PRISMA 2020 27-item checklist, an expanded checklist that details reporting recommendations for each item, the PRISMA 2020 abstract checklist, and the revised flow diagrams for original and updated reviews.
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            Diagnostic and Statistical Manual of Mental Disorders

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              Default Bayes factors for ANOVA designs

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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                Developmental Medicine & Child Neurology
                Develop Med Child Neuro
                Wiley
                0012-1622
                1469-8749
                May 2024
                October 30 2023
                May 2024
                : 66
                : 5
                : 654-666
                Affiliations
                [1 ] Department of Clinical and Experimental Sciences University of Brescia Brescia Italy
                [2 ] Istituto di Ricovero e Cura a Carattere Scientifico Neuromed Pozzilli Italy
                [3 ] Department of Human Neurosciences, Faculty of Medicine and Dentistry Sapienza University of Rome Rome Italy
                Article
                10.1111/dmcn.15794
                37899708
                bbd56536-e049-45a1-aecd-5d582e825a08
                © 2024

                http://creativecommons.org/licenses/by/4.0/

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