Literature DB >> 26696867

Commentary: Cortical responses to salient nociceptive and not nociceptive stimuli in vegetative and minimal conscious state.

Antonino Naro1, Rocco S Calabrò1.   

Abstract

Entities:  

Keywords:  DOC; LEP; MCS; VS; pain perception

Year:  2015        PMID: 26696867      PMCID: PMC4672151          DOI: 10.3389/fnhum.2015.00657

Source DB:  PubMed          Journal:  Front Hum Neurosci        ISSN: 1662-5161            Impact factor:   3.169


× No keyword cloud information.
We read with great interest the work by de Tommaso et al. (2015) assessing cortical responsiveness to nociceptive and multimodal sensory stimuli in patients affected by chronic disorders of consciousness (DOC). In their valuable work, the authors attempted to assign each patient to the most appropriate DOC category by using auditory, visual, somatosensory, and nociceptive laser stimuli. Interestingly, the motor responsiveness to nociceptive stimuli assessed through the Coma Recovery Scale-Revised and the Nociception Coma Scale-Revised correlated with each evoked response, but Laser Evoked Potentials (LEPs). The latter were recognizable in all of the patients, independently from the preservation of other sensory modalities and the motor responsiveness to nociceptive stimuli. Hence, LEP absence should not be considered as a demonstration of the inability to experience pain, since the preservation does not per se indicate a conscious pain perception in DOC (de Tommaso et al., 2015). However, it is to note that we should be aware in interpreting authors' findings since these are based on a very limited number of patients (i.e., only 4 MCS and 5 VS). Moreover, since the presence vs. absence of LEPs was based on a subjective visual identification of the event-related potential waveforms, the possibility of misinterpretations (mainly due to very low signal-to-noise ratio) should be taken into account. Conscious pain perception in DOC patients is a very thorny matter of ethical and clinical debate. Indeed, it is not easy to clinically assess pain perception in the vegetative state (VS) (characterized by non-conscious reflexive behavioral patterns) and minimally conscious state (MCS) patients (characterized by reproducible but fluctuant conscious behavioral patterns), although several clinical scales have been ad hoc employed to improve diagnostic accuracy (Chatelle et al., 2012). In addition, functional neuroimaging studies have shown that some DOC individuals can show residual complex brain activations that do not correspond to their behavioral output (e.g., Kassubek et al., 2003; Boly et al., 2008). Thus, a potential pain experience should be considered even in VS individuals, independently from their communication skills. Although LEPs are commonly used when studying nociceptive pathways, their role concerning pain assessment in DOC individuals could be at first glance limited by the following issues: (i) the basic LEP parameters, including amplitude and latency, cannot give unique information concerning conscious pain perception in DOC patients (de Tommaso et al., 2015); (ii) LEPs mainly constitute a marker of relevant-stimulus dependent arousal (Mouraux and Iannetti, 2009); (iii) LEPs depend on the selective activation of thermo-nociceptive afferents; and (iv) LEP reflect the activity of multiple cortical assemblies within different cortical areas that process either nociceptive or somatosensory inputs (Garcia-Larrea et al., 2003). Nevertheless, the presence or the absence of LEPs could be somehow useful in determining whether or not a patient has the ability to experience pain, although LEPs are not considered a specific marker of pain perception. To this end, some correlations between perceived pain intensity and single-LEP features have been documented (Iannetti et al., 2005; Huang et al., 2013). In our opinion, further LEP protocols should be fostered in an attempt to more reliably assess pain-perception in DOC patients and reach a more reliable differential diagnosis. In fact, recent studies in healthy individuals have suggested that LEP-related γ-band oscillatory activity (GBO) may have a role in modulating pain intensity within primary somatosensory cortex (Gross et al., 2007; Zhang et al., 2012). It has been recently showed that fronto-parietal GBO and the associated sensory-motor integration processes may reflect the functionality of the fronto-cingulate-parietal network involved in pain perception and pain-gating processes at cortical level, independently from the patient's ability to communicate (Naro et al., 2015a,b). Unfortunately, GBO analysis presents some limiting factors, including low signal-to-noise ratio, high inter-individual variability, and contamination of ocular movements and/or muscle artifacts. Nonetheless, the evaluation of LEP-related GBO might contribute to uncover residual pain perception even in those totally non-communicative patients, even though it is still debated whether or not GBO can be reliably assessed at single-subject level. Future studies should be fostered in an attempt to shed some light on the role of combined LEP-GBO analysis in pain perception assessment in DOC patients.

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
  12 in total

Review 1.  Brain generators of laser-evoked potentials: from dipoles to functional significance.

Authors:  L Garcia-Larrea; M Frot; M Valeriani
Journal:  Neurophysiol Clin       Date:  2003-12       Impact factor: 3.734

2.  Gamma-band oscillations in the primary somatosensory cortex--a direct and obligatory correlate of subjective pain intensity.

Authors:  Z G Zhang; L Hu; Y S Hung; A Mouraux; G D Iannetti
Journal:  J Neurosci       Date:  2012-05-30       Impact factor: 6.167

3.  Nociceptive laser-evoked brain potentials do not reflect nociceptive-specific neural activity.

Authors:  A Mouraux; G D Iannetti
Journal:  J Neurophysiol       Date:  2009-04-01       Impact factor: 2.714

4.  Shaping thalamo-cortical plasticity: a marker of cortical pain integration in patients with post-anoxic unresponsive wakefulness syndrome?

Authors:  Antonino Naro; Antonino Leo; Margherita Russo; Angelo Quartarone; Placido Bramanti; Rocco Salvatore Calabrò
Journal:  Brain Stimul       Date:  2014-09-08       Impact factor: 8.955

5.  Single-trial laser-evoked potentials feature extraction for prediction of pain perception.

Authors:  Gan Huang; Ping Xiao; Li Hu; Yeung Sam Hung; Zhiguo Zhang
Journal:  Conf Proc IEEE Eng Med Biol Soc       Date:  2013

6.  Operculoinsular cortex encodes pain intensity at the earliest stages of cortical processing as indicated by amplitude of laser-evoked potentials in humans.

Authors:  G D Iannetti; L Zambreanu; G Cruccu; I Tracey
Journal:  Neuroscience       Date:  2005       Impact factor: 3.590

7.  Moving Toward Conscious Pain Processing Detection in Chronic Disorders of Consciousness: Anterior Cingulate Cortex Neuromodulation.

Authors:  Antonino Naro; Antonino Leo; Placido Bramanti; Rocco Salvatore Calabrò
Journal:  J Pain       Date:  2015-07-21       Impact factor: 5.820

8.  Perception of pain in the minimally conscious state with PET activation: an observational study.

Authors:  Mélanie Boly; Marie-Elisabeth Faymonville; Caroline Schnakers; Philippe Peigneux; Bernard Lambermont; Christophe Phillips; Patrizio Lancellotti; Andre Luxen; Maurice Lamy; Gustave Moonen; Pierre Maquet; Steven Laureys
Journal:  Lancet Neurol       Date:  2008-10-03       Impact factor: 44.182

9.  Cortical responses to salient nociceptive and not nociceptive stimuli in vegetative and minimal conscious state.

Authors:  Marina de Tommaso; Jorge Navarro; Crocifissa Lanzillotti; Katia Ricci; Francesca Buonocunto; Paolo Livrea; Giulio E Lancioni
Journal:  Front Hum Neurosci       Date:  2015-01-29       Impact factor: 3.169

10.  Gamma oscillations in human primary somatosensory cortex reflect pain perception.

Authors:  Joachim Gross; Alfons Schnitzler; Lars Timmermann; Markus Ploner
Journal:  PLoS Biol       Date:  2007-05       Impact factor: 8.029

View more
  1 in total

1.  Response: Commentary: Cortical responses to salient nociceptive and not nociceptive stimuli in vegetative and minimal conscious state.

Authors:  Marina de Tommaso
Journal:  Front Hum Neurosci       Date:  2016-01-29       Impact factor: 3.169

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.