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      The search for pain biomarkers in the human brain

      review-article
      1 , 2 , 3
      Brain
      Oxford University Press
      pain, neuroimaging, EEG, fMRI, biomarkers

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          Abstract

          Do current neuroimaging-based biomarkers developed to ‘objectively’ assess pain perception truly relate to pain? Mouraux and Iannetti critically review the evidence, and examine the utility of brain biomarkers for achieving mechanism-based patient stratification, predicting treatment responses and offering personalized treatments.

          Abstract

          Non-invasive functional brain imaging is used more than ever to investigate pain in health and disease, with the prospect of finding new means to alleviate pain and improve patient wellbeing. The observation that several brain areas are activated by transient painful stimuli, and that the magnitude of this activity is often graded with pain intensity, has prompted researchers to extract features of brain activity that could serve as biomarkers to measure pain objectively. However, most of the brain responses observed when pain is present can also be observed when pain is absent. For example, similar brain responses can be elicited by salient but non-painful auditory, tactile and visual stimuli, and such responses can even be recorded in patients with congenital analgesia. Thus, as argued in this review, there is still disagreement on the degree to which current measures of brain activity exactly relate to pain. Furthermore, whether more recent analysis techniques can be used to identify distributed patterns of brain activity specific for pain can be only warranted using carefully designed control conditions. On a more general level, the clinical utility of current pain biomarkers derived from human functional neuroimaging appears to be overstated, and evidence for their efficacy in real-life clinical conditions is scarce. Rather than searching for biomarkers of pain perception, several researchers are developing biomarkers to achieve mechanism-based stratification of pain conditions, predict response to medication and offer personalized treatments. Initial results with promising clinical perspectives need to be further tested for replicability and generalizability.

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          Most cited references104

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          Functional imaging of brain responses to pain. A review and meta-analysis (2000).

          Brain responses to pain, assessed through positron emission tomography (PET) and functional magnetic resonance imaging (fMRI) are reviewed. Functional activation of brain regions are thought to be reflected by increases in the regional cerebral blood flow (rCBF) in PET studies, and in the blood oxygen level dependent (BOLD) signal in fMRI. rCBF increases to noxious stimuli are almost constantly observed in second somatic (SII) and insular regions, and in the anterior cingulate cortex (ACC), and with slightly less consistency in the contralateral thalamus and the primary somatic area (SI). Activation of the lateral thalamus, SI, SII and insula are thought to be related to the sensory-discriminative aspects of pain processing. SI is activated in roughly half of the studies, and the probability of obtaining SI activation appears related to the total amount of body surface stimulated (spatial summation) and probably also by temporal summation and attention to the stimulus. In a number of studies, the thalamic response was bilateral, probably reflecting generalised arousal in reaction to pain. ACC does not seem to be involved in coding stimulus intensity or location but appears to participate in both the affective and attentional concomitants of pain sensation, as well as in response selection. ACC subdivisions activated by painful stimuli partially overlap those activated in orienting and target detection tasks, but are distinct from those activated in tests involving sustained attention (Stroop, etc.). In addition to ACC, increased blood flow in the posterior parietal and prefrontal cortices is thought to reflect attentional and memory networks activated by noxious stimulation. Less noted but frequent activation concerns motor-related areas such as the striatum, cerebellum and supplementary motor area, as well as regions involved in pain control such as the periaqueductal grey. In patients, chronic spontaneous pain is associated with decreased resting rCBF in contralateral thalamus, which may be reverted by analgesic procedures. Abnormal pain evoked by innocuous stimuli (allodynia) has been associated with amplification of the thalamic, insular and SII responses, concomitant to a paradoxical CBF decrease in ACC. It is argued that imaging studies of allodynia should be encouraged in order to understand central reorganisations leading to abnormal cortical pain processing. A number of brain areas activated by acute pain, particularly the thalamus and anterior cingulate, also show increases in rCBF during analgesic procedures. Taken together, these data suggest that hemodynamic responses to pain reflect simultaneously the sensory, cognitive and affective dimensions of pain, and that the same structure may both respond to pain and participate in pain control. The precise biochemical nature of these mechanisms remains to be investigated.
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            Corticostriatal functional connectivity predicts transition to chronic back pain

            The mechanism of brain reorganization in pain chronification is unknown. In a longitudinal brain imaging study, sub–acute back pain (SBP) patients were followed over one year. When pain persisted (SBPp, in contrast to recovering SBP, and healthy controls), brain gray matter density decreased. Importantly, initially greater functional connectivity of nucleus accumbens with prefrontal cortex predicted pain persistence, implying that corticostriatal circuitry is causally involved in the transition from acute to chronic pain.
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              Moving differently in pain: a new theory to explain the adaptation to pain.

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                Author and article information

                Journal
                Brain
                Brain
                brainj
                Brain
                Oxford University Press
                0006-8950
                1460-2156
                December 2018
                20 November 2018
                20 November 2018
                : 141
                : 12
                : 3290-3307
                Affiliations
                [1 ]Institute of Neuroscience, UCLouvain, Brussels, Belgium
                [2 ]Department of Neuroscience, Physiology and Pharmacology, University College London, London, UK
                [3 ]Neuroscience and Behaviour Laboratory, Istituto Italiano di Tecnologia, Rome, Italy
                Author notes
                Correspondence to: Giandomenico Iannetti Neuroscience and Behaviour Laboratory Istituto Italiano di Tecnologia Viale Regina Elena 291 00161, Rome, Italy E-mail: giandomenico.iannetti@ 123456iit.it
                Article
                awy281
                10.1093/brain/awy281
                6262221
                30462175
                e0d3a76a-a183-47d6-8820-70011d893ca2
                © The Author(s) (2018). Published by Oxford University Press on behalf of the Guarantors of Brain.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 29 September 2018
                : 4 October 2018
                Page count
                Pages: 18
                Funding
                Funded by: ERC 10.13039/100010663
                Funded by: Wellcome Trust 10.13039/100004440
                Funded by: ERC 10.13039/100010663
                Categories
                Review Article

                Neurosciences
                pain,neuroimaging,eeg,fmri,biomarkers
                Neurosciences
                pain, neuroimaging, eeg, fmri, biomarkers

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