European journal of pain : EJP
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The current study interviewed patients with chronic pain to: (1) identify the most common words used by patients in the samples to describe the "quality" of their pain (i.e. sharp, dull) and (2) evaluate the validity of existing pain quality measures. Two-hundred and thirteen individuals with pain associated with spinal cord injury (SCI) or multiple sclerosis (MS) were asked to describe their pain. Consistent with previous research that has shown that patients with different types of pain problems describe their pain using different pain quality descriptors, there was variability in the frequency of pain descriptors used by the study participants. ⋯ Regarding the validity of existing pain measures, only one pain quality measure assessed all 14 of the most common pain descriptors volunteered by the sample. Also, although a number of pain quality measures have been developed to discriminate neuropathic from nociceptive pain, there was surprisingly little overlap in descriptors between these measures. The results of the current study and other studies using similar procedures would be useful for evaluating and developing existing and future pain quality measures.
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To study the effects of occupational class, physical and psychosocial working conditions, health behaviours, and pain in the low back and the neck on sciatic pain among middle-aged employees. ⋯ Manual occupational class in both genders and semi-professional occupations in men, unhealthy behaviours and previous pain both in the neck and the lower back predicted sciatica, while physical and psychosocial working conditions had no independent effect.
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Pain among children is common, yet far less studied compared to that among adults. Little has been reported regarding various types of pain in a national community sample of German children. ⋯ The rather high pain prevalence suggests pain among children may be a potential public health issue. Further studies are required to investigate the characteristics and correlational attributes of children suffering most frequently from pain and children from families with low socioeconomic status.
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Patients with Alzheimer's disease (AD) are administered fewer analgesics and report less clinical pain compared with their cognitively-intact peers, prompting much speculation about the likely impact of neurodegeneration on pain perception and processing. This study used functional connectivity analysis to examine the impact of AD on the integrated functioning of brain regions mediating the sensory, emotional, and cognitive aspects of pain. Fourteen patients with AD and 15 controls attended two experimental sessions. ⋯ Between-group comparisons revealed enhanced functional connectivity between the DLPFC and the anterior mid cingulate cortex, periaqueductal grey, thalamus, hypothalamus, and several motor areas in patients with AD compared with control group. Likewise, inter-regional functional connectivity across most regions of the predefined pain network was shown to be greater in the patient group, with the enhanced functional connectivity centred on three nodes: the DLPFC-R, hypothalamus, and PAG. The results of this study support previous research suggesting an interplay between pain and cognitive processes in patients with AD.
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Somatostatin (SST) in spinal cord has been linked with the inhibition of nociceptive neurotransmission in several experimental paradigms. The SST2 receptor (SSTR2) is the main SST receptor subtype in the superficial dorsal horn (DH) and is activated, besides to the naïve peptide, by the SST synthetic analogue octreotide (OCT). In the present work, we have studied the central effects of SSTR2 activation on capsaicin (CAP)-induced glutamate release in mouse DH. ⋯ A subset of them was also found to express the CAP receptor TRPV1. These data show that the SST analogue OCT inhibits CAP-mediated activation of non-peptidergic nociceptive PAFs in lamina II. Our data indicate that SSTR2a plays an important role in the pre-synaptic modulation of central excitatory nociceptive transmission in mouse.