Additional (Positron Emission Tomography)PET Scan of Brain in Patients Undergoing PET Scan for Diseases Unrelated to Brain

Background and Significance:

Despite advancement in pain management, pain relief and patient satisfaction are still inadequate in many patients. Functional imaging techniques have recently made it possible to identify the main cerebral components of the human nociceptive system. These comprise at least two main human nociceptive components working in parallel called the medial and lateral pain systems. This has provided a physical construct for the concept of the human pain matrix. Careful study of these areas of the human brain has the potential to drive development of new classes of analgesic compounds. PET is an imaging technique that can quantify increases in nerve cell activity in selective regions of the brain (1-5). PET provides the means to measure tissue concentrations of labeled drugs in brain and other tissues and also to measure changes in receptor occupancy.

Earlier studies have examined the pattern of increased brain activity that follows experimentally-induced acute pain (2) and chronic pain syndromes (1,3,5). Distal pain pathways (e.g. spinothalamic tract) project to the thalamus and then discrete regions of the cortex via thalamocortical projections. Among cortical areas involved in sensation, perception, and attention in both humans and monkeys are anterior cingulate gyrus, insular cortex, primary somatosensory cortex, and secondary somatosensory cortex. PET studies with experimental human pain also demonstrate activation in brain areas related to sensory-motor integration. However, depending on the type of noxious stimulation, different areas of brain are activated (2). Components of the lateral system such as the primary somatosensory (SI) cortex do appear to be frequently activated with tonic (non-phasic experimental pain) and phasic pain (67% and 69% of studies show activations, respectively). But only 23% of studies of chronic clinical pain studies demonstrate activation of SI.

We have performed the first clinical study (IRB study #05121504) to investigate the change in brain activity associated with significant postoperative pain (6). This was an IRB-approved study with just one patient to establish that the methods we have developed will be sensitive enough for a more complete randomized clinical trial. We determined that postsurgical pain is associated with increased activity in the contralateral primary somatosensory cortex. Other brain regions showing increased postsurgical activity were the contralateral parietal cortex, bilateral pulvinar and ipsilateral medial dorsal nucleus of the thalamus, contralateral putamen, contralateral superior temporal gyrus, ipsilateral fusiform gyrus, ipsilateral posterior lobe and contralateral anterior cerebellar lobe. We have received permission from the IRB to perform a larger study with 21 patients (IRB study #07050273).

Although fMRI has also been used for functional brain imaging, the advantages of PET over fMRI are (7):