The imaging method known as fMRI is one of the most commonly used imaging methods in chronic pain research. There are many chronic pain disorders of which the etiology is unknown due to a lack of understanding of the structural abnormalities and their association with different disorders. fMRI is a very useful non-invasive technique for obtaining information related to neural networks and their activities [17,18].

Fibromyalgia is a common chronic pain disorder. It is characterized by allodynia all over the body and a feeling of exhaustion with no specific cause. Fibromyalgia commonly accompanies other disorders, such as mood disorder or sleep disorder. Fibromyalgia studies are mostly focused on abnormal activities that occur in the central nervous system. Numerous studies have reported that fibromyalgia patients have distinctively more activity in the pain matrix compared to control groups. According to the latest research, predictions of pain and perceptions of pain both have a meaningful positive correlation with hyperactivity in the brain areas of the motor cortex and cingulate cortex; the patient group in this line of research showed distinct activity in the frontal and temporal areas [19]. Moreover, increased activity was noted in the medial frontal cortex, cerebellum, dorsal ACC, dorsolateral PFC, and claustrum, all of which are areas related to pain anticipation and attention and all of which have a significant correlation with pain catastrophe [20]. The areas of the anterior and mid-cingulate cortex, middle frontal cortex, SMA, thalamus, anterior insula, and basal ganglia displayed more activity in fibromyalgia patients [21,22]. Overall, fibromyalgia patients showed increased neural activity in pain-related areas.

Chronic back pain is a widespread pain disorder that afflicts a broad range of the population. It has been estimated that nearly 80% the human population has experienced chronic back pain at least once in their life [23]. However, the pathological causes of this type of pain remain unidentified. In this area of research, neuro-imaging techniques have been used to investigate the causes. According to Baliki et al. [24], chronic back pain influences the deactivation of the default mode network (DMN) during the resting state. It has also been reported that the posterior cingulate cortex (PCC) plays an important role as an affective component of pain mediation, as much as the ACC, which is known to be responsible for pain mediation [25]. In another study, the medial PFC showed significantly increased activity in chronic back pain patients [26].

Complex regional pain syndrome (CRPS) is a chronic pain disorder that accompanies sensory, motor, and autonomic dysfunctions. Its origin as well has yet to be identified. This lack of knowledge delays the proper type of treatment for CRPS patients [26-28]. Maihöfner et al. [26] observed activations in the S1 and S2 cortex, insula, PFC, and in the ACC during pin-prick stimulation of CRPS patients who experience hyperalgesia. They found that the S2 cortex is also involved in the processing of non-painful stimuli. Another report found that children and teenagers with CRPS showed distinct activation patterns in the central nervous system when stimulated with mechanical and thermal stimuli; especially noted was decreased activity during a painful state [29].

There are many other chronic pain studies involving patients with unidentified chronic pain. Malinen et al. [30] studied 10 patients who suffered severely from unknown chronic pain. They found that during a resting period, these patients showed abnormal temporal and spatial fluctuations and connectivity disturbances in the pain matrix, particularly the lower insula and the ACC. Diabetic patients who suffered from neuropathic pain also displayed significantly different brain activity from healthy control subjects during the resting period [31]. Disturbances in the DMN of chronic pain patients have been noted in many studies [24,30,31]. Another report showed that when patients feel depressed, the activities of the PFC, subgenual ACC, and hippocampus are all more intense, as is the level of perceived pain [32]. Such studies give deeper insight into the high correlation between chronic pain and mood disorders.

MRS allows us to explore not only the structural information but also the biochemical information of the brain. There are few MRS studies pertaining to chronic pain. A handful of studies suggest the important role of glutamate in chronic pain. Harris et al. [33] reported that the levels of glutamate and combined glutamate, both known to play an important role in pain neurotransmission, were significantly higher in the right posterior insula of fibromyalgia patients. They also found that glutamate and combined glutamate levels are negatively correlated with pain threshold. Moreover, glutamergic abnormalities were found in the ACC and insula of migraine patients. Such abnormalities were suggested to be responsible for the chronic nature of the patients' migraines [34]. There have also been reports that N-acetyl aspartate and glucose were decreased in the dorsolateral PFC of chronic back pain patients [35,36]. When such findings achieve more reliable congruence, accounting for this information may lead to more objective diagnoses of chronic patients.

Using VBM, the volume of brain tissue can be measured. By comparing the gray matter volume of chronic pain patients to that of healthy controls, structural differences, if they exist, in the brains of pain patients can be estimated. Research on chronic pain using VBM includes a few conflicting results, but thus far, researchers generally agree that chronic pain patients have decreased gray matter volume in the regions considered as the pain matrix. Chronic tension-type headache patients showed an overall decrease in their gray matter volume in the pain matrix [37], while chronic back pain patients also showed reduced gray matter density in the bilateral dorsolateral PFC and right thalamus compared to healthy controls [38]. CRPS patients also showed overall decrease in gray matter volume. Gray matter reduction in the right insula, right ventromedial PFC, and right nucleus accumbens was particularly more severe compared to that in other regions [39]. Gray matter intensity in fibromyalgia patients was significantly reduced in the postcentral gyrus, amygdala, hippocampus, superior frontal gyrus, and anterior cingulate gyrus as well [40]. Burgmer et al. [41] also reported decreased gray matter volume in the PFC, amygdala, and ACC. A study of female fibromyalgia patients also found significantly decreased gray matter density in the left parahippocampal gyrus, bilateral mid/posterior cingulate gyrus, left insula, and medial frontal cortex [42]. Kim et al. [43] also reported decreased gray matter volumes in the bilateral insula, bilateral motor/premotor cortex, bilateral PFC, left dorsal ACC, right dorsal posterior cingulate cortex, right inferior and superior parietal cortex, and orbitofrontal cortex in migraine patients. Amputees who experience phantom limb sensations had reduced gray matter in the anterior and posterior cingulate regions, SMA, and midbrain [44]. However, other studies report increased gray matter volume in some brain regions, as well as reports of gray matter reduction. Chronic back pain patients showed substantial decreases in the somatosensory cortex and brainstem, whereas the volume of gray matter in the bilateral basal ganglia and left thalamus increased significantly [45]. Another report found that fibromyalgia patients had increased gray matter volumes in their left orbitofrontal cortex, left cerebellum and bilateral striatum with decreased gray matter volume in their right superior temporal gyrus and left posterior thalamus [46]. In addition, Teutsch et al. [47] observed a number of modulations, including an increase in gray matter in the middle cingulate cortex and somatosensory cortex when noxious stimuli were applied repetitively to healthy subjects. Although it is too soon to conclude anything regarding a tendency toward an increase in gray matter in chronic pain patients at this point, increased gray matter volumes were observed mostly in the left hemisphere.

The DTI method provides quantitative information on chronic pain processing in the central nervous system by monitoring the motions of water molecules. It can be an effective marker for the structural evolution of long-term disease [48]. Chronic pain studies using a DTI technique are not yet as prevalent as studies that utilize other imaging techniques. Using a DTI method, Rocca et al. [49] investigated normal-appearing brain tissue in migraine patients. They reported no significant differences in fractional anisotropy (FA) and mean diffusivity. Later in 2006, they investigated the influence of normal-appearing white matter and gray matter separately in migraine patients. They found a reduction in the mean diffusivity of the gray matter in migraine patients, whereas no significant difference was noted in the mean diffusivity of their white matter. Moreover, no distinct FA difference was noted in both the white and gray matter of these patients [50]. Lutz et al. [40] reported that white matter FA was decreased in the bilateral thalamus, bilateral insula and thalamocortical tracts, whereas it was increased in the postcentral gyrus, amygdala, hippocampus, superior frontal gyrus and anterior cingulate gyrus. They also suggested that the perception of both pain intensity and fatigue was associated with the white matter FA in certain regions of the pain matrix, implying its possible application in pain diagnosis. CRPS patients showed decreased white matter FA in left callosal fiber tract in lateral ACC [39]. If structural changes are consistently observed in patients, diagnosing chronic pain disorders and estimating the degree of suffering can be standardized.