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Our corneal pain system is unique in its principal role of protecting, sustaining and restoring the optical tear layer without which our vision would be non-functional. To meet this existential need, the human dry eye alarm evolved into the most powerful, sensitive and complex pain system in the body, incorporating sensors that are unusually vulnerable to being exposed to the noxious environment. Like other damaged nociceptive systems, it is capable of failing and becoming a disease in its own right known as neuropathic pain.1 Indeed, the features of corneal nerves associated with pain parallel the well-defined properties of somatic neuropathic pain defined as ongoing pain as a direct consequence of a lesion or disease affecting the somatosensory system. Nevertheless, a recent PubMed search (http://www.ncbi.nlm.nih.gov/pubmed) using key words cornea, neuropathic, pain came up empty except for references to herpes zoster. Here we provide an overview of disorders of the corneal pain system in the context of neuropathic pain as it relates to dry eye disease (DED) and other disorders affecting the corneal sensory system characterised by otherwise inadequately explained chronic pain.
What is dry eye disease?
Although the definition of DED is ambiguous and often contradictory, its most consistent clinical feature is chronic dry eye-like pain (DELP).
Dry eye symptoms
DELP is a unique type of corneal pain that we associate with excessive tear film evaporation. Unlike pain experienced elsewhere in the body, that of dry eye is characterised by its sensitivity to environmental evaporative factors in being exacerbated by circumstances that promote tear film evaporation and are mitigated by those that suppress it. Thus, in addition to mechanisms commonly associated with neuropathic pain, specialised corneal nociceptors tuned to tear film evaporation have been shown to play a central role in generating chronic sensations of dry eye (see below). Moreover, we believe that it is appropriate to distinguish them from symptoms caused by the mechanical consequences of dry ocular surfaces such as scratchy or foreign body-like and others such as burning when they are not highly sensitive to tear evaporation. The reasons for our arbitrary decision to highlight symptoms associated with evaporation of the pre-corneal tear layer will become apparent below.
Although patients with chronic corneal evaporative symptoms as a group have lower tear metrics than those who are asymptomatic,2 the weak relationship between DELP and tear metrics3 ,4 questions the assumption of a direct causal relationship. Moreover, the validity of highlighting Meibomian gland dysfunction (MGD) to explain the disparity between signs and symptoms has been challenged by the recent report of its similarly weak relationship with dry eye symptoms.5 On the other hand, dry eye symptoms are keyed to the sensitivity of specialised evaporation-sensitive (cold) receptors located in afferent corneal nerve terminals6 known as TRPM8 channels that in murine models are responsive to cooling7 and the presence of hyperosmotic tears,8 and others described as innocuous cold afferents.9 It should be noted that different results have been obtained on the effects of hyperosmolality6 ,8 that may reflect differences in the experimental set-up or others that can alter the responsivity of the cold-sensitive afferents (including genetic background). Hypertonicity and increased rate of cooling at the corneal surface that occurs with evaporative thinning of the overlying tear film drive the nociceptive activity that sustains basal tear secretion.9–11 When thinning of the tear layer exceeds certain programmed thresholds, the escalating activity of these nerves triggers the release of fresh tears that normally restores the tear film thickness, thereby silencing the dry eye alarm. However, if the tearing response is inadequate, the escalating alarm activity breaches conscious levels and triggers the maximum release of available tears. Notably, damaged nociceptors in other body parts usually demonstrate enhanced activity to cold typical of many neuropathic conditions.12
Physiological corneal sensitisation and evaporative hyperalgesia
Hyperalgesia is the pain state characterised by increased sensitivity and responsiveness of nociceptors to their noxious stimuli. Proinflammatory cytokines released during inflammation are classic nociceptor sensitizers13 ,14 presumably for those of corneas as well. As the major corneal noxious stimulus, tear evaporation also appears to be the dominant type of corneal hyperalgesia for which we propose the neogilistic term corneal evaporative hyperalgesia (CEH). CEH is unlikely to be clinically problematic when there is no underlying inflammation or nerve damage. It is logical to assume that the sensitivities of the cold and osmotic corneal nerve receptors increase with the greater concentrations of and (possibly) increased sensitivity of nociceptors to proinflammatory cytokines as has been demonstrated in non-ocular tissues.15 In such cases the thickness of the thermal insulating and diluting tear film required to avoid triggering the ‘sensitised’ dry eye alarm must also be greater. This suggests that when the increased thickness of the tear film required to maintain the silence of the sensitised dry eye alarm becomes unsustainable, DELP can be experienced even in the presence of normally adequate tears metrics assuming that the neural-mediated tear secretory function of the lacrimal glands16 remains adequate.
The scleral lens: a diagnostic tool for CEH
The unique capability of scleral lenses to instantly and completely block corneal surface evaporation on their insertion points to symptoms they suppress as representing CEH. Moreover, by maintaining an optimal hydrating environment and protecting the external corneal surface from the friction of blinking (thereby avoiding the activation of sensitised low-threshold C-mechanoreceptors), corneal symptoms experienced while these devices are worn could be expected to represent spontaneous pain (the exception being chemical hyperalgesia as these devices are permeable to fumes).
(Neuropathic) Disorders of the peripheral dry dye alarm
Although the traditional model of DED assumes that the dry eye alarm is a passive participant, cold receptors elsewhere in the body have been shown to be capable of becoming autonomous drivers of neuropathic nociceptor hyperactivity.17 We suggest that the cascade involved in the expression of evaporative corneal hyperalgesia can be similarly driven by dysfunctional nociceptor elements.
Tear deficiency and chronic DELP
It has been assumed that otherwise unexplained chronic DELP is caused by insufficient tears because they are identical to those associated with dry eyes and some of these eyes exhibit vital staining of their exposed surfaces. However, these symptoms can also be experienced despite the presence of adequate tears as reported a study of 52 eyes in which tear volumes did not differ significantly from preoperative values over a period of 6 months following laser-assisted in situ keratomileusis (LASIK).18 Moreover, it is possible that the exposed ocular surfaces may be more vulnerable to desiccating stress by neurotrophic effects of corneal nerve damage from the procedure. Nevertheless, it is not surprising that studies have found reduced tears in these eyes19 presumably consequent to the disruption of afferent neural pathways of the lacrimal functional unit.
In our opinion, the role of Meibomian glands in the pathoetiology of chronic DELP is also debatable. Although MGD is associated with increased tear evaporation,20 the relationship between chronic DELP and MGD is weak,5 suggesting that the function of Meibomian glands may not be a significant factor as an initiating cause in chronic DELP. On the other hand, interventions that improve Meibomian gland function can temporarily reduce these symptoms.21 How can these findings be reconciled? We suggest that the missing part of the equation may be due to the effects of corneal sensitisation. While non-sensitised corneas appear to be agnostic to MGD, that may not be true of sensitised corneas since they could be expected to be more symptomatically responsive to changes in tear film evaporation; both positive and negative. Increased concentrations of proinflammatory cytokines in the tears of these patients22 ,23 suggest the presence of corneal sensitisation.
When is cornea-based chronic DELP pain neuropathic?
Hyperosmotic tears, a marker of tear deficiency,24–26 have been shown to induce inflammation in human corneal epithelial cells,27 increase the local ability to concentrate human neutrophils28 and enhance the sensitivity of cold transducers in corneal nociceptors.29 Nevertheless, the tear osmolarity distribution curves of symptomatic patients include some that are not hyperosmolar. This should be considered in the context of a progressive or chronic process whereby the nerves are either sensitised by inflammatory molecules damage. Many diseases affect nerves involved in chronic pain throughout the body (eg, diabetes, fibromyalgia) or from local damage (eg, LASIK). The above observation is consistent with anecdotal observations of the presence in some patients with chronic DELP of tears that are too abundant to be explained by hyperevaporating tears (PR, personal observations). Should future studies confirm the presence of elevated levels of proinflammatory cytokines in non-hypertonic tears of patients reporting chronic DELP, their possible source could be neuroinflammation caused by prolonged periods of corneal nociceptor hyperactivity (peripheral sensitisation) as has been shown in other tissues (see reviews30 ,31). Moreover, the typical paucity of external signs of inflammation in these eyes has also been noted in other types of peripheral neuropathies characterised by neuroinflammation and peripheral sensitisation.32 Being more sensitive to noxious stimuli, neuropathically sensitised corneas might also be expected to be more responsive to localised areas of hyperosmolarity occurring in areas of tear film break-up33 that would be asymptomatic in non-sensitised corneas.
Age-related dry eye disease
These corneas are characterised by negative symptoms of reduced tactile sensitivity related to lower corneal nerve densities34 and positive symptoms of evaporative hyperalgesia. The juxtaposition of opposite sensory features was also reported in the skin of healthy elderly subjects in whom it was found that although the overall activity of the C-fibres was reduced by their attrition, that of the surviving nerves was increased,35 indicating ongoing hyperactivity. If similar age-related changes occur in the corneal nerves, it could explain the presence of chronic dry eye symptoms in this cohort considering the far greater density of corneal nociceptors compared with skin. Moreover, the effect of aging on enhancing central pain-modulating processing36 may also be a factor in amplifying the intensity of CEH. Unexplained, chronic corneal evaporative hyperalgesia is consistent with neuropathic pain.
Neuropathic pain following corneal nerve injury
Pain following non-ocular surgery is typically generated by inherently hypersensitive ectopic pacemakers located in regenerating nociceptor fibre terminals and dorsal root ganglia37 in which its phenotype has transitioned from transmission to regeneration.38 Healing is accompanied by their return to the transmitting phenotype accompanied by pruning of redundant regenerating nerve fibres, microneuromas and their ectopic pain signal generators and the termination of ectopic pacemaker expression in their somata. Nevertheless, unexplained chronic pain following otherwise uneventful non-ocular surgical procedures that persists long after complete healing has taken place indicates the presence of neuropathic pain.39
DELP is the dominant symptom experienced by patients following the extensive corneal axotomies performed during laser keratorefractive surgery. Although they typically resolve within several months, symptoms can persist as long as a year40 and sometimes longer in which case their levels typically reach higher levels of intensity41 and in our experience can be permanent.
Neuropathic eye pain and the brain
Peripheral injuries trigger complex changes in the central nociceptive system leading to central sensitisation that enhances the sensitivity and responsiveness of the brain regions involved in sensory processing through neuroplastic processes.42 ,43 In some cases, these physiological responses progress to neuropathic centralised pain.
Physiological central sensitisation
In contrast to all other sensory systems that adapt to sustained applications of constant stimuli, that of pain is amplified both peripherally (peripheral sensitisation) and centrally (central sensitisation). Central sensitisation is the physiological phenomenon that describes the augmentation of incoming trains of peripheral afferent pain signals in the dorsal horn44 and its equivalent in the trigeminal brainstem45 by activity-driven feed-back and feed-forward mechanisms. The result is sustained elevated excitability levels in relevant synapses through adaptive molecular and cellular neuroplastic changes.46 Its upper limits are controlled by responsive descending inhibitory pain signals47 that dominate the background of the central nociceptive system and serve to extinguish central sensitisation when afferent pain signals cease (see review).47
The dynamic responsiveness of central sensitisation to increased peripheral pain activity triggered by nerve injuries and inflammation is a function of the remarkable neuroplasticity of the somatosensory nervous system.48 Nevertheless, these changes can become entrenched and counterproductive; a phenomenon described as maladaptive plasticity.42 Inappropriately sustained synaptic membrane hyperexcitability in the central nociceptive pathways can be caused by an imbalance between excitation and inhibition promoted by a compromised inhibitory system (disinhibition).49 ,50 The consequent facilitation of central pain signals amplifies and distorts incoming pain signals such as those generated by tear film evaporation (central CEH), that can result in painful responses to normally non-noxious stimuli (allodynia), and spontaneous discharges in the central nociceptive pathways (spontaneous pain).51
Pathologically entrenched synaptic hyperexcitability in the central pain pathways results in sustained amplification and distortion of incoming pain signals (central hyperalgesia) and/or spontaneous pain long after the triggering noxious insult has resolved. Involvement of the eyes in this pain syndrome points to malfunctions in the trigeminal brainstem, which is the target of ascending corneal nociceptive projections in murine models.52
Our use of the term oculofacial pain (OFP) describes neuropathic pain generated and/or sustained in the central trigeminal circuitry and projected to its receptive field including (and sometimes limited to) that of its ophthalmic division. Because centralised pain is expressed through neurological mechanisms remote from its origins (see review53), its apparent peripheral trigger is an illusion responsible for the striking disparity between symptoms and signs. Moreover, as the centre for processing corneal hyperalgesia,54 maintaining corneal surface wetness homeostasis55 and monitoring aversive light intensity,56 dysfunctional synaptic excitability levels in the trigeminal brainstem can, in addition to generating projected spontaneous pain, impair tear production and increase the pain of photosensitivity (neuropathic photophobia)—see below.
Clinical observations of over 200 patients (PR) of presumed centralised OFP have provided further insights into symptoms that these patients can experience. We identified the components of OFP as spontaneous when they were experienced during lid closure in a dark room or during scleral lens wear. Patient descriptors of spontaneous pain included burning hot, sharp, cutting, needle-like, foreign body, pins and needles and pounding, pressure/aching. It was often described as radiating to and from the eyes and/or orbits, ears and receptive fields of the maxillary and mandibular divisions of the trigeminal nerve. Comorbid headaches were common and most often characterised as new and less commonly as an exacerbation of long-standing ones. Tactile allodynia of skin innervated by the ophthalmic branch of the trigeminal nerve was reported by a few patients. Notably, hypersensitivity to sound (hyperacusis), although rarely volunteered, was common. Tinnitus, vertigo and/or alterations in smell and taste were also described. On the other hand, in some patients’ symptoms included and were sometimes dominated by those of CEH in which case they appeared to differ from those generated solely in the cornea by their greater intensity and more common association with chemical and occasionally cold corneal hyperalgesia. Symptoms were limited to those of neuropathic photophobia in a few patients (see below).
Allodynia was most often reported as otherwise unexplained painful photophobia typically characterised by increased sensitivity to lights of computer screens and fluorescent and metal halide fixtures (characterised by high-frequency flicker) and less to incandescent lights (PR, personal observations). The association of photophobia with centralised trigeminal pain has been previously reported and in the absence of a visible peripheral cause we consider it being a neuropathic symptom and describe it as photoallodynia.57 ,58 It also appeared to differ from peripherally triggered photoallodynia in the failure of cycloplegia to mitigate symptoms (PR, personal observations) consistent with the findings in a murine model.59 Based on these observations, we speculate that, while we believe that neuropathic photophobia is associated with the activation of the corneal-trigeminal pathways similar to that associated with corneal trauma,60 it differs in being sustained by neuropathic disorders involving relevant pathways in the brainstem.59 These symptoms appear to share certain properties with those described by migrainous patients in whom exposure to light exacerbates their headache61 and who have been reported to be more sensitive to high-frequency flickering light.62
Centralised mechano-hyperalgesia associated with OFP
Many patients in our cohort of OFP were inexplicably intolerant to wearing scleral lenses. Although this response was typically experienced during the initial fitting process, it also appeared after the devices had been worn comfortably; sometimes for several years (personal observations). Some of these patients also experienced an unusually painful reaction to the application of Schirmer's strips (PR, personal observations) consistent with secondary hyperalgesia associated with centralised neuropathic pain.63
OFP following laser keratorefractive surgery
Since neuropathic pain is known to follow surgical incisions of the skin64 which is far less densely innervated than the cornea, it is not surprising that the massive corneal axotomies performed during laser keratorefractive procedures can trigger this disease in vulnerable patients. We identified a cohort (n=21) who developed severe neuropathic eye pain consistent with its centralisation following keratorefractive surgery. The duration of the pain at the initial consultation ranged from 2 to 15 years (unpublished data). Eighty-one per cent of these patients reported significant neuropathic photophobia. An unexpected finding was that the onset of the centralised pain following the resolution of postoperative pain was often delayed for periods ranging from days to years. If validated, these findings suggest that some currently asymptomatic post-keratorefractive surgery patients are at risk for developing this devastating complication. Although not described as such, the neuropathic centralised pain state following LASIK has been previously described41 as has the delayed onset of chronic pain following surgery of other body parts.65
Responses to topical corneal anaesthesia: a diagnostic test for centralised corneal pain
Most patients with OFP reported incomplete suppression of their eye symptoms during total topical corneal anaesthesia. Two examples are provided below.
The experience of a 28-year-old physician provides an informative example. Her chronic, bilateral OFP of 4 years was triggered by a minor chemical injury reported to have rapidly healed and was described as consisting of two distinct components: symptoms of CEH and spontaneous sharp, needle-like sensations that she localised to her eyes and face. Topical corneal anaesthesia suppressed symptoms of CEH as expected but failed to do so for those of spontaneous needle-like pain. That response, the normal appearance of her corneal nerves and absence of inflammatory cells in laser scanning confocal microscope images of her corneas suggested that the source of her spontaneous eye pain was located central to the trigeminal ganglion.
In contrast, a 51-year-old otherwise healthy man developed OFP 5 years after LASIK at which time confocal microscope images revealed striking morphological signs of active corneal axon degeneration/regeneration and inflammation. He reported total suppression of his spontaneous and hyperalgesic oculofacial symptoms including dental pain during corneal anaesthesia. This patient's symptoms suggested possible involvement of corneal polymodal nociceptive afferents66 ,67 and a key role of corneal nociceptor activity in sustaining the central neuropathic process. Differences in the symptom patterns of these two patients reflect the diversity of mechanisms involved in the pathogenesis of peripherally triggered centralised pain.
OFP and comorbid disorders
Fibromyalgia is now believed to be a brain disorder characterised by aberrant central pain facilitation and a state of hyperalgesia68 believed to be sustained by impaired descending inhibition.69 In our experience, the OFP syndrome, whether or not preceded by a noxious insult in the trigeminal sensory receptive field, was often associated with symptoms of fibromyalgia and/or associated comorbidities such as irritable bowel syndrome,70 chronic fatigue, temporomandibular disorders,71 multichemical sensitivities,72 pelvic pain and urological disorders,73 carpal tunnel syndrome74 and sleep disorders75 all of which have been linked to neuropathic central sensitisation.76 In our opinion, this suggests that OFP may also reflect a hypersensitive pain state in some patients.77
Some patients in our cohort were diagnosed with small fibre neuropathy that could serve as driver of centralised pain and that has also been reported in patients with fibromyalgia.78 The disparity between dry eye symptoms and tear metrics in this disease has been previously reported.79
OFP and blepharospasm
The association of blepharospasm and OFP was reported in a case series of five patients (four women and one male).80 In vivo confocal microscopy revealed strikingly abnormal corneal nerve morphology in all, of whom one had previously undergone LASIK. All these patients reported spontaneous pain, chronic dry eye-like symptoms and photophobia in the absence of vital dye staining of their exposed corneal surface. Dysfunctional activity in the basal ganglia–thalamocortical circuitry has been observed in patients with pain and cervical dystonia.81
While studies have reported lower tear volumes in patients with Sjogren's syndrome (SS),82 this has not been a uniform finding.83 Moreover, signs and symptoms of dry eye were not found to be related to the level of autoimmune activity in this disease.84 The weak correlation between symptoms and signs of dry eye in these patients was also consistent with our informal observations that although all patients who were referred to us with this diagnosis suffered from disabling chronic dry eye symptoms and most from desiccating DED, some had normal tear metrics and ocular surfaces. On the other hand, a few patients in the latter group did develop severe dry eyes over time (PR, personal observations), suggesting that the discordance between symptoms and signs may be more significant in the early phases of the disease. If validated, these observations could be interpreted as supporting corneal sensitisation as a cause of chronic DELP in SS that can occur prior to the onset of tear deficiency. This hypothesis could be further tested by measuring both the levels of proinflammatory cytokines in the tears of these patients (which have been shown to be elevated in past studies85) and their osmolarities. The finding of elevated levels of proinflammatory cytokines in non-hyperosmolar tears would point to another source of inflammation such as neuroinflammation caused by the hyperactivity of dysfunctional corneal nociceptors. This would also be consistent with the increased incidence of peripheral neuropathies in this disease.86 Moreover, these corneas could also be expected to be hypersensitive to tear evaporation accelerators such as MGD, a known complication of SS.87 ,88
The foregoing comments are consistent with the increased prevalence of signs and symptoms of central nervous system disorders in associated syndromes.89
Cognitive and affective complications of neuropathic OFP
Chronic pain is associated with numerous brain-related changes that can impair memory, alter reward processing and compromise cognitive functions.90 Many of our patients with long-standing OFP also reported a significant deterioration of their cognitive and executive functions and working memory consistent with reports of fibromyalgia patients.91 In this context, the management of these patients should take into account the bidirectional effects of depression and chronic pain.92 ,93 Moreover, it has been shown that patients diagnosed as having DED are burdened by low self-assessment scores of their health and well-being.94
Does mitochondrial dysfunction play a role in OFP?
The diversity of systemic diseases associated with centralised corneal pain suggests that they may share underlying pathogenetic vulnerabilities. Reports of mitochondrial dysfunction in patients with SS95 and fibromyalgia96 and in those with chronic neuropathic pain97 suggest a possible link, whether one of association or causation.
If validated, our suggestion that chronic dry eye-like symptoms are promoted and sustained by CEH that can be neuropathic in some patients expands our conceptual horizons of these enigmatic diseases in which the role of tear deficiency is relegated to the level of an associated complication from its current assigned role as the underlying cause. We also suggest that the typical disparity between symptoms and signs in the so-called DED are consequences of the varying relationship between levels of corneal sensitisation and compromised tear production each of which in our opinion is a complication of the disease that can evolve along different pathways and timelines.
Separately we describe a previously overlooked oculofacial trigeminal pain syndrome similarly characterised by a striking discordance between the high-intensity levels of its symptoms and paucity of external signs. As the location of the first synapse of primary corneal afferents that transmit noxious corneal sensations, the homeostatic corneal surface wetness control centre and the centre for monitoring the averseness of ambient light levels the trigeminal brainstem would appear to be the location of the neuropathic disease capable of causing trigeminal-projected pain and otherwise unexplained photophobia. The various clinical expressions of this sensory disease reflect the complexity of overlapping networks of interactive pathogenetic cascades adding to the bewilderment of clinicians many of whom take refuge in the belief that these symptoms are imaginary or fabricated.
If the neuropathic paradigm is validated, may open new avenues for the development of targeted treatments for this spectrum of enigmatic diseases.
The authors are grateful to Todd Margolis, M.D., PhD, Carlos Belmonte Martinez, PhD and Kazuo Tsubota, M.D., PhD for their support of this review and helpful suggestions.
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