Taste Disorders
Summary
Taste disorders are frequently encountered in specialized outpatient clinics. However, they occur less often than olfactory disorders. Most patients with taste disorders suffer considerably, which can present as gustatory loss, or decreased or changed gustatory perception. Within this chapter, we present the different causes, diagnostic procedures, and possible therapies for taste disorders.
Introduction
Talking about taste always requires clarification between the medical term taste and “taste” as it is used in daily language. Taste used in everyday language means the sensations one experiences during eating or drinking. This is composed of texture, retronasal smell, and “pure” taste inputs. The physiological definition of taste is restricted to the five qualities sweet, sour, salty, bitter, and umami (the taste of glutamate). As a consequence, most people confuse olfaction and gustation. For example, most patients with olfactory dysfunction complain of smell and taste alteration, while testing reveals that olfaction but not the five basic tastes are affected.1
In clinical practice, patients rarely present with taste disorders restricted to the five basic tastes. The reason for this low incidence is not clear. One explanation could be that many taste disorders are transient, and patients only seek medical advice for long-lasting or permanent taste disorders. Another explanation could be that many patients with taste disorders have concomitant, more troublesome health problems (e.g., facial paresis, stroke) and forget to mention the taste disorder. Taste assessment is far from a routine procedure, and the low incidence of taste deficits may simply reflect the fact that this sense is rarely tested. Finally, taste is represented by three cranial nerves per side, making taste innervation redundant. This could lead to a higher resistance of taste to trauma and injury, thus explaining the few taste disorders observed in clinical practice. An intact sense of taste is significant in the regulation of nourishment, the recognition of poisonous and rotten food, and even for the experience of the hedonic aspects of a common meal.
Recent routine taste testing in a large sample of the general population showed that measurable taste impairment is more frequent than previously thought. In a cohort of 761 healthy individuals aged 5 to 89 years, reduced taste function was measured in 5%, despite the fact that these individuals considered their taste capacity to be normal. Most of these cases were hypogeusia; ageusia was observed rarely.2 While taking the patient’s history, it is therefore important to ask specific questions such as, “Do you have problems tasting sweet, sour, salty, or bitter flavors?” The isolated question, “Do you have taste problems?” is too vague and will be answered too often with no, even when taste problems exist.3
Taste problems can be an important sign or symptom in daily clinical practice, as several case vignettes report. Severe taste disorders can occur after laryngoscopy,4 stroke,5 temporal bone fracture,6 dissection of the brain-supplying arteries,7 in celiac disease,8 or even as a paraneoplastic symptom.9 Such severe taste disorders can lead to anorexia, weight loss, and impairment of well-being. An isolated impairment of gustatory sensitivity to salt was recently identified as a risk factor for arterial hypertension.10
There is confusion between smell and taste symptoms. Taste disorders can be the first symptom of underlying pathologies.
Typical Clinical Findings
Taste disorders do not have a distinct pathognomonic clinical finding that can be identified easily. The clinical presentations are rather heterogeneous, and here we try to describe the different types of gustatory disorders that can be present and how they can be diagnosed.
Patient History
The patient’s history, as in many medical problems, is key to understanding the disorder. When it comes to taste disorders, it must be remembered that patients do not always rate their gustatory function correctly.11 Sometimes patients do not even notice taste deficiency.12 Thus, asking about taste function is mandatory but unreliable, and becomes meaningful only with concurrent testing. When taking a history, emphasis should be put on specific questions about tasting the different qualities, production of saliva, swallowing and chewing capacity, orofacial pain, former infections or surgery in the head and neck region (especially the middle ear), diseases of the salivary glands, hearing or vestibular impairment, and oral hygiene. In addition, drug intake (and when this intake began), comorbidities (e.g., diabetes, thyroid dysfunction, Sicca syndrome [Sjögren disease], cancer), and former radiochemotherapy should be ascertained.13
Classification of Taste Disorders
Taste disorders can be clinically classified as quantitative or qualitative disorders. The most important quantitative taste disorders are ageusia, a complete loss of taste, and hypogeusia, a diminished taste. The most important qualitative taste disorders are dysgeusia and parageusia, characterized by a distorted sense of taste or an ongoing bad taste even in the absence of a taste stimulant. The dysgeusia taste is often described as bitter, sour, or metallic. Phantogeusia is a gustatory hallucination and is encountered in patients with epilepsy or psychotic disorders. Difficulty identifying a tastant that has been properly perceived is termed taste agnosia. It is assumed that the anteromedial temporal lobe has an important role in recognizing taste quality.14 Despite the dichotomous classification in clinical practice, quantitative and qualitative taste disorders often coexist. The main difference between qualitative and quantitative taste disorders is that the latter can be tested objectively and assessed psychophysically, whereas qualitative disorders cannot yet be assessed by any available technique. Qualitative taste disorders are comparable to tinnitus in hearing: a frequent, bothersome complaint that may occur with or without hypoacousis and cannot be measured. Qualitative taste disorders (dysgeusia, phantogeusia, parageusia) are much more frequently encountered in a clinical setting than quantitative taste disorders ( Table 15.1 ). An alternative way to classify taste disorders is to distinguish between central or peripheral taste disorders ( Fig. 15.1 ) according to the site of the lesion. Finally, taste disorders can be classified according to their cause ( Table 15.2 ). Congenital ageusia has never been reported to the best of our knowledge (unlike congenital anosmia, which is frequent15). Selective taste deficiencies such as ageusia for a single taste quality seem to be rare (except for bitter). Only a few reports of these exist, and it is not clear if this is a result of under-reporting or the particular biological importance of an intact taste function preventing such isolated and congenital ageusia.16,17
A careful patient history, testing of each modality, and clinical work-up is important for patients with taste disorders.
Pathophysiology
Often, we do not know the exact pathological mechanism underlying taste disorders, which is reflected by the classification systems. Two of the three classification systems presented here are clinical and observational classifications without any explanation about the underlying mechanism. We observe patients with medication side effects, but barely know any molecular details about the disorders. In contrast, the pathological mechanism seems clear in situations where a lesion is visible or documented (as seen in Fig. 15.1 ). In these cases, the taste pathway is directly injured.
Etiology of Taste Disorders
To determine etiology of taste disorders the following differential diagnostic approach has been shown to be useful:
Is the taste disorder caused by drugs or toxins?
Is the taste disorder caused by local factors in the oral cavity, for instance atrophy of the mucosa, physical or chemical injuries, alteration of the composition of saliva, or otorhinolaryngological or dental diseases (e.g., Candida albicans)?
Is the taste disorder caused by a disease of the peripheral nervous system?
Is the taste disorder caused by a disease of the central nervous system?
Is the taste disorder caused by a systemic disease?
Did the taste disorder occur after any distinct event (e.g., infection, surgery, etc.)?
Taste Disorder Caused by Lesions of the Peripheral Nervous System
Taste disorders caused by peripheral nervous system disease can occur because of an isolated or combined lesion of one of the cranial nerves VII, IX, or X, such as occur in polyneuritis cranialis or Guillain–Barré syndrome.18 Taste disorders can also occur in polyneuropathy.
Taste disorders affect 31 to 46% of patients with acute facial palsy, with no difference in incidence between the idiopathic form (Bell palsy) and borreliacaused palsy. Compared with clinical signs and symptoms, and especially analysis of cerebrospinal fluid, taste results were of poor clinical value in differentiating among the causes of facial palsy.19 Isolated peripheral cranial nerve lesions with resulting taste disorder have a wide differential diagnosis, including dissection of the brain-supplying arteries and local or systemic diseases affecting peripheral nerves. Further, lesions of the skull base or cerebellopontine angle, as well as traumatic skull fractures, might lead to taste disorders.20 However, the most frequent cause of isolated peripheral taste disorder is surgical (iatrogenic) damage to one of the taste nerves ( Fig. 15.1 ). The procedures most frequently associated with taste disorders are otological surgery with damage to the chorda tympani,21 tonsillectomy and microlaryngoscopy22 with damage to the lingual branch of the glossopharyngeal nerve, and oral or dental surgery with damage to the lingual nerve.23 Unless the nerve is accidentally severed, most cases of surgically induced taste disorders are transient because peripheral nerves regenerate. This process takes a long time and patients often suffer from dysgeusia for many months or years.
In polyneuropathy, prominent taste disorders can occur and have been reported in cases of diphtheria, porphyries, systemic lupus erythematosus, or amyloidosis.13 In a recent observational study of 53 patients with polyneuropathy, 43% demonstrated significant taste disorder on taste strip testing. The disorder was more severe in patients with diabetic polyneuropathy.24 There are also reports of some degree of taste disorder in patients with trigeminal neuropathy, based on the fact that gustatory nerve fibers run via the trigeminal nerve.25 This raises an interesting issue about interaction between the chemical senses. As mentioned, trigeminal lesions seem to influence taste function subclinically. The converse also seems to be true, with taste loss affecting lingual trigeminal function.26 Likewise, olfactory impairment influences taste function subclinically.27 Taken together, these observations make interpretation of selective chemosensory disorders difficult.
Generally, taste disorders due to peripheral nerve disease are accompanied by additional signs and symptoms such as pain, altered oral perceptions, and foreign body feelings in the pharynx or oral cavity; swallowing disorders; palpable masses; or palatal or facial palsy. Taste disorders can occur after dental procedures,28 after surgical treatment of vestibular Schwannoma,29 or following manipulation of the lingual nerve. In the case of carotid gustatory syndrome, a transient metallic taste perception emerges after compression of the carotid artery, probably due to a misconnection within the glossopharyngeal nerve between afferent impulses from carotid baroreceptors and sensory impulses from taste fibers.30