ABSTRACT
Huntington's disease (HD) is a degenerative genetic disorder with autosomal-dominant transmission. The triad of symptoms of this disease consists of psychiatric disorders, jerky movements, and dementia. Oropharyngeal dysphagia, which is more evident with disease progression, is also present. Few studies have addressed the swallowing characteristics using objective analysis in this population. The purpose of this research was to describe the swallowing endoscopic findings of the pharyngeal phase in HD. This is a cross-sectional study addressing a clinical case which included two individuals of the same family, male, 32 and 63 years old, designated as individual A and individual B, with progression of the disease for five and 13 years, respectively. Consistent liquid, nectar, and puree were offered during the evaluation. There was presence of posterior oral spillage in liquid and nectar, small amount of pharyngeal residues, and no laryngeal penetration or aspiration in the individuals with HD in this study.
Keywords: Deglutition Disorders; Huntington’s Disease; Neurodegenerative Diseases; Chorea; Endoscopy
INTRODUCTION
Huntington's disease (HD) is a degenerative genetic disorder with autosomal-dominant transmission1-3. The triad of symptoms of this disease consists of psychiatric disorders, jerky movements, and dementia. Oropharyngeal dysphagia is more evident with disease progression and compromises the swallowing function.
In the descriptions of this disease in the literature, there are studies on swallowing which investigate the characteristics of the oral and pharyngeal phases using videofluoroscopy (VFD) and fiberoptic endoscopic evaluation of swallowing (FEES), as well as the risks of aspiration associated with bronchopulmonary infections, airway obstruction, dehydration, and malnutrition4,5.
Although the clinical assessments of swallowing provide relevant information on the condition of oral feeding in patients with oropharyngeal dysphagia, the variability found in their accuracy shows the importance of conducting supplemental exams to objectively assess swallowing in the diagnosis of dysphagia. Also, there are few studies addressing this diagnosis in this population. They verified the swallowing of individuals using videofluoroscopy, and identified postural changes, inadequate movement of the tongue, multiple swallowing, pharyngeal residue after swallowing, and residues in the valleculae and pyriform sinuses6,7. The presence of penetration and/or laryngotracheal aspiration was observed only in the advanced stages of the disease4.
In this paper we used Fiberoptic Endoscopic Evaluation of Swallowing (FEES)8, which is an excellent method to analyze the pharyngeal phase of swallowing, identifying posterior oral spillage, pharyngeal residue, penetration, and aspiration. The main purpose of this study was to describe the swallowing endoscopic findings of the pharyngeal phase in HD.
CASE REPORT
This descriptive study addresses the clinical case of two individuals of the same family, male, 32 and 63 years old, designated as individual A and individual B, respectively. The individuals were referred to the Dysphagia Center due to complaints of speech and swallowing. Both of them signed the Informed Consent Form. The individuals were diagnosed with HD confirmed by genetic testing, with progression of the disease for five and 13 years, respectively. They presented weight loss and gagging. Functional activities such as dressing, brushing teeth, and bathing were compromised. During the evaluation, both individuals presented hyperkinetic dysarthria, postural instability, and involuntary movements of the head and upper and lower limbs. These signals were worse in the A individual, who is younger than the B individual. In the clinical assessment of swallowing, the individuals presented difficulties in labial sealing, oral incoordination, compensatory maneuvers of the head, and disorder in oral transit time, but no clinical signs suggestive of penetration and/or laryngotracheal aspiration. The individuals were referred to FEES, which was performed by an Ear, Nose and Throat Physician (ENT) and accompanied by a speech-language pathologist. The patients were positioned with support to minimize involuntary movement. During the endoscopy examination, no structural disorder was found in the nasopharynx, oropharynx, and hipopharynx. Disorders in the vocal folds were also not found. We used consistent liquid, nectar, and puree in volumes of 3-10 mL. The results show that both individuals presented laryngeal and pharyngeal sensitivity, posterior oral spillage for liquid and nectar (Figures 1 and 2), absence of salivary stasis, pharyngeal residues in small quantity, presence of pharyngeal clearance, and absence of laryngeal penetration and/or laryngotracheal aspiration.
DISCUSSION
According to few authors, dysphagia is a common complication of Huntington's disease, which is often responsible for episodes of respiratory impairment9. Clinical assessment provides information on the presence, nature, and severity of dysphagia4,10, but supplementary exams through objective assessment of swallowing are needed for its diagnosis8.
In this study, we used the FEES method because it provides easy visualization of the pharyngeal phase of swallowing11,12 in agreement with videofluoroscopy findings. It is known that the oral phase in HD can become poor and compromise the oral transit time. However, the presence of posterior oral spillage can also provide us with some information on the coordination of the oral phase, and this parameter can be identified in the FEES and in the videofluoroscopy13. In both tests, the presence of involuntary movement present in HD further complicates the oral control and the presence of posterior oral spillage.
Other studies using swallowing videofluoroscopy in liquid and puree consistencies verified involuntary movements of the tongue, presence of posterior oral spillage, and pharyngeal residue, corroborating the findings of this study6,14.
These results on posterior oral spillage and pharyngeal residue found in both individuals were also identified by another authors7 as the most prevalent signs in HD. The FEES is an excellent method for the research of these symptoms because it can clearly identify the presence of pharyngeal residue, penetration, and aspiration.
Penetration and/or tracheal aspiration were not observed in either of the individuals, showing once again agreement with other studies that used videofluoroscopy15. Also, the literature reports the presence of these signs only in advanced stages of the disease. In addition to the progression of the disease, other aspects that should be considered and that can increase the risk of tracheal aspiration are also related to the amount of pharyngeal residue4.
There are no studies in the literature describing oropharyngeal dysphagia by the progression of the disease in this population due to the particular manifestations of each individual. New studies with larger samples and different periods of the disease should be conducted to provide additional information on the characteristics and management of swallowing in this population. This demonstrates that there is little knowledge on dysphagia, its most frequent findings during the course of the disease, and its prevalence in HD7.
FINAL COMMENTS
The use of FEES in assessing the pharyngeal phase of swallowing in HD identified findings consistent with those of VFD for this population. This does not preclude the use of VFD as an important tool to assessment oral phase of swallowing in this population. However, because it provides the possibility to confirm or exclude the presence of pharyngeal residue, laryngeal penetration, and aspiration in this population, the FEES is a more accessible evaluation method in present context of the country. This study identified the presence of posterior oral spillage and small amount of pharyngeal residues, and no presence of penetration or aspiration in individuals with HD.
-
Study carried out at Dysphagia Research Center of the Universidade Estadual Paulista – UNESP - Marília (SP), Brazil.
-
Financial support: none.
REFERENCES
-
1 Gusella JF, MacDonald ME. Huntington’s disease. Semin Cell Biol. 1995;6(1):21-8. http://dx.doi.org/10.1016/1043-4682(95)90011-X PMid:7620118.
» http://dx.doi.org/10.1016/1043-4682(95)90011-X - 2 Yorkston KM, Miller RM, Strand EA. Management of speech and swallowing in degenerative diseases. Tucson: Communication Skill Builders; 1995.
-
3 Pringsheim T, Wiltshire K, Day L, Dykeman J, Steeves T, Jette N. The incidence and prevalence of Huntington’s disease: a systematic review and meta‐analysis. Mov Disord. 2012;27(9):1083-91. http://dx.doi.org/10.1002/mds.25075 PMid:22692795.
» http://dx.doi.org/10.1002/mds.25075 -
4 Hamilton A, Heemskerk AW, Loucas M, Twiston-Davies R, Matheson KY, Simpson SA, et al. Oral feeding in Huntington’s disease: a guideline document for speech and language therapists. Neurodegener Dis Manag. 2012;2(1):45-53. http://dx.doi.org/10.2217/nmt.11.77
» http://dx.doi.org/10.2217/nmt.11.77 -
5 Hamakawa S, Koda C, Umeno H, Yoshida Y, Nakashima T, Asaoka K, et al. Oropharyngeal dysphagia in a case of Huntington’s disease. Auris Nasus Larynx. 2004;31(2):171-6. http://dx.doi.org/10.1016/j.anl.2003.11.001 PMid:15121228.
» http://dx.doi.org/10.1016/j.anl.2003.11.001 -
6 Heemskerk AW, Roos RA. Dysphagia in Huntington’s disease: a review. Dysphagia. 2011;26(1):62-6. http://dx.doi.org/10.1007/s00455-010-9302-4 PMid:20838817.
» http://dx.doi.org/10.1007/s00455-010-9302-4 -
7 Kagel MC, Leopold NA. Dysphagia in Huntington’s disease: a 16-year retrospective. Dysphagia. 1992;7(2):106-14. http://dx.doi.org/10.1007/BF02493441 PMid:1533361.
» http://dx.doi.org/10.1007/BF02493441 - 8 Marinque D. Avaliação otorrinolaringológica da deglutição. In: Furkin AM, Santini CS. Disfagias orofaríngeas. Carapicuiba: Pró-fono; 1999. p. 49-66.
-
9 Leopold NA, Kagel MC. Dysphagia in Huntington’s disease. Arch Neurol. 1985;42(1):57-60. http://dx.doi.org/10.1001/archneur.1985.04060010063017 PMid:3155611.
» http://dx.doi.org/10.1001/archneur.1985.04060010063017 - 10 Langmore SE. Issues in the management of dysphagia. Folia Phoniatr. 1999;51(1):220-30.
-
11 Langmore SE, Schatz K, Olson N. Endoscopic and videofluoroscopic evaluations of swallowing and aspiration. Ann Otol Rhinol Laryngol. 1991;100(8):678-81. http://dx.doi.org/10.1177/000348949110000815 PMid:1872520.
» http://dx.doi.org/10.1177/000348949110000815 -
12 Kelly AM, Drinnan MJ, Leslie P. Assessing penetration and aspiration: how do videofluoroscopy and fiberoptic endoscopic evaluation of swallowing compare? Laryngoscope. 2007;117(10):1723-7. http://dx.doi.org/10.1097/MLG.0b013e318123ee6a PMid:17906496.
» http://dx.doi.org/10.1097/MLG.0b013e318123ee6a -
13 Dodds WJ, Logemann JA, Stewart ET. Radiologic assessment of abnormal oral and pharyngeal phases of swallowing. AJR Am J Roentgenol. 1990;154(5):965-74. http://dx.doi.org/10.2214/ajr.154.5.2108570 PMid:2108570.
» http://dx.doi.org/10.2214/ajr.154.5.2108570 - 14 Barsottini OGP. Doença de Huntington: o que é preciso saber. Einstein. 2007;5(3):83-8.
-
15 Lee TH, Lee JS, Kim WJ. High resolution impedance manometric findings in dysphagia of Huntington’s disease. World journal of gastroenterology. WJG. 2012;18(14):1695-9. http://dx.doi.org/10.3748/wjg.v18.i14.1695 PMid:22529701.
» http://dx.doi.org/10.3748/wjg.v18.i14.1695
Publication Dates
-
Publication in this collection
23 June 2016 -
Date of issue
Jul-Aug 2016
History
-
Received
26 Feb 2015 -
Accepted
04 Aug 2015