INTRODUCTIONCaffeine is the most used psychoactive substance in the world1. About 80% of the general population uses this substance daily, be it through coffee, tea, chocolate, soft drinks or caffeine-based drugs. Coffee is the richest source of caffeine2. After oral intake, caffeine is quickly eliminated with a half-life of four to six hours3.
The moderate intake of coffee is defined as daily intake that ranges from 200 to 300 milligrams2. Excessive intake is defined above 600 mg/day4. One cup of Brazilian coffee (60ml) normally has 50.4 mg caffeine2, and according to the authors it may vary from 85 mg to 125 mg5.
Under experimental conditions, caffeine, in moderate doses, produces excellent physical and intellectual performance, increase in concentration and reduction in time of response to sensorial stimuli6. Conversely, high doses may cause perceptible signs of mental confusion and induction of mistakes in intellectual tasks, anxiety, nervousness, muscle tremors, tachycardia and tinnitus3,6. Sudden interruption of caffeine intake may lead to withdrawal syndrome. The most common symptoms are fatigue, anxiety and depression, nausea, vomiting, headache and reduced concentration7,8. The occurrence of anxiety with sudden suspension of caffeine may be present even in subjects that take low doses of the substance (50 to 150 mg/day)9.
Instructions about coffee intake interruption before vestibular tests vary from service to service. Some authors recommend that the patients interrupt coffee intake 72 hours before the test10,11. Others indicate interruption for 48 hours12,13 or for 24 hours14,15. There are those that recommend no intake on the exam day16,17 and other that make no restrictions to intake18-20.
It is essential to maintain the patient calm during the performance of the vestibular test because stress and anxiety may lead to changes in tracing, especially caloric hyperreflexia21,22, inducing the mistaken diagnosis of vestibular disease18. The present study aims at assessing the effect of moderate doses of coffee in the vestibular test.
METHODSThe present study was a comparative, transversal, matched analysis in which the studied group comprised patients that had taken caffeine, according to their own habits, and the control group was the same patients without the use of the substance. Considering that among the foods that contain caffeine coffee is the one that contributes the most to its intake2, researchers defined the concentration of caffeine based on daily coffee intake of participants.
The study comprised subjects sent from different primary care centers in Belo Horizonte with otorhinolaryngologists' referral to perform vestibular test.
Nineteen patients with vestibular symptoms that used to drink coffee everyday were enrolled in the study. None of them had been previously submitted to the test or had clinical presentation compatible with central labyrinth pathology.
First, patients were submitted to vestibular test following the instruction provided by the Service of Audiology, Hospital das Clínicas, Medical School, UFMG, which were: interruption of non-essential drugs and alcoholic drinks for 72 hours before the test; cigarette and caffeine (coffee, chocolate, soft drinks) for 24 hours before the test, and fasting for 3 hours before the test. Next, the same subjects underwent the vestibular test a second time, but a different examiner performed it the second time. Vestibular tests were performed by different examiners so that patients were not used to it in the second time. Thus, patients were alert in both tests. Examiners were previously trained so that the first and second tests were exactly the same.
The instructions were the same, except for no interruption of caffeine intake in the second test.
Vectoelectronystagmography was the method used to record ocular movements, applying the triangular placement of electrodes 23. We used the equipment brand Contronic do Brasil version5. The assessment of balance comprised the following steps: clinical examination with Frenzel lenses, ocular motricity test and caloric test. We assessed saccadic oculomotor movement, tracking and optokinetic movements, in addition to spontaneous and semi-spontaneous nystagmus. Vestibular assessment included caloric test in temperatures of 30°C and 44°C with water. Data generated for the study were analyzed using the statistical program EPI-INFO 6.04. For the statistical comparison, we applied McNemar test for matched analysis. The level of statistical significance for the study was 5%.
The project and the consent forms were analyzed and approved by the Research Ethics Committee, Federal University of Minas Gerais. All involved subjects agreed to participate in the study and in the dissemination of results, in compliance with Resolution nº196 of 1996.
RESULTSThe mean age of participants was 49.5 years, ranging from 21 to 76 years. All subjects were female patients. Mean daily consumption of coffee in the studied population was three cups (Table 1).
The assessment of the most frequent clinical symptoms in relation to vestibular test, with and without coffee intake, are presented in Graph 1. Three patients did not respond to the questionnaire. The highest prevalence of headache and anxiety occurred in patients submitted to the vestibular test with suspension of coffee (p=0.01).
Considering the choice of the patient, 13 (68.4%) preferred to be submitted to the vestibular test with habitual coffee intake. Among the 13 patients, the complaints related with sudden suspension of the drink were anxiety (92.3%), headache (69.3%), nausea and vomiting (38.5%), and more marked vertigo during the test (38.5%). Graph 2 demonstrated that the frequency of withdrawal syndrome has increased with daily dose of caffeine in those patients.
In the result of the vestibular test, no abnormality was observed concerning calibration or measurement of the oculomotor movements with and without coffee suspension. As to caloric test, there was no statistically significant difference between the results found with and without coffee, considering as normal the number of labyrinthic predominance and directional predominance of the nystagmus up to 33%. The matched analysis of data referring to caloric test is demonstrated in Table 2.
DISCUSSIONIn agreement with previous studies, dizziness is the most frequent complaint in female gender and it predominates in the 5th and 6th decades of life in both genders19,24.
The preference of the vestibular test performed with habitual coffee intake (68.4%) may be justified by the higher occurrence of anxiety and headache associated with the test when the instruction to interrupt the intake of caffeine was given (p=0.01).
Caffeine withdrawal syndrome may occur after sudden interruption of intake in those used to moderate or low doses of caffeine20, 21. In this study, most participants were used to take daily moderate doses of caffeine (three cups a day)2. The complaints of anxiety and headache increased as a result of increased doses of caffeine intake. Thus, these symptoms present in the test after previous interruption of coffee intake could be manifestations of caffeine withdrawal syndrome, which could negatively interfere in the results of the vestibular test. Anxiety can cause changes to the tracing of vectoelectronystagmography, leading to misdiagnosis of vestibular disease18.
The vestibular test is a type of test that may generate some uneasiness in the patient. In the present study, the test with instructions to interrupt coffee intake was the first one to be performed. Thus, anxiety could have been associated with two factors: 1) fear of the exam; 2) caffeine withdrawal syndrome. The highest frequency of headache in the test with previous interruption of caffeine intake, conversely, would not be justified by lack of knowledge about the test. It is interesting to notice that headache is an important symptom in caffeine withdrawal syndrome12.
The pharmacological actions of caffeine are well known. In moderate doses, it maintains the subject alert, with greater and more constant intellectual activity, favoring complex association of ideas and reducing the time of reaction to sensorial stimuli6. The improvement in the process of vestibular compensation has been demonstrated25-27. In high doses, caffeine is toxic to the vestibular system. It may cause impairment of the systems of convergence and accommodation, reduction in saccadic movements and peripheral vestibular dysfunction28.
The influence of psychological factors during the performance of a vestibular test has been considered in the quality of the test. To maintain the patient relaxed, and at the same time alert, is essential for the success of the exam. In this study, the result of the vestibular test was similar with and without coffee intake. Therefore, interruption of low and moderate doses of caffeine before the vestibular test should be reassessed, given that in subjects used to take such drinks daily the interruption may trigger undesirable anxiety reactions in subjects that are going to be submitted to the vestibular test.
CONCLUSIONIn the present study, the results of the vestibular test after the intake of moderate doses of coffee were similar to the results with suspension of coffee intake up to 24 hours before the test. Interruption proved to be unnecessary. As to coffee intake instruction before the vestibular test, moderate intake (up to 3 cups/ 24 hours) may be allowed, with restriction for the last intake up to 6 hours before the test (caffeine half-life).
REFERENCES1. Gilbert RM. In: Spiller GA. The methylxanthine beverages and foods: chemistry, consumption, and health effects. New York: Alan R. Liss; 1984. p.185-213.
2. Camargo MCR, Toledo MCF. Teor de cafeína em cafés brasileiros. Ciênc Tecnol Aliment 1999; 18: 421-4.
3. Augello DE. In: Silva P. Farmacologia. 6a ed. Rio de Janeiro: Guanabara Koogan; 2002. p. 428-9.
4. Laranjeira RR, Nicastri S. In: Almeida OP, Dractu L, Laranjeira RR. Manual de Psiquiatra. Rio de Janeiro: Guanabara Koogan; 1996; p. 83-112.
5. Jaffe JH. In: Gilman AG, Goodman LS, Rall TW, Murad F. Goodman & Gilman: as bases farmacológicas da terapêutica. 7ª ed. Rio de Janeiro: Guanabara Koogan; 1987. p.348-62.
6. Rall TW. In: Gilman AG, Goodman LS, Rall TW, Murad F. Goodman & Gilman: as bases farmacológicas da terapêutica. 7ª ed. Rio de Janeiro: Guanabara Koogan; 1987. p.390-4.
7. Juliano LM, Griffiths RR. A critical review of caffeine withdrawal: empirical validation of symptoms and signs, incidence, severity, and associated features. Psychopharmacology 2004; 176: 1-29.
8. Manual Diagnóstico e Estatístico de Transtornos Mentais. 4ª ed. Porto Alegre: Artes Médicas Sul; 2000. [http://www.psiqweb.med.br/dsm/ansie4.html#substancia]
9. Griffiths RR, Evans SM, Heishman SJ, Preston KL, Sannerud CA, Wolf B, Woodson PP. Low-dose caffeine physical dependence in humans. J Pharmacol Exp Ther 1990; 255:1123-32.
10. Flores MR, Franco ES. Vectoeletronistagmografia computadorizada: nistagmo estimulação com ar em indivíduos sem queixa. Arq Otorrinolaringol 2003; 7: 301-8.
11. Silva LV, Caovilla HH. Nistagmografia computadorizada e auto-rotação cefálica na neurite vestibular. Acta Awho 2002. [http://www.actaawho.com.br/]
12. Mangabeira-Albernaz PL, Ganança MM, Caovilla HH, Ito TI, Novo NF, Juliano I. Aspectos clínicos e terapêuticos das vertigens. Acta AWHO 1986; 5 (Suppl 2): 49-109. Apud: Silveira SR, Taguchi CK, Ganança FF. Análise comparativa de duas linhas de tratamento para pacientes portadores de disfunção vestibular periférica com idade superior a sessenta anos. Acta AWHO 2002. [http://www.actaawho.com.br/]
13. Mota PHM, Franco ES, Pinto ESM, Arieta AM. Estudo de equilíbrio no idoso por meio da eletronistagmografia. Acta Awho 2002. [http://www.actaawho.com.br/]
14. Assunção ARM, Albertino S, Lima MAMT. Auto-rotação cefálica ativa em pacientes com tontura/ vertigem. Rev Bras ORL 2002; 68: 57-63.
15. Mor R, Fragoso M, Taguchi CK, Figueiredo JFFR. Vestibulometria & Fonoaudiologia: como realizar e interpretar. São Paulo: Lovise; 2001. p.186.
16. Caovilla HH, Ganança MM, Munhoz MSL, Silva MLG, Ganança FF, Ganança CF. In:Caovilla HH, Ganança MM, Munhoz MSL, Silva MLG. Equilibriometria clínica. São Paulo: Atheneu; 1999. p. 40-78.
17. Gushikem P, Caovilla HH, Ganança MM. Avaliação otoneurológica em idosos com tontura. Acta AWHO 2002. [http://www.actaawho.com.br/]
18. Barber HO, Stockwell CW. Manual of eletronystagmography. 2nd ed. St Louis: The CV Mosby Company; 1980. p. 69-113.
19. Desmond AL. Vestibular function: evolution and treatment. New York: Thieme; 2004. p. 97-8.
20. Jacobson GP, Newman CW, Kartush JM. Handbook of balance function testing. San Diego, London: Singular Publishing Group; 1997. p. 156.
21. Aschan G, Bergst M, Stahl J. Nystagmography. Acta Otolaryngol 1956; 46:1-103.
22. Reisco-MacClure JS. Caloric test: methods and interpretation. Ann Otol Rhinol Laryngol 1964; 73:829-37.
23. Pansini M, Padovan I. Three derivations in electronystagmography. Acta Oto-Laryng. Stockh 1969; 67: 303-9.
24. Ganança FF, Ganança CF. In: Ganança MM. Vertigem tem cura? São Paulo: Lemos editorial; 1998. p. 37-48.
25. Darlington CL, Smith PF. Pre-treatment with a Ca 2+ channel antagonist facilitates vestibular compensation. NeuroReport, 1992; 3: 143-5.
26. Ganança MM. In: Ganança MM, Vieira RM, Caovilla HH. Princípios em Otoneurologia. Vol. 1. São Paulo: Editora Atheneu; 1998. p. 114-5.
27. Gilchrist DP, Smith PF, Darlington CL. ACTH (4-10) accelerates ocular motor recovery in the guinea pig following vestibular deafferentation. Neurosci Lett 1990; 118:14-6.
28. Ganança MM, Caovilla HH Munhoz MSL, Silva MLG, Ganança FF, Ganança CF.O que esperar da equilibriometria. In: Caovilla HH, Ganança MM, Munhoz MSL, Silva MLG. Equilibriometria clínica. São Paulo: Atheneu; 1999. p. 23-9.
29. Brandt T. Vertigo: its a multisensory syndromes. 2nd ed., Springer; 1999. p. 57-60.
1 Speech therapist, Hospital das Clínicas, UFMG.
2 Speech therapist, Hospital das Clínicas, UFMG.
3 Ph.D. in Tropical Medicine, Medical School, UFMG. Otoneurologist, Joint Professor, Department of Ophthalmology, Otorhinolaryngology and Speech and Hearing Therapy, Medical School, UFMG.
4 Master in Linguistics, FALE-UFMG, Speech Therapist, Assistant Professor, School of Speech and Hearing Therapy, UFMG.
Federal University of Minas Gerais.
Address correspondence to: Denise Ustch Gonçalves. Avenida Alfredo Balena 190 sala 3005 Santa Efigênia Belo Horizonte MG.
The present article was submitted through SGP on June 10, 2005 and approved on September 21, 2005.