Subscribe to RSS
DOI: 10.1055/s-0042-1755268
Evaluation of the complete Sniffin Sticks Test versus its subtests in differentiating Parkinson's disease patients from healthy controls
Avaliação do Sniffin Sticks Test completo versus seus subtestes na diferenciação de pacientes com doença de Parkinson de controles sem a doençaAbstract
Background Hyposmia is one of the most common, as well as the first nonmotor condition in Parkinson disease (PD). The sniffin sticks test (SST) evaluates three different aspects of olfactory function: threshold (T), discrimination (D), and identification (I). The sum of the scores of these three subtests produce a global score of olfaction, the Threshold-Discrimination-Identification (TDI) score.
Objective The aim of this study was to investigate if the TDI score or one of its subtests is better to discriminate PD patients from controls.
Methods We recruited 27 PD patients and 17 healthy age-matched controls (HC) who were evaluated through a clinical interview, the Montreal Cognitive Assessment and Movement Disorders Society – Unified Parkinson Disease Rating Scale. The olfaction was assessed using the complete SST.
Results The performance of PD patients on the olfactory test was significantly worse when compared with the HC (T: 3.0 vs. 6.5, p < 0.001; D: 8.1 vs. 11.2, p < 0.001; I: 7.3 vs. 11.7, p < 0.001; TDI: 18.8 vs. 29.9, p < 0.001). The prevalence of olfaction impairment in our study (PD: 100%, and HC: 56%) was greater than that found in the literature. Cognition influenced the performance on TDI. The olfactory subtests were impaired proportionally between patients and controls. Furthermore, D and I were correlated, but only in PD patients. The TDI showed a tendency to better discriminate PD patients from HC, when compared with its subtests.
Conclusions Although the complete olfactory evaluation is time consuming, it seems to be a superior tool to identify olfaction impairment in PD patients, when compared with the isolated subtests.
Resumo
Antecendentes Hiposmia é um dos sintomas mais comuns da doença de Parkinson (DP), além de ser um de seus primeiros sintomas não-motores. O Sniffin Sticks Test avalia três diferentes aspectos da função olfatória: limiar (L), discriminação (D) e identificação (I). A soma dos escores desses três subtestes produz um escore global do olfato, o Threshold-Discrimination-Identification (TDI).
Objetivo O objetivo deste estudo foi investigar se o TDI ou um de seus subtestes seria melhor em discriminar pacientes com DP de controles saudáveis.
Métodos Foram recrutados 27 pacientes com DP e 17 controles saudáveis de mesma faixa etária, que foram avaliados através de uma entrevista clínica, a Montreal Cognitive Assessment e Movement Disorders Society – Unified Parkinson Disease Rating Scale. O olfato foi examinado através da bateria completa do Sniffin Sticks Test (SST).
Resultados Os pacientes com DP tiveram pior performance no teste olfatório quando comparados com os controles (L: 3,0 vs. 6,5; p < 0,001; D: 8,1 vs. 11,2; p < 0,001; I: 7,3 vs. 11,7; p < 0,001; TDI: 18,8 vs. 29,9; p < 0,001). A prevalência de comprometimento olfatório no nosso estudo (DP: 100%, e controles: 56%) foi maior do que a reportada na literatura. A cognição influenciou a performance no TDI. Os subtestes olfatórios foram afetados proporcionalmente entre pacientes e controles. Além disso, D e I se correlacionaram, mas apenas em pacientes de DP. O TDI mostrou uma tendência em melhor discriminar pacientes de DP dos controles, quando comparado com os seus subtestes.
Conclusões Embora a avaliação olfatória completa consuma tempo, ela parece ser superior aos subtestes isolados para identificar comprometimento olfatório em pacientes com DP.
Authors' Contributions
CRMR: conceptualization; BSFO, ST: data collection and writing; CRMR, YFFB: review and editing.
Publication History
Received: 21 May 2021
Accepted: 22 October 2021
Article published online:
18 October 2022
© 2022. Academia Brasileira de Neurologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit (https://creativecommons.org/licenses/by/4.0/)
Thieme Revinter Publicações Ltda.
Rua do Matoso 170, Rio de Janeiro, RJ, CEP 20270-135, Brazil
-
References
- 1 Berendse HW, Roos DS, Raijmakers P, Doty RL. Motor and non-motor correlates of olfactory dysfunction in Parkinson's disease. J Neurol Sci 2011; 310 (1-2): 21-24
- 2 Postuma RB, Berg D, Stern M. et al. MDS clinical diagnostic criteria for Parkinson's disease. Mov Disord 2015; 30 (12) 1591-1601
- 3 Beach TG, White III CL, Hladik CL. et al; Arizona Parkinson's Disease Consortium. Olfactory bulb α-synucleinopathy has high specificity and sensitivity for Lewy body disorders. Acta Neuropathol 2009; 117 (02) 169-174
- 4 Landis BN, Konnerth CG, Hummel T. A study on the frequency of olfactory dysfunction. Laryngoscope 2004; 114 (10) 1764-1769
- 5 Hummel T, Kobal G, Gudziol H, Mackay-Sim A. Normative data for the “Sniffin' Sticks” including tests of odor identification, odor discrimination, and olfactory thresholds: an upgrade based on a group of more than 3,000 subjects. Eur Arch Otorhinolaryngol 2007; 264 (03) 237-243
- 6 Doty RL, Shaman P, Applebaum SL, Giberson R, Siksorski L, Rosenberg L. Smell identification ability: changes with age. Science 1984; 226 (4681): 1441-1443
- 7 Ortiz J, Medina A, Pineda H, Gomez P, Medina R, Avila C. Implementation of sniffin sticks test in Honduran patients with Parkinson's disease: A matched case control study. Mov Disord 2018; 33: S102
- 8 Baba T, Kikuchi A, Hirayama K. et al. Severe olfactory dysfunction is a prodromal symptom of dementia associated with Parkinson's disease: a 3 year longitudinal study. Brain 2012; 135 (Pt 1): 161-169
- 9 Fullard ME, Tran B, Xie SX. et al. Olfactory impairment predicts cognitive decline in early Parkinson's disease. Parkinsonism Relat Disord 2016; 25: 45-51
- 10 Camargo CHF, Jobbins VA, Serpa RA, Berbetz FA, Sabatini JS, Teive HAG. Association between olfactory loss and cognitive deficits in Parkinson's disease. Clin Neurol Neurosurg 2018; 173 (August): [Internet] 120-123 DOI: 10.1016/j.clineuro.2018.08.018.
- 11 Masala C, Solla P, Liscia A. et al. Correlation among olfactory function, motors' symptoms, cognitive impairment, apathy, and fatigue in patients with Parkinson's disease. J Neurol 2018; 265 (08) 1764-1771 DOI: 10.1007/s00415-018-8913-9. [Internet]
- 12 Cecchini MP, Federico A, Zanini A. et al. Olfaction and taste in Parkinson's disease: the association with mild cognitive impairment and the single cognitive domain dysfunction. J Neural Transm (Vienna) 2019; 126 (05) 585-595 DOI: 10.1007/s00702-019-01996-z. [Internet]
- 13 Krismer F, Pinter B, Mueller C. et al. Sniffing the diagnosis: Olfactory testing in neurodegenerative parkinsonism. Parkinsonism Relat Disord 2017; 35: 36-41 DOI: 10.1016/j.parkreldis.2016.11.010. [Internet]
- 14 Wolz M, Hähner A, Meixner L. et al. Accurate detection of Parkinson's disease in tremor syndromes using olfactory testing. Eur Neurol 2014; 72 (1-2): 1-6
- 15 Mahlknecht P, Pechlaner R, Boesveldt S. et al. Optimizing odor identification testing as quick and accurate diagnostic tool for Parkinson's disease. Mov Disord 2016; 31 (09) 1408-1413
- 16 Boesveldt S, de Muinck Keizer RJO, Knol DL, Wolters ECh, Berendse HW. Extended testing across, not within, tasks raises diagnostic accuracy of smell testing in Parkinson's disease. Mov Disord 2009; 24 (01) 85-90
- 17 Boesveldt S, Verbaan D, Knol DL. et al. A comparative study of odor identification and odor discrimination deficits in Parkinson's disease. Mov Disord 2008; 23 (14) 1984-1990