- Research article
- Open Access
- Open Peer Review
Nystagmus as an early ocular alteration in Machado-Joseph disease (MJD/SCA3)
© Raposo et al.; licensee BioMed Central Ltd. 2014
- Received: 11 November 2013
- Accepted: 17 January 2014
- Published: 22 January 2014
Machado-Joseph disease (MJD), also named spinocerebellar ataxia type 3 (SCA3) is the most common autosomal dominant ataxia worldwide. Although nystagmus is one of the most frequently reported ocular alterations in MJD patients its behaviour during the course of the disease, namely in its early stages, has only recently started to be investigated. The main goal of this work was to characterize the frequency of nystagmus in symptomatic and presymptomatic carriers of the MJD mutation, and investigate its usefulness as an early indicator of the disease.
We conducted an observational study of Azorean MJD family members, comprising a total of 158 subjects which underwent neurological evaluation. Sixty eight were clinically and molecularly diagnosed with MJD, 48 were confirmed asymptomatic carriers and 42 were confirmed non-carriers of the MJD mutation. The frequency of nystagmus was calculated for the 3 groups.
Nystagmus was present in 88% of the MJD patients. Seventeen percent of the at-risk subjects with a carrier result in the molecular test and none of the 42 individuals who received a non-carrier test result displayed nystagmus (p < 0.006). Although not reaching statistical significance, symptomatic subjects showing nystagmus had a tendency for a higher length of the CAG tract in the expanded allele, when compared to individuals who did not have nystagmus.
The frequency of nystagmus in asymptomatic carriers and its absence in non-carriers of the mutation, suggests that nystagmus may appear before gait disturbance and can thus be considered an early sign of MJD.
- Spinocerebellar ataxia
- Presymptomatic subjects
- Clinical trials
Machado-Joseph disease (MJD; MIM #109150; ORPHA98757), also known as spinocerebellar ataxia type 3 (SCA3), is the most frequent autosomal dominant ataxia worldwide . The MJD gene (ATXN3) was mapped to 14q32.1 and the causative mutation was identified as a coding unstable CAG expansion [2, 3]; normal alleles consensually range from 12 to 44 CAGs, whereas well established limits for expanded alleles comprise from 61 to 87 repeats .
With an average onset in adulthood (around 40 years), MJD is characterized by a wide range of clinical manifestations, including ataxia, progressive external ophtalmoplegia, pyramidal and extrapyramidal signs, dystonia with rigidity and distal muscular atrophies [5, 6]. Gait ataxia is reported as the initial complaint in the majority of MJD patients ; in some of the cases, other symptoms, such as diplopia have been reported as preceding gait instability . Ocular alterations are clinical features commonly described in SCAs, occurring as a consequence of cerebellar and brainstem degeneration . Amongst such alterations is nystagmus, a clinical sign associated with vestibular nuclei, found to be damaged in MJD post-mortem brains . Nystagmus is one of the most frequently reported ocular alterations in MJD patients [7, 11, 12]; its behaviour during the course of the disease, namely in its early stages, has only recently started to be investigated .
The main goal of this work was to characterize the frequency of nystagmus in symptomatic and presymptomatic carriers of the MJD mutation and investigate its usefulness as an early indicator of the disease. The availability of molecular testing to detect asymptomatic carriers of the MJD mutation, associated with biological and/or refined clinical markers of the disease process, would enable an early intervention with prophylactic treatment, which should lead to prevention, or at least delayed onset or slowed progression, by allowing intervention before the appearance of motor symptoms .
From 1996 to 2011, 158 subjects belonging to 21 Azorean MJD families performed the molecular test for MJD, either in the context of molecular diagnosis (N = 68) or predictive testing (PT) (N = 90). Subjects were asked for written informed consent to participate in research concerning the analysis of the clinical variability of MJD. During this period the molecular tests have been conducted by two distinct Portuguese genetic diagnosis laboratories.
Three main groups were defined for this study:
Group 1- subjects with a clinical and molecular diagnosis of MJD (N = 68). This group corresponds to individuals that were already symptomatic at the time of their first observation, and for which a molecular confirmation of MJD was subsequently obtained; Group 2- subjects with a normal neurological evaluation, who were confirmed as carriers of the ATXN3 mutation in the molecular test (N = 48). Group 2 was therefore formed by subjects that were submitted to a neurological examination upon entering the PT program (before taking the molecular test) and were asymptomatic at that time. Some of the subjects from this group developed motor symptoms during the observational period of the study. For genotype-phenotype analysis these subjects were clustered with patients from group 1, constituting the pool of “symptomatic subjects” (N = 87).
Group 3- subjects with a normal pre-test clinical evaluation and that subsequently received a negative result in the molecular test (non-carriers of the ATXN3 mutation) (N = 42).
This study is part of a larger project which was approved by the Ethics Committee of the Hospital do Divíno Espírito Santo (São Miguel Island, Azores – Portugal).
Neurological examination was performed by two experienced neurologists, following the protocol established by Coutinho . The examination included the evaluation of nystagmus, which consists in small, horizontal, saccade-like movements that lead the eye away from the target trajectory and, after a delay, bring it back onto the target [9, 15]. The evaluation of nystagmus followed the ICARS procedure . The age at onset and the duration of disease were also assessed. Onset corresponded to the age of appearance of the first symptoms (such as gait disturbance) reported by the patient and/or a close relative. Disease duration was calculated as the time elapsed between the age at onset and the last neurological evaluation available. Time from onset was calculated as the difference between age at first neurological observation and reported age at onset of ataxia.
Differences in the frequency of nystagmus among the three study groups were measured by the Fisher’s Exact Test. Unrelated subjects (N = 46) from the pool of symptomatic subjects were analysed for the following variables: CAG length of the normal and expanded allele, age at onset and disease duration. Pearson correlation test was performed to evaluate the relationship between the CAG repeat length of normal and expanded alleles and age at onset. Univariate and multivariate linear regression were used to test the effect of several predictors on age at onset, namely: the number of CAGs in expanded and normal alleles, gender, island of origin, molecular diagnosis laboratory, and presence/absence of nystagmus. The best model was used to predict the age at onset for all members of group 2. The results were accepted as statistically significant whenever p < 0.05. All analyses were performed with PASW Statistics 18 .
Frequency of nystagmus in symptomatic and presymptomatic MJD carriers
Characterization of the studied subjects according to group assignment
48 ± 15 [16–82]
30 ± 9 [18–59]
36 ± 12 [18–60]
20 ± 5 [13–28]
22 ± 5 [13–27]
17 ± 4 [13–27]
23 ± 4 [13–31]
71 ± 4 [61–80]
71 ± 4 [63–80]
From the 68 patients in group 1, only eight (12%) failed to present nystagmus at the first neurological examination; five out of these eight, however, presented nystagmus at the last observation performed in the course of this study, increasing to 96% the number of patients who presented nystagmus. The remaining three patients were lost from follow-up, therefore preventing the verification of the presence of nystagmus at a later stage of the disease.
Using information on unrelated symptomatic subjects with available CAG data, a negative correlation between the size of the expanded allele and the age at onset was observed (N = 42, r = -0.667, p < 0.0005). The explanation of the age at onset variance provided by the CAG length in expanded allele was 45% (t = -5.740, p < 0.0005). An improvement of the model using additional predictors (CAG repeat number in normal allele, gender, island of origin and genotyping laboratory) raised the explanation of the age at onset to 48% (p < 0.0005). Individuals showing nystagmus had a tendency for a higher CAG length in expanded allele, when compared to individuals who did not have nystagmus [71.54 ± 0.67 and 69.71 ± 0.97 (mean ± standard error), respectively]; this tendency, however, failed to reach significance. The presence/absence of nystagmus did not improve significantly the prediction of the age at onset when adding this variable to the number of CAG repeats in the expanded allele as well as the other predictors previously mentioned.
The present study confirmed nystagmus as a very frequent sign in MJD patients (up to 96% of the MJD patients from the studied series), which is in agreement with previous studies where this sign has been reported with frequencies that vary between 55 and 92% [7, 8, 18, 19]. Considering the genotype-phenotype results, a long term follow-up study would be needed to understand if there is a correlation between CAG repeat length in expanded allele and the age of appearance of nystagmus.
The present study further shows that nystagmus is also observed in carriers of the MJD mutation, before the manifestation of gait disturbance, indicating that it can be an early sign of the disease, which should be monitored in mutation carriers even before motor signs appear. Recently a higher rate of horizontal gaze-evoked nystagmus in MJD carriers than non-carriers (ten [39%] of 26 vs one [5%] of 20; p = 0 · 013) has been described . From ataxia clinical scales currently being applied, the complementary use of one that includes the evaluation of nystagmus, such as ICARS  or NESSCA  is important, to avoid the under-estimation of this clinical sign and the failure to detect early alterations. In other SCAs, early detection of impaired eye movements in presymptomatic individuals has been a matter of study. Slowing of horizontal saccades was observed in SCA1, 2, 6 and 7 [19, 21–24] whereas a decrease in pursuit gain was found in SCA6 . The present study is based in the qualitative analysis of nystagmus, i.e., presence or absence of this clinical sign; although reasonable information about oculomotor movements might be obtained with such qualitative measure, the use of semi-quantitative techniques such as oculographic evaluations, should improve the characterization of nystagmus types as well as the study of other ocular features, which might help to further understand the importance of eye abnormalities in early stages of MJD.
The presence of nystagmus in asymptomatic MJD carriers suggests that the detection of this sign might be useful in the identification of early stages of MJD, potentially facilitating the enrolment of presymptomatic individuals in future preventive clinical trials.
This work was funded by FEDER funds through the Operational Competitiveness Programme – COMPETE and by National Funds through FCT – Fundação para a Ciência e a Tecnologia under the project FCOMP-01-0124-FEDER-028753 (PTDC/DTP/PIC/0370/2012); and by a PhD fellowship M3.1.2/F/006/2011 (Raposo M) from Fundo Regional para a Ciência (FRC).
- Bettencourt C, Lima M: Machado-Joseph Disease: from first descriptions to new perspectives. Orphanet J Rare Dis. 2011, 6: 35-10.1186/1750-1172-6-35.View ArticlePubMedPubMed CentralGoogle Scholar
- Takiyama Y, Nishizawa M, Tanaka H, Kawashima S, Sakamoto H, Karube Y, Shimazaki H, Soutome M, Endo K, Ohta S: The gene for Machado-Joseph disease maps to human chromosome 14q. Nat Genet. 1993, 4: 300-304. 10.1038/ng0793-300.View ArticlePubMedGoogle Scholar
- Kawaguchi Y, Okamoto T, Taniwaki M, Aizawa M: CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32. 1. Nat Genet. 1994, 8: 221-228. 10.1038/ng1194-221.View ArticlePubMedGoogle Scholar
- Maciel P, Costa MC, Ferro A, Rousseau M, Santos CS, Gaspar C, Barros J, Rouleau GA, Coutinho P, Sequeiros J: Improvement in the molecular diagnosis of Machado-Joseph disease. Arch Neurol. 2001, 58: 1821-1827. 10.1001/archneur.58.11.1821.View ArticlePubMedGoogle Scholar
- Coutinho P, Andrade C: Autosomal dominant system degeneration in Portuguese families of the Azores Islands. A new genetic disorder involving cerebellar, pyramidal, extrapyramidal and spinal cord motor functions. Neurology. 1978, 28: 703-709. 10.1212/WNL.28.7.703.View ArticlePubMedGoogle Scholar
- Lima L, Coutinho P: Clinical criteria for diagnosis of Machado-Joseph disease: report of a non-Azorena Portuguese family. Neurology. 1980, 30: 319-322. 10.1212/WNL.30.3.319.View ArticlePubMedGoogle Scholar
- Coutinho P: Doença de Machado-Joseph: Tentativa de Definição. 1992, Porto: Universidade do Porto, 247-Google Scholar
- Globas C, du Montcel ST, Baliko L, Boesch S, Depondt C, DiDonato S, Durr A, Filla A, Klockgether T, Mariotti C, Melegh B, Rakowicz M, Ribai P, Rola R, Schmitz-Hubsch T, Szymanski S, Timmann D, Van de Warrenburg BP, Bauer P, Schols L: Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6. Mov Disord. 2008, 23: 2232-2238. 10.1002/mds.22288.View ArticlePubMedGoogle Scholar
- Rodríguez-Labrada R, Velázquez-Pérez L: Eye movement abnormalities. Spinocerebellar Ataxias. Edited by: José G. 2012, Croatia: InTech Europe, 59-76.Google Scholar
- Sequeiros J, Coutinho P: Epidemiology and clinical aspects of Machado-Joseph disease. Adv Neurol. 1993, 61: 139-153.PubMedGoogle Scholar
- Vale J, Bugalho P, Silveira I, Sequeiros J, Guimarães J, Coutinho P: Autosomal dominant cerebellar ataxia: frequency analysis and clinical characterization of 45 families from Portugal. Eur J Neurol. 2010, 17: 124-128. 10.1111/j.1468-1331.2009.02757.x.View ArticlePubMedGoogle Scholar
- Jardim LB, Pereira ML, Silveira I, Ferro A, Sequeiros J, Giugliani R: Neurologic findings in Machado-Joseph disease: relation with disease duration, subtypes, and (CAG)n. Arch Neurol. 2001, 58: 899-904. 10.1001/archneur.58.6.899.View ArticlePubMedGoogle Scholar
- Jacobi H, Reetz K, du Montcel ST, Bauer P, Mariotti C, Nanetti L, Rakowicz M, Sulek A, Durr A, Charles P, Filla A, Antenora A, Schöls L, Schicks J, Infante J, Kang J-S, Timmann D, Di Fabio R, Masciullo M, Baliko L, Melegh B, Boesch S, Bürk K, Peltz A, Schulz JB, Dufaure-Garé I, Klockgether T: Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data. Lancet Neurol. 2013, 12: 650-658. 10.1016/S1474-4422(13)70104-2.View ArticlePubMedGoogle Scholar
- Paulsen JS, Hayden M, Stout JC, Langbehn DR, Aylward E, Ross CA, Guttman M, Nance M, Kieburtz K, Oakes D, Shoulson I, Kayson E, Johnson S, Penziner E: Preparing for preventive clinical trials: the Predict-HD study. Arch Neurol. 2006, 63: 883-890. 10.1001/archneur.63.6.883.View ArticlePubMedGoogle Scholar
- Leigh R, Zee D: The Neurology of Eye Movements. 2006, New York: Oxford University Press, 4Google Scholar
- Trouillas P, Takayanagi T, Hallett M, Currier RD, Subramony SH, Wessel K, Bryer A, Diener HC, Massaquoi S, Gomez CM, Coutinho P, Ben Hamida M, Campanella G, Filla A, Schut L, Timann D, Honnorat J, Nighoghossian N, Manyam B: International cooperative ataxia rating scale for pharmacological assessment of the cerebellar syndrome. The ataxia neuropharmacology committee of the world federation of neurology. J Neurol Sci. 1997, 145: 205-211. 10.1016/S0022-510X(96)00231-6.View ArticlePubMedGoogle Scholar
- SPSS (SPSS Inc: PASW Statistics for Windows, Version 18.0. 2009, Chicago: SPSS IncGoogle Scholar
- Rivaud-Pechoux S, Dürr A, Gaymard B, Cancel G, Ploner CJ, Agid Y, Brice A, Pierrot-Deseilligny C: Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type I. Ann Neurol. 1998, 43: 297-302. 10.1002/ana.410430306.View ArticlePubMedGoogle Scholar
- Bürk K, Fetter M, Abele M, Laccone F, Brice A, Dichgans J, Klockgether T: Autosomal dominant cerebellar ataxia type I: oculomotor abnormalities in families with SCA1, SCA2, and SCA3. J Neurol. 1999, 246: 789-797. 10.1007/s004150050456.View ArticlePubMedGoogle Scholar
- Kieling C, Rieder CRM, Silva ACF, Saute JAM, Cecchin CR, Monte TL, Jardim LB: A neurological examination score for the assessment of spinocerebellar ataxia 3 (SCA3). Eur J Neurol. 2008, 15: 371-376. 10.1111/j.1468-1331.2008.02078.x.View ArticlePubMedGoogle Scholar
- Klostermann W, Zühlke C, Heide W, Kömpf D, Wessel K: Slow saccades and other eye movement disorders in spinocerebellar atrophy type 1. J Neurol. 1997, 244: 105-111. 10.1007/s004150050058.View ArticlePubMedGoogle Scholar
- Seifried C, Velázquez-Pérez L, Santos-Falcón N, Abele M, Ziemann U, Almaguer LE, Martínez-Góngora E, Sánchez-Cruz G, Canales N, Pérez-González R, Velázquez-Manresa M, Viebahn B, Stuckrad-Barre S, Klockgether T, Fetter M, Auburger G: Saccade velocity as a surrogate disease marker in spinocerebellar ataxia type 2. Ann N Y Acad Sci. 2005, 1039: 524-527. 10.1196/annals.1325.059.View ArticlePubMedGoogle Scholar
- Christova P, Anderson JH, Gomez CM: Impaired eye movements in presymptomatic spinocerebellar ataxia type 6. Arch Neurol. 2008, 65: 530-536. 10.1001/archneur.65.4.530.View ArticlePubMedGoogle Scholar
- Oh AK, Jacobson KM, Jen JC, Baloh RW: Slowing of voluntary and involuntary saccades: an early sign in spinocerebellar ataxia type 7. Ann Neurol. 2001, 49: 801-804. 10.1002/ana.1059.View ArticlePubMedGoogle Scholar
- Takeichi N, Fukushima K, Sasaki H, Yabe I, Tashiro K, Inuyama Y: Dissociation of smooth pursuit and vestibulo-ocular reflex cancellation in SCA-6. Neurology. 2000, 54: 860-866. 10.1212/WNL.54.4.860.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2377/14/17/prepub
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