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Spinocerebellar Ataxia Type 3 Phenotypically Resembling Parkinson Disease in a Black Family FREE

Katrina Gwinn-Hardy, MD; Andrew Singleton, PhD; Padraig O'Suilleabhain, MD; Michael Boss, PhD; David Nicholl, MD; Amanda Adam, BS; Jennifer Hussey, BA; P. Critchley, MD; John Hardy, PhD; Matthew Farrer, PhD
[+] Author Affiliations

From the Department of Pharmacology, Mayo Clinic Jacksonville, Jacksonville, Fla (Drs Gwinn-Hardy, Singleton, Hardy, and Farrer and Mss Adam and Hussey); the Departments of Neurology, University of Texas Southwestern Medical Center at Dallas (Dr O'Suilleabhain), Queen Elizabeth Hospital, Birmingham, England (Dr Nicholl), and the Leicester Royal Infirmary, Leicester, England (Dr Critchley); and Athena Diagnostics Corporation, Worcester, Mass (Dr Boss).


Arch Neurol. 2001;58(2):296-299. doi:10.1001/archneur.58.2.296.
Text Size: A A A
Published online

ABSTRACT

Background  Machado-Joseph disease (MJD), also known as spinocerebellar ataxia type 3 (SCA3), can present with parkinsonism. However, classically, atypical features, including pyramidal and cerebellar signs, peripheral neuropathy, and/or anterior horn cell dysfunction, are also seen. Levodopa responsiveness is unusual in this disorder.

Objective  To determine the cause of apparent parkinsonism suggestive of Parkinson disease (PD) in a large family of African origin.

Methods  We studied a large family in which apparent autosomal dominant parkinsonism suggestive of PD occurs in order to find the causal genetic mutation. Affected and unaffected family members were screened for the presence of a pathogenic expansion at the MJD/SCA3 locus using a polymerase chain reaction polyacrylamide gel electrophoresis–based assay.

Results  Three of the 4 individuals who were examined have a phenotype reminiscent of PD. Specifically, they have at least 2 of the cardinal features, are levodopa responsive, and have no atypical features. All affected family members were shown to possess pathogenic expansions in the MJD/SCA3 gene.

Conclusions  Parkinsonism suggestive of PD due to MJD/SCA3 has not been previously reported, to our knowledge. However, atypical, though also levodopa-responsive, parkinsonism has been previously reported to occur in African American families, suggesting that that this phenotype is associated with African ancestry. In this regard, it is perhaps significant that all the individuals with parkinsonism have relatively low numbers of repeats (normal, 16-34; pathologic, 60-84). In families in which linkage analysis is being performed to determine a locus for autosomal dominant parkinsonism suggestive of PD, evaluation for the MJD/SCA3 mutation is indicated.

Figures in this Article

THERE ARE 3 usual typical phenotypes of Machado-Joseph disease (MJD) (also known as spinocerebellar ataxia type 3 [SCA3]): type 1, which is characterized by pyramidal and extrapyrimidal signs and early age at onset; type 2, which is characterized by cerebellar and pyramidal signs; and type 3, which is characterized by cerebellar signs and anterior horn cell degenerative symptoms.1 A rare, fourth variant, with parkinsonism and peripheral neuropathy, has also been described.2 In all the variants described previously, the parkinsonian features occur in combination with features such as dystonia, ataxia, spasticity, or peripheral neuropathy. The latter findings often predominate and, if seen in an individual with parkinsonism in clinical practice, would rule out the diagnosis of typical Parkinson disease (PD).2,3 We describe a family of sub-Saharan African descent living in Antigua, the United States, and England. Most living affected individuals in the family appear to have parkinsonism suggestive of PD on standard neurological examination, but they demonstrate a segregating SCA3 repeat expansion on molecular analysis.

METHODS

Genomic DNA was isolated from whole blood using genomic DNA purification kits (Wizard). Polymerase chain reaction amplification was performed in a 25-µL reaction containing 25 ng of genomic DNA, 10 pmol of both forward and reverse oligonucleotide custom primers (F 5′-CCAGTGACTACTTTGATTCG-3′, 5′ labeled with Tet; R 5′-TGGCCTTTCACATGGATGTGAA-3′ (Life Technologies, Rockville, Md), 1 × manufacturer's buffer, 1 × Q solution (Qiagen Inc, Valencia, Calif), 200-µmol/L deoxynucleotide trisphosphates (Amersham Pharmacia Biotech Inc, Piscataway, NJ), and 0.2 U of Taq DNA polymerase (Qiagen Inc). Polymerase chain reaction was run on a commercially available machine (Touchdown; Hybaid, Franklin, Mass) using the following conditions: 5 minutes of denaturation at 95°C, followed by 35 cycles at 95°C for 30 seconds, 55°C for 20 seconds, and 72°C for 30 seconds, and then by a final 10-minute incubation at 72°C. Five microliters of each reaction was run on a 2% agarose gel to confirm amplification and to exclude the possibility of pathogenic extensions beyond the ladder size (500 base pairs [bp])used on the automated sequencer. One microliter of the polymerase chain reaction product at a dilution of 1:50 was electrophoresed on a 6% polacrylamide gel using an automated sequencer (ABI377 96XL; Applied Biosystems, Foster City, Calif). Sizing was performed using a 50- to 500-bp tetramethylrhodamine ladder (TAMRA; Applied Biosystems) according to the manufacturer's instructions. Also, to confirm that extensions were uninterrupted repeats, polymerase chain reaction was performed on each case using exactly the same conditions as mentioned earlier but using an unlabeled forward primer. The resulting products were then sequenced with these primers and a reaction kit (BigDye Terminator Ready Reaction Kit; Applied Biosystems) and analyzed using an automated sequencer (ABI377 96XL; Applied Biosystems) according to the manufacturer's instructions.

CLINICAL DESCRIPTIONS

The family tree, along with the number of repeats at the SCA3 locus, is shown in Figure 1. A summary of the clinical characteristics and repeat length is presented in Table 1. The clinical characteristics of those individuals who were examined by one or more of us are presented in detail below.

Place holder to copy figure label and caption

An abbreviated pedigree is shown. The phenotype of living affected individuals is given in Table 1. The phenotype of other individuals is per family report. Historically, the family settled on Monserrat in the Caribbean 2 generations ago, coming from Ireland before that. Earlier emigration information is not known. Squares symbols indicate males, circles females; diagonal lines through symbols, deceased; question mark, unknown phenotype; solid symbols, parkinsonism; half-darkened symbol, foot dystonia; and arrow, the proband. The SCA3 (spinocerebellar ataxia type 3) repeat length is indicated below the symbol for living affected individuals.

Graphic Jump Location
Table Graphic Jump Location Phenotypic and Genotypic Characteristics of Affected Individuals in the Antigua Family
PROBAND (2001, CORIELL CELL REPOSITORIES NO. GM 15904)

A previously well 36-year-old woman noted the insidious onset and gradual progression of motor slowing for 5 years. Her legs "would not keep up with her trunk when walking." Her handwriting became small, and she had muscle tightness but no resting tremor. She had no change in voice or vision and no autonomic complaints. She underwent a trial of baclofen, with minor benefit in the stiffness, although she never had spasticity. She subsequently began taking pramipexole (1 mg 3 times daily), which has resulted in marked improvement, and she has gone from being wheelchair bound to walking freely. Results of magnetic resonance imaging, measurement of serum ceruloplasmin levels, human T-lymphotropic virus 1 and cerebrospinal fluid studies, and electromyography with nerve conduction studies were normal.

On examination in the "on" state, her mental status was normal. She had masked facies, though a normal blink rate. Her speech was normal. Rigidity was prominent in the left upper extremity, and mild but present in the right upper extremity, neck, and both lower extremities. Deep tendon reflexes were normal. She had mild stooped posture and steppage gait. Alternate motion rates were slow, with breakdown of movement in the lower extremities and borderline breakdown in the hands. No tremor was seen.

3002

The 60-year-old father of the proband noted symptoms of resting tremor when he was approximately 30 years old. His sister, who is a nurse, also noted at that time that his walk was slower and that his face was masked, as their father's had been. Since then, he has had gradually progressive slowness in his movements and difficulty with balance. The right-sided tremor continues to occur intermittently when he is at rest, and a resting tremor has also developed in his right foot. There is no postural or activation tremor. He feels stiff all over, especially in his lower extremities. He needs assistance with most activities of daily living. His greatest current difficulty is walking, and he tends to fall forward almost daily. He needs full assistance to ambulate. Carbidopa-levodopa therapy (10/100 3 taken times daily) helped at the time it was initiated, but the dosage has not been changed in many years, and he feels that the medication is not helping as much lately. Nonetheless, he feels that he cannot function without it. His medical history is significant only for controlled hypertension.

His examination was performed in the "on" state. The findings of his mental status examination were normal. His handwriting was slow and deliberate, with mild micrographia. His speech was severely hypophonic. He had occasional drooling. His extraocular movements were saccadic but full. There was marked tremor of his chin on the right side. His motor examination revealed a severe breakdown of movement with rapid alternating movements bilaterally, worse on the right than on the left, in all extremities. He could not tap his right foot voluntarily at all, and he could barely tap his left foot. His strength was normal, as was sensation to light touch, pinprick, and vibration throughout. His deep tendon reflexes were normal throughout, and his toes were down-going bilaterally to plantar reflex testing. Rigidity was moderate in his upper extremities, severe in his lower extremities, and markedly severe in his neck. He needed full assistance to stand from a seated position and to take small, hesitant, deliberate steps. He would have fallen spontaneously if not fully supported. He sat backward, with a large fall onto the furniture, and could not control the impact.

3012

The 65-year-old half-uncle of the proband developed parkinsonism at 57 years of age characterized by a resting tremor of his left upper extremity, mild bradykinesia, and a reduced arm swing. Throughout the course of his illness, his major complaint has been a coarse, predominantly left-sided tremor that affected both upper and lower extremities. He has been receiving levodopa replacement therapy for 7 years, with good effect, but over the last year, he has developed levodopa-related motor fluctuations without dyskinesias. At the time of examination, he was taking 900 mg/d of levodopa (Madopar).

On examination in the "on" state, his mental status was normal. His cranial nerves were normal except for slowed saccades. His eye movements were full. He had moderate masked facies and moderate hypophonia. There was intermittent resting tremor in all 4 extremities, more marked on the left side of his body. His posture was slightly stooped, with absence of a postural response on pull testing. His gait was slightly hesitant, with a reduced arm swing. There was a mild degree of bradykinesia, with no rigidity. Strength, sensation, and deep tendon reflexes were normal.

3018

A 51-year-old woman has had difficulty with back pain and stiffness since her teens. These symptoms have been attributed to scoliosis and have not been formally evaluated or treated. She has noted in the past 10 to 12 months that her left foot involuntarily turns inward, especially first thing in the morning. This is only moderately bothersome to her, and she has not sought the help of a physician.

The findings of her mental status examination were normal. Her cranial nerve examination was significant for saccadic pursuits. Scoliosis was apparent during the gait examination. She had left foot dystonia while in repose, which worsened slightly when she was ambulating. The results of the rest of the neurological examination were normal.

COMMENT

Parkinsonian features have been previously reported as the predominant phenotype of the MJD/SCA3 mutation (MJD type 4), usually accompanied by robust atypical features.2,4 However, 3 of the 4 individuals from the pedigree described herein have a phenotype suggestive of PD. Specifically, they have at least 2 of the cardinal features, are levodopa responsive, and have no atypical features. Although more extensive testing (eg, electromyography with nerve conduction studies) might be revealing, this was done in 1 of the 4 individuals, and the results were normal. Furthermore, we suspect that if these patients walked into the standard neurology practice today, they would be diagnosed as having PD. While there has been no neuropathologic examination to date in this kindred, we would expect it to be unlikely that they would have Lewy body disease.5 To our knowledge, the remarkable combination of symptoms in MJD/SCA3 that were found in our kindred has not been previously documented, although it is of interest that an atypical, though also levodopa-responsive, parkinsonism has been previously reported to occur in African American families.4 Thus, the parkinsonian phenotype encompassing both "typical" (this work) and "atypical" (see reference 5) features may be associated with African ancestry, although this theory clearly will require further investigation in more families of diverse ethnic origin before a secure conclusion can be reached. In this regard, it is perhaps significant that all the individuals with parkinsonism have relatively low numbers of repeats (normal, 16-34; pathologic, 60-84),6,7 although this is likely not the only factor.

These observations are of importance for 3 reasons. First, MJD/SCA3 should particularly be considered in the differential diagnosis of parkinsonism that is suggestive of PD in blacks. Second, our findings may imply the possibility of genetic modifiers, which influence the phenotype of the mutant allele in different racial groups. Finally, these results emphasize that in other studies in which familial parkinsonism is being studied, care should be exercised in identifying individuals in which the mutations is at the MJD/SCA3 locus. In those families in which linkage analysis is being performed to determine a locus for autosomal dominant parkinsonism that is suggestive of PD, evaluation for the MJD/SCA3 mutation is particularly important.

ARTICLE INFORMATION

Accepted for publication September 1, 2000.

This work was supported by grants from the American Parkinson Disease Association Inc, Staten Island, NY (Dr Gwinn-Hardy); and the Udall Parkinson's Disease Research Center of the Johns Hopkins School of Medicine and the US Public Health Service, National Institutes of Health, Bethesda, Md (Drs Gwinn-Hardy and Farrer and Ms Hussey).

Thanks to the members of the family, without whom this work would not be possible. Thanks to Valerie Thomas for help in collecting and preparing the samples and to G. E. M. Thomas, MD, on Antigua for helping us to investigate her patient.

Corresponding author and reprints: Katrina Gwinn-Hardy, MD, Mayo Clinic Jacksonville, 4500 San Pablo Rd, Jacksonville, FL 32224 (e-mail: gwinn.katrina@mayo.edu).

REFERENCES

Romanul  FCFowler  HLRadvany  JFeldman  RGFeingold  M Azorean disease of the nervous system. N Engl J Med.1977;296:1505-1508.
Tuite  PJRogaeva  EASt George-Hyslop  PHLang  AE Dopa-responsive parkinsonism phenotype of Machado-Joseph disease: confirmation of 14q CAG expansion. Ann Neurol.1995;38:684-687.
Rosenberg  RN Joseph disease: an autosomal dominant motor system degeneration. Adv Neurol.1984;41:179-193.
Subramony  SHCurrier  RD Intrafamilial variability in Machado-Joseph disease. Mov Disord.1996;11:741-743.
Sachdev  HSForno  LSKane  CA Joseph disease: a multisystem degenerative disorder of the nervous system. Neurology.1982;32:192-195.
Maciel  PGaspar  CDeStefano  AL  et al Correlation between CAG repeat length and clinical features in Machado-Joseph disease. Am J Hum Genet.1995;57:54-61.
Maruyama  HNakamura  SMatsuyama  Z  et al Molecular features of the CAG repeats and clinical manifestation of Machado-Joseph disease. Hum Mol Genet.1995;4:807-812.

Figures

Place holder to copy figure label and caption

An abbreviated pedigree is shown. The phenotype of living affected individuals is given in Table 1. The phenotype of other individuals is per family report. Historically, the family settled on Monserrat in the Caribbean 2 generations ago, coming from Ireland before that. Earlier emigration information is not known. Squares symbols indicate males, circles females; diagonal lines through symbols, deceased; question mark, unknown phenotype; solid symbols, parkinsonism; half-darkened symbol, foot dystonia; and arrow, the proband. The SCA3 (spinocerebellar ataxia type 3) repeat length is indicated below the symbol for living affected individuals.

Graphic Jump Location

Tables

Table Graphic Jump Location Phenotypic and Genotypic Characteristics of Affected Individuals in the Antigua Family

References

Romanul  FCFowler  HLRadvany  JFeldman  RGFeingold  M Azorean disease of the nervous system. N Engl J Med.1977;296:1505-1508.
Tuite  PJRogaeva  EASt George-Hyslop  PHLang  AE Dopa-responsive parkinsonism phenotype of Machado-Joseph disease: confirmation of 14q CAG expansion. Ann Neurol.1995;38:684-687.
Rosenberg  RN Joseph disease: an autosomal dominant motor system degeneration. Adv Neurol.1984;41:179-193.
Subramony  SHCurrier  RD Intrafamilial variability in Machado-Joseph disease. Mov Disord.1996;11:741-743.
Sachdev  HSForno  LSKane  CA Joseph disease: a multisystem degenerative disorder of the nervous system. Neurology.1982;32:192-195.
Maciel  PGaspar  CDeStefano  AL  et al Correlation between CAG repeat length and clinical features in Machado-Joseph disease. Am J Hum Genet.1995;57:54-61.
Maruyama  HNakamura  SMatsuyama  Z  et al Molecular features of the CAG repeats and clinical manifestation of Machado-Joseph disease. Hum Mol Genet.1995;4:807-812.

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