Title |
Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2
|
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Published in |
Neurology, May 2018
|
DOI | 10.1212/wnl.0000000000005660 |
Pubmed ID | |
Authors |
Erik Boot, Nancy J. Butcher, Sean Udow, Connie Marras, Kin Y. Mok, Satoshi Kaneko, Matthew J. Barrett, Paolo Prontera, Brian D. Berman, Mario Masellis, Boris Dufournet, Karine Nguyen, Perrine Charles, Eugénie Mutez, Teodor Danaila, Aurélia Jacquette, Olivier Colin, Sophie Drapier, Michel Borg, Ania M. Fiksinski, Elfi Vergaelen, Ann Swillen, Annick Vogels, Annika Plate, Claudia Perandones, Thomas Gasser, Kristien Clerinx, Frédéric Bourdain, Kelly Mills, Nigel M. Williams, Nicholas W. Wood, Jan Booij, Anthony E. Lang, Anne S. Bassett, Nicola Tambasco, Gabriela M Repetto, Rosemarie Fritsch, Barber M Tinselboer, Jacob AS Vorstman, Luis A Pellene, Stephen G Reich, Claudia Schulte, Annet Dekker |
Abstract |
To delineate the natural history, diagnosis, and treatment response of Parkinson disease (PD) in individuals with 22q11.2 deletion syndrome (22q11.2DS), and to determine if these patients differ from those with idiopathic PD. In this international observational study, we characterized the clinical and neuroimaging features of 45 individuals with 22q11.2DS and PD (mean follow-up 7.5 ± 4.1 years). 22q11.2DS PD had a typical male excess (32 male, 71.1%), presentation and progression of hallmark motor symptoms, reduced striatal dopamine transporter binding with molecular imaging, and initial positive response to levodopa (93.3%). Mean age at motor symptom onset was relatively young (39.5 ± 8.5 years); 71.4% of cases had early-onset PD (<45 years). Despite having a similar age at onset, the diagnosis of PD was delayed in patients with a history of antipsychotic treatment compared with antipsychotic-naive patients (median 5 vs 1 year, p = 0.001). Preexisting psychotic disorders (24.5%) and mood or anxiety disorders (31.1%) were common, as were early dystonia (19.4%) and a history of seizures (33.3%). Major clinical characteristics and response to standard treatments appear comparable in 22q11.2DS-associated PD to those in idiopathic PD, although the average age at onset is earlier. Importantly, treatment of preexisting psychotic illness may delay diagnosis of PD in 22q11.DS patients. An index of suspicion and vigilance for complex comorbidity may assist in identifying patients to prioritize for genetic testing. |
X Demographics
Geographical breakdown
Country | Count | As % |
---|---|---|
United States | 3 | 15% |
Canada | 2 | 10% |
Ireland | 1 | 5% |
Netherlands | 1 | 5% |
Chile | 1 | 5% |
Belgium | 1 | 5% |
United Kingdom | 1 | 5% |
Unknown | 10 | 50% |
Demographic breakdown
Type | Count | As % |
---|---|---|
Members of the public | 15 | 75% |
Practitioners (doctors, other healthcare professionals) | 3 | 15% |
Scientists | 2 | 10% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
---|---|---|
Unknown | 95 | 100% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Bachelor | 15 | 16% |
Student > Doctoral Student | 10 | 11% |
Student > Ph. D. Student | 8 | 8% |
Researcher | 8 | 8% |
Student > Master | 7 | 7% |
Other | 19 | 20% |
Unknown | 28 | 29% |
Readers by discipline | Count | As % |
---|---|---|
Medicine and Dentistry | 28 | 29% |
Psychology | 8 | 8% |
Neuroscience | 7 | 7% |
Agricultural and Biological Sciences | 7 | 7% |
Biochemistry, Genetics and Molecular Biology | 4 | 4% |
Other | 10 | 11% |
Unknown | 31 | 33% |