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. 2014 May 22;16:31–38. doi: 10.1007/8904_2014_315

Table 1.

Demographics, clinical features, and medication use in GBA-PD and IPD

GBA-PD (n = 34) IPD (n = 60) p value
Women, n (%) 17 (50.0) 28 (46.7) 0.76
Age of onset, years 57.5 (48, 65) 59 (51, 66) 0.44
Time to first evaluation, years 2.4 (1.0, 5.7) 2.0 (1.4, 5.0) 0.90
Duration of disease, years 9.3 (5.9, 15.1) 8.4 (7.0, 12.5) 0.99
Duration of clinical follow-up, years 5.1 (3.1, 9.2) 5.4 (3.0, 8.5) 0.83
Education, n (%) 0.28
High School 4 (11.8) 2 (1.8)
Undergraduate 13 (38.2) 27 (48.2)
Graduate 17 (50.0) 27 (48.2) (n = 56)
UPDRS III at last visit 20.5 (15, 30) 16 (13, 26.5) (n = 52) 0.26
Levodopa equivalents at last visit, mg 715.8 (400, 1,000) 598.5 (432.5, 887.5) 0.22
Dopamine agonist at last visit, n (%) 12 (35.3) 26 (43.3) 0.29
Mentation consistently >1, n (%) 9 (26.5) 7 (11.7) 0.07
Cholinesterase inhibitor >6 months, n (%) 14 (41.2) 9 (15.0) 0.005
Hallucinations >1, n (%) 17(50.0) 18 (30.0) 0.054
Hallucinations >1 for 6 months, n (%) 9 (26.5) 4 (6.7) 0.01
Antipsychotic >6 months, n (%) 6 (17.7) 7 (11.7) 0.54

Continuous variables are reported as medians with interquartile ranges. GBA-PD Parkinson disease with heterozygous GBA mutations, IPD idiopathic Parkinson disease, UPDRS Unified Parkinson’s Disease Rating Scale