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. Author manuscript; available in PMC: 2017 Jan 1.
Published in final edited form as: Mov Disord. 2015 Aug 13;31(1):79–85. doi: 10.1002/mds.26374

Table 1.

Descriptive statistics and GRS regression summaries for PD, SWEDD and healthy controls.

Part A. Descriptive statistics
Subset PD SWEDD Controls
Total in analyses (N) 367 55 165
Age in years (mean, SD) 64.256,
9.598
63.018, 10.117 63.794, 1.588
Females (%) 33.242 34.545 33.333
Family history of PD (%) 25.068 30.909 5.454
N370S carriers (%) 1.912* 1.818 0.606
G2019S carriers (%) 1.3624 0 0
SNCA multiplication (%) 0 1 0
Common variant GRS (mean, SD
in Z units)
0.511, 1.034 0.323, 0.976 0, 1
Common and rare variant GRS
(mean, SD in Z units)
0.596, 1.201 0.347, 1.065 0, 1
Part B. GRS logistic regression
models
Subset Odds ratio
of trend
95%
confidence
interval
P-value of
trend
AUC AUC confidence
interval
PD versus controls, common
variant GRS
1.691 1.372, 2.083 8.39E-07 0.741 0.698-0.784
SWEDD versus controls,
common variant GRS
1.371 0.971, 1.934 0.073 0.696 0.608-0.784
PD and SWEDD versus controls,
common variant GRS
1.617 1.328, 1.969 1.69E-06 0.716 0.674-0.759
PD versus controls, common and
rare variant GRS
1.736 1.413, 2.134 1.59E-07 0.748 0.706-0.791
SWEDD versus controls,
common and rare variant GRS
1.359 0.970, 1.904 0.075 0.694 0.606-0.782
PD and SWEDD versus controls,
common and rare variant GRS
1.701 1.396, 2.074 1.40E-07 0.733 0.691-0.775

Star denotes one missing genotype. Odds ratios and other summary statistics are based on a single standard deviation (Z) change in the GRS distribution from the mean of the healthy controls. Age refers to onset in cases and age at last clinic visit in controls. Family history refers to any first or second degree relatives with PD from self-report.