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Table 1 Study group demographics

From: Association of ABI3 and PLCG2 missense variants with disease risk and neuropathology in Lewy body disease and progressive supranuclear palsy

Group

Study population

Total N

Mean age ± SD

Female

N

%

LBD-NP

Low

263

80.84 ± 11.13

128

48.67

Intermediate

287

79.63 ± 10.33

163

56.79

High

423

78.04 ± 7.92

268

63.36

Combined LBD-NP

973

79.27 ± 9.66

559

57.45

PSP

PSP series 1

230

74.8 ± 7.06

105

45.65

PSP series 2

810

75.47 ± 7.45

376

46.42

Combined PSP

1040

75.32 ± 7.37

481

46.25

Controls

 

3351

80.6 ± 7.1

1844

55.03

  1. All LBD-NP and PSP participants had neuropathologic diagnosis. Controls had either clinical or neuropathologic diagnosis. “Combined LBD-NP” refers to the combined group of LBD-NP patients from all sub-categories. The sub-categories of “High”, “Intermediate”, or “Low” refers to the likelihood of diagnosing typical clinical DLB-CL based on the 2017 DLB-CL Consortium neuropathologic criteria [17]. All control and a subset of 230 PSP (series 1) cases were genotyped in our prior study [8]. All LBD-NP and an additional 810 PSP cases (series 2) were genotyped in this study
  2. PSP progressive supranuclear palsy, LBD-NP Lewy body disease, neuropathologic diagnosis