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. Author manuscript; available in PMC: 2020 Jan 1.
Published in final edited form as: Alzheimer Dis Assoc Disord. 2019 Jan-Mar;33(1):15–20. doi: 10.1097/WAD.0000000000000284

Table 1.

Table 1a. Sample Characteristics with Comparisons of Depression statusa

Depressive symptoms (n = 54) No depressive symptoms (n = 300)
Age, y (SD) 71.37 (5.40) 72.48 (5.47)
Education, y (SD) 15.00 (2.73) 15.75 (2.80)
MMSE, scoreb(SD) 28.78 (1.53) 28.86 (1.36)
GDS (SD) 3.06 (2.33)* 0.73 (0.96)
Sex, % female 70.4* 50.3
APOE ε4, % positive 31.5 35.3
Table 1b. Sample Characteristics with Comparisons of Preclinical AD status
Preclinical AD statusc Stage 2 or 3 Preclinical AD statusd
Biomarker positive(n = 107) Biomarker negative (n=249) Biomarker positive(n = 47) Biomarker negative (n=309)
Age, y (SD) 74.94 (6.49)* 72.09 (5.49) 75.69 (5.95)* 72.53 (5.84)
Education, y (SD) 15.93 (3.09) 15.47 (2.83) 14.91 (2.68) 15.67 (2.85)
MMSE, scoreb (SD) 28.61 (1.50)* 29.07 (1.19) 28.57 (1.61)* 28.95 (1.28)
GDS (SD) 0.99 (1.23) 0.96 (1.40) 1.04 (1.20) 1.03 (1.49)
Sex, % female 49.5 55.8 51.1 57.0
APOE ε4, % positive 49.5* 27.3 53.2* 31.5
a

Two participants were not included due to missing information.

b

Scored 1–30; 30 is a perfect score.

c

Preclinical AD here represents an abnormal biomarker result from PET-PiB neuroimaging, or CSF assay (using only abnormal Aβ1–42 as a cutoff), or both, in cognitively normal persons.

d

Stage 2 or 3 Preclinical AD represents both abnormal Aβ1–42 and tau levels

*

P < 0.01, compared to the group with no depressive symptoms (table 1a) or no preclinical AD (table 1b)

Abbreviations: MMSE, Mini-Mental Status Exam; APOE ε4, ApolipoproteinE ε4.