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Table 1 Baseline characteristics of the study population (n = 203) based on clinical diagnosis. Values are listed as the mean (± standard deviation) and dichotomous data as n (%)

From: Amyloid-β misfolding as a plasma biomarker indicates risk for future clinical Alzheimer’s disease in individuals with subjective cognitive decline

 

Total population n = 203

Non-converted SCD

SCD to MCI/AD

p value

Characteristics

n = 180 (89%)

n = 23 (11%)

 

Age, year

60 (±9)

67 (±8)

< 0.001

Female

74 (41%)

14 (61%)

0.072

MMSE

28 (±1)

28 (±1)

0.036

APOE ε4 carrier (reported)

61 (34%)

16 (70%)

<  0.001

ε4 homozygotes

51 (84%)

12 (75%)

ε4 heterozygotes

10 (16%)

4 (25%)

Follow-up duration, y

2.7 (±2.1)

Time to progression, y

2.5 (±2.2)

CSF Aβ42, pg/ml

1053 (±246)

800 (±203)

<  0.001

Plasma Aβ40, pg/ml

208 (± 36)

203 (±34)

0.346

Plasma Aβ42, pg/ml

10 (±2)

9 (±2)

0.003

Plasma Aβ42/40 ratio

49 (±7)

44 (±7)

0.002

  1. Abbreviations: MCI mild cognitive impairment, MMSE Mini-Mental State Examination, SCD subjective cognitive decline