Table 1.
Overview of demographic data, plasma amyloid levels (pg/ml) and methodology of studies included in our meta‐analyses in alphabetic order of first author names
Study | Subjects | m | f | Age | Plasma Aβ42 | Plasma Aβ40 | Aβ42/Aβ40 | Methods | Study design | Data used in meta‐analyses |
---|---|---|---|---|---|---|---|---|---|---|
n | n | n | mean ± SD | mean ± SD | mean ± SD | mean ± SD | ||||
Coppus et al. (2012) | DS 264 | 169 | 95 | 50.6 ± 4.4 | 51 ± 14.8 | 326.4 ± 101.3 | 0.16 ± 0.05 | xMAP technology (Innogenetics) | Longitudinal clinical assessments: plasma samples collected at baseline only |
Groups: DS versus DS.D
|
DS.D 62 | 36 | 26 | 54 ± 5.9 | 50 ± 17.5 | 352.3 ± 103.5 | 0.15 ± 0.06 | Aβ values from baseline | |||
Fortea et al. (2018) | DS 233 | 14.12 ± 3.18 | 343.83 ± 60.95 | Simoa | Cross‐sectional design |
Groups: DS versus DS.D
|
||||
DS.D 49 | 28 | 21 | 54.88*, * | 14.79 ± 3.42 | 384.39 ± 79.87 | |||||
Fortea et al. (2018) | DS 194 | 105 | 89 | 37.05*, * | 14.22 ± 3.12 | 341.52 ± 60.19 | Simoa | Cross‐sectional design |
Groups: DS versus NC
|
|
NC 67 | 20 | 47 | 52.02*, * | 9.41 ± 1.51 | 196.77 ± 26.58 | |||||
Head et al. (2011) | DS 26 | 17 | 9 | 45.1 ± 9.67 | 20.59 ± 8.27 | 275.76 ± 104.63 | 0.09 ± 0.102 | ELISA: BAN50 + BC05/ BA27 | Cross‐sectional design | Groups: DS versus DS.D |
DS.D 52 | 26 | 26 | 53.3 ± 5.05 | 23.78 ± 17.22 | 289.61 ± 98.96 | 0.08 ± 0.072 | ||||
Head et al. (2011) | DS 17 | 9 | 8 | 44.1 ± 5.77 | 32.88 ± 18.57 | 327.71 ± 117.80 | 0.10 ± 0.041 | ELISA: BAN50 + BC05/ BA27 | Cross‐sectional design |
Groups: DS versus NC
|
NC 11 | 5 | 6 | 46.5 ± 6.63 | 19.82 ± 6.72 | 196.97 ± 40.20 | 0.10 ± 0.033 | ||||
Iulita et al. (2016) | DS 21 | 10 | 11 | 34 ± 9.62 | 16.62 ± 7.79 | 228.4 ± 109.065 | ELISA: Multi‐ | Longitudinal | Groups: DS versus DS.D | |
DS.D 10 | 6 | 4 | 52 ± 6.32 | 17.75 ± 7.27 | 258.5 ± 93.29 | spot V‐PLEX Aβ peptide Panel (6E10) | design; plasma samples and clinical data collected at multiple visits |
Aβ values from baseline |
||
NC 31 | 16 | 15 | 38 ± 11.14 | 9.14 ± 5.01 | 90.17 ± 46.77 | |||||
Jones et al. (2009) | DS 39 | 48.8 ± 7.62 | 27.07 ± 11.43 | 121.32 ± 50.71 | ELISA (commercial biosource) | Cross‐sectional design | Groups: DS versus DS.D | |||
DS.D 21 | 54 ± 5.045 | 27.85 ± 16.63 | 125.6 ± 84.14 | |||||||
Matsuoka et al. (2009) | DS 145 | 89** | 59** | 54.2 ± 3.6** | 1,527.03 ± 2,599.10 | 1,246.75 ± 1,662.34 | ELISA: 82E1 + 1C3/ 1A10 | Cross‐sectional design (using data from a longitudinal study on vitamin E) | Groups: DS versus DS.D | |
DS.D 52 | 33 | 19 | 56 ± 3.9 | 1,887.34 ± 2,972.97 | 1,047.62 ± 1,389.61 | |||||
Prasher et al. (2010) | DS 83 | 52 | 31 | 49 ± 10.2 | 33.8 ± 15 | 177.8 ± 67.8 | 0.23 ± 0.23 | ELISA: 6E10 + R165/ R162 | Longitudinal cognitive assessments; plasma samples collected at last visit only |
Groups: DS versus DS.D
|
DS.D 44 | 30 | 14 | 56.8 ± 4.9 | 33.2 ± 15.9 | 179.6 ± 59.7 | 0.21 ± 0.13 | ||||
Schupf et al. (2001) | DS 97 | 51.9 ± 6.6 | 22.4 ± 6.1 | 132.1 ± 44.4 | ELISA: 6E10 + R165/ R162 | Cross‐sectional design | Groups: DS versus DS.D | |||
NC 64 | 51.5 ± 7.1 | 14.2 ± 4.5 | 84.7 ± 19.6 | |||||||
Schupf et al. ( 2010) | DS 164 | 55 | 109 | 50.3 ± 5.2 | 33.4 ± 8.59 | 150.1 ± 53.79 | 0.25 ± 0.13 | ELISA: 6E10 + R165/ R162 | Longitudinal design with DS subjects without AD at baseline; plasma samples collected at multiple visits |
Groups: DS versus DS.D
|
DS.D 61 | 18 | 43 | 53.7 ± 5.4 | 25.8 ± 21.77 | 172.1 ± 52.33 | 0.16 ± 0.08 | Aβ values from follow‐up | |||
Startin et al. (2019) | DS 24 | 17 | 7 | 45.25 ± 10.90 | 25.42 ± 8.46 | 308.93 ± 105.75 | 0.086 ± 0.019 | Simoa | Cross‐sectional design | Groups: DS versus DS.D |
DS.D 7 | 5 | 2 | 52 ± 10.36 | 27.07 ± 8.19 | 363.71 ± 116.14 | 0.076 ± 0.015 | ||||
Startin et al. (2019) | DS 31 | 22 | 9 | 46.77 ± 10.99 | 25.79 ± 8.29 | 321.30 ± 108.69 | 0.083 ± 0.019 | Simoa | Cross‐sectional design | Groups: DS versus NC |
NC 27 | 16 | 11 | 49.26 ± 10.4 | 15.72 ± 7.43 | 148.39 ± 75.75 | 0.110 ± 0.023 |
The studies by Head et al. (2011), Fortea et al. (2018), and Startin et al. (2019) were split into two rows each due to the use of different samples for comparisons of DS versus NC and DS.D versus DS groups. All amyloid values have been converted to pg/ml whenever necessary, using 1 pg/mL = 0.222 pmol/L for Aβ42 and 0.231 pmol/L for Aβ40. Values reported as standard errors (SE) were converted to SD: SD = SE * √n.
Abbreviations: AD = Alzheimer's disease; aDS = DS subjects who are asymptomatic for AD; Down syndrome; DS.D = Down syndrome with dementia; NC = normal controls, pDS = DS subjects who are in the prodromal stage of AD but do not fulfil criteria for AD diagnosis; SD = standard deviation.
Indicates median values;
Values were calculated for a total of 148 subjects, not 145 (3 were subsequently excluded).