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. 2017 Feb 7;9:18. doi: 10.3389/fnagi.2017.00018

Table 2.

Subgroup analysis for studies included in the analysis.

Subgroup analysis Pooled OR (95% CI), P-value for the heterogeneity Q test, I2 statistics (%), number of estimates in included studies (n)
n Risk estimates of cognitive impairment and dementia
Mean age
≥65 years 12 0.80 (0.71–0.91); I2 = 54.7, P = 0.012
< years 3 0.79 (0.51–1.21); I2 = 70.8, P = 0.032
Sex
Female 4 0.82 (0.64–1.06); I2 = 71.9, P = 0.014
Male 2 1.18 (0.85–1.63); I2 = 0.0, P = 0.571
Combined 9 0.71 (0.66–0.78); I2 = 0.0, P = 0.567
Geographic location
Europe 7 0.84 (0.70–0.99); I2 = 60.8, P = 0.018
United States 2 0.78 (0.58–1.04); I2 = 21.9, P = 0.258
China 6 0.71 (0.64–0.78); I2 = 38.0, P = 0.153
Study design
Cohort 9 0.80 (0.69–0.92); I2 = 67.5, P = 0.002
Cross-sectional 6 0.80 (0.67–0.95); I2 = 23.5, P = 0.257
Study quality scorea
Full marks 7 0.91 (0.81–1.02); I2 = 28.1, P = 0.214
Not full marks 8 0.71 (0.65–0.77); I2 = 40.9, P = 0.106
Disease type
Cognitive impairment 10 0.82 (0.72–0.93); I2 = 57.8, P = 0.011
Dementia 5 0.73 (0.54–0.83); I2 = 56.9, P = 0.054
Dietary assessment method
FFQ 3 0.79 (0.65–0.96); I2 = 30.2, P = 0.239
Others 12 0.79 (0.69–0.91); I2 = 61.2, P = 0.003

OR, odds ratio; CI, confidence interval; FFQ, food frequency questionnaire.

aFull mark was defined as nine points for cohort studies and five points for cross-sectional studies based on the Newcastle–Ottawa Scale.