| Cognitive performance of treatment group as compared to control group (estimated mean difference)c |
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Total study population (n = 1685) | Matched sample 1:1 (n = 478)d |
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Model 1e | Model 2f | Model 3g | Model 4h |
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Mean | 95%CI | P value | Mean | 95%CI | P value | Mean | 95%CI | P value | Mean | 95% CI | P value |
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First measurement | −0.35 | − 0.46 to − 0.24 | < 0.001 | 0.03 | −0.10 to 0.16 | 0.68 | −0.05 | − 0.20 to 0.10 | 0.53 | − 0.05 | −0.17 to 0.08 | 0.49 |
Second measurement | −0.45 | −0.56 to − 0.34 | < 0.001 | −0.07 | − 0.21 to − 0.06 | 0.28 | −0.07 | − 0.22 to 0.08 | 0.36 | − 0.07 | −0.20 to 0.06 | 0.28 |
Third measurement | −0.51 | −0.64 to − 0.39 | < 0.001 | −0.14 | − 0.28 to 0.00 | 0.06 | − 0.09 | −0.26 to 0.07 | 0.27 | −0.08 | − 0.23 to 0.07 | 0.29 |
- Abbreviations: 95%CI 95% confidence interval
- a Cognitive performance was measured as a composite score of two tests (z-score): the Ruff Figural Fluency Test (RFFT) and the Visual Association Test (VAT) [20, 22]
- b Treatment group included persons who had pharmacological treatment of vascular risk factors for the first time at the first measurement of cognitive function
- c Estimated mean difference was calculated as mean cognitive performance of treatment group minus control group
- d The sample (N = 478) was matched on the following characteristics: age, gender, educational level and treatable vascular risk
- e Model 1 is unadjusted; − 2*log likelihood: 8851.36
- f Model 2 is adjusted for propensity score for treatment of vascular risk factors; − 2*log likelihood: 8752.82
- g Model 3 is unadjusted; − 2*log likelihood: 2521.53
- h Model 4 is adjusted for age, educational level, interaction age x measurement, treatable vascular risk; − 2*log likelihood: 2319.52