There was a 2.1‐fold higher hazard for cognitive impairment in the MBI‐psychosis group relative to the No Psychosis group in APOE ε4 non‐carriers, but this did not reach statistical significance (95% CI: 1–4.4, p = 0.05).
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Late-life onset psychotic symptoms and incident cognitive impairment in people without dementia: Modification by genetic risk for Alzheimer's disease.
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