Key result
Incident TIA shows no association with long-term all-cause dementia risk vs. matched controls.
Why the study?
Does a first incident transient ischemic attack increase the long-term incidence of all-cause dementia in adults >60 years?
Cohort (n=1,782)
Does a first incident transient ischemic attack increase the long-term incidence of all-cause dementia in adults >60 years?
Answers are grounded in this paper and cite their sources.
Incident TIA in older adults is not associated with an increased long-term risk of dementia, potentially because the event prompts behavioral and medical modifications that lower cardiovascular risk.
Background The association between transient ischemic attack (TIA) and dementia is incompletely characterized. Determining the cognitive sequalae of TIA is important as it can function as an early warning sign or additional risk factor for dementia. We sought to determine the long‐term incidence of post‐TIA dementia and examined whether TIA prompts changes in vascular risk factors. Methods Nested matched longitudinal cohort study within the community‐based Framingham Heart Study. A prospectively collected sample of participants without dementia or transient ischemic attack were matched on age and sex (5:1) to participants with first incident TIA >60 years. The primary outcome of interest was the 20‐year incidence of all‐cause dementia. Results The study matched 297 participants with TIA, 141 (47%) men, mean age 72.7±7.7 years, with 1485 controls without TIA. People with TIA were more likely to have hypertension, coronary heart disease, and atrial fibrillation. Over a median of 8.9 years of follow up, 57 (19%) participants with TIA and 353 (24%) controls without TIA developed dementia (hazard ratio [HR], 0.93 [95% CI, 0.71–1.24], P =0.63). Adjusting for stroke and accounting for the competing risk of death did not alter this association. Participants with TIA were more likely to have a reduction in the frequency of smoking (18% to 11%, P =0.025), an increase in anticoagulant use from 3% to 18%, ( P =0.0005), and a marginal increase in aspirin use (46% to 61%, P =0.052). Conclusions We found no significant difference in dementia incidence over a 20‐year follow‐up period compared with matched TIA‐free controls. Our findings suggest that TIA prompts treatment changes and behavioral shifts that lower cardiovascular risk. Whether these are sufficient to mitigate subsequent dementia risk remains to be tested in prospective randomized studies.
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Lioutas et al. (2025) conducted a cohort in Transient ischemic attack (n=1,782). Transient ischemic attack vs. Matched controls without TIA was evaluated on 20-year incidence of all-cause dementia (HR 0.93, 95% CI 0.71-1.24, p=0.63). Incident transient ischemic attack was not associated with a significantly different risk of all-cause dementia compared with matched TIA-free controls (HR 0.93; 95% CI 0.71-1.24; P=0.63).
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