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Association between symptoms reported in a population questionnaire and future ischemic stroke: the ARIC study
Lloyd E Chambless1, James F Toole, F Javier Nieto
1Department of Biostatistics, School of Public Health, University of North Carolina, Chapel Hill, NC 27514, USA. wchambliss@unc.edu
Neuroepidemiology
|January 24, 2004
Summary
Self-reported stroke symptoms significantly increase the risk of future ischemic stroke. Individuals reporting prior transient ischemic attack/stroke symptoms faced a 2.8-fold higher hazard rate for incident ischemic stroke.
Area of Science:
- Neurology
- Epidemiology
- Cardiovascular Disease Research
Background:
- Early identification of individuals at high risk for ischemic stroke is crucial for preventative strategies.
- The predictive value of self-reported transient ischemic attack (TIA) or stroke symptoms for future stroke events requires further investigation.
Purpose of the Study:
- To assess the association between computer-diagnosed symptoms from a questionnaire and the incidence of first hospitalized ischemic stroke.
- To evaluate the predictive power of self-reported prior TIA/stroke symptoms on future ischemic stroke risk.
Main Methods:
- Analysis of 11,804 participants from the Atherosclerosis Risk in Communities Study with no baseline stroke history.
- Utilized a symptom questionnaire for computer-derived diagnosis and tracked incident ischemic stroke over up to 11 years.
- Statistical adjustments for age, locale, sex, and race were applied.
Main Results:
- Participants reporting prior TIA/stroke symptoms had a 2.8 times higher hazard rate for incident ischemic stroke (95% CI: 1.9-4.1).
- Increased relative risk was observed in younger individuals, women, African-Americans, non-smokers, and those with lower white blood cell counts.
- 265 strokes occurred between 1987-1998 among the study cohort.
Conclusions:
- Self-reported baseline symptoms suggestive of TIA/stroke are a significant predictor of future ischemic stroke.
- The findings highlight specific demographic and clinical factors associated with elevated stroke risk in individuals with prior symptoms.