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Multicenter Study
. 2018 Nov 1;75(11):1375-1382.
doi: 10.1001/jamaneurol.2018.1935.

Association Between Midlife Risk Factors and Late-Onset Epilepsy: Results From the Atherosclerosis Risk in Communities Study

Affiliations
Multicenter Study

Association Between Midlife Risk Factors and Late-Onset Epilepsy: Results From the Atherosclerosis Risk in Communities Study

Emily L Johnson et al. JAMA Neurol. .

Abstract

Importance: The incidence of epilepsy is higher in older age than at any other period of life. Stroke, dementia, and hypertension are associated with late-onset epilepsy; however, the role of other vascular and lifestyle factors remains unclear.

Objective: To identify midlife vascular and lifestyle risk factors for late-onset epilepsy.

Design, setting, and participants: The Atherosclerosis Risk in Communities (ARIC) study is a prospective cohort study of 15 792 participants followed up since 1987 to 1989 with in-person visits, telephone calls, and surveillance of hospitalizations (10 974 invited without completing enrollment). The ARIC is a multicenter study with participants selected from 4 US communities. This study included 10 420 black or white participants from ARIC with at least 2 years of Medicare fee-for-service coverage and without missing baseline data. Data were analyzed betweeen April 2017 and May 2018.

Exposures: Demographic, vascular, lifestyle, and other possible epilepsy risk factors measured at baseline (age 45-64 years) were evaluated in multivariable survival models including demographics, vascular risk factors, and lifestyle risk factors.

Main outcomes and measures: Time to development of late-onset epilepsy (2 or more International Classification of Diseases, Ninth Revision codes for epilepsy or seizures starting at 60 years or older in any claim [hospitalization or outpatient Medicare through 2013]), with first code for seizures after at least 2 years without code for seizures.

Results: Of the 10 420 total participants (5878 women [56.4%] and 2794 black participants [26.8%]; median age 55 years at first visit), 596 participants developed late-onset epilepsy (3.33 per 1000 person-years). The incidence was higher in black than in white participants (4.71; 95% CI, 4.12-5.40 vs 2.88; 95% CI, 2.60-3.18 per 1000 person-years). In multivariable analysis, baseline hypertension (hazard ratio [HR], 1.30; 95% CI, 1.09-1.55), diabetes (HR, 1.45; 95% CI, 1.17-1.80), smoking (HR, 1.09; 95% CI, 1.01-1.17), apolipoprotein E ε4 genotype (1 allele HR, 1.22; 95% CI, 1.02-1.45; 2 alleles HR, 1.95; 95% CI, 1.35-2.81), and incident stroke (HR, 3.38; 95% CI, 2.78-4.10) and dementia (HR, 2.56; 95% CI, 2.11-3.12) were associated with an increased risk of late-onset epilepsy, while higher levels of physical activity (HR, 0.90; 95% CI, 0.83-0.98) and moderate alcohol intake (HR, 0.72; 95% CI, 0.57-0.90) were associated with a lower risk. Results were similar after censoring individuals with stroke or dementia.

Conclusions and relevance: Potentially modifiable risk factors in midlife and the APOE ε4 genotype were positively associated with risk of developing late-onset epilepsy. Although stroke and dementia were both associated with late-onset epilepsy, vascular and lifestyle risk factors were significant even in the absence of stroke or dementia.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Krauss is a consultant and investigator for Eisai Laboratory and SK Bios and an investigator for UCB Pharma. No other disclosures are reported.

Figures

Figure 1.
Figure 1.. Identification of Cases of Late-Onset Epilepsy
Definition 1 includes participants with 2 or more International Classification of Diseases, Ninth Revision (ICD-9) codes for seizures, epilepsy, or convulsions, with at least 2 years of Atherosclerosis Risk in Communities (ARIC) hospitalization or Medicare data prior to first seizure-related code, and first seizure at 60 years or older. Definition 2 includes participants with at least 1 epilepsy-related ICD-9 code and at least 1 antiepileptic drug prescription and includes only participants with Medicare Part D information available. CMS indicates Centers for Medicare and Medicaid Services; FFS, fee-for-service, RR, risk ratio.
Figure 2.
Figure 2.. Hazard Ratios (95% CIs) of Midlife Risk Factors for Late-Onset Epilepsy
All covariates and visit 1 age are included in same model, with stroke and dementia as time-varying exposures based on date of stroke or dementia diagnosis. HS indicates high school; MD, Maryland; MS, Mississippi; MN, Minnesota; NC, North Carolina.
Figure 3.
Figure 3.. Hazard Ratios (95% CIs) for Late-Onset Epilepsy by Life’s Simple Seven (LSS) Score
Hazard ratios are adjusted for race/ethnicity, center, sex, age at visit 1, and education level. The LSS score evaluates controlled blood pressure, glucose and cholesterol levels, healthy weight, healthy diet, exercise, and smoking status. The LSS score from 0-14 is calculated from total number of healthy LSS characteristics per Folsom et al (eTable 1 in the Supplement).

Comment in

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