Association between ischemic stroke and seropositive rheumatoid arthritis in Korea: A nationwide longitudinal cohort study

• Published in: PloS one 2021-05, Vol.16 (5), p.e0251851-e0251851
• Main Authors: Lee, Dong Hyun, Sheen, Seung Hun, Lee, Dong-Geun, Jang, Jae-Won, Lee, Dong Chan, Shin, Seung-Ho, Han, In-Bo, Hong, Je Beom, Kim, Hakyung, Sohn, Seil
• Format: Article
• Language: English
• Subjects: Age; Arthritis; Biology and Life Sciences; Codes; Cohort analysis; Comorbidity; Complications and side effects; Computer programs; Data acquisition; Diabetes; Drafting software; Editing; Funding; Genomes; Gloss; Graduate schools; Graduate studies; Health care facilities; Health insurance; Health risks; Hospitals; Hypertension; Inflammatory diseases; Ischemia; Medical prognosis; Medical screening; Medicine and Health Sciences; Metabolic disorders; Methodology; Mortality; Neurosurgery; Patients; People and Places; Public health; Rheumatoid arthritis; Risk factors; Software; Spine; Stroke; Stroke (Disease); Visualization
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0251851

The purpose of this longitudinal follow-up study was to investigate the risk of ischemic stroke nationwide in patients with seropositive rheumatoid arthritis (RA) and controls who were matched in age and sex. Patient data were collected from the National Health Insurance Service (NHIS) Health Screening (HEALS) cohort. Using the International Classification of Diseases code M05 (seropositive RA), with a prescription of any disease-modifying anti-rheumatic drug (DMARD), RA was identified. A total of 2,765 patients and 13,825 control subjects were included in our study. The 12-year incidence of ischemic stroke in each group was calculated using the Kaplan-Meier method. The risk ratio of ischemic stroke was estimated using Cox proportional hazards regression. Sixty-four patients (2.31%) in the seropositive RA group and 512 (3.70%) in the control group experienced ischemic stroke (P < 0.001) during the follow-up period. The hazard ratio of ischemic stroke in the seropositive RA group was 1.32 (95% confidence interval (CI), 1.02-1.73) after adjusting for age and sex. The adjusted hazard ratio of ischemic stroke in the seropositive RA group was 1.40 (95% CI, 1.07-1.82) after adjusting for demographics and comorbid medical disorders. According to the subgroup analysis, the hazard ratios of ischemic stroke risks in the female and hypertensive subgroups were 1.44 (95% CI, 1.05-1.97) and 1.66 (95% CI, 1.16-2.38), respectively. In the non-diabetes and non-dyslipidemia subgroups, the corresponding hazard ratios of ischemic stroke were 1.47 (95% CI, 1.11-1.95) and 1.43 (95% CI, 1.07-1.91). Seropositive RA patients have an increased risk of ischemic stroke. In female, hypertension, non-diabetes, and non-dyslipidemia RA subgroups, even without the traditional risk factors for stroke (except for hypertension), increased the risk, which could be potentially attributed to RA.