Key result
High visit-to-visit total cholesterol variability was associated with a significantly increased risk of incident atrial fibrillation (HR 1.15) compared to the lowest variability quartile.
Why the study?
Long-term variability of cardiometabolic risk factors is linked to cardiovascular disease, but the effect of long-term total cholesterol variability on incident AF had not been examined.
Does high visit-to-visit total cholesterol variability increase the risk of incident atrial fibrillation in adults?
Cohort (n=160,165)
Does high visit-to-visit total cholesterol variability increase the risk of incident atrial fibrillation in adults?
High visit-to-visit total cholesterol variability is independently associated with an increased risk of incident atrial fibrillation.
Should not yet change AF risk assessment; leaves open whether cholesterol variability is a modifiable target.
BACKGROUND: Long-term variability of cardiometabolic risk factors have been suggested as the risk factors for cardiovascular disease and mortality. However, the effect of long-term variability of total cholesterol (TC) on incident atrial fibrillation (AF) has not been examined. METHODS AND FINDINGS: We explored whether visit-to-visit TC variability are associated with the risk of incident AF in 160,165 Korean adults, using the population-based Korean National Health Insurance Service-Health Screening Cohort (NHIS-HEALS) database, over a median duration of 8.4 years. TC variability was measured as coefficients of variance (TC-CV), standard deviation (TC-SD), and variability independent of the mean (TC-VIM). Kaplan-Meier analysis demonstrated a decreased disease-free probability in the highest quartile group of TC variability compared to that in the other groups. In the multivariate Cox proportional hazard analysis, the risk of AF increased significantly in the highest quartile group of TC variability. After multivariate adjustment for confounding variables including mean TC levels, the hazard ratio for incident AF was 1.15 (95% confidence interval 1.05-1.25; P = 0.0035) when comparing the highest with the lowest TC variability quartile (TC-CV). These relationships were consistent with TC variability defined using TC-SD or TC-VIM. Subgroup analyses, including age, sex, body mass index, and cardiometabolic disorders, showed similar results. CONCLUSIONS: The present study is the first to demonstrate that high TC variability was associated with an increased risk of AF.
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Roh et al. (2019) conducted a cohort in Atrial fibrillation (n=160,165). High total cholesterol variability (highest quartile) vs. Lowest total cholesterol variability (lowest quartile) was evaluated on Incident atrial fibrillation (HR 1.15, 95% CI 1.05-1.25, p=0.0035). High visit-to-visit total cholesterol variability was associated with a significantly increased risk of incident atrial fibrillation (HR 1.15) compared to the lowest variability quartile.
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