Key result
Lower circulating n-6 polyunsaturated fatty acid levels on admission were independently associated with an increased risk of all-cause death and worsening heart failure (HR 0.996).
Why the study?
Does lower circulating n-6 PUFA level on admission predict adverse clinical outcomes in patients with acute decompensated heart failure?
Cohort (n=685)
No
Does lower circulating n-6 PUFA level on admission predict adverse clinical outcomes in patients with acute decompensated heart failure?
Hazard Ratio: 0.996 (95% CI 0.993–0.999)
p-value: p=0.027
Lower circulating n-6 PUFA levels on admission are independently associated with worse clinical outcomes in patients with acute decompensated heart failure, suggesting potential utility for risk stratification.
May aid risk stratification in acute decompensated HF; leaves open whether n-6 PUFA supplementation alters outcomes.
BACKGROUND: Circulating polyunsaturated fatty acid (PUFA) levels are associated with clinical outcomes in cardiovascular diseases including coronary artery disease and chronic heart failure (HF). However, their clinical implications in acute decompensated HF (ADHF) remain unclear. The aim of this study was to investigate the clinical roles of circulating PUFAs in patients with ADHF. METHODS: Circulating levels of PUFAs, eicosapentaenoic acid (EPA), docosahexaenoic acid (DHA), arachidonic acid (AA) and dihomo-gamma linoleic acid (DGLA), were measured on admission in 685 consecutive ADHF patients. Adverse events were defined as all-cause death and worsening HF. RESULTS: During a median follow-up period of 560 days, 262 (38.2%) patients had adverse events. Although patients with adverse events had lower n-6 PUFA (AA + DGLA) level than those without, n-3 PUFA (EPA + DHA) level was comparable between the groups. Kaplan-Meier analyses showed that lower n-6 PUFA level on admission was significantly associated with the composite of all-cause death and worsening HF, all-cause death, cardiovascular death and worsening HF (p < 0.001, p = 0.005, p = 0.021, p = 0.019, respectively). In a multivariate Cox model, lower n-6 PUFA level was independently associated with increased risk of adverse events (HR 0.996, 95% CI: 0.993-0.999, p = 0.027). CONCLUSIONS: Lower n-6 but not n-3 PUFA level on admission was significantly related to worse clinical outcomes in ADHF patients. Measurement of circulating n-6 PUFA levels on admission might provide information for identifying high risk ADHF patients.
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Nagai et al. (2016) conducted a cohort in Acute Decompensated Heart Failure (n=685). Circulating n-6 polyunsaturated fatty acids vs. Higher n-6 PUFA levels was evaluated on Composite of all-cause death and worsening heart failure (HR 0.996, 95% CI 0.993-0.999, p=0.027). Lower circulating n-6 polyunsaturated fatty acid levels on admission were independently associated with an increased risk of all-cause death and worsening heart failure (HR 0.996).
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