Division of Cardiology Osaka Rosai Hospital Osaka Japan.
Division of Cardiology Osaka General Medical Center Osaka Japan.
J Am Heart Assoc. 2022 Oct 4;11(19):e026301. doi: 10.1161/JAHA.122.026301. Epub 2022 Sep 21.
Background An association between uric acid (UA) and cardiovascular diseases, including heart failure (HF), has been reported. However, whether UA is a causal risk factor for HF is controversial. In particular, the prognostic value of lowering UA in patients with HF with preserved ejection fraction (HFpEF) is unclear. Methods and Results We enrolled patients with HFpEF from the PURSUIT-HFpEF (Prospective Multicenter Observational Study of Patients With Heart Failure With Preserved Ejection Fraction) registry. We investigated whether UA was correlated with the composite events, including all-cause mortality and HF rehospitalization, in patients with hyperuricemia and HFpEF (UA >7.0 mg/dL). Additionally, we evaluated whether lowering UA for 1 year (≥1.0 mg/dL) in them reduced mortality or HF rehospitalization. We finally analyzed 464 patients with hyperuricemia. In multivariable Cox regression analysis, UA was an independent determinant of composite death and rehospitalization (hazard ratio [HR], 1.15 [95% CI, 1.03-1.27], =0.015). We divided them into groups with severe and mild hyperuricemia according to median estimated value of serum UA (8.3 mg/dL). Cox proportional hazards models revealed the incidence of all-cause mortality was significantly higher in the group with severe hyperuricemia than in the group with mild hyperuricemia (HR, 1.73 [95% CI, 1.19-2.25], =0.004). The incidence of all-cause mortality was significantly decreased in the group with lowering UA compared with the group with nonlowering UA (HR, 1.71 [95% CI, 1.02-2.86], =0.041). The incidence of urate-lowering therapy tended to be higher in the group with lowering UA than in the group with nonlowering UA (34.9% versus 24.6%, =0.06). Conclusions UA is a predictor for the composite of all-cause death and HF rehospitalization in patients with hyperuricemia and HFpEF. In these patients, lowering UA, including the use of urate-lowering therapy, may improve prognosis.
尿酸(UA)与心血管疾病(包括心力衰竭(HF))之间存在关联。然而,UA 是否是 HF 的因果危险因素仍存在争议。特别是,HF 射血分数保留(HFpEF)患者降低 UA 的预后价值尚不清楚。
我们从 PURSUIT-HFpEF(HFpEF 患者前瞻性多中心观察性研究)登记处招募了 HFpEF 患者。我们研究了在高尿酸血症和 HFpEF(UA > 7.0mg/dL)患者中,UA 是否与包括全因死亡率和 HF 再入院在内的复合事件相关。此外,我们评估了在 1 年内(≥1.0mg/dL)降低 UA 是否降低死亡率或 HF 再入院率。我们最终分析了 464 例高尿酸血症患者。多变量 Cox 回归分析显示,UA 是复合死亡和再入院的独立决定因素(危险比 [HR],1.15[95%CI,1.03-1.27],=0.015)。我们根据血清 UA 的中位数估计值将他们分为严重高尿酸血症和轻度高尿酸血症组。Cox 比例风险模型显示,严重高尿酸血症组的全因死亡率显著高于轻度高尿酸血症组(HR,1.73[95%CI,1.19-2.25],=0.004)。与非降低 UA 组相比,降低 UA 组的全因死亡率显著降低(HR,1.71[95%CI,1.02-2.86],=0.041)。与非降低 UA 组相比,降低 UA 组降尿酸治疗的发生率更高(34.9%比 24.6%,=0.06)。
UA 是高尿酸血症和 HFpEF 患者全因死亡和 HF 再住院复合事件的预测因子。在这些患者中,降低 UA,包括使用降尿酸治疗,可能改善预后。