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达格列净治疗心力衰竭与体重指数的相关性:DELIVER 试验。

Dapagliflozin for heart failure according to body mass index: the DELIVER trial.

机构信息

British Heart Foundation Cardiovascular Research Centre, University of Glasgow, 126 University Place, Glasgow G12 8TA, UK.

Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

出版信息

Eur Heart J. 2022 Nov 1;43(41):4406-4417. doi: 10.1093/eurheartj/ehac481.

Abstract

AIMS

Obesity is common and associated with unique phenotypic features in heart failure with preserved ejection fraction (HFpEF). Therefore, understanding the efficacy and safety of new therapies in HFpEF patients with obesity is important. The effects of dapagliflozin were examined according to body mass index (BMI) among patients in the Dapagliflozin Evaluation to Improve the LIVEs of Patients With PReserved Ejection Fraction Heart Failure trial.

METHODS AND RESULTS

Body mass index was analysed by World Health Organization (WHO) categories and as a continuous variable using restricted cubic splines. Body mass index ranged from 15.2 to 50 kg/m2 with a mean value of 29.8 (standard deviation ± 6.1) kg/m2. The proportions, by WHO category, were: normal weight 1343 (21.5%); overweight 2073 (33.1%); Class I obesity 1574 (25.2%); Class II obesity 798 (12.8%); and Class III obesity 415 (6.6%). Compared with placebo, dapagliflozin reduced the risk of the primary outcome to a similar extent across these categories: hazard ratio (95% confidence interval): 0.89 (0.69-1.15), 0.87 (0.70-1.08), 0.74 (0.58-0.93), 0.78 (0.57-1.08), and 0.72 (0.47-1.08), respectively (P-interaction = 0.82). The placebo-corrected change in Kansas City Cardiomyopathy Questionnaire total symptom score with dapagliflozin at 8 months was: 0.9 (-1.1, 2.8), 2.5 (0.8, 4.1), 1.9 (-0.1, 3.8), 2.7 (-0.5, 5.8), and 8.6 (4.0, 13.2) points, respectively (P-interaction = 0.03). The placebo-corrected change in weight at 12 months was: -0.88 (-1.28, -0.47), -0.65 (-1.04, -0.26), -1.42 (-1.89, -0.94), -1.17 (-1.94, -0.40), and -2.50 (-4.4, -0.64) kg (P-interaction = 0.002).

CONCLUSIONS

Obesity is common in patients with HFpEF and is associated with higher rates of heart failure hospitalization and worse health status. Treatment with dapagliflozin improves cardiovascular outcomes across the spectrum of BMI, leads to greater symptom improvement in patients with obesity, compared with those without, and has the additional benefit of causing modest weight loss.

摘要

目的

肥胖在射血分数保留型心力衰竭(HFpEF)患者中较为常见,并伴有独特的表型特征。因此,了解新疗法在肥胖 HFpEF 患者中的疗效和安全性非常重要。在 Dapagliflozin Evaluation to Improve the LIVEs of Patients With PReserved Ejection Fraction Heart Failure 试验中,根据患者的体重指数(BMI)来评估 dapagliflozin 的疗效。

方法和结果

采用世界卫生组织(WHO)类别和限制性立方样条对 BMI 进行分析。BMI 范围为 15.2 至 50kg/m2,平均值为 29.8(标准差±6.1)kg/m2。按照 WHO 类别,患者的比例为:正常体重 1343 例(21.5%);超重 2073 例(33.1%);I 类肥胖 1574 例(25.2%);II 类肥胖 798 例(12.8%);III 类肥胖 415 例(6.6%)。与安慰剂相比,dapagliflozin 降低了主要终点的风险,其效果在这些类别中大致相似:风险比(95%置信区间):0.89(0.69-1.15)、0.87(0.70-1.08)、0.74(0.58-0.93)、0.78(0.57-1.08)和 0.72(0.47-1.08)(P 交互作用=0.82)。dapagliflozin 治疗 8 个月后,堪萨斯城心肌病问卷总症状评分的安慰剂校正变化为:0.9(-1.1,2.8)、2.5(0.8,4.1)、1.9(-0.1,3.8)、2.7(-0.5,5.8)和 8.6(4.0,13.2)分(P 交互作用=0.03)。治疗 12 个月后,安慰剂校正的体重变化为:-0.88(-1.28,-0.47)、-0.65(-1.04,-0.26)、-1.42(-1.89,-0.94)、-1.17(-1.94,-0.40)和-2.50(-4.4,-0.64)kg(P 交互作用=0.002)。

结论

肥胖在 HFpEF 患者中较为常见,与心力衰竭住院率较高和健康状况较差有关。dapagliflozin 治疗可改善 BMI 谱内的心血管结局,与无肥胖的患者相比,肥胖患者的症状改善更大,并且还具有适度减轻体重的额外益处。

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