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射血分数保留的心力衰竭体重变化:TOPCAT 研究结果。

Weight changes in heart failure with preserved ejection fraction: findings from TOPCAT.

机构信息

Centre d'Investigations Cliniques Plurithématique 1433, F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists), Université de Lorraine, Inserm, Inserm U1116, CHRU Nancy - Hopitaux de Brabois, Institut Lorrain du Coeur Et Des Vaisseaux Louis Mathieu, 4 rue du Morvan, 54500, Vandoeuvre les Nancy, France.

Cardiovascular Research and Development Center, Department of Surgery and Physiology, Faculty of Medicine, University of Porto, Porto, Portugal.

出版信息

Clin Res Cardiol. 2022 Apr;111(4):451-459. doi: 10.1007/s00392-021-01962-4. Epub 2021 Nov 10.

Abstract

BACKGROUND

Weight loss has been associated with poor outcomes in patients with heart failure (HF). However, few data are available for patients with heart failure with preserved ejection fraction (HFpEF). The impact of weight gain on outcomes has not been frequently reported either.

AIMS

To study post-randomization weight changes and how these could impact outcomes and the effect of spironolactone in patients with HFpEF enrolled in the TOPCAT-Americas trial (N = 1767).

METHODS

Mixed-effects regressions and time-updated Cox models to assess the factors associated with weight changes and their impact on subsequent outcomes.

RESULTS

Over a median follow-up of 3 years, 824 (47%) patients experienced weight loss ≥ 5% and 390 (22%) experienced weight loss ≥ 10%. Patients experiencing weight loss were older and more frequently women with severe HF symptoms. Spironolactone slightly reduced body weight before 12 months of follow-up: β =  - 0.55 (- 0.82 to - 0.29) kg, without effect on weight afterwards: β = 0.01 (- 0.66 to 0.68) kg; treatment-by-time interaction P = 0.0015. Spironolactone did not increase the odds of weight loss but reduced the odds of weight gain. Weight loss ≥ 5% was associated with a higher risk of cardiovascular and all-cause death irrespective of baseline body mass index: HR = 1.47, 95%CI = 1.07-2.01 and HR = 1.84, 95%CI = 1.46-2.31, respectively. Weight gain was not associated with an increased risk of any outcome.

CONCLUSION

Weight loss ≥ 5% was frequent and independently associated with an increased risk of subsequent mortality. Spironolactone induced only slight body weight reductions early after its introduction and up to a maximum of 8-12 months of follow-up. Association between body weight changes and subsequent death. Legend: HR, hazard ratio from time-updated Cox models. Model adjusted on age, sex, race, NYHA class, systolic blood pressure, diabetes, atrial fibrillation, previous myocardial infarction, previous heart failure hospitalization, estimated glomerular filtration rate, diuretic use, and baseline weight.

摘要

背景

体重减轻与心力衰竭(HF)患者的不良预后相关。然而,关于射血分数保留的心力衰竭(HFpEF)患者的数据很少。体重增加对结局的影响也没有经常报道。

目的

研究随机分组后体重的变化以及这些变化如何影响结局,并研究螺内酯对入选 TOPCAT-Americas 试验(N=1767)的 HFpEF 患者的影响。

方法

混合效应回归和时间更新 Cox 模型评估与体重变化相关的因素及其对随后结局的影响。

结果

在中位数为 3 年的随访期间,824 名(47%)患者经历了体重减轻≥5%,390 名(22%)患者经历了体重减轻≥10%。体重减轻的患者年龄较大,且更常伴有严重 HF 症状。螺内酯在随访前 12 个月内略微减轻体重:β=−0.55(−0.82 至−0.29)kg,但之后体重没有变化:β=0.01(−0.66 至 0.68)kg;治疗与时间的交互作用 P=0.0015。螺内酯并未增加体重减轻的几率,但降低了体重增加的几率。体重减轻≥5%与心血管和全因死亡风险增加相关,无论基线 BMI 如何:HR=1.47,95%CI=1.07-2.01 和 HR=1.84,95%CI=1.46-2.31。体重增加与任何结局的风险增加无关。

结论

体重减轻≥5%很常见,且与随后的死亡风险增加独立相关。螺内酯仅在引入后早期和最多 8-12 个月的随访期内引起轻微的体重减轻。体重变化与随后死亡之间的关联。图例:HR,时间更新 Cox 模型的风险比。模型调整因素为年龄、性别、种族、纽约心脏协会(NYHA)心功能分级、收缩压、糖尿病、心房颤动、既往心肌梗死、既往心力衰竭住院、估计肾小球滤过率、利尿剂使用和基线体重。

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