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在非糖尿病心力衰竭患者中,较低的低密度脂蛋白胆固醇与较高的死亡率相关。

Lower low density lipoprotein cholesterol associates to higher mortality in non-diabetic heart failure patients.

作者信息

Gouveia R, Madureira S, Elias C, Neves A, Soares P Ribeirinho, Soares-Carreira M, Pereira J, Ribeiro A, Amorim M, Almeida J, Araújo J P, Lourenco P

机构信息

Internal Medicine Department, Centro Hospitalar e Universitário de São João, Porto, Portugal.

Heart Failure Clinic, Internal Medicine Department, Centro Hospitalar Universitário de São João, Porto, Portugal.

出版信息

Int J Cardiol Cardiovasc Risk Prev. 2023 Jul 16;18:200197. doi: 10.1016/j.ijcrp.2023.200197. eCollection 2023 Sep.

DOI:10.1016/j.ijcrp.2023.200197
PMID:37521244
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10374454/
Abstract

BACKGROUND

In patients with established heart failure (HF) low total cholesterol levels associate with worse prognosis. Evidence concerning the impact of Low-density lipoprotein cholesterol (LDL-c) in HF is scarce. We aimed to evaluate the prognostic impact of LDL-c in patients with HF, both with and without diabetes (DM).

METHODS

We retrospectively analyzed outpatients with chronic HF with systolic dysfunction followed in our HF clinic from January/2012 to May/2018. LDL-c was calculated using the Friedewald's formula. Patients without a complete lipid profile were excluded. The endpoint under analysis was all-cause mortality. Patients were followed until January/2021. A Cox-regression analysis was used to study the prognostic impact of LDL-c. The LDL-c cut-off used was 100 mg/dL (mean value). Analysis was stratified according to the coexistence of DM. Multivariate models were built adjusting for age, sex, coronary artery disease, atherosclerotic non-coronary artery disease, arterial hypertension, smoking status, statin use, severity of systolic dysfunction, creatinine clearance and evidence-based therapy.

RESULTS

We studied 522 chronic HF patients, mean age was 70 years, 66.5% males. Severe systolic dysfunction was present in 42.7%, 30.5% had coronary heart disease, 60.5% had arterial hypertension, 41.6% had DM. A total of 92.0% were treated with beta blocker, 87.5% with an ACEi/ARB and 29.1% with a MRA. During a median follow-up of 53 (interquartile range 33-73) months, 235 (45%) patients died. Patients with LDL-c ≤100 mg/dL presented increased multivariate-adjusted risk of all-cause mortality: HR = 1.58 (95% CI: 1.08-2.30), p = 0.02. When patients were stratified according to DM, LDL-c ≤100 mg/dL was independently associated with increased death risk - HR = 1.55 (95% CI:1.05-2.30), p = 0.03 in patients without DM; in patients with DM no association was detected - multivariate-adjusted HR = 1.18 (95% CI: 0.77-1.80), p = 0.44.

CONCLUSION

Non-DM HF patients with LDL-c>100 mg/dL have a 35% reduction in the mortality risk when compared with those with lower values. The "cholesterol paradox" in HF also applies to LDL-c in non-DM patients.

摘要

背景

在已确诊的心力衰竭(HF)患者中,总胆固醇水平较低与预后较差相关。关于低密度脂蛋白胆固醇(LDL-c)对HF影响的证据很少。我们旨在评估LDL-c在有和没有糖尿病(DM)的HF患者中的预后影响。

方法

我们回顾性分析了2012年1月至2018年5月在我们的HF诊所随访的慢性HF合并收缩功能障碍的门诊患者。使用Friedewald公式计算LDL-c。排除没有完整血脂谱的患者。分析的终点是全因死亡率。对患者随访至2021年1月。使用Cox回归分析研究LDL-c的预后影响。使用的LDL-c临界值为100mg/dL(平均值)。根据DM的共存情况进行分层分析。建立多变量模型,对年龄、性别、冠状动脉疾病、非冠状动脉粥样硬化疾病、动脉高血压、吸烟状况、他汀类药物使用、收缩功能障碍的严重程度、肌酐清除率和循证治疗进行调整。

结果

我们研究了522例慢性HF患者,平均年龄70岁,男性占66.5%。42.7%存在严重收缩功能障碍,30.5%患有冠心病,60.5%患有动脉高血压,41.6%患有DM。共有92.0%的患者接受了β受体阻滞剂治疗,87.5%接受了ACEi/ARB治疗,29.1%接受了MRA治疗。在中位随访53(四分位间距33 - 73)个月期间,235例(45%)患者死亡。LDL-c≤100mg/dL的患者全因死亡率的多变量调整风险增加:HR = 1.58(95%CI:1.08 - 2.30),p = 0.02。当根据DM对患者进行分层时,LDL-c≤100mg/dL与死亡风险增加独立相关 - 在无DM的患者中HR = 1.55(95%CI:1.05 - 2.30),p = 0.03;在有DM的患者中未检测到相关性 - 多变量调整HR = 1.18(95%CI:0.77 - 1.80),p = 0.44。

结论

与LDL-c值较低的非DM HF患者相比,LDL-c>100mg/dL的患者死亡风险降低35%。HF中的“胆固醇悖论”也适用于非DM患者的LDL-c。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c83/10374454/8e4e800a73f4/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c83/10374454/3686515072d5/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c83/10374454/8e4e800a73f4/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c83/10374454/3686515072d5/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c83/10374454/8e4e800a73f4/gr2.jpg

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