MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1016/j.jacc.2017.08.057

Медицинская библиотека · Journal of the American College of Cardiology · 2017

The PCSK9-LDL Receptor Axis and Outcomes in Heart Failure: BIOSTAT-CHF Subanalysis.

Bayes-Genis Antoni, Núñez Julio, Zannad Faiez, Ferreira João Pedro, Anker Stefan D, Cleland John G, Dickstein Kenneth, Filippatos Gerasimos, Lang Chim C, Ng Leong L, Ponikowski Piotr, Samani Nilesh J, van Veldhuisen Dirk J, Zwinderman Aeilko H, Metra Marco, Lupón Josep, Voors Adriaan A

СтатьяМногоцентровое исследованиеНаблюдательное исследованиеПеревод в очереди

Аннотация

BACKGROUND

Proprotein convertase subtilisin/kexin type 9 (PCSK9) binds low-density lipoprotein receptor (LDLR), preventing its recycling. PCSK9 is a risk predictor and a biotarget in atherosclerosis progression.

OBJECTIVES

The aim of this study was to determine whether the PCSK9-LDLR axis could predict risk in patients with heart failure (HF).

METHODS

The BIOSTAT-CHF (Biology Study to Tailored Treatment in Chronic Heart Failure) is a multicenter, multinational, prospective, observational study that included patients with worsening HF signs and/or symptoms. The primary endpoints were all-cause mortality and the composite of mortality or unscheduled hospitalizations for HF. We implemented Cox proportional hazard regression to determine the simultaneously adjusted effect of PCSK9 and LDLR on both outcomes when added to the previously validated BIOSTAT-CHF risk scores.

RESULTS

This study included 2,174 patients (mean age: 68 ± 12 years; 53.2% had a history of ischemic heart disease). Median (interquartile range) PCSK9 and LDLR levels were 1.81 U/ml (1.45 to 2.18) and 2.98 U/ml (2.45 to 3.53), respectively. During follow-up, 569 deaths (26.2%) and 896 (41.2%) composite endpoints were ascertained. A multivariable analysis, which included BIOSTAT-CHF risk scores, LDLR, and statin treatment as covariates, revealed a positive linear association between PCSK9 levels and the risk of mortality (hazard ratio [HR]: 1.24; 95% confidence interval [CI]: 1.04 to 1.49; p = 0.020) and the composite endpoint (HR: 1.21; 95% CI: 1.05 to 1.40; p = 0.010). A similar analysis for LDLR revealed a negative association with mortality (HR: 0.86; 95% CI: 0.76 to 0.98; p = 0.025) and the composite endpoint (HR: 0.92; 95% CI: 0.83 to 1.01; p = 0.087). Including PCSK9 and LDLR improved risk score performance.

CONCLUSIONS

The PCSK9-LDLR axis was associated with outcomes in patients with HF. Future studies must assess whether PCSK9 inhibition will result in better outcomes in HF.

Для цитирования: Bayes-Genis Antoni, Núñez Julio, Zannad Faiez, Ferreira João Pedro, Anker Stefan D, Cleland John G, Dickstein Kenneth, Filippatos Gerasimos, Lang Chim C, Ng Leong L, Ponikowski Piotr, Samani Nilesh J, van Veldhuisen Dirk J, Zwinderman Aeilko H, Metra Marco, Lupón Josep, Voors Adriaan A. The PCSK9-LDL Receptor Axis and Outcomes in Heart Failure: BIOSTAT-CHF Subanalysis.. Journal of the American College of Cardiology. 2017. DOI: 10.1016/j.jacc.2017.08.057.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.