The Metabolic Vulnerability Index A Novel Marker for Mortality Prediction in Heart Failure

被引:8
|
作者
Conners, Katherine M. [1 ]
Shearer, Joseph J. [1 ]
Joo, Jungnam [2 ]
Park, Hoyoung [1 ]
Manemann, Sheila M. [3 ]
Remaley, Alan T. [4 ]
Otvos, James D. [4 ]
Connelly, Margery A. [5 ]
Sampson, Maureen [6 ]
Bielinski, Suzette J. [3 ]
Wolska, Anna [4 ]
Turecamo, Sarah [1 ]
Roger, Veronique L. [1 ,7 ]
机构
[1] Natl Heart Lung & Blood Inst, NIH, Epidemiol & Community Hlth Branch, Heart Dis Phen Lab, Bethesda, MD USA
[2] Natl Heart Lung & Blood Inst, NIH, Off Biostat Res, Bethesda, MD USA
[3] Dept Quantitat Hlth Sci, Div Epidemiol, Mayo Clin, Rochester, MN USA
[4] Natl Heart Lung & Blood Inst, NIH, Translat Vasc Med Branch, Lipoprotein Metab Lab, Bethesda, MD USA
[5] LabCorp, Morrisville, NC USA
[6] NIH, Clin Ctr, Dept Lab Med, Bethesda, MD USA
[7] Natl Heart Lung & Blood Inst, Epidemiol & Community Hlth Branch, Epidemiol & Community Hlth Branch Heart, 31 Ctr Dr, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
heart failure; inflammation; malnutrition; metabolomics; mortality; NMR; MEDICAL-RECORDS-LINKAGE; CARDIOVASCULAR-DISEASE; RISK SCORE; GLYCA; EPIDEMIOLOGY; SURVIVAL; INFLAMMATION; ASSOCIATION; BIOMARKER; HISTORY;
D O I
10.1016/j.jchf.2023.06.013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Inflammation and protein energy malnutrition are associated with heart failure (HF) mortality. The metabolic vulnerability index (MVX) is derived from markers of inflammation and malnutrition and measured by nuclear magnetic resonance spectroscopy. MVX has not been examined in HF. OBJECTIVES The authors sought to examine the prognostic value of MVX in patients with HF. METHODS The authors prospectively assembled a population-based cohort of patients with HF from 2003 to 2012 and measured MVX scores with a nuclear magnetic resonance scan from plasma collected at enrollment. Patients were divided into 4 MVX score groups and followed until March 31, 2021. RESULTS The authors studied 1,382 patients (median age: 78 years; 48% women). The median MVX score was 64.6. Patients with higher MVX were older, more likely to be male, have atrial fibrillation, have higher NYHA functional class, and have HF duration of >18 months. Higher MVX was associated with mortality independent of Meta-analysis Global Group in Chronic Heart Failure score, ejection fraction, and other prognostic biomarkers. Compared to those with the lowest MVX, the HRs for MVX groups 2, 3, and 4 were 1.2 (95% CI: 0.9-1.4), 1.6 (95% CI: 1.3-2.0), and 1.8 (95% CI: 1.4-2.2), respectively (Ptrend < 0.001). Measures of model improvement document the added value of MVX in HF for classifying the risk of death beyond the Meta-analysis Global Group in Chronic Heart Failure score and other biomarkers. CONCLUSIONS In this HF community cohort, MVX was strongly associated with mortality independently of established clinical factors and improved mortality risk classification beyond clinically validated markers. These data underscore the potential of MVX to stratify risk in HF. (J Am Coll Cardiol HF 2024;12:290-300) Published by Elsevier on behalf of the American College of Cardiology Foundation.
引用
收藏
页码:290 / 300
页数:11
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