Body Composition, Coronary Microvascular Dysfunction, and Future Risk of Cardiovascular Events Including Heart Failure

被引:18
|
作者
Souza, Ana Carolina do A. H. [1 ]
Rosenthal, Michael H. [3 ,4 ]
Moura, Filipe A. [1 ,2 ]
Divakaran, Sanjay [1 ,2 ]
Osborne, Michael T. [5 ,6 ]
Hainer, Jon [1 ,2 ]
Dorbala, Sharmila [1 ,2 ]
Blankstein, Ron [1 ,2 ]
Carli, Marcelo F. Di [1 ,2 ]
Taqueti, Viviany R. [1 ,2 ,7 ]
机构
[1] Brigham & Womens Hosp, Dept Med, Cardiovasc Imaging Program, Boston, MA USA
[2] Brigham & Womens Hosp, Dept Radiol, Cardiovasc Imaging Program, Boston, MA USA
[3] Brigham & Womens Hosp, Dana Farber Canc Inst, Dept Imaging, Boston, MA USA
[4] Brigham & Womens Hosp, Dept Radiol, Boston, MA USA
[5] Massachusetts Gen Hosp, Cardiovasc Imaging Res Ctr, Dept Med, Boston, MA USA
[6] Massachusetts Gen Hosp, Dept Med, Cardiol Div, Boston, MA USA
[7] Brigham & Womens Hosp, Cardiac Stress Lab, 75 Francis St, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
body composition; cardiometabolic disease; coronary microvascular dysfunction; heart failure; ischemia and no obstructive coronary artery disease; lean body mass; obesity; PRESERVED EJECTION FRACTION; SKELETAL-MUSCLE; FLOW RESERVE; EXERCISE INTOLERANCE; OLDER PATIENTS; DISEASE; OBESITY; INFLAMMATION; ANGIOGRAPHY; VALIDATION;
D O I
10.1016/j.jcmg.2023.07.014
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Body mass index (BMI) is a controversial marker of cardiovascular prognosis, especially in women. Coronary microvascular dysfunction (CMD) is prevalent in obese patients and a better discriminator of risk than BMI, but its association with body composition is unknown. OBJECTIVES The authors used a deep learning model for body composition analysis to investigate the relationship between CMD, skeletal muscle (SM), subcutaneous adipose tissue (SAT), and visceral adipose tissue (VAT), and their contribution to adverse outcomes in patients referred for evaluation of coronary artery disease. METHODS Consecutive patients (n = 400) with normal perfusion and preserved left ventricular ejection fraction on cardiac stress positron emission tomography were followed (median, 6.0 years) for major adverse events, including death and hospitalization for myocardial infarction or heart failure. Coronary flow reserve (CFR) was quantified as stress/rest myocardial blood flow from positron emission tomography. SM, SAT, and VAT cross-sectional areas were extracted from abdominal computed tomography at the third lumbar vertebra using a validated automated algorithm. RESULTS Median age was 63, 71% were female, 50% non-White, and 50% obese. Compared with the nonobese, patients with obesity (BMI: 30.0-68.4 kg/m(2)) had higher SAT, VAT, and SM, and lower CFR (all P < 0.001). In adjusted analyses, decreased SM but not increased SAT or VAT was significantly associated with CMD (CFR <2; OR: 1.38; 95% CI: 1.08-1.75 per -10 cm(2)/m(2) SM index; P < 0.01). Both lower CFR and SM, but not higher SAT or VAT, were independently associated with adverse events (HR: 1.83; 95% CI: 1.25-2.68 per -1 U CFR and HR: 1.53; 95% CI: 1.20-1.96 per -10 cm(2)/m(2) SM index, respectively; P < 0.002 for both), especially heart failure hospitalization (HR: 2.36; 95% CI: 1.31-4.24 per -1 U CFR and HR: 1.87; 95% CI: 1.30-2.69 per -10 cm(2)/m(2) SM index; P < 0.004 for both). There was a significant interaction between CFR and SM (adjusted P = 0.026), such that patients with CMD and sarcopenia demonstrated the highest rate of adverse events, especially among young, female, and obese patients (all P < 0.005). CONCLUSIONS In a predominantly female cohort of patients without flow -limiting coronary artery disease, deficient muscularity, not excess adiposity, was independently associated with CMD and future adverse outcomes, especially heart failure. In patients with suspected ischemia and no obstructive coronary artery disease, characterization of lean body mass and coronary microvascular function may help to distinguish obese phenotypes at risk for cardiovascular events. (J Am Coll Cardiol Img 2024;17:179-191) (c) 2024 by the American College of Cardiology Foundation.
引用
收藏
页码:179 / 191
页数:13
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