健康受试者的心肌灌注和氧化代谢:血管舒张应激11c -醋酸PET的性别特异性见解

IF 3.1 3区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Sang-Geon Cho, Hyung Yoon Kim, Ki Seong Park, Jahae Kim, Jang Bae Moon, Nuri Lee, Hyukjin Park, Jae Yeong Cho, Hyun Ju Yoon, Youngkeun Ahn, Joon-Hyung Doh, Eun-Seok Shin, Kye Hun Kim, Ho-Chun Song
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引用次数: 0

摘要

背景:11c -乙酸盐正电子发射断层扫描(PET)可以同时定量心肌血流量(MBF)和氧化代谢;然而,在血管扩张剂压力下,性别特异性的规范性数据仍然没有充分定义。我们的目标是在健康个体中描述这些参数。结果:18名健康个体(9男9女,年龄/性别匹配,中位年龄43岁[范围34-65])超声心动图正常,无潜在心血管疾病,接受了为期一天的静息应激动态11c -醋酸酯PET与腺苷。应激MBF中位数为2.73 (2.24 ~ 3.11)mL/min/g,休息MBF中位数为0.99 (0.82 ~ 1.14)mL/min/g。应激型kmono为0.074 (0.063 ~ 0.082)/min,休息型kmono为0.061 (0.050 ~ 0.068)/min。外心功、心肌总耗氧量(MVO₂)和MEE分别为4.24 (3.75-5.54)× 10 5 mL·mmHg/min、16.5 (14.9-20.9)mL/min和17.7%(14.0-24.2%)。与男性相比,女性的校正休息MBF (1.14 vs. 0.96 mL/min/g, p = 0.032)、应激kmono (0.078 vs. 0.070 /min, p = 0.005)和总MVO₂(17.6 vs. 15.5 mL/min, p = 0.003)显著高于男性。尽管心脏外功相似,但女性的心肌外效率明显较低(15.5%比20.3%,p = 0.009)。MBF与氧化代谢在两性中呈正相关。结论:本研究评估了参考范围,并显示了血管舒张应激11C-acetate PET在心肌灌注和氧化代谢方面的显著性别差异。这些发现为临床实践中评估灌注代谢异常提供了有价值的生理框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Myocardial perfusion and oxidative metabolism in healthy subjects: sex-specific insights from vasodilatory stress <sup>11</sup>C-acetate PET.

Myocardial perfusion and oxidative metabolism in healthy subjects: sex-specific insights from vasodilatory stress <sup>11</sup>C-acetate PET.

Myocardial perfusion and oxidative metabolism in healthy subjects: sex-specific insights from vasodilatory stress <sup>11</sup>C-acetate PET.

Myocardial perfusion and oxidative metabolism in healthy subjects: sex-specific insights from vasodilatory stress 11C-acetate PET.

Background: 11C-acetate positron emission tomography (PET) enables simultaneous quantification of myocardial blood flow (MBF) and oxidative metabolism; however, sex-specific normative data under vasodilator stress remain insufficiently defined. We aimed to characterize these parameters in healthy individuals.

Results: Eighteen healthy individuals (9 males and 9 females, age/sex-matched; median age 43 years [range 34-65]) with normal echocardiography and no underlying cardiovascular disease underwent one-day rest-stress dynamic 11C-acetate PET with adenosine. Median stress MBF was 2.73 (2.24-3.11) mL/min/g and rest MBF 0.99 (0.82-1.14) mL/min/g. Stress kmono was 0.074 (0.063-0.082)/min, and rest kmono was 0.061 (0.050-0.068)/min. External cardiac work, total myocardial oxygen consumption (MVO₂), and MEE were 4.24 (3.75-5.54) × 10⁵ mL·mmHg/min, 16.5 (14.9-20.9) mL/min, and 17.7% (14.0-24.2%), respectively. Compared to males, females exhibited significantly higher corrected rest MBF (1.14 vs. 0.96 mL/min/g, p = 0.032), stress kmono (0.078 vs. 0.070 /min, p = 0.005), and total MVO₂ (17.6 vs. 15.5 mL/min, p = 0.003). Despite similar external cardiac work, myocardial external efficiency was significantly lower in females (15.5% vs. 20.3%, p = 0.009). MBF and oxidative metabolism were positively correlated in both sexes.

Conclusions: This study assesses reference ranges and demonstrates significant sex-based differences in myocardial perfusion and oxidative metabolism using vasodilatory stress 11C-acetate PET. These findings provide a valuable physiological framework for assessing perfusion-metabolism abnormalities in clinical practice.

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来源期刊
EJNMMI Research
EJNMMI Research RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING&nb-
CiteScore
5.90
自引率
3.10%
发文量
72
审稿时长
13 weeks
期刊介绍: EJNMMI Research publishes new basic, translational and clinical research in the field of nuclear medicine and molecular imaging. Regular features include original research articles, rapid communication of preliminary data on innovative research, interesting case reports, editorials, and letters to the editor. Educational articles on basic sciences, fundamental aspects and controversy related to pre-clinical and clinical research or ethical aspects of research are also welcome. Timely reviews provide updates on current applications, issues in imaging research and translational aspects of nuclear medicine and molecular imaging technologies. The main emphasis is placed on the development of targeted imaging with radiopharmaceuticals within the broader context of molecular probes to enhance understanding and characterisation of the complex biological processes underlying disease and to develop, test and guide new treatment modalities, including radionuclide therapy.
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