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应激期熵相对于标准 PET 心肌灌注成像变量的增量预后价值。

Incremental prognostic value of stress phase entropy over standard PET myocardial perfusion imaging variables.

机构信息

Departments of Medicine (Division of Artificial Intelligence in Medicine), Imaging, and Biomedical Sciences, Cedars-Sinai Medical Center, 8700 Beverly Blvd., Los Angeles, CA, 90048, USA.

Department of Cardiology, Nihon University, Tokyo, Japan.

出版信息

Eur J Nucl Med Mol Imaging. 2023 Oct;50(12):3619-3629. doi: 10.1007/s00259-023-06323-z. Epub 2023 Jul 10.

DOI:10.1007/s00259-023-06323-z
PMID:37428217
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10547643/
Abstract

PURPOSE

Phase analysis can assess left ventricular dyssynchrony. The independent prognostic value of phase variables over positron emission tomography myocardial perfusion imaging (PET-MPI) variables including myocardial flow reserve (MFR) has not been studied. The aim of this study was to explore the prognostic value of phase variables for predicting mortality over standard PET-MPI variables.

METHODS

Consecutive patients who underwent pharmacological stress-rest Rb PET study were enrolled. All PET-MPI variables including phase variables (phase entropy, phase bandwidth, and phase standard deviation) were automatically obtained by QPET software (Cedars-Sinai, Los Angeles, CA). Cox proportional hazard analyses were used to assess associations with all-cause mortality (ACM).

RESULTS

In a total of 3963 patients (median age 71 years; 57% male), 923 patients (23%) died during a median follow-up of 5 years. Annualized mortality rates increased with stress phase entropy, with a 4.6-fold difference between the lowest and highest decile groups of entropy (2.6 vs. 12.0%/year). Abnormal stress phase entropy (optimal cutoff value, 43.8%) stratified ACM risk in patients with normal and impaired MFR (both p < 0.001). Among three phase variables, only stress phase entropy was significantly associated with ACM after the adjustment of standard clinical and PET-MPI variables including MFR and stress-rest change of phase variables, whether modeled as binary variables (adjusted hazard ratio, 1.44 for abnormal entropy [> 43.8%]; 95%CI, 1.18-1.75; p < 0.001) or continuous variables (adjusted hazard ratio, 1.05 per 5% increase; 95%CI, 1.01-1.10; p = 0.030). The addition of stress phase entropy to the standard PET-MPI variables significantly improved the discriminatory power for ACM prediction (p < 0.001), but the other phase variables did not (p > 0.1).

CONCLUSION

Stress phase entropy is independently and incrementally associated with ACM beyond standard PET-MPI variables including MFR. Phase entropy can be obtained automatically and included in clinical reporting of PET-MPI studies to improve patient risk prediction.

摘要

目的

相位分析可评估左心室不同步。相位变量对正电子发射断层扫描心肌灌注成像(PET-MPI)变量(包括心肌血流储备(MFR))的独立预后价值尚未得到研究。本研究的目的是探讨相位变量预测死亡率的预后价值,超过标准的 PET-MPI 变量。

方法

连续入组接受药物应激-静息 Rb PET 研究的患者。所有 PET-MPI 变量,包括相位变量(相位熵、相位带宽和相位标准差),均由 QPET 软件(Cedars-Sinai,洛杉矶,CA)自动获得。Cox 比例风险分析用于评估与全因死亡率(ACM)的相关性。

结果

共 3963 例患者(中位年龄 71 岁;57%为男性),中位随访 5 年期间 923 例(23%)患者死亡。年度死亡率随应激相位熵增加而增加,熵值最低和最高十分位数组之间存在 4.6 倍差异(2.6%与 12.0%/年)。异常应激相位熵(最佳截断值为 43.8%)在 MFR 正常和受损的患者中分层 ACM 风险(均 p<0.001)。在三个相位变量中,仅应激相位熵在调整包括 MFR 和应激-静息相位变量变化在内的标准临床和 PET-MPI 变量后与 ACM 显著相关,无论是作为二分类变量(校正风险比,异常熵[>43.8%]的 1.44;95%CI,1.18-1.75;p<0.001)还是连续变量(校正风险比,每增加 5%的 1.05;95%CI,1.01-1.10;p=0.030)。将应激相位熵添加到标准 PET-MPI 变量中可显著提高 ACM 预测的区分能力(p<0.001),但其他相位变量则不然(p>0.1)。

结论

应激相位熵与包括 MFR 在内的标准 PET-MPI 变量独立且递增相关,与 ACM 相关。相位熵可以自动获得,并包含在 PET-MPI 研究的临床报告中,以提高患者风险预测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ed9/10547643/bbeb19363b3e/259_2023_6323_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ed9/10547643/c1509c0cc19e/259_2023_6323_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ed9/10547643/a2f728b32c06/259_2023_6323_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ed9/10547643/bbeb19363b3e/259_2023_6323_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ed9/10547643/c1509c0cc19e/259_2023_6323_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ed9/10547643/a2f728b32c06/259_2023_6323_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ed9/10547643/bbeb19363b3e/259_2023_6323_Fig3_HTML.jpg

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