期刊论文详细信息
The Journal of Nuclear Medicine
Comparison of Exogenous Ketone Administration Versus Dietary Carbohydrate Restriction on Myocardial Glucose Suppression: A Crossover Clinical Trial
article
Senthil Selvaraj1  Kenneth B. Margulies1  Supritha Dugyala2  Erin Schubert2  Ann Tierney3  Zoltan Arany1  Daniel A. Pryma2  Svati H. Shah4  J. Eduardo Rame1  Daniel P. Kelly5  Paco E. Bravo1 
[1] Division of Cardiology, Department of Medicine, Perelman School of Medicine of the University of Pennsylvania;Division of Nuclear Medicine, Department of Radiology, Perelman School of Medicine of the University of Pennsylvania;Department of Biostatistics, Perelman School of Medicine of the University of Pennsylvania;Division of Cardiology, Department of Medicine, Duke Molecular Physiology Institute, Duke University School of Medicine;Department of Cardiology, Thomas Jefferson University
关键词: ketogenic diet;    ketone ester;    FDG;    PET;    myocardial glucose uptake;   
DOI  :  10.2967/jnumed.121.262734
学科分类:医学(综合)
来源: Society of Nuclear Medicine
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【 摘 要 】

The ketogenic diet (KD) is the standard of care to achieve myocardial glucose suppression (MGS) for assessing inflammation using 18F-FDG PET. However, failure to suppress physiologic glucose uptake remains a significant diagnostic barrier. Although extending the duration of KD may be effective, exogenously delivered ketones may provide a convenient, reliable, and same-day alternative. The aims of our study were to determine whether exogenous ketone administration is noninferior to the KD to achieve MGS and whether serum β-hydroxybutyrate (BHB) levels can predict MGS. Methods: KEETO-CROSS (Ketogenic Endogenous versus Exogenous Therapies for myoCaRdial glucOse SuppresSion) is a crossover, noninferiority trial of the KD (endogenous ketosis) versus ketone ester ([KE] exogenous ketosis) drink. Twenty healthy participants were enrolled into 3 arms: weight-based KE drink, 24-h KD, and 72-h KD (n = 18 completed all arms). The primary outcome was achievement of complete MGS on PET (noninferiority margin 5%). The area under receiver-operating-characteristics (AUROC) of endogenous BHB levels (analyzed in a laboratory and by point-of-care device) for predicting MGS was analyzed in 37 scans completed on the KD. Results: The mean age was 30 ± 7 y, 50% were women, and 45% were nonwhite. The median achieved BHB levels (mmol/L) were 3.82 (25th–75th percentile, 2.55–4.97) (KE drink), 0.77 (25th–75th percentile, 0.58–1.02) (25th–75th percentile, 24-h KD), and 1.30 (25th–75th percentile, 0.80–2.24) (72-h KD). The primary outcome was achieved in 44% (KE drink), 78% (24-h KD), and 83% (72-h KD) of participants (noninferiority P = 0.97 and 0.98 for KE vs. 24-h and 72-h KD). Endogenous BHB levels robustly predicted MGS (AUROC, 0.88; 95% CI 0.71, 1.00). A BHB of 0.58 or more correctly classified 92% of scans. A point-of-care device provided comparable predictive value. Conclusion: In healthy volunteers, KE was inferior to KD for achieving MGS. Serum BHB is a highly predictive biomarker for MGS and can be clinically implemented upstream of 18F-FDG PET, with rapid facilitation by point-of-care testing, to reduce false-positive scans.

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