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American Heart Association

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Final ID: Sa1033

Utility of Splenic Switch-off Evaluated by Myocardial Positron Emission Tomography as a Predictor in Patients with Hemodialysis and Renal Transplantation

Abstract Body (Do not enter title and authors here): Background
Hemodialysis (HD) is a cause of arteriosclerosis, and approximately half of the deaths are due to cardiovascular disease. Myocardial flow reserve (MFR) derived from 13N-ammonia positron emission tomography (NH3-PET) is a prognostic factor for patients with ischemic heart disease. In NH3-PET imaging, the splenic switch-off (SSO) sign, which demonstrates the decrease in splenic 13N-ammonia uptake during adenosine stress, is a hemodynamic indicator of a favorable response to adenosine. This phenomenon is owing to the fact that adenosine receptor stimulation produces coronary artery dilation while producing vasoconstriction in the splenic circulation. Previous study indicated SSO was a predictor of coronary artery event in patients with heart transplantation.
Hypothesis
We hypothesized that patients with HD had arteriosclerosis of the systemic blood vessels, and splenic reactivity to adenosine was reduced. Therefore, the aim of this study was to compare the splenic blood flow assessed by NH3-PET among patients with HD, non-HD and renal transplantation, and examine its prognostic value for major adverse cardiac event (MACE).
Methods
100 patients (HD: 40, non-HD: 50, renal transplantation: 10) who underwent NH3-PET were enrolled. Using NH3-PET projection images, we placed an ROI on the spleen and measured the mean standardized uptake value (SUV). The spleen ratio (SR) was defined as the mean SUV of the spleen at stress divided by that at rest, and compared among the three groups using the Kruskal–Wallis test. The endpoint was the occurrence of MACEs comprising acute coronary syndrome, heart failure hospitalization, and all-cause mortality. SSO was determined by a cutoff obtained using receiver operating characteristic (ROC) analysis for the SR. The patients were divided into two groups according to the presence or absence of SSO, and the frequency of MACE was compared by Kaplan-Meier and log-rank test.
Results
Patients with HD had reduced MFR (1.7±0.6 vs. 2.1±0.6, p=0.0057). The SR was significantly higher in the HD group than the non-HD group (0.92±0.16 vs. 0.78±0.21, p=0.014). The ROC curve analysis of the SR for MACE demonstrated a cutoff value of 0.96. Patients without SSO had higher rate of MACE than with SSO (p=0.0074).
Conclusions
Splenic blood flow reactivity to adenosine in patients with HD was reduced compared to those with non-HD. SSO might be related with the endothelial function of systemic blood vessels and was a prognostic factor for MACE.
  • Yamamoto, Atsushi  ( Tokyo Women's Medical University , Tokyo , Japan )
  • Sakai, Shuji  ( Tokyo Women's Medical University , Tokyo , Japan )
  • Yamaguchi, Junichi  ( TOKYO WOMEN'S MEDICAL UNIVERSITY , Tokyo , Japan )
  • Nagao, Michinobu  ( Tokyo Women's Medical University , Tokyo , Japan )
  • Kikuchi, Haruka  ( Tokyo Women's Medical University , Tokyo , Japan )
  • Imakado, Risa  ( Tokyo Women's Medical University , Tokyo , Japan )
  • Nakao, Risako  ( Tokyo Women's Medical University , Tokyo , Japan )
  • Maekawa, Yui  ( Tokyo Women's Medical University , Tokyo , Japan )
  • Matsuo, Yuka  ( Tokyo Women's Medical University , Tokyo , Japan )
  • Sakai, Akiko  ( Tokyo Women's Medical University , Tokyo , Japan )
  • Momose, Mitsuru  ( Momose Clinic , Tokyo , Japan )
  • Author Disclosures:
    Atsushi Yamamoto: DO NOT have relevant financial relationships | Shuji Sakai: No Answer | Junichi Yamaguchi: DO NOT have relevant financial relationships | Michinobu Nagao: DO NOT have relevant financial relationships | Haruka Kikuchi: No Answer | Risa Imakado: No Answer | Risako Nakao: No Answer | Yui Maekawa: No Answer | Yuka Matsuo: No Answer | Akiko Sakai: DO NOT have relevant financial relationships | Mitsuru Momose: No Answer
Meeting Info:

Scientific Sessions 2025

2025

New Orleans, Louisiana

Session Info:

Imaging Challenges in MR, CT, PET and Echo

Saturday, 11/08/2025 , 02:30PM - 03:30PM

Abstract Poster Board Session

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