Rotating Frame Relaxation Time Mapping for the Visualization of the Sinoatrial Node Without Contrast Agent
Li, Yi; Casula, Victor; Huhta, Tarja; Mailhiot, Sarah; Tolkkinen, Katja; Karjalainen, Jouni; Liimatainen, Timo (2025-06-29)
Li, Yi
Casula, Victor
Huhta, Tarja
Mailhiot, Sarah
Tolkkinen, Katja
Karjalainen, Jouni
Liimatainen, Timo
John Wiley & Sons
29.06.2025
Y. Li, V. Casula, T. Huhta, et al., “ Rotating Frame Relaxation Time Mapping for the Visualization of the Sinoatrial Node Without Contrast Agent,” NMR in Biomedicine 38, no. 8 (2025): e70083, https://doi.org/10.1002/nbm.70083.
https://creativecommons.org/licenses/by/4.0/
© 2025 The Author(s). NMR in Biomedicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium,provided the original work is properly cited.
https://creativecommons.org/licenses/by/4.0/
© 2025 The Author(s). NMR in Biomedicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium,provided the original work is properly cited.
https://creativecommons.org/licenses/by/4.0/
Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:oulu-202508125287
https://urn.fi/URN:NBN:fi:oulu-202508125287
Tiivistelmä
Abstract
Late gadolinium-enhanced cardiovascular magnetic resonance (LGE-CMR) has been used to visualize the sinoatrial node (SAN) structure. In this study, we aimed to investigate the rotating frame relaxation (RAFF2 and T1ρ) time mapping to characterize the SAN structure in the heart ex vivo without a contrast agent. Ex vivo swine heart tissues were scanned on a 7 T vertical bore preclinical and a 3 T clinical MRI system. The contrast between the SAN and the surrounding atria was assessed using TRAFF2, T1ρ, T1, and T2 relaxation time mappings, as well as magnetization transfer (MT) imaging. Masson's trichrome stained histological sections were prepared to validate the location of the SAN. Relative relaxation time difference (RRTD) and MT contrast (MTC) were calculated for the SAN and remote myocardium areas. Significant differences between the SAN and myocardium were observed in all endogenous MRI contrasts. TRAFF2 and T1ρ showed the highest contrast between the SAN and myocardium, although the differences in contrast among TRAFF2, T1ρ and T2 were not significant at 3 T. Furthermore, SAN sizes determined based on TRAFF2 and T1ρ maps were highly correlated with the corresponding fibrous structures in the histological sections. The 3D reconstruction of 2D TRAFF2 maps revealed the SAN region with increased relaxation time compared to the surrounding myocardium, located lateral to the crista terminalis. This study demonstrates the potential of TRAFF2 and T1ρ for visualizing the SAN in the swine heart without the use of contrast agents. Detection of the SAN location using TRAFF2 and T1ρ relaxation time mapping could offer a non-invasive alternative to LGE-CMR.
Late gadolinium-enhanced cardiovascular magnetic resonance (LGE-CMR) has been used to visualize the sinoatrial node (SAN) structure. In this study, we aimed to investigate the rotating frame relaxation (RAFF2 and T1ρ) time mapping to characterize the SAN structure in the heart ex vivo without a contrast agent. Ex vivo swine heart tissues were scanned on a 7 T vertical bore preclinical and a 3 T clinical MRI system. The contrast between the SAN and the surrounding atria was assessed using TRAFF2, T1ρ, T1, and T2 relaxation time mappings, as well as magnetization transfer (MT) imaging. Masson's trichrome stained histological sections were prepared to validate the location of the SAN. Relative relaxation time difference (RRTD) and MT contrast (MTC) were calculated for the SAN and remote myocardium areas. Significant differences between the SAN and myocardium were observed in all endogenous MRI contrasts. TRAFF2 and T1ρ showed the highest contrast between the SAN and myocardium, although the differences in contrast among TRAFF2, T1ρ and T2 were not significant at 3 T. Furthermore, SAN sizes determined based on TRAFF2 and T1ρ maps were highly correlated with the corresponding fibrous structures in the histological sections. The 3D reconstruction of 2D TRAFF2 maps revealed the SAN region with increased relaxation time compared to the surrounding myocardium, located lateral to the crista terminalis. This study demonstrates the potential of TRAFF2 and T1ρ for visualizing the SAN in the swine heart without the use of contrast agents. Detection of the SAN location using TRAFF2 and T1ρ relaxation time mapping could offer a non-invasive alternative to LGE-CMR.
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