Association of resting left ventricular global longitudinal strain with myocardial perfusion abnormalities evaluated by 13N‐ammonia positron emission tomography in patients with stable angina pectoris and normal left ventricular ejection fraction

Aims Little is known about whether resting left ventricular global longitudinal strain (GLS) impairment is associated with myocardial perfusion abnormalities evaluated using 13N‐ammonia positron emission tomography (13N‐NH3‐PET)‐myocardial perfusion imaging (MPI). This study aimed to investigate the...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Echocardiography (Mount Kisco, N.Y.) N.Y.), 2022-12, Vol.39 (12), p.1555-1562
Hauptverfasser: Yamabe, Sayuri, Yamada, Akira, Kawada, Yuka, Ueda, Sayano, Hoshino, Naoki, Hoshino, Meiko, Takada, Kayoko, Sakaguchi, Eirin, Ito, Ryuta, Kakuno, Motohiko, Sakakibara, Takashi, Ohshima, Satoru, Sarai, Masayoshi, Izawa, Hideo
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Aims Little is known about whether resting left ventricular global longitudinal strain (GLS) impairment is associated with myocardial perfusion abnormalities evaluated using 13N‐ammonia positron emission tomography (13N‐NH3‐PET)‐myocardial perfusion imaging (MPI). This study aimed to investigate the correlation between resting GLS and myocardial perfusion parameters in patients with a normal left ventricular ejection fraction (LVEF). We evaluated whether resting GLS can predict myocardial perfusion abnormalities in these patients. Methods and Results We selected 157 patients with suspected stable angina pectoris who underwent both ATP‐stress NH3‐PET‐MPI and 2‐dimentional speckle tracing echocardiography. All subjects had a preserved LVEF and no known history of myocardial infarction. Patients were stratified into Group N (normal perfusion; summed stress score [SSS], 0–3; n = 101), Group M (mildly to moderately abnormal perfusion; SSS, 4–11; n = 41), or Group S (severely abnormal perfusion; SSS, 12+; n = 15). GLS was more impaired as myocardial perfusion abnormality severity increased (–17.9 ± 2.9% for Group N, –16.8 ± 3.1% for Group M, and –14.2 ± 3.5% for Group S; p 
ISSN:0742-2822
1540-8175
DOI:10.1111/echo.15487