Added prognostic value of left ventricular shape by gated SPECT imaging in patients with suspected coronary artery disease and normal myocardial perfusion.


Journal

Journal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology
ISSN: 1532-6551
Titre abrégé: J Nucl Cardiol
Pays: United States
ID NLM: 9423534

Informations de publication

Date de publication:
08 2019
Historique:
received: 26 07 2017
revised: 29 09 2017
pubmed: 27 10 2017
medline: 21 10 2020
entrez: 27 10 2017
Statut: ppublish

Résumé

Left ventricular (LV) remodeling is associated with adverse cardiovascular events. We evaluated the added prognostic value of LV shape index (SI) assessed by gated single-photon emission tomography (SPECT) in patients without known coronary artery disease (CAD). We studied 674 patients with normal myocardial perfusion and normal LV ejection fraction (EF) on stress gated SPECT imaging. An automated software program was used to calculate end-diastolic and end-systolic LVSI. An LVSI ≤ 0.54 at end-systole was considered normal. Follow-up was 96% complete with a median follow-up of 37 months. During follow-up, 25 events occurred (3.8% cumulative event rate). Event-free survival was lower in patients with abnormal end-systolic LVSI (P < .001). Age (P = .021), diabetes (P = .048), and end-systolic LVSI (P < .001) were independent predictors of events. LVSI added prognostic information increasing the global chi-square of the model including age and diabetes from 15.15 to 25.97 (P < .001). The effect of diabetes on hazard ratio increased with increasing values of end-systolic LVSI. The probability of events at 48 months predicted by Weibull analysis progressively increased with increasing values of end-systolic LVSI and was higher in patients with diabetes as compared to those without. Decision curve analyses indicate that the model including end-systolic LVSI resulted in an increased net benefit between 5% and 30% threshold probability, indicating superior estimation of outcomes at low threshold probability levels. The evaluation of LVSI may identify patients with early-stage LV remodeling and at higher risk of adverse cardiac events, even in the presence of normal myocardial perfusion.

Sections du résumé

BACKGROUND
Left ventricular (LV) remodeling is associated with adverse cardiovascular events. We evaluated the added prognostic value of LV shape index (SI) assessed by gated single-photon emission tomography (SPECT) in patients without known coronary artery disease (CAD).
METHODS AND RESULTS
We studied 674 patients with normal myocardial perfusion and normal LV ejection fraction (EF) on stress gated SPECT imaging. An automated software program was used to calculate end-diastolic and end-systolic LVSI. An LVSI ≤ 0.54 at end-systole was considered normal. Follow-up was 96% complete with a median follow-up of 37 months. During follow-up, 25 events occurred (3.8% cumulative event rate). Event-free survival was lower in patients with abnormal end-systolic LVSI (P < .001). Age (P = .021), diabetes (P = .048), and end-systolic LVSI (P < .001) were independent predictors of events. LVSI added prognostic information increasing the global chi-square of the model including age and diabetes from 15.15 to 25.97 (P < .001). The effect of diabetes on hazard ratio increased with increasing values of end-systolic LVSI. The probability of events at 48 months predicted by Weibull analysis progressively increased with increasing values of end-systolic LVSI and was higher in patients with diabetes as compared to those without. Decision curve analyses indicate that the model including end-systolic LVSI resulted in an increased net benefit between 5% and 30% threshold probability, indicating superior estimation of outcomes at low threshold probability levels.
CONCLUSIONS
The evaluation of LVSI may identify patients with early-stage LV remodeling and at higher risk of adverse cardiac events, even in the presence of normal myocardial perfusion.

Identifiants

pubmed: 29071670
doi: 10.1007/s12350-017-1090-x
pii: 10.1007/s12350-017-1090-x
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1148-1156

Commentaires et corrections

Type : CommentIn

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Auteurs

Valeria Gaudieri (V)

Institute of Biostructure and Bioimaging, National Council of Research, Naples, Italy.

Carmela Nappi (C)

Department of Advanced Biomedical Sciences, University Federico II, Naples, Italy.

Wanda Acampa (W)

Institute of Biostructure and Bioimaging, National Council of Research, Naples, Italy.
Department of Advanced Biomedical Sciences, University Federico II, Naples, Italy.

Emilia Zampella (E)

Department of Advanced Biomedical Sciences, University Federico II, Naples, Italy.

Roberta Assante (R)

Department of Advanced Biomedical Sciences, University Federico II, Naples, Italy.

Teresa Mannarino (T)

Department of Advanced Biomedical Sciences, University Federico II, Naples, Italy.

Andrea Genova (A)

Department of Advanced Biomedical Sciences, University Federico II, Naples, Italy.

Giovanni De Simini (G)

Department of Advanced Biomedical Sciences, University Federico II, Naples, Italy.

Michele Klain (M)

Department of Advanced Biomedical Sciences, University Federico II, Naples, Italy.

Guido Germano (G)

Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
David Geffen School of Medicine, UCLA, Los Angeles, CA, USA.

Mario Petretta (M)

Department of Translational Medical Sciences, University Federico II, Via Pansini 5, 80131, Naples, Italy.

Alberto Cuocolo (A)

Department of Advanced Biomedical Sciences, University Federico II, Naples, Italy. cuocolo@unina.it.

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