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Impact of Metabolic Syndrome and Its Components on Clinical Severity and Long-Term Prognosis in Patients With Premature Myocardial Infarction

BACKGROUND: The effects of metabolic syndrome (MS) on premature myocardial infarction (PMI) are not clear to date. This study aimed to investigate the impact of MS and its components on clinical severity and long-term prognosis in patients with PMI. METHODS: We enrolled 772 patients aged ≤45 years o...

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Autores principales: Gao, Jing, Wang, Yuan, Yang, Ya-Nan, Wu, Xiao-Yuan, Cui, Yan, Zou, Zhong-He, Cui, Zhuang, Liu, Yin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9279730/
https://www.ncbi.nlm.nih.gov/pubmed/35846283
http://dx.doi.org/10.3389/fendo.2022.920470
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author Gao, Jing
Wang, Yuan
Yang, Ya-Nan
Wu, Xiao-Yuan
Cui, Yan
Zou, Zhong-He
Cui, Zhuang
Liu, Yin
author_facet Gao, Jing
Wang, Yuan
Yang, Ya-Nan
Wu, Xiao-Yuan
Cui, Yan
Zou, Zhong-He
Cui, Zhuang
Liu, Yin
author_sort Gao, Jing
collection PubMed
description BACKGROUND: The effects of metabolic syndrome (MS) on premature myocardial infarction (PMI) are not clear to date. This study aimed to investigate the impact of MS and its components on clinical severity and long-term prognosis in patients with PMI. METHODS: We enrolled 772 patients aged ≤45 years old who were diagnosed with acute myocardial infarction (AMI) at our hospital consecutively between 2015 and 2020. The patients were divided into an MS group and non-MS group. The parameters of clinical severity were compared using regression analysis. Patients were followed for median of 42 months for major adverse cardiovascular events (MACE). RESULTS: Hyperglycemia was associated with multi-vessel disease [odds ratio(OR)=1.700, 95% confidence interval (CI)=1.172-2.464, P=0.005] and Syntax score ≥33 (OR=2.736, 95% CI=1.241-6.032, P=0.013). Increased MACE were observed in the MS group(17.9% vs 10.3%, P=0.004).The Kaplan-Meier curve also showed significant differences (P< 0.001). MS was an independent risk factor for MACE. Of each component of MS, BMI ≥28 kg/m(2) (hazard ratio [HR]=2.022, 95% CI =1.213-3.369, P=0.007] and hyperglycemia (HR=2.904, 95% CI=1.847-4.567, P<0.001) were independent risk factors for MACE. CONCLUSIONS: In patients with PMI, 1) hyperglycemia usually indicates more severe lesions; 2) MS as a whole was an independent risk factor for MACE; 3) BMI ≥28.0 kg/m(2) and hyperglycemia were associated with MACE.
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spelling pubmed-92797302022-07-15 Impact of Metabolic Syndrome and Its Components on Clinical Severity and Long-Term Prognosis in Patients With Premature Myocardial Infarction Gao, Jing Wang, Yuan Yang, Ya-Nan Wu, Xiao-Yuan Cui, Yan Zou, Zhong-He Cui, Zhuang Liu, Yin Front Endocrinol (Lausanne) Endocrinology BACKGROUND: The effects of metabolic syndrome (MS) on premature myocardial infarction (PMI) are not clear to date. This study aimed to investigate the impact of MS and its components on clinical severity and long-term prognosis in patients with PMI. METHODS: We enrolled 772 patients aged ≤45 years old who were diagnosed with acute myocardial infarction (AMI) at our hospital consecutively between 2015 and 2020. The patients were divided into an MS group and non-MS group. The parameters of clinical severity were compared using regression analysis. Patients were followed for median of 42 months for major adverse cardiovascular events (MACE). RESULTS: Hyperglycemia was associated with multi-vessel disease [odds ratio(OR)=1.700, 95% confidence interval (CI)=1.172-2.464, P=0.005] and Syntax score ≥33 (OR=2.736, 95% CI=1.241-6.032, P=0.013). Increased MACE were observed in the MS group(17.9% vs 10.3%, P=0.004).The Kaplan-Meier curve also showed significant differences (P< 0.001). MS was an independent risk factor for MACE. Of each component of MS, BMI ≥28 kg/m(2) (hazard ratio [HR]=2.022, 95% CI =1.213-3.369, P=0.007] and hyperglycemia (HR=2.904, 95% CI=1.847-4.567, P<0.001) were independent risk factors for MACE. CONCLUSIONS: In patients with PMI, 1) hyperglycemia usually indicates more severe lesions; 2) MS as a whole was an independent risk factor for MACE; 3) BMI ≥28.0 kg/m(2) and hyperglycemia were associated with MACE. Frontiers Media S.A. 2022-06-30 /pmc/articles/PMC9279730/ /pubmed/35846283 http://dx.doi.org/10.3389/fendo.2022.920470 Text en Copyright © 2022 Gao, Wang, Yang, Wu, Cui, Zou, Cui and Liu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Gao, Jing
Wang, Yuan
Yang, Ya-Nan
Wu, Xiao-Yuan
Cui, Yan
Zou, Zhong-He
Cui, Zhuang
Liu, Yin
Impact of Metabolic Syndrome and Its Components on Clinical Severity and Long-Term Prognosis in Patients With Premature Myocardial Infarction
title Impact of Metabolic Syndrome and Its Components on Clinical Severity and Long-Term Prognosis in Patients With Premature Myocardial Infarction
title_full Impact of Metabolic Syndrome and Its Components on Clinical Severity and Long-Term Prognosis in Patients With Premature Myocardial Infarction
title_fullStr Impact of Metabolic Syndrome and Its Components on Clinical Severity and Long-Term Prognosis in Patients With Premature Myocardial Infarction
title_full_unstemmed Impact of Metabolic Syndrome and Its Components on Clinical Severity and Long-Term Prognosis in Patients With Premature Myocardial Infarction
title_short Impact of Metabolic Syndrome and Its Components on Clinical Severity and Long-Term Prognosis in Patients With Premature Myocardial Infarction
title_sort impact of metabolic syndrome and its components on clinical severity and long-term prognosis in patients with premature myocardial infarction
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9279730/
https://www.ncbi.nlm.nih.gov/pubmed/35846283
http://dx.doi.org/10.3389/fendo.2022.920470
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