Association of triglyceride levels with adverse cardiovascular events in patients with ST-segment elevation myocardial infarction.

MACE STEMI Triglyceride

Journal

Heliyon
ISSN: 2405-8440
Titre abrégé: Heliyon
Pays: England
ID NLM: 101672560

Informations de publication

Date de publication:
Jun 2023
Historique:
received: 09 05 2023
revised: 13 06 2023
accepted: 13 06 2023
medline: 24 7 2023
pubmed: 24 7 2023
entrez: 24 7 2023
Statut: epublish

Résumé

Although there is an established association between elevated triglyceride (eTG, ≥175 mg/dl) levels and adverse cardiovascular events, some studies have suggested that eTG levels may be linked to neutral or even improved clinical outcomes, particularly among patients with acute myocardial infarction. However, these studies had certain limitations, including small sample sizes, heterogeneous study populations, and inadequate statistical adjustments. To address these limitations, we conducted an analysis of 5347 patients with ST-segment elevation myocardial infarction (STEMI) between March 2003 and December 2020, using a prospective registry-based cohort from two large, regional STEMI centers. We used a triglyceride level of 175 mg/dl as the cutoff point for eTG levels. Of the study participants, 24.5% (n = 1312) had eTG levels. These patients were more likely to be younger, male, and have a higher number of cardiovascular risk factors compared to those with low TG levels. Despite these unfavorable cardiovascular risk profiles, patients with eTG levels had lower unadjusted risks of 1-year major adverse cardiac events (MACE) -a composite of myocardial infarction, stroke, and death- than those with low TG levels (8.8% vs. 11%, p = 0.034). However, after adjusting for certain clinical factors and lipid profile, eTG levels were not associated with a lower 1-year MACE (aHR: 1.10 (0.71-1.70), p = 0.7). In conclusion, a quarter of STEMI patients had eTG levels and these patients had comparable long-term cardiovascular outcomes compared to those with low TG levels after controlling for clinical factors and lipid profile.

Identifiants

pubmed: 37484361
doi: 10.1016/j.heliyon.2023.e17308
pii: S2405-8440(23)04516-4
pmc: PMC10361356
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e17308

Informations de copyright

© 2023 Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Mehmet Yildiz (M)

The Carl and Edyth Lindner Center for Research and Education at The Christ Hospital, Cincinnati, OH, USA.

Michael D Miedema (MD)

Minneapolis Heart Institute Foundation, Minneapolis, MN, USA.

Avinash Murthy (A)

Prairie Heart Institute at St John's Hospital, Springfield, IL, USA.

Timothy D Henry (TD)

The Carl and Edyth Lindner Center for Research and Education at The Christ Hospital, Cincinnati, OH, USA.

Seth Bergstedt (S)

Minneapolis Heart Institute Foundation, Minneapolis, MN, USA.

Brynn K Okeson (BK)

Minneapolis Heart Institute Foundation, Minneapolis, MN, USA.

Christian W Schmidt (CW)

Minneapolis Heart Institute Foundation, Minneapolis, MN, USA.

Lucas Volpenhein (L)

The Carl and Edyth Lindner Center for Research and Education at The Christ Hospital, Cincinnati, OH, USA.

Santiago Garcia (S)

Minneapolis Heart Institute Foundation, Minneapolis, MN, USA.

Scott W Sharkey (SW)

Minneapolis Heart Institute Foundation, Minneapolis, MN, USA.

Frank V Aguirre (FV)

Prairie Heart Institute at St John's Hospital, Springfield, IL, USA.

Classifications MeSH