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Article: Triglyceride levels and its association with all-cause mortality and cardiovascular outcomes among patients with heart failure

TitleTriglyceride levels and its association with all-cause mortality and cardiovascular outcomes among patients with heart failure
Authors
Issue Date6-Feb-2025
PublisherSpringer Nature
Citation
Nature Communications, 2025, v. 16, n. 1, p. 1408 How to Cite?
AbstractRemnant cholesterol, identified by triglyceride-rich lipoprotein, is a significant causal risk factor for ischemic heart diseases. The association of triglyceride levels with all-cause and cause-specific outcomes in heart failure (HF) remains unexplored. Using a previously validated territory-wide clinical information registry, all eligible patients diagnosed with HF (N = 127124) from 2000 to 2020 were included. In this population-based cohort (mean age: 71.4 ± 12.2 years, 51.8% male), the association between triglyceride levels and risk of all-cause mortality and cardiovascular disease was a U-shapedḍ curve. High triglyceride levels (≥3.0 mmol/L) were associated with atherosclerotic cardiovascular disease admission or death; conversely, lower triglyceride levels (<1.2 mmol/L) were associated with higher risks of HF readmission or death. The risk of adjusted all-cause mortality reached a nadir between triglyceride levels of 1.2 mmol/L and 3.0 mmol/L. Results were externally validated in BIOSTAT-CHF. Our findings have important implications for defining the role of triglyceride levels in contributing to the diverse outcomes in patients with HF.
Persistent Identifierhttp://hdl.handle.net/10722/368599

 

DC FieldValueLanguage
dc.contributor.authorRen, Qing Wen-
dc.contributor.authorTeng, Tiew Hwa Katherine-
dc.contributor.authorOuwerkerk, Wouter-
dc.contributor.authorTse, Yi Kei-
dc.contributor.authorTsang, Christopher Tze Wei-
dc.contributor.authorWu, Mei Zhen-
dc.contributor.authorTse, Hung Fat-
dc.contributor.authorVoors, Adriaan A.-
dc.contributor.authorTromp, Jasper-
dc.contributor.authorLam, Carolyn S.P.-
dc.contributor.authorYiu, Kai Hang-
dc.date.accessioned2026-01-15T00:35:28Z-
dc.date.available2026-01-15T00:35:28Z-
dc.date.issued2025-02-06-
dc.identifier.citationNature Communications, 2025, v. 16, n. 1, p. 1408-
dc.identifier.urihttp://hdl.handle.net/10722/368599-
dc.description.abstractRemnant cholesterol, identified by triglyceride-rich lipoprotein, is a significant causal risk factor for ischemic heart diseases. The association of triglyceride levels with all-cause and cause-specific outcomes in heart failure (HF) remains unexplored. Using a previously validated territory-wide clinical information registry, all eligible patients diagnosed with HF (N = 127124) from 2000 to 2020 were included. In this population-based cohort (mean age: 71.4 ± 12.2 years, 51.8% male), the association between triglyceride levels and risk of all-cause mortality and cardiovascular disease was a U-shapedḍ curve. High triglyceride levels (≥3.0 mmol/L) were associated with atherosclerotic cardiovascular disease admission or death; conversely, lower triglyceride levels (<1.2 mmol/L) were associated with higher risks of HF readmission or death. The risk of adjusted all-cause mortality reached a nadir between triglyceride levels of 1.2 mmol/L and 3.0 mmol/L. Results were externally validated in BIOSTAT-CHF. Our findings have important implications for defining the role of triglyceride levels in contributing to the diverse outcomes in patients with HF.-
dc.languageeng-
dc.publisherSpringer Nature-
dc.relation.ispartofNature Communications-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleTriglyceride levels and its association with all-cause mortality and cardiovascular outcomes among patients with heart failure-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1038/s41467-025-56790-1-
dc.identifier.pmid39915479-
dc.identifier.scopuseid_2-s2.0-85218290669-
dc.identifier.volume16-
dc.identifier.issue1-
dc.identifier.spage1408-
dc.identifier.eissn2041-1723-
dc.identifier.issnl2041-1723-

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