98%
921
2 minutes
20
Aims/hypothesis: Recent evidence shows decreasing trends for ischaemic heart disease over time in the general population as well as in those with type 2 diabetes. As type 2 diabetes has been associated with an increased risk of both ischaemic and non-ischaemic heart failure, a greater proportion of people with type 2 diabetes could now be presenting with non-ischaemic heart failure phenotypes. We aimed to investigate the risk of incident ischaemic and non-ischaemic heart failure in people with type 2 diabetes.
Methods: We used the Clinical Practice Research Datalink primary care data, linked to hospital and mortality records, to identify newly diagnosed adults with type 2 diabetes between 2000 and 2021, who were matched to up to four people without diabetes by sex, year of birth, and general practice. Ischaemic heart failure was defined as incident heart failure at or following an ischaemic heart disease event; non-ischaemic HF was defined as incident heart failure in the absence of prevalent ischaemic heart disease. We used Poisson and Royston-Parmar models to estimate, respectively, the incidence rates and the hazard ratios (adjusted for sociodemographic and clinical confounders) for ischaemic and non-ischaemic heart failure, comparing people with type 2 diabetes to those without diabetes.
Results: In a cohort of 1,621,090 people (mean age, 60.1 years; 52.8% women; 532,185 with type 2 diabetes), during a median follow-up of 5.8 (interquartile range: 2.6-10.3) years, a heart failure event occurred in 20,016 (3.8%) people with type 2 diabetes (ischaemic: 5046; non-ischaemic: 14,970) and in 29,835 (2.7%) without diabetes (7001 and 22,834, respectively). Age-standardised rates were higher for non-ischaemic (3.18 [95% CI: 3.09-3.27] vs. 2.08 [2.03-2.12] per 1000 person-years in men with type 2 diabetes vs. without diabetes; and 2.47 [2.39-2.54] vs. 1.57 [1.53-1.61], respectively, in women) than ischaemic (corresponding estimates: 1.57 [1.51-1.63] vs. 0.95 [0.92-0.98] and 0.80 [0.76-0.84] vs. 0.46 [0.44-0.48]) heart failure. Comparing people with type 2 diabetes versus those without diabetes, the hazard ratios were larger for ischaemic (adjusted hazard ratio: 1.36 [1.28-1.45] and 1.30 [1.20-1.42] in men and women, respectively) than non-ischaemic (1.12 [1.07-1.16] and 1.10 [1.06-1.14], respectively) heart failure.
Conclusions/interpretations: The higher rates of non-ischaemic heart failure highlight the need for early prevention before ischaemic heart disease develops, regardless of type 2 diabetes. Meanwhile, the greater excess risk of ischaemic heart failure in those with type 2 diabetes suggests suboptimal post-ischaemic prevention in this group.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12304495 | PMC |
http://dx.doi.org/10.1002/dmrr.70072 | DOI Listing |
J Palliat Care
September 2025
Department of Healthcare Administration and Policy, School of Public Health, University of Nevada, Las Vegas, NV, USA.
ObjectivesRecently, atrial fibrillation (AF) has contributed to an increase in cardiovascular deaths in the U.S. Palliative care (PC) and atrial ablation (AA) procedure can elevate quality of life of high-risk AF patients, who are associated with multiple comorbidities.
View Article and Find Full Text PDFPLoS One
September 2025
Biobank of Jiangsu Cancer Hospital, Jiangsu Institute of Cancer Research & The Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, Jiangsu, PR China.
Heart failure (HF) and lung cancer (LC) often coexist, yet their shared molecular mechanisms are unclear. We analyzed transcriptome data from the NCBI Gene Expression Omnibus (GEO) database (GSE141910, GSE57338) to identify 346 HF‑related differentially expressed genes (DEGs), then combined weighted gene co-expression network analysis (WGCNA) pinpointed 70 hub candidates. Further screening of these 70 hub candidates in TCGA lung cancer cohorts via LASSO, Random Forest, and multivariate Cox regression suggested CYP4B1 as the only independent prognostic marker.
View Article and Find Full Text PDFPLoS One
September 2025
Department of Cardiology, Fuzhou University Affiliated Provincial Hospital, Fujian Provincial Hospital, Fuzhou, Fujian, China.
Introduction: Kidney stone disease is associated with numerous cardiovascular risk factors. However, the findings across studies are non-uniformly consistent, and the control of confounding variables remains suboptimal. This study aimed to investigate the association between kidney stone and cardiovascular disease.
View Article and Find Full Text PDFAm J Physiol Heart Circ Physiol
September 2025
Division of Pediatric Critical Care, Department of Pediatrics, University of California, San Francisco, USA.
Right ventricular (RV) failure is the primary cause of death among patients with pulmonary arterial hypertension (PAH). Patients with congenital heart disease-associated PAH (CHD-PAH) demonstrate improved outcomes compared to patients with other forms of PAH, which is related to the maintenance of an adaptively hypertrophied RV. In an ovine model of CHD-PAH, we aimed to elucidate the cellular, microvascular, and transcriptional adaptations to congenital pressure overload that support RV function.
View Article and Find Full Text PDFJCI Insight
September 2025
Department of Pharmacology, University of Michigan, Ann Arbor, United States of America.
Cardiac hypertrophy is a common adaptation to cardiovascular stress and often a prelude to heart failure. We examined how S-palmitoylation of the small GTPase, Ras-related C3 botulinum toxin substrate 1 (Rac1), impacts cardiomyocyte stress signaling. Mutation of the cysteine-178 palmitoylation site impaired activation of Rac1 when overexpressed in cardiomyocytes.
View Article and Find Full Text PDF