Wenbo Ding | PubMed Health

PubMed2025

Risk of Cardiovascular Disease Mortality in Patients With Diagnosed Cancer and Associated Genetic and Proteomic Mechanisms: A UK Biobank-Based Cohort Study.

BACKGROUND: Previous studies have identified a link between cancer and cardiovascular disease; however, the underlying genetic and proteomic mechanisms remain unclear. Therefore, this study aimed to investigate the association between cancer diagnosis and cardiovascular mortality and to explore the potential mechanisms involved. METHODS: A total of 379 944 participants without cardiovascular disease at baseline, including 65 047 individuals with cancer, were recruited from the UK Biobank database. The primary end point was cardiovascular death. Multivariate Cox regression was performed to evaluate the risk of cardiovascular death in populations with and without cancer. Genome-wide association studies, phenome-wide association studies, and proteomic analyses were applied to investigate the underlying genetic and proteomic mechanisms. RESULTS: Multivariate Cox regression analysis showed an increased risk of cardiovascular death in the group with cancer (hazard ratio, 1.50 [95% CI, 1.40-1.61]) after multivariable adjustment. Proteomic analysis confirmed a strong association between cancer and cardiovascular disease, primarily involving pathways related to complement and coagulation cascades, and various inflammatory processes. In contrast, genome-wide association studies and phenome-wide association studies revealed only a limited number of shared genetic variations between cancer and cardiovascular conditions, such as hypertension and cardiac dysrhythmias. CONCLUSIONS: Cardiovascular risk is increased in patients with cancer and may be related to altered expression of inflammation- and coagulation-related proteins. In clinical practice, it is recommended to emphasize the management of endocrine, kidney, and inflammation-related risk factors in the population with cancer.

Humans↗

PubMed2025

Intraspecific divergence within Microcystis aeruginosa mediates the dynamics of freshwater harmful algal blooms under climate warming scenarios.

Intraspecific biodiversity can have ecosystem-level consequences and may affect the accuracy of ecological forecasting. For example, rare genetic variants may have traits that prove beneficial under future environmental conditions. The cyanobacterium responsible for most freshwater harmful algal blooms worldwide, Microcystis aeruginosa, occurs in at least three types. While the dominant type occurs in eutrophic environments and is adapted to thrive in nutrient-rich conditions, two additional types have recently been discovered that inhabit oligotrophic and eutrophic environments and have genomic adaptations for survival under nutrient limitation. Here, we show that these oligotrophic types are widespread throughout the Eastern USA. By pairing an experimental warming study with gene expression analyses, we found that the eutrophic type may be most susceptible to climate warming. In comparison, oligotrophic types maintained their growth better and persisted longer under warming. As a mechanistic explanation for these patterns, we found that oligotrophic types responded to warming by widespread elevated expression of heat shock protein genes. Reduction of nutrient loading has been a historically effective mitigation strategy for controlling harmful algal blooms. Our results suggest that climate warming may benefit oligotrophic types of M. aeruginosa, potentially reducing the effectiveness of such mitigation efforts. In-depth study of intraspecific variation may therefore improve forecasting for understanding future whole ecosystem dynamics.

Microcystis↗