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TRIB1: a multifaceted regulator of cardiometabolic health
Valeria Prete1,2, Paola Di Pietro1, Angela Carmelita Abate1
1Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University of Salerno, Baronissi, Italy.
Insights
Tribbles homolog 1 (Trib1) is a potential therapeutic biomarker for cardiovascular diseases (CVDs). Research highlights its role in lipid metabolism, inflammation, and insulin signaling, offering new avenues for CVD risk assessment and prevention.
Area of Science:
- Biomedical research
- Genetics
- Cardiovascular medicine
Background:
- Cardiovascular diseases (CVDs) are a leading global cause of death, driven by risk factors like dyslipidemia, atherosclerosis, diabetes, and obesity.
- Genome-wide association studies (GWASs) have identified the 8q24 locus, including the TRIB1 gene, associated with cardiometabolic traits.
Purpose of the Study:
- To review the role of Tribbles homolog 1 (Trib1) as a therapeutic biomarker in cardiovascular diseases (CVDs).
- To explore Trib1's association with lipid metabolism, atherosclerosis, obesity, and diabetes.
- To analyze in vitro and in vivo studies and elucidate Trib1's molecular mechanisms in CVD.
Main Methods:
- Literature review of in vitro and in vivo studies.
- Analysis of genome-wide association studies (GWASs) data.
- Exploration of molecular mechanisms underlying Trib1 function.
Main Results:
- Trib1 is linked to key cardiometabolic traits including plasma lipid levels (triglycerides, LDL, HDL, total cholesterol) and glycated hemoglobin.
- Emerging evidence suggests Trib1's involvement in regulating plasma lipid levels, inflammation, and insulin signaling.
- Trib1 presents potential as a novel biomarker for CVD risk assessment.
Conclusions:
- Trib1 plays a crucial role in pathways relevant to cardiovascular health.
- Targeting Trib1 may offer new therapeutic strategies for preventing and managing CVDs.
- Further research into Trib1's mechanisms can enhance CVD risk stratification and treatment.
Abstract:
Cardiovascular diseases (CVDs) are the leading cause of morbidity and mortality worldwide. The rising prevalence of CVD is primarily driven by several risk factors, including dyslipidemia, atherosclerosis, diabetes, and obesity. Many current studies are focused on unraveling the underlying pathophysiological mechanisms that govern these risk factors, with the main goal of identifying novel biomarkers and therapeutic targets to prevent the onset of CVD in the population. In recent decades, genome-wide association studies (GWASs) have linked the 8q24 locus containing the TRIB1 (Tribbles homolog 1) gene to various cardiometabolic traits in humans, such as plasma triglycerides, LDL cholesterol, HDL cholesterol, total cholesterol, adiponectin, and glycated hemoglobin levels. Emerging research has investigated the role of Trib1 in regulating plasma lipid levels, inflammation, and insulin signaling, opening new avenues for the potential therapeutic role of Trib1 in CVD risk assessment. Accordingly, this review aims to explore the crucial role of Trib1 as a therapeutic biomarker in CVDs, with a focus on its association with lipid metabolism, atherosclerosis, obesity, and diabetes, analyzing in vitro and in vivo studies and offering insights into its underlying molecular mechanisms.
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