ArticleScience China. Life sciences2025
Global burden of atherosclerotic cardiovascular disease attributed to lifestyle and metabolic risks.
Article in Science China. Life sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.
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Who cites it
17 citing papers in PubMed, 2 syntheses or guidelines pooled it.
- Cardiovascular Benefit and Gastrointestinal Risk of Colchicine in Secondary Prevention: Risk Associated with Dose and Treatment Duration.American journal of cardiovascular drugs : drugs, devices, and other interventions · 2026Pooled it
- Metabolic score for insulin resistance and the incidence of cardiovascular disease: a meta-analysis of cohort studies.Frontiers in endocrinology · 2025Pooled it
- An oral-gut microbial metabolite linksGut microbes · 2026Article
- Effects of ursodeoxycholic acid on statin-induced impaired glucose tolerance: study protocol for a randomized controlled trial.BMJ open · 2026Article
- Behavior Change Content and Implementation of Large Language Model-Driven Conversational Agents in Cardiometabolic Care: Scoping Review.Journal of medical Internet research · 2026Article
- Precision medicine for atherosclerotic cardiovascular disease: Integrative genomics maps risk loci and AI-predicted functional consequences.Clinical and translational medicine · 2026Article
- High-density lipoprotein antioxidant function is associated with lipid profiles and lipid-lowering therapy.Science China. Life sciences · 2026Article
- MASLD as a systemic metabolic disease: expanding the scope of cardiovascular-kidney-metabolic (CKM) syndrome.Science China. Life sciences · 2026Review
- The Role of Long Non-Coding RNA in Atherosclerosis: Mechanism and Intervention of Traditional Chinese Medicine.International journal of molecular sciences · 2026Review
- Association of Composite Metabolic Indices With Incident Carotid Plaque: A Chinese Cohort Study.Journal of the American Heart Association · 2026Article
- Iron and Copper Homeostasis in Cardiometabolic Disease: Therapeutic Potential of Chelators.Pharmaceuticals (Basel, Switzerland) · 2026Review
- Association between the triglyceride glucose index:Chinese visceral adiposity index (TyG-CVAI) and new-onset cardiovascular disease in middle-aged and older adults-insights from the China Health and Retirement Longitudinal Study (CHARLS).Cardiovascular diabetology · 2026Article
- The role of tetramethylpyrazine and paeoniflorin in modulating iron metabolism and ferroptosis: innovative strategies for atherosclerosis treatment.Frontiers in pharmacology · 2026Article
- RNA-Targeted Therapeutics for Lipid Metabolic Disorders: From Bench to Bedside.Research (Washington, D.C.) · 2026Article
- Multimodal Cardiovascular Risk Discrimination: Clinical, Biochemical, and Doppler Ultrasound Insights from a Contemporary Atherosclerotic Cardiovascular Disease Cohort.Anatolian journal of cardiology · 2025Article
- Sentrin-specific protease 3 (SENP3)-mediated Krüppel-like factor 4 (KLF4) deSUMOylation regulates vascular smooth muscle cell phenotypic switching in atherosclerosis.Molecular biomedicine · 2025Article
- Sex-Related Differences in Predictors of Acute Coronary Syndrome in Kosovo: A Cross-Sectional Study.Journal of clinical medicine · 2025Article
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Atherosclerotic cardiovascular disease (ASCVD) continues to increase globally as the most common cardiovascular disease. Lifestyle and metabolic risks are major contributors to the increase in the burden of ASCVD. However, the epidemiological characterization of the burden of ASCVD due to lifestyle and metabolic risks has not been adequately documented. We analyzed data from the 2021 Global Burden of Disease Study to assess the disability-adjusted life years (DALYs) and age-standardized DALY rate (ASDR) attributed to ASCVD induced by lifestyle and metabolic risks. This study also analyzes temporal trends and inequalities in disease burden. Lifestyle and metabolic risks led to an increase in the DALYs and a decrease in the ASDR for ASCVD. High systolic blood pressure (SBP) was the primary contributor to the burden of ischemic heart disease (IHD) and ischemic stroke (IS), whereas high fasting plasma glucose (FPG) was the primary contributor to the burden of peripheral artery disease (PAD). High FPG and high body mass index (BMI) are primary risk factors that contribute to a more rapid increase in the burden of ASCVD. Over 32 years, high SDI regions reduced ASCVD burden linked to lifestyle and metabolic risks, while low SDI regions saw increases. ASCVD attributable to lifestyle and metabolic risks remains a major global public health concern. Although the burden of ASCVD caused by lifestyle and metabolic risks has improved in developed countries, developing countries still need to take effective measures to reduce the disease burden. Furthermore, while high SBP remains the leading contributor to the ASCVD burden, it is also crucial to recognize that high FPG and high BMI are becoming significant drivers of the growth in the ASCVD burden. This highlights the need for a paradigm shift in ASCVD prevention and control strategies-from single risk management to comprehensive metabolic network regulation.
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40553416What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.