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REFLECTIONS
                                                                                                                   Dyslipidaemia
     Dyslipidaemia Global Newsletter #9 2025


     Various tools and strategies are highlighted for the diagnosis   surgery, and pharmacotherapy. Future advancements in clinical
     and management of SMD. The authors describe several        risk scores, polygenic risk scores (PRS), and microbiome-based
     diagnostic tools and/or biomarkers that can be used to assess   treatments hold promise for further personalising risk assessment,
                                                                                                                   Dyslipidaemia
     each SMD component. Management of SMD involves lifestyle   predicting SMD progression, and guiding preventive interventions
     changes, i.e. improved diet quality, calorie restriction, and   even earlier in life.
     regular physical activity. Additionally, metabolic/bariatric surgery
     is an option for severe obesity, and pharmacotherapy includes
     modern agents like GLP-1 receptor agonists, SGLT2 inhibitors,
     lipid-lowering medications like statins and PCSK9 inhibitors,
     antihypertensives, and anti-inflammatory drugs like low-dose
     colchicine. High-intensity statins are also the first-line therapy
     for achieving reductions in LDL-C, apoB, and non-HDL-C.
     Several future therapies have been found effective in treating
     hypertriglyceridaemia (antisense oligonucleotides, siRNA-
     based therapies, monoclonal antibodies targeting apoCIII and
     ANGPTL3) but further studies are required to establish whether
     targeting these pathways will result in reducing the residual
     cardiovascular risk in individuals with SMD-related dyslipidaemia.  CLICK HERE
                                                                         TO VIEW A SHORT VIDEO DISCUSSING
     This EAS consensus statement provides a comprehensive,              THE MAIN POINTS OF THE GUIDELINES
     pathophysiology-based staging system for SMD, emphasising           FROM @GUIDELINECENTRAL.
     its multiorgan nature and progressive course. The prevalence
     data from the UK Biobank underscore the significant burden of
     early-stage SMD in the population. The proposed framework           CLICK HERE
     aims to facilitate a holistic and individually tailored approach to   FOR THE LINK TO FULL ARTICLE
     clinical management, integrating lifestyle modifications, metabolic


     Coronary artery calcium testing-too early, too late, too often.
     Zheutlin AR, et al. JAMA Cardiol. 2025;10(5):503-509.

     Coronary artery calcium (CAC) testing is a valuable tool used to assess the burden of advanced atherosclerosis and improve
     individual-level risk prediction for future ASCVD. Measured by a computed tomography (CT) scan in under 15 minutes with low
     radiation exposure, the CAC score quantifies calcium deposition in atherosclerotic lesions and is compared to normative data by
     age, sex, and race. While traditional ASCVD risk factors (such as diabetes, smoking, etc.) are associated with CAC, the score offers
     additional insight into incident ASCVD risk, particularly for adults without a history of ASCVD and not taking statin therapy.

                      Clinical scenarios for when a CAC level of 0 may impact clinical decision-making

        Scenario    Description

           1        Statin-naive patients hesitant to initiate statin therapy and require more information regarding their individual
                    risk vs benefit of statin therapy

                    Patients previously trialed on statin therapy who were unable to tolerate statin therapy due to side effects and are
           2
                    considering retrialing statin therapy
                    Adults aged 55-80 y for men or 60-80 y for women who do not have significant cardiovascular risk factors and
           3
                    are unclear whether a statin is likely to benefit them
                    Adults aged 40-55 y with a calculated 10-y risk of ASCVD of 5% to <7.5% by the PCE that have other factors
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                    that increase their ASCVD risk

     ASCVD, atherosclerotic cardiovascular disease; PCE, pooled cohort equation.


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