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REFLECTIONS
                                                                                                                   Dyslipidaemia
     Dyslipidaemia Global Newsletter #7 2024


     New epidemiological data has shown that the relationship
     between baseline Lp(a) level and ASCVD events is continuous                                                   Dyslipidaemia
     and log-linear, with increased risk even at “lower-risk” levels
     (25–50 nmol/L). Despite differences in Lp(a) levels among
     racial/ethnic groups as observed in UK Biobank, Lp(a)-
     attributable risk is similar, eliminating previous race-based
     definitions of elevated Lp(a). The NLA clarifies that because
     accepted conversion factors to adjust for Lp(a)-C in LDL-C
     calculation have proven inaccurate, this leads to undertreatment
     of high-risk patients and such adjustments should not be used.

     With regards to management and treatment, the NLA
     recommends adoption of a healthy lifestyle as the foundation
     of management for all adults and children. In addition, statins
     remain first-line therapy for mitigating LDL-C-driven ASCVD risk
     in both secondary and high-risk primary prevention patients.
     Although statins do not lower Lp(a) and may slightly increase
     it, statins clearly lower ASCVD risk and remain the standard
     of care. A PCSK-9i may be a good choice if a high-risk patient
     needs additional LDL-C lowering after a maximally tolerated
     statin therapy to address residual risk from both LDL-C and
     Lp(a). Aspirin remains a key recommendation for the secondary
     prevention of ASCVD and recent studies have suggested
     that individuals with genetically predicted elevated Lp(a) may
     derive net benefit from aspirin therapy due to its purported
     prothrombotic characteristics.

     Finally, for patients with high Lp(a), apheresis, the only FDA-
     approved therapy for treating high Lp(a), is recommended,
     although the NLA comments that it is not available at all centres
     and can be expensive and time-consuming.

     The NLA notes that although Lp(a) is an established
     independent causal risk factor for cardiovascular disease,
     and despite the high prevalence of Lp(a) elevation (~1 of 5
     individuals), measurement rates are low, warranting improved
     screening strategies for cardiovascular disease prevention and
     a need for specific Lp(a)-lowering therapies in the future.








                                                                           WATCH
                                                                           PROF. KOSCHINKSKY, LEADING
                                                                           AUTHOR OF THE NLA UPDATE,
                                                                           DISCUSS THE ABCS OF
                                                                           LIPOPROTEIN(A) FROM A RECENT
             CLICK HERE                                                    LECTURE FOR THE AMERICAN HEART
             FOR THE LINK TO FULL ARTICLE                                  ASSOCIATION. (1 HR)




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