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Letter to the Editor
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Disponible online el 10 de septiembre de 2024
When “old” lipid lowering therapies not should be discontinued
Cuándo no se deben suspender las terapias hipolipemiantes «antiguas»
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Francesco Sbrana
Autor para correspondencia
Francesco.sbrana@ftgm.it

Corresponding author.
, Beatrice Dal Pino
Lipoapheresis Unit and Reference Center for Inherited Dyslipidemias, Fondazione Toscana Gabriele Monasterio, Pisa, Italy
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Dear Editor,

We read with interest Vila À et al. titled “Observational study of patients from a Lipid Unit on lipid-modifying therapy for primary and secondary prevention: ULFI Study1 highlighting that factors associated with therapeutic lipid lowering success were the presence of arteriosclerotic cardiovascular disease, the intensity of lipid-lowering treatment (LLT), diabetes mellitus, and low to moderate alcohol consumption but we have to consider that low adherence to LLT is one of the main reasons beyond the failure in achieving the recommended lipid targets in several patients. The ULFI study is in agree with the SANTORINI study2 who reported that a considerable proportion of subjects at high and very high cardiovascular risk fail to reach the LDL-cholesterol goals established by the guidelines (<70 and <55mg/dL, respectively) although prescribing attitudes changed over time, with a rising, trend toward more aggressive LLT interventions. Recently, ESC indications3 highlighting the importance of periodic reassessment of chronic cardiovascular therapy especially after a lengthy period of treatment. However, between the several discussed cardiovascular medications, some further considerations need to be made regarding the LLT:

  • i)

    Niacin treatment, although able to increase HDL cholesterol levels especially in familial hypoalphalipoproteinemia, increase the frequency of serious adverse events with an unfavorable risk/benefit ration and the fish oil supplementation (<1g/day) has an irrelevant therapeutic effect although a very high daily dose is not recommended, especially in patients with heart disease, due to the risk of atrial fibrillation.4

  • ii)

    Statin-associated muscle symptoms (SAMS) are a major determinant of poor treatment adherence and/or statin discontinuation but this condition can benefit from coenzyme Q10 supplementation especially when CPK values are high before start statin therapy.5 Moreover, SAMS could be the opportunity to identify, through vitamin D dosage, states of vitamin deficiency in order to start specific therapy.

  • iii)

    Among patients with atherosclerotic cardiovascular disease (ASCVD), hypertriglyceridemia is common, and is associated with higher ASCVD risk across a range of TG.6 Lowering triglycerides with fibrates reduces the risk of cardiovascular events by the same amount as LDL-C-lowering therapies when measured per unit change of non-HDL-C. Combinations of statins with gemfibrozil may enhance the risk for myopathy but this risk seems to be small using fenofibrate and routinary monitoring CPK.7

  • iv)

    Simvastatin has a good safety profile, especially in chronic kidney disease,8 and adding ezetimibe allowed an LDL-cholesterol reduction great then 50% in a large number of high cardiovascular risk subjects.

All strategies, according to the operative international lipid expert panel indication and with protocol to valorized the therapeutic adherence,1,9 have a role to improve the LLT effectiveness don’t forget, in the era of “new” lipid-lowering drugs, cornerstone data regarding “old” LLT.

Funding sources

No financial support was received.

Author approval

All authors have seen and approved the study submitted.

No part of the submitted work has been published or is under consideration for publication elsewhere.

Authors’ contribution

FS and BDP: contributed to conception or design, drafted and critically revised the manuscript. All authors read and approved the final version of the manuscript.

Notes

Data have not been presented at any congress.

Consent for publication

The patient signed the informed consent from form for anonymous medical data usage in our paper.

Conflict of interest

No conflict of interest for each author.

Acknowledgements

None.

References
[1]
À. Vila, E. Pons, P.T. García, D. Vidal, S. López, A. Grau.
Observational study of patients from a Lipid Unit on lipid-modifying therapy for primary and secondary prevention: ULFI study.
Clin Investig Arterioscler, 35 (2023), pp. 272-279
[2]
K.K. Ray, I. Haq, A. Bilitou, C. Aguiar, M. Arca, D.L. Connolly, et al.
Evaluation of contemporary treatment of high- and very high-risk patients for the prevention of cardiovascular events in Europe—methodology and rationale for the multinational observational SANTORINI study.
Atheroscler Plus, 13 (2021), pp. 24-30
[3]
K.A. Krychtiuk, B.J. Gersh, J.B. Washam, C.B. Granger.
When cardiovascular medicines should be discontinued.
Eur Heart J, 45 (2024), pp. 2039-2051
[4]
M. Lombardi, S. Carbone, M.G. Del Buono, J.G. Chiabrando, G.M. Vescovo, M. Camilli, et al.
Omega-3 fatty acids supplementation and risk of atrial fibrillation: an updated meta-analysis of randomized controlled trials.
Eur Heart J Cardiovasc Pharmacother, 7 (2021), pp. e69-e70
[5]
K. A. Folkers, R. Nakamura, G.P. Littarru, H. Zellweger, J.B. Brunkhorst, C.W. Williams Jr., et al.
Effect of coenzyme Q on serum levels of creatine phosphokinase in preclinical muscular dystrophy.
Proc Natl Acad Sci USA, 71 (1974), pp. 2098-2102
[6]
P.R. Lawler, G. Kotrri, M. Koh, S.G. Goodman, M.E. Farkouh, D.S. Lee, et al.
Real-world risk of cardiovascular outcomes associated with hypertriglyceridaemia among individuals with atherosclerotic cardiovascular disease and potential eligibility for emerging therapies.
Eur Heart J, 41 (2020), pp. 86-94
[7]
F. Mach, C. Baigent, A.L. Catapano, K.C. Koskinas, M. Casula, L. Badimon, et al.
2019 ESC/EAS Guidelines for the management of dyslipidaemias: lipid modification to reduce cardiovascular risk.
Eur Heart J, 41 (2020), pp. 111-188
[8]
Sharp Collaborative Group.
Study of Heart and Renal Protection (SHARP): randomized trial to assess the effects of lowering low-density lipoprotein cholesterol among 9438 patients with chronic kidney disease.
Am Heart J, 160 (2010),
[9]
B. Dal Pino, F. Sbrana.
Therapeutic adherence in hyperlipidemia: when one size doesn’t fit all.
Eur J Intern Med, 112 (2023), pp. 143-145
Copyright © 2024. Sociedad Española de Arteriosclerosis
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