Novel RNA-targeting antisense therapy is shown to reduce lipoprotein(a) levels in 286 patients with existing atherosclerotic disease by upwards of 80% in a phase 2 clinical trial.
References
Tsimikas, S. et al. J. Am. Coll. Cardiol. 71, 177–192 (2018).
Tsimikas, S. et al. N. Engl. J. Med. 382, 244–255 (2020).
Paré, G. et al. Circulation 139, 1472–1482 (2019).
Clarke, R. et al. N. Engl. J. Med. 361, 2518–2528 (2009).
Burgess, S. et al. JAMA Cardiol. 3, 619–627 (2018).
Thanassoulis, G. et al. N. Engl. J. Med. 368, 503–512 (2013).
de Oliveira Sá, M. P. B. et al. Curr. Atheroscler. Rep. 22, 2 (2020).
Boffa, M. B. & Koschinsky, M. L. Nat. Rev. Cardiol. 16, 305–318 (2019).
Willeit, P. et al. Lancet 392, 1311–1320 (2018).
Wilson, D. P. et al. J. Clin. Lipidol. 13, 374–392 (2019).
Varvel, S., McConnell, J. P. & Tsimikas, S. Arterioscler. Thromb. Vasc. Biol. 36, 2239–2245 (2016).
O’Donoghue, M. L. et al. Circulation 139, 1483–1492 (2019).
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D. J. R. serves on the Scientific Advisory Board for Alnylam, which makes small interfering RNA therapeutics, and for Novartis, which has licensed AKCEA-APO(a)-LRx.
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Bajaj, A., Rader, D.J. Antisense oligonucleotides for atherosclerotic disease. Nat Med 26, 471–472 (2020). https://doi.org/10.1038/s41591-020-0835-2
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DOI: https://doi.org/10.1038/s41591-020-0835-2
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