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. 2020 Jul 23;19:173. doi: 10.1186/s12944-020-01272-0

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© The Author(s) 2020

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 2 — a. Non-linear relationship and tertile points between Lp(a) and ARAS adjusted covariates. Illustration: External image: the x-axis is Lp(a) concentration. The y-axis is the incidence of ARAS, with the shaded area representing a 95% confidence interval. (linear trend, P = 0.028). Internal image: the x-axis is Lp(a) concentration. The y-axis is the incidence of ARAS when dividing Lp(a) concentrations into three tertiles. The reference group (low Lp(a)) was set to 1.0. b. Population-based ARAS prevalence corresponding to different concentrations of Lp(a) levels in patients with low LDL-c levels. Illustration: Blue color indicates the prevalence of ARAS at different Lp(a) levels among a low LDL-c population.