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. 2022 Nov 30;14:157. doi: 10.1186/s13148-022-01377-6

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© The Author(s) 2022

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. 1 — Analysis of relative histone acetylation changes in lymphocytes (A) and monocytes (B) between study timepoints. A The change in the fluorescence levels for lymphocytes was statistically significant between the first and both the second and the third timepoints. B In monocytes, we observed a statistically significant decrease in detected fluorescence between the first and the third timepoints. The change was not statistically significant between the first and second timepoints. We did not observe statistically significant differences in the levels of fluorescence intensity between the second and third timepoints in neither lymphocytes (A) nor monocytes (B)