Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2024 Oct 23;14:25091. doi: 10.1038/s41598-024-76084-8

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, 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 you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. 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-nc-nd/4.0/.

PMC Copyright notice

Fig. 4 — Plasma levels of six antioxidant-related proteins and correlations between the levels and average weekly alcohol consumption in 162 young adults. (A) The six applicable antioxidant-related gene proteins, namely those of the genes BNIP3, CCL5, MT3, PDLIM1, SOD1, and TTN, were selected. Only the SOD1 plasma level was significantly downregulated in the heavier-drinking group between any two of the three drinking groups. Plasma levels of BNIP3 and CCL5 were significantly downregulated in the heavier-drinking group between at least two of the three groups (*p < 0.05, **p < 0.001; n.s., not significant; Wilcoxon Kruskal–Wallis test). (B) Plasma levels of BNIP3, SOD1, and TTN were negatively correlated with average weekly alcohol consumption. Associations with p < 0.05 are shown in bold.