Elevated Alcohol Consumption and Chronic Inflammation Predict Cardiovascular Risk Among Black Americans: Examination of a Dual-Risk Model Using Epigenetic Risk Markers.

IF 4.1 Q3 GENETICS & HEREDITY
Steven R H Beach, Robert A Philibert, Mei-Ling Ong, Man-Kit Lei, Kaixiong Ye
{"title":"Elevated Alcohol Consumption and Chronic Inflammation Predict Cardiovascular Risk Among Black Americans: Examination of a Dual-Risk Model Using Epigenetic Risk Markers.","authors":"Steven R H Beach, Robert A Philibert, Mei-Ling Ong, Man-Kit Lei, Kaixiong Ye","doi":"10.3390/epigenomes9040040","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Heart disease may take a greater toll on Black Americans than White Americans despite similar levels of traditional risk factors. Elevated alcohol consumption (EAC) and chronic inflammation are two potentially important additional risk factors to consider. Both are relevant to understanding health disparities in cardiovascular health.</p><p><strong>Methods: </strong>Couples with a Black preadolescent or early adolescent child living in the home were recruited and followed. In waves 5 and 6 of data collection, biological samples were also collected allowing the characterization of elevated alcohol consumption, chronic inflammation, and cardiac risk using DNA methylation indices. 383 individual partners comprising 221 couples were examined across the two waves of data, yielding 661 person-wave observations from 383 individuals.</p><p><strong>Results: </strong>EAC at wave 5 forecast increased cardiac risk at W6 (R<sup>2</sup> change = 0.276), β = -0.193, <i>p</i> = 0.001. However, chronic inflammation at wave 5 did not add significantly to the baseline model, β = -0.042, <i>p</i> = 0.549. Conversely, the slope of change for chronic inflammation was associated with slope of change in cardiac risk (R<sup>2</sup> change = 0.111), b = -0.014, <i>p</i> = <0.001, but EAC change was not significantly associated with change in cardiac risk, b = -0.001, <i>p</i> = 0.185.</p><p><strong>Conclusions: </strong>Elevated alcohol consumption may be an important risk factor for increased cardiac risk over time in middle age. If so, it could be an important avenue for preventative intervention to decrease cardiac risk. Future research should examine whether similar associations are observed for other racial or minoritized groups and for non-minoritized groups.</p>","PeriodicalId":55768,"journal":{"name":"Epigenomes","volume":"9 4","pages":""},"PeriodicalIF":4.1000,"publicationDate":"2025-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12551029/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Epigenomes","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/epigenomes9040040","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Heart disease may take a greater toll on Black Americans than White Americans despite similar levels of traditional risk factors. Elevated alcohol consumption (EAC) and chronic inflammation are two potentially important additional risk factors to consider. Both are relevant to understanding health disparities in cardiovascular health.

Methods: Couples with a Black preadolescent or early adolescent child living in the home were recruited and followed. In waves 5 and 6 of data collection, biological samples were also collected allowing the characterization of elevated alcohol consumption, chronic inflammation, and cardiac risk using DNA methylation indices. 383 individual partners comprising 221 couples were examined across the two waves of data, yielding 661 person-wave observations from 383 individuals.

Results: EAC at wave 5 forecast increased cardiac risk at W6 (R2 change = 0.276), β = -0.193, p = 0.001. However, chronic inflammation at wave 5 did not add significantly to the baseline model, β = -0.042, p = 0.549. Conversely, the slope of change for chronic inflammation was associated with slope of change in cardiac risk (R2 change = 0.111), b = -0.014, p = <0.001, but EAC change was not significantly associated with change in cardiac risk, b = -0.001, p = 0.185.

Conclusions: Elevated alcohol consumption may be an important risk factor for increased cardiac risk over time in middle age. If so, it could be an important avenue for preventative intervention to decrease cardiac risk. Future research should examine whether similar associations are observed for other racial or minoritized groups and for non-minoritized groups.

Abstract Image

Abstract Image

Abstract Image

饮酒增加和慢性炎症预测美国黑人心血管风险:使用表观遗传风险标记的双风险模型检验
背景:尽管传统的危险因素水平相似,但美国黑人患心脏病的人数可能比白人多。酒精摄入量增加(EAC)和慢性炎症是需要考虑的两个潜在的重要风险因素。两者都与理解心血管健康的健康差异有关。方法:对家中有黑人青春期前或青春期早期儿童的夫妇进行招募和随访。在数据收集的第5和第6波中,还收集了生物样本,使用DNA甲基化指数来表征酒精摄入量升高、慢性炎症和心脏风险。包括221对夫妇在内的383名个人伴侣通过两波数据进行了检查,从383个人中获得了661人波观察结果。结果:第5波EAC预测W6时心脏风险增加(R2变化= 0.276),β = -0.193, p = 0.001。然而,第5波慢性炎症对基线模型没有显著增加,β = -0.042, p = 0.549。相反,慢性炎症的变化斜率与心脏风险的变化斜率相关(R2变化= 0.111),b = -0.014, p = p = 0.185。结论:随着时间的推移,酒精摄入量升高可能是中年心脏病风险增加的重要危险因素。如果是这样,它可能是预防性干预降低心脏风险的重要途径。未来的研究应审查是否在其他种族或少数群体和非少数群体中观察到类似的联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Epigenomes
Epigenomes GENETICS & HEREDITY-
CiteScore
3.80
自引率
0.00%
发文量
38
审稿时长
11 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书