The longevity factor spermidine is part of a highly heritable complex erythrocyte phenotype associated with longevity

IF 7.8 1区 医学 Q1 Biochemistry, Genetics and Molecular Biology Aging Cell Pub Date : 2024-09-07 DOI:10.1111/acel.14311
Cameron J. Kaminsky, Jericha Mill, Viharkumar Patel, Dylan Pierce, Amelia Haj, Aaron S. Hess, Lingjun Li, Thomas Raife
{"title":"The longevity factor spermidine is part of a highly heritable complex erythrocyte phenotype associated with longevity","authors":"Cameron J. Kaminsky,&nbsp;Jericha Mill,&nbsp;Viharkumar Patel,&nbsp;Dylan Pierce,&nbsp;Amelia Haj,&nbsp;Aaron S. Hess,&nbsp;Lingjun Li,&nbsp;Thomas Raife","doi":"10.1111/acel.14311","DOIUrl":null,"url":null,"abstract":"<p>Extreme longevity in humans is known to be a heritable trait. In a well-established twin erythrocyte metabolomics and proteomics database, we identified the longevity factor spermidine and a cluster of correlated molecules with high heritability estimates. Erythrocyte spermidine is 82% heritable and significantly correlated with 59 metabolites and 22 proteins. Thirty-eight metabolites and 19 proteins were &gt;20% heritable, with a mean heritability of 61% for metabolites and 49% for proteins. Correlated metabolites are concentrated in energy metabolism, redox homeostasis, and autophagy pathways. Erythrocyte mean cell volume (MCV), an established heritable trait, was consistently negatively correlated with the top 25 biomolecules most strongly correlated with spermidine, indicating that smaller MCVs are associated with higher concentrations of spermidine and correlated molecules. Previous studies have linked larger MCVs with poorer memory, cognition, and all-cause mortality. Analysis of 432,682 unique patient records showed a linear increase in MCV with age but a significant deviation toward smaller than expected MCVs above age 86, suggesting that smaller MCVs are associated with extreme longevity. Consistent with previous reports, a subset of 78,158 unique patient records showed a significant skewing toward larger MCV values in a deceased cohort compared to an age-matched living cohort. Our study supports the existence of a complex, heritable phenotype in erythrocytes associated with health and longevity.</p>","PeriodicalId":55543,"journal":{"name":"Aging Cell","volume":"23 12","pages":""},"PeriodicalIF":7.8000,"publicationDate":"2024-09-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11634715/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Aging Cell","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/acel.14311","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0

Abstract

Extreme longevity in humans is known to be a heritable trait. In a well-established twin erythrocyte metabolomics and proteomics database, we identified the longevity factor spermidine and a cluster of correlated molecules with high heritability estimates. Erythrocyte spermidine is 82% heritable and significantly correlated with 59 metabolites and 22 proteins. Thirty-eight metabolites and 19 proteins were >20% heritable, with a mean heritability of 61% for metabolites and 49% for proteins. Correlated metabolites are concentrated in energy metabolism, redox homeostasis, and autophagy pathways. Erythrocyte mean cell volume (MCV), an established heritable trait, was consistently negatively correlated with the top 25 biomolecules most strongly correlated with spermidine, indicating that smaller MCVs are associated with higher concentrations of spermidine and correlated molecules. Previous studies have linked larger MCVs with poorer memory, cognition, and all-cause mortality. Analysis of 432,682 unique patient records showed a linear increase in MCV with age but a significant deviation toward smaller than expected MCVs above age 86, suggesting that smaller MCVs are associated with extreme longevity. Consistent with previous reports, a subset of 78,158 unique patient records showed a significant skewing toward larger MCV values in a deceased cohort compared to an age-matched living cohort. Our study supports the existence of a complex, heritable phenotype in erythrocytes associated with health and longevity.

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
长寿因子亚精胺是与长寿相关的高遗传性复杂红细胞表型的一部分。
众所周知,人类的极度长寿是一种遗传性状。在一个完善的双胞胎红细胞代谢组学和蛋白质组学数据库中,我们发现了长寿因子亚精胺和一组具有高遗传率估计值的相关分子。红细胞亚精胺的遗传率为 82%,与 59 种代谢物和 22 种蛋白质显著相关。38种代谢物和19种蛋白质的遗传率大于20%,代谢物的平均遗传率为61%,蛋白质的平均遗传率为49%。相关代谢物主要集中在能量代谢、氧化还原平衡和自噬途径中。红细胞平均体积(MCV)是一种既定的遗传性状,它与与亚精胺相关性最强的前 25 种生物大分子一直呈负相关,表明较小的 MCV 与较高浓度的亚精胺和相关分子有关。以前的研究表明,较大的 MCV 与较差的记忆力、认知能力和全因死亡率有关。对 432,682 份独特病历的分析表明,MCV 随年龄呈线性增长,但在 86 岁以上,MCV 显著偏向于小于预期值,这表明较小的 MCV 与极度长寿有关。与之前的报告一致,78,158 份独特患者记录的子集显示,与年龄匹配的在世患者队列相比,已故患者队列的 MCV 值明显偏向于更大。我们的研究证实,红细胞中存在一种与健康和长寿相关的复杂遗传表型。
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 去求助
来源期刊
Aging Cell
Aging Cell 生物-老年医学
CiteScore
14.40
自引率
2.60%
发文量
212
审稿时长
8 weeks
期刊介绍: Aging Cell, an Open Access journal, delves into fundamental aspects of aging biology. It comprehensively explores geroscience, emphasizing research on the mechanisms underlying the aging process and the connections between aging and age-related diseases.
期刊最新文献
Issue Information Aging research from bench to bedside and beyond: What we learned from Sammy Basso Featured Cover Additional Cover Additional Cover
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1