探索血管虚弱在了解接受血液透析的终末期肾病患者血压变化和死亡风险中的作用。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Szu-Ying Lee MD, Chia-Ter Chao MD, PhD
{"title":"探索血管虚弱在了解接受血液透析的终末期肾病患者血压变化和死亡风险中的作用。","authors":"Szu-Ying Lee MD,&nbsp;Chia-Ter Chao MD, PhD","doi":"10.1002/clc.24281","DOIUrl":null,"url":null,"abstract":"<p>Dong et al. investigated the relationship between interdialytic home blood pressure variability (BPV) and mortality in individuals with end-stage kidney disease (ESKD) undergoing hemodialysis.<span><sup>1</sup></span> Their study revealed a notable correlation between increasing home BPV and a stepwise escalation in the risk of all-cause mortality among this population. In the discussion, the authors attributed this association to comorbid cardiovascular diseases, diabetes, systemic inflammation, and higher vascular stiffness. We believe that a more comprehensive characterization of vascular integrity impairment is needed to explain this BPV-outcome association.</p><p>Our team previously introduced the concept of vascular frailty, which elucidates vascular structural and functional degeneration leading to physical frailty or the coexistence of both phenotypes.<span><sup>2</sup></span> Vascular tissues are exquisitely susceptible to adverse consequences related to tissue senescence from chronological aging and metabotoxic stimuli, particularly uremic toxins. Vascular frailty manifests through structural degenerations such as vascular calcification and atherosclerosis, as well as functional perturbations like increased stiffness and vasomotor dysfunction. Uremic toxins predispose individuals with chronic kidney disease to developing physical frailty<span><sup>3</sup></span> and contribute to the pathogenesis of vascular frailty by inducing vascular calcification and increasing vascular stiffness,<span><sup>4</sup></span> thereby leading to higher BPV. It is widely acknowledged that ESKD patients are prone to developing vascular calcification over time. Moreover, individuals with ESKD exhibit accelerated aging and heightened tissue wear, culminating in physical frailty that significantly elevates mortality risk. Our previous findings demonstrated that ESKD patients with frailty faced a significantly higher risk of mortality compared with those without.<span><sup>5</sup></span></p><p>From this perspective, we recommend that the authors consider incorporating additional features of vascular frailty, such as measurements of vascular calcification severity and evidence of autonomic dysfunction, in their assessments of these patients. Doing so will facilitate a more thorough understanding of the mechanisms underlying the BPV-outcome association.</p><p>Szu-Ying Lee and Chia-Ter Chao are responsible for drafting of this manuscript.</p><p>The authors declare no conflict of interest.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/clc.24281","citationCount":"0","resultStr":"{\"title\":\"Exploring the role of vascular frailty in understanding blood pressure variability and mortality risk among end-stage kidney disease patients undergoing hemodialysis\",\"authors\":\"Szu-Ying Lee MD,&nbsp;Chia-Ter Chao MD, PhD\",\"doi\":\"10.1002/clc.24281\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Dong et al. investigated the relationship between interdialytic home blood pressure variability (BPV) and mortality in individuals with end-stage kidney disease (ESKD) undergoing hemodialysis.<span><sup>1</sup></span> Their study revealed a notable correlation between increasing home BPV and a stepwise escalation in the risk of all-cause mortality among this population. In the discussion, the authors attributed this association to comorbid cardiovascular diseases, diabetes, systemic inflammation, and higher vascular stiffness. We believe that a more comprehensive characterization of vascular integrity impairment is needed to explain this BPV-outcome association.</p><p>Our team previously introduced the concept of vascular frailty, which elucidates vascular structural and functional degeneration leading to physical frailty or the coexistence of both phenotypes.<span><sup>2</sup></span> Vascular tissues are exquisitely susceptible to adverse consequences related to tissue senescence from chronological aging and metabotoxic stimuli, particularly uremic toxins. Vascular frailty manifests through structural degenerations such as vascular calcification and atherosclerosis, as well as functional perturbations like increased stiffness and vasomotor dysfunction. Uremic toxins predispose individuals with chronic kidney disease to developing physical frailty<span><sup>3</sup></span> and contribute to the pathogenesis of vascular frailty by inducing vascular calcification and increasing vascular stiffness,<span><sup>4</sup></span> thereby leading to higher BPV. It is widely acknowledged that ESKD patients are prone to developing vascular calcification over time. Moreover, individuals with ESKD exhibit accelerated aging and heightened tissue wear, culminating in physical frailty that significantly elevates mortality risk. Our previous findings demonstrated that ESKD patients with frailty faced a significantly higher risk of mortality compared with those without.<span><sup>5</sup></span></p><p>From this perspective, we recommend that the authors consider incorporating additional features of vascular frailty, such as measurements of vascular calcification severity and evidence of autonomic dysfunction, in their assessments of these patients. Doing so will facilitate a more thorough understanding of the mechanisms underlying the BPV-outcome association.</p><p>Szu-Ying Lee and Chia-Ter Chao are responsible for drafting of this manuscript.</p><p>The authors declare no conflict of interest.</p>\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-05-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/clc.24281\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/clc.24281\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/clc.24281","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0

摘要

Dong 等人研究了接受血液透析的终末期肾病(ESKD)患者的透析间期家庭血压变异性(BPV)与死亡率之间的关系1。在讨论中,作者将这种关联归因于合并心血管疾病、糖尿病、全身炎症和较高的血管僵硬度。2 血管组织极易受到慢性衰老和代谢毒性刺激(尤其是尿毒症毒素)导致的组织衰老的不良后果的影响。血管衰弱表现为血管钙化和动脉粥样硬化等结构性退化,以及僵硬度增加和血管运动功能障碍等功能性紊乱。尿毒症毒素使慢性肾脏病患者易患体质虚弱3 ,并通过诱导血管钙化和增加血管僵硬度4 从而导致更高的血压升高,从而促进血管虚弱的发病机制。众所周知,随着时间的推移,ESKD 患者容易出现血管钙化。此外,ESKD 患者的衰老速度加快,组织磨损加剧,最终导致身体虚弱,大大增加了死亡风险。我们之前的研究结果表明,与没有虚弱症状的 ESKD 患者相比,有虚弱症状的 ESKD 患者面临的死亡风险明显更高5。从这个角度出发,我们建议作者在评估这些患者时考虑纳入更多的血管虚弱特征,如血管钙化严重程度的测量和自主神经功能障碍的证据。这样做将有助于更透彻地了解 BPV 与结果之间的关联机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploring the role of vascular frailty in understanding blood pressure variability and mortality risk among end-stage kidney disease patients undergoing hemodialysis

Dong et al. investigated the relationship between interdialytic home blood pressure variability (BPV) and mortality in individuals with end-stage kidney disease (ESKD) undergoing hemodialysis.1 Their study revealed a notable correlation between increasing home BPV and a stepwise escalation in the risk of all-cause mortality among this population. In the discussion, the authors attributed this association to comorbid cardiovascular diseases, diabetes, systemic inflammation, and higher vascular stiffness. We believe that a more comprehensive characterization of vascular integrity impairment is needed to explain this BPV-outcome association.

Our team previously introduced the concept of vascular frailty, which elucidates vascular structural and functional degeneration leading to physical frailty or the coexistence of both phenotypes.2 Vascular tissues are exquisitely susceptible to adverse consequences related to tissue senescence from chronological aging and metabotoxic stimuli, particularly uremic toxins. Vascular frailty manifests through structural degenerations such as vascular calcification and atherosclerosis, as well as functional perturbations like increased stiffness and vasomotor dysfunction. Uremic toxins predispose individuals with chronic kidney disease to developing physical frailty3 and contribute to the pathogenesis of vascular frailty by inducing vascular calcification and increasing vascular stiffness,4 thereby leading to higher BPV. It is widely acknowledged that ESKD patients are prone to developing vascular calcification over time. Moreover, individuals with ESKD exhibit accelerated aging and heightened tissue wear, culminating in physical frailty that significantly elevates mortality risk. Our previous findings demonstrated that ESKD patients with frailty faced a significantly higher risk of mortality compared with those without.5

From this perspective, we recommend that the authors consider incorporating additional features of vascular frailty, such as measurements of vascular calcification severity and evidence of autonomic dysfunction, in their assessments of these patients. Doing so will facilitate a more thorough understanding of the mechanisms underlying the BPV-outcome association.

Szu-Ying Lee and Chia-Ter Chao are responsible for drafting of this manuscript.

The authors declare no conflict of interest.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
×
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:481959085
Book学术官方微信