定量评估慢性肾病对血浆 P-Tau217 浓度的影响

IF 7.7 1区 医学 Q1 CLINICAL NEUROLOGY
Joshua A Bornhorst,Carly S Lundgreen,Stephen D Weigand,Daniel J Figdore,Heather Wiste,Michael Griswold,Prashanthi Vemuri,Jonathan Graff-Radford,David S Knopman,Petrice Cogswell,Clifford R Jack,Ronald C Petersen,Alicia Algeciras-Schimnich
{"title":"定量评估慢性肾病对血浆 P-Tau217 浓度的影响","authors":"Joshua A Bornhorst,Carly S Lundgreen,Stephen D Weigand,Daniel J Figdore,Heather Wiste,Michael Griswold,Prashanthi Vemuri,Jonathan Graff-Radford,David S Knopman,Petrice Cogswell,Clifford R Jack,Ronald C Petersen,Alicia Algeciras-Schimnich","doi":"10.1212/wnl.0000000000210287","DOIUrl":null,"url":null,"abstract":"BACKGROUND AND OBJECTIVES\r\nChronic kidney disease (CKD) is known to be associated with increased plasma phosphorylated tau217 (p-tau217) concentrations, potentially confounding the utility of plasma p-tau217 measurements as a marker of amyloid pathology in individuals with suspected Alzheimer disease (AD). In this study, we quantitatively investigate the relationship of plasma p-tau217 concentrations vs estimated glomerular filtration rate (eGFR) in individuals with CKD with and without amyloid pathology.\r\n\r\nMETHODS\r\nThis was a retrospective examination of data from 2 observational cohorts from either the Mayo Clinic Study of Aging or the Alzheimer's Disease Research Center cohorts. p-Tau217 was determined using the ALZpath Simoa p-tau217 immunoassay and an immunoprecipitation mass spectrometry assay that simultaneously measures p-tau217 and nonphosphorylated-tau217 (np-tau217) to determine %p-tau217 ([p-tau217/nonphosphorylated-tau217]) × 100%) (C2N Diagnostics). Amyloid positivity was defined by amyloid-PET and a centiloid of ≥25. Log-log linear regression fits were used to quantitatively predict increases in plasma p-tau217 associated with decreasing eGFR.\r\n\r\nRESULTS\r\nParticipants (n = 202, mean age of 78 years, 38% female) with diagnoses of cognitive unimpairment (n = 109), mild cognitive impairment (n = 71), and dementia (n = 22) were included. In all, 114 (56%) of all participants were amyloid-PET positive (A+). In addition, 86 (43%) of all participants were classified as having CKD (CKD stages 3-4). p-Tau217 concentrations were significantly higher in A- participants with an eGFR of <60 (mL/min/1.73 m2), as compared with those with eGFR >60 A- participants. For an eGFR of 45 vs 60 in the A- cohort, the calculated percentage changes were +31%, +55%, and +19%, for ALZpath p-tau217, C2N p-tau217, and C2N %p-tau217, respectively. For the A+ cohort, the corresponding calculated percentage changes were +17%, +15%, and -5%, respectively.\r\n\r\nDISCUSSION\r\nCKD was associated with increased p-tau217 concentrations when measuring p-tau217 by ALZpath and C2N methodologies, but the effect was mitigated by the use of %p-tau217. These results indicate limitations for the utility of plasma p-tau217 measurements in individuals with significant renal impairment (eGFR <45 or CKD stage 3b or greater). Determination of eGFR should be considered to avoid inaccurate classification of the presence of AD-related pathology by plasma p-tau217 in individuals with CKD.\r\n\r\nCLASSIFICATION OF EVIDENCE\r\nThis study provides Class II evidence that in individuals with CKD stage 3 (especially stage 3b) or higher, p-tau217 concentrations are increased, with a greater increase in amyloid-PET-negative individuals.","PeriodicalId":19256,"journal":{"name":"Neurology","volume":"99 1","pages":"e210287"},"PeriodicalIF":7.7000,"publicationDate":"2025-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Quantitative Assessment of the Effect of Chronic Kidney Disease on Plasma P-Tau217 Concentrations.\",\"authors\":\"Joshua A Bornhorst,Carly S Lundgreen,Stephen D Weigand,Daniel J Figdore,Heather Wiste,Michael Griswold,Prashanthi Vemuri,Jonathan Graff-Radford,David S Knopman,Petrice Cogswell,Clifford R Jack,Ronald C Petersen,Alicia Algeciras-Schimnich\",\"doi\":\"10.1212/wnl.0000000000210287\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"BACKGROUND AND OBJECTIVES\\r\\nChronic kidney disease (CKD) is known to be associated with increased plasma phosphorylated tau217 (p-tau217) concentrations, potentially confounding the utility of plasma p-tau217 measurements as a marker of amyloid pathology in individuals with suspected Alzheimer disease (AD). In this study, we quantitatively investigate the relationship of plasma p-tau217 concentrations vs estimated glomerular filtration rate (eGFR) in individuals with CKD with and without amyloid pathology.\\r\\n\\r\\nMETHODS\\r\\nThis was a retrospective examination of data from 2 observational cohorts from either the Mayo Clinic Study of Aging or the Alzheimer's Disease Research Center cohorts. p-Tau217 was determined using the ALZpath Simoa p-tau217 immunoassay and an immunoprecipitation mass spectrometry assay that simultaneously measures p-tau217 and nonphosphorylated-tau217 (np-tau217) to determine %p-tau217 ([p-tau217/nonphosphorylated-tau217]) × 100%) (C2N Diagnostics). Amyloid positivity was defined by amyloid-PET and a centiloid of ≥25. Log-log linear regression fits were used to quantitatively predict increases in plasma p-tau217 associated with decreasing eGFR.\\r\\n\\r\\nRESULTS\\r\\nParticipants (n = 202, mean age of 78 years, 38% female) with diagnoses of cognitive unimpairment (n = 109), mild cognitive impairment (n = 71), and dementia (n = 22) were included. In all, 114 (56%) of all participants were amyloid-PET positive (A+). In addition, 86 (43%) of all participants were classified as having CKD (CKD stages 3-4). p-Tau217 concentrations were significantly higher in A- participants with an eGFR of <60 (mL/min/1.73 m2), as compared with those with eGFR >60 A- participants. For an eGFR of 45 vs 60 in the A- cohort, the calculated percentage changes were +31%, +55%, and +19%, for ALZpath p-tau217, C2N p-tau217, and C2N %p-tau217, respectively. For the A+ cohort, the corresponding calculated percentage changes were +17%, +15%, and -5%, respectively.\\r\\n\\r\\nDISCUSSION\\r\\nCKD was associated with increased p-tau217 concentrations when measuring p-tau217 by ALZpath and C2N methodologies, but the effect was mitigated by the use of %p-tau217. These results indicate limitations for the utility of plasma p-tau217 measurements in individuals with significant renal impairment (eGFR <45 or CKD stage 3b or greater). Determination of eGFR should be considered to avoid inaccurate classification of the presence of AD-related pathology by plasma p-tau217 in individuals with CKD.\\r\\n\\r\\nCLASSIFICATION OF EVIDENCE\\r\\nThis study provides Class II evidence that in individuals with CKD stage 3 (especially stage 3b) or higher, p-tau217 concentrations are increased, with a greater increase in amyloid-PET-negative individuals.\",\"PeriodicalId\":19256,\"journal\":{\"name\":\"Neurology\",\"volume\":\"99 1\",\"pages\":\"e210287\"},\"PeriodicalIF\":7.7000,\"publicationDate\":\"2025-01-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Neurology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1212/wnl.0000000000210287\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1212/wnl.0000000000210287","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景与目的慢性肾脏疾病(CKD)与血浆磷酸化tau217 (p-tau217)浓度升高有关,这可能会混淆血浆p-tau217测量作为疑似阿尔茨海默病(AD)患者淀粉样蛋白病理标志物的应用。在这项研究中,我们定量研究了伴有和不伴有淀粉样蛋白病理的CKD患者血浆p-tau217浓度与肾小球滤过率(eGFR)的关系。方法回顾性分析来自梅奥临床衰老研究或阿尔茨海默病研究中心的2个观察性队列的数据。p-Tau217采用ALZpath Simoa p-Tau217免疫分析法和免疫沉淀质谱法测定,同时测量p-Tau217和非磷酸化-tau217 (np-tau217),以确定% p-Tau217 ([p-Tau217 /非磷酸化-tau217]) × 100%) (C2N Diagnostics)。淀粉样蛋白阳性由淀粉样蛋白- pet和≥25的centiloid来定义。对数-对数线性回归拟合用于定量预测血浆p-tau217升高与eGFR降低相关。结果纳入诊断为认知功能正常(n = 109)、轻度认知功能障碍(n = 71)和痴呆(n = 22)的参与者(n = 202,平均年龄78岁,女性38%)。所有参与者中有114人(56%)为淀粉样蛋白pet阳性(A+)。此外,所有参与者中有86人(43%)被归类为CKD (CKD 3-4期)。p-Tau217浓度在eGFR为60的A-参与者中显著升高。在A-队列中,eGFR为45 vs 60时,ALZpath p-tau217、C2N p-tau217和C2N %p-tau217的计算百分比变化分别为+31%、+55%和+19%。对于A+队列,相应的计算百分比变化分别为+17%,+15%和-5%。当使用ALZpath和C2N方法测量p-tau217时,ckd与p-tau217浓度增加有关,但使用%p-tau217可以减轻这种影响。这些结果表明血浆p-tau217测量在严重肾功能损害(eGFR <45或CKD 3b期或以上)个体中的应用存在局限性。应考虑eGFR的测定,以避免CKD患者血浆p-tau217对ad相关病理的不准确分类。证据分类:本研究提供的II类证据表明,在CKD 3期(尤其是3b期)或更高阶段的个体中,p- ta217浓度升高,淀粉样蛋白pet阴性个体中p- ta217浓度升高更大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantitative Assessment of the Effect of Chronic Kidney Disease on Plasma P-Tau217 Concentrations.
BACKGROUND AND OBJECTIVES Chronic kidney disease (CKD) is known to be associated with increased plasma phosphorylated tau217 (p-tau217) concentrations, potentially confounding the utility of plasma p-tau217 measurements as a marker of amyloid pathology in individuals with suspected Alzheimer disease (AD). In this study, we quantitatively investigate the relationship of plasma p-tau217 concentrations vs estimated glomerular filtration rate (eGFR) in individuals with CKD with and without amyloid pathology. METHODS This was a retrospective examination of data from 2 observational cohorts from either the Mayo Clinic Study of Aging or the Alzheimer's Disease Research Center cohorts. p-Tau217 was determined using the ALZpath Simoa p-tau217 immunoassay and an immunoprecipitation mass spectrometry assay that simultaneously measures p-tau217 and nonphosphorylated-tau217 (np-tau217) to determine %p-tau217 ([p-tau217/nonphosphorylated-tau217]) × 100%) (C2N Diagnostics). Amyloid positivity was defined by amyloid-PET and a centiloid of ≥25. Log-log linear regression fits were used to quantitatively predict increases in plasma p-tau217 associated with decreasing eGFR. RESULTS Participants (n = 202, mean age of 78 years, 38% female) with diagnoses of cognitive unimpairment (n = 109), mild cognitive impairment (n = 71), and dementia (n = 22) were included. In all, 114 (56%) of all participants were amyloid-PET positive (A+). In addition, 86 (43%) of all participants were classified as having CKD (CKD stages 3-4). p-Tau217 concentrations were significantly higher in A- participants with an eGFR of <60 (mL/min/1.73 m2), as compared with those with eGFR >60 A- participants. For an eGFR of 45 vs 60 in the A- cohort, the calculated percentage changes were +31%, +55%, and +19%, for ALZpath p-tau217, C2N p-tau217, and C2N %p-tau217, respectively. For the A+ cohort, the corresponding calculated percentage changes were +17%, +15%, and -5%, respectively. DISCUSSION CKD was associated with increased p-tau217 concentrations when measuring p-tau217 by ALZpath and C2N methodologies, but the effect was mitigated by the use of %p-tau217. These results indicate limitations for the utility of plasma p-tau217 measurements in individuals with significant renal impairment (eGFR <45 or CKD stage 3b or greater). Determination of eGFR should be considered to avoid inaccurate classification of the presence of AD-related pathology by plasma p-tau217 in individuals with CKD. CLASSIFICATION OF EVIDENCE This study provides Class II evidence that in individuals with CKD stage 3 (especially stage 3b) or higher, p-tau217 concentrations are increased, with a greater increase in amyloid-PET-negative individuals.
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
Neurology
Neurology 医学-临床神经学
CiteScore
12.20
自引率
4.00%
发文量
1973
审稿时长
2-3 weeks
期刊介绍: Neurology, the official journal of the American Academy of Neurology, aspires to be the premier peer-reviewed journal for clinical neurology research. Its mission is to publish exceptional peer-reviewed original research articles, editorials, and reviews to improve patient care, education, clinical research, and professionalism in neurology. As the leading clinical neurology journal worldwide, Neurology targets physicians specializing in nervous system diseases and conditions. It aims to advance the field by presenting new basic and clinical research that influences neurological practice. The journal is a leading source of cutting-edge, peer-reviewed information for the neurology community worldwide. Editorial content includes Research, Clinical/Scientific Notes, Views, Historical Neurology, NeuroImages, Humanities, Letters, and position papers from the American Academy of Neurology. The online version is considered the definitive version, encompassing all available content. Neurology is indexed in prestigious databases such as MEDLINE/PubMed, Embase, Scopus, Biological Abstracts®, PsycINFO®, Current Contents®, Web of Science®, CrossRef, and Google Scholar.
×
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