Frederikke Kragh Clemmensen, Fernando Gonzalez-Ortiz, Mathias Holsey Gramkow, Cristano Santos, Henrik Zetterberg, Kaj Blennow, Steen Gregers Hasselbalch, Kristian Steen Frederiksen, Anja Hviid Simonsen
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Patients were dichotomized by cerebrospinal fluid (CSF) amyloidosis (Aβ+ = 29, Aβ− = 18). We compared intra- and inter-individual variability (coefficient of variation [CV]) in the plasma p-tau217/BD-tau ratio with p-tau217 alone and tested if kidney function, glycated hemoglobin, and body mass index (BMI) affected the variability. Finally, we compared the p-tau217/BD-tau ratio with CSF p-tau217.</p>\n </section>\n \n <section>\n \n <h3> RESULTS</h3>\n \n <p>We found that for Aβ+ individuals, the intra-individual variability of the plasma p-tau217/BD-tau ratio (CV 7.1% [95% confidence interval {CI} 5.6;8.4]) was lower than for p-tau217 alone (CV 9.4% [95% CI 7.4;11.5]). At the group level, the variability in the p-tau217/BD-tau ratio was reduced in both Aβ+ (CV 15.1% [95% CI 11.7;18.7]) and Aβ− (CV 18.4% [95% CI 13.0;23.8]) individuals compared to p-tau217 alone (Aβ+ CV 19.1 [15.0;23.4], Aβ− 27.1 [18.4;36.0]). Adjusting for estimated glomerular filtration rate, hemoglobin A1C, and BMI further reduced the inter-individual variability of p-tau217/BD-tau in the Aβ+ group. CSF p-tau217 showed higher correlation with plasma p-tau217/BD-tau (rho = 0.53, <i>p</i> = 0.0005) than with p-tau217 alone (rho = 0.37, <i>p</i> = 0.02).</p>\n </section>\n \n <section>\n \n <h3> DISCUSSION</h3>\n \n <p>Our findings suggest that using the ratio of plasma p-tau217 to plasma BD-tau and accounting for the influence of peripheral confounders improves biomarker stability, which is important for the interpretation of longitudinal biomarker changes and to prevent misclassification.</p>\n </section>\n \n <section>\n \n <h3> HIGHLIGHTS</h3>\n \n <div>\n <ul>\n \n <li>The plasma p-tau217/BD-tau ratio lowered short-term intra- and, especially, inter-individual variability compared to the variability in plasma p-tau217 alone.</li>\n \n <li>Plasma BD-tau did not correlate with eGFR, HbA1c, or BMI, while plasma p-tau217 was significantly negatively associated with BMI.</li>\n \n <li>Adjusting for eGFR, HbA1c, and BMI further reduced the inter-individual variability of p-tau217/BD-tau.</li>\n \n <li>Additionally, CSF p-tau217 correlated better with plasma p-tau217/BD-tau than with p-tau217 alone.</li>\n </ul>\n </div>\n </section>\n </div>","PeriodicalId":53225,"journal":{"name":"Alzheimer''s and Dementia: Translational Research and Clinical Interventions","volume":"11 3","pages":""},"PeriodicalIF":6.8000,"publicationDate":"2025-08-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://alz-journals.onlinelibrary.wiley.com/doi/epdf/10.1002/trc2.70143","citationCount":"0","resultStr":"{\"title\":\"The plasma p-tau217/BD-tau ratio improves biomarker short-term variability in memory clinic patients\",\"authors\":\"Frederikke Kragh Clemmensen, Fernando Gonzalez-Ortiz, Mathias Holsey Gramkow, Cristano Santos, Henrik Zetterberg, Kaj Blennow, Steen Gregers Hasselbalch, Kristian Steen Frederiksen, Anja Hviid Simonsen\",\"doi\":\"10.1002/trc2.70143\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> INTRODUCTION</h3>\\n \\n <p>Assessment of short-term intra- and inter-individual variability for Alzheimer's disease (AD) plasma biomarkers is essential for clinically relevant interpretation of biomarker levels. 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引用次数: 0
摘要
评估阿尔茨海默病(AD)血浆生物标志物的短期个体内和个体间变异性对于生物标志物水平的临床相关解释至关重要。我们假设在苏氨酸217位点磷酸化的血浆tau蛋白(p-tau217)的可变性可以通过将其与tau标记物血浆脑源性tau蛋白(BD-tau)结合作为p-tau217/BD-tau比值来降低。方法对记忆门诊患者在36天内连续采集3份血样。脑脊液(CSF)淀粉样变患者分为Aβ+ = 29, Aβ−= 18。我们比较了血浆p-tau217/BD-tau比值与单独p-tau217的个体内变异性和个体间变异性(变异系数[CV]),并检测了肾功能、糖化血红蛋白和体重指数(BMI)是否影响这种变异性。最后,我们比较了p-tau217/BD-tau与CSF p-tau217的比值。结果我们发现,在Aβ+个体中,血浆p-tau217/BD-tau比值的个体内变异性(CV为7.1%[95%可信区间{CI} 5.6;8.4])低于单独p-tau217的个体内变异性(CV为9.4%[95%可信区间{CI} 7.4;11.5])。在组水平上,与单独使用p-tau217 (Aβ+ CV 19.1 [15.0;23.4], Aβ−27.1[18.4;36.0])相比,Aβ+个体(CV 15.1% [95% CI 11.7;18.7])和Aβ−个体(CV 18.4% [95% CI 13.0;23.8]) p-tau217/ bb -tau比值的变异性降低。调整估计的肾小球滤过率、血红蛋白A1C和BMI进一步降低了Aβ+组中p-tau217/BD-tau的个体间变异性。脑脊液p-tau217与血浆p-tau217/BD-tau的相关性(rho = 0.53, p = 0.0005)高于单独p-tau217 (rho = 0.37, p = 0.02)。我们的研究结果表明,使用血浆p-tau217与血浆BD-tau的比例,并考虑外周混杂因素的影响,可以提高生物标志物的稳定性,这对于解释纵向生物标志物变化和防止错误分类很重要。与单独使用血浆p-tau217相比,血浆p-tau217/BD-tau比值降低了短期内,特别是个体间的变异性。血浆BD-tau与eGFR、HbA1c或BMI无关,而血浆p-tau217与BMI呈显著负相关。调整eGFR、HbA1c和BMI进一步降低了p-tau217/BD-tau的个体间变异性。此外,CSF p-tau217与血浆p-tau217/BD-tau的相关性优于单独的p-tau217。
The plasma p-tau217/BD-tau ratio improves biomarker short-term variability in memory clinic patients
INTRODUCTION
Assessment of short-term intra- and inter-individual variability for Alzheimer's disease (AD) plasma biomarkers is essential for clinically relevant interpretation of biomarker levels. We hypothesized that the variability of plasma tau phosphorylated at threonine 217 (p-tau217) could be reduced by combining it with a tau marker, plasma brain-derived tau (BD-tau), as the p-tau217/BD-tau ratio.
METHODS
Three consecutive blood samples were collected from memory clinic patients within 36 days. Patients were dichotomized by cerebrospinal fluid (CSF) amyloidosis (Aβ+ = 29, Aβ− = 18). We compared intra- and inter-individual variability (coefficient of variation [CV]) in the plasma p-tau217/BD-tau ratio with p-tau217 alone and tested if kidney function, glycated hemoglobin, and body mass index (BMI) affected the variability. Finally, we compared the p-tau217/BD-tau ratio with CSF p-tau217.
RESULTS
We found that for Aβ+ individuals, the intra-individual variability of the plasma p-tau217/BD-tau ratio (CV 7.1% [95% confidence interval {CI} 5.6;8.4]) was lower than for p-tau217 alone (CV 9.4% [95% CI 7.4;11.5]). At the group level, the variability in the p-tau217/BD-tau ratio was reduced in both Aβ+ (CV 15.1% [95% CI 11.7;18.7]) and Aβ− (CV 18.4% [95% CI 13.0;23.8]) individuals compared to p-tau217 alone (Aβ+ CV 19.1 [15.0;23.4], Aβ− 27.1 [18.4;36.0]). Adjusting for estimated glomerular filtration rate, hemoglobin A1C, and BMI further reduced the inter-individual variability of p-tau217/BD-tau in the Aβ+ group. CSF p-tau217 showed higher correlation with plasma p-tau217/BD-tau (rho = 0.53, p = 0.0005) than with p-tau217 alone (rho = 0.37, p = 0.02).
DISCUSSION
Our findings suggest that using the ratio of plasma p-tau217 to plasma BD-tau and accounting for the influence of peripheral confounders improves biomarker stability, which is important for the interpretation of longitudinal biomarker changes and to prevent misclassification.
HIGHLIGHTS
The plasma p-tau217/BD-tau ratio lowered short-term intra- and, especially, inter-individual variability compared to the variability in plasma p-tau217 alone.
Plasma BD-tau did not correlate with eGFR, HbA1c, or BMI, while plasma p-tau217 was significantly negatively associated with BMI.
Adjusting for eGFR, HbA1c, and BMI further reduced the inter-individual variability of p-tau217/BD-tau.
Additionally, CSF p-tau217 correlated better with plasma p-tau217/BD-tau than with p-tau217 alone.
期刊介绍:
Alzheimer''s & Dementia: Translational Research & Clinical Interventions (TRCI) is a peer-reviewed, open access,journal from the Alzheimer''s Association®. The journal seeks to bridge the full scope of explorations between basic research on drug discovery and clinical studies, validating putative therapies for aging-related chronic brain conditions that affect cognition, motor functions, and other behavioral or clinical symptoms associated with all forms dementia and Alzheimer''s disease. The journal will publish findings from diverse domains of research and disciplines to accelerate the conversion of abstract facts into practical knowledge: specifically, to translate what is learned at the bench into bedside applications. The journal seeks to publish articles that go beyond a singular emphasis on either basic drug discovery research or clinical research. Rather, an important theme of articles will be the linkages between and among the various discrete steps in the complex continuum of therapy development. For rapid communication among a multidisciplinary research audience involving the range of therapeutic interventions, TRCI will consider only original contributions that include feature length research articles, systematic reviews, meta-analyses, brief reports, narrative reviews, commentaries, letters, perspectives, and research news that would advance wide range of interventions to ameliorate symptoms or alter the progression of chronic neurocognitive disorders such as dementia and Alzheimer''s disease. The journal will publish on topics related to medicine, geriatrics, neuroscience, neurophysiology, neurology, psychiatry, clinical psychology, bioinformatics, pharmaco-genetics, regulatory issues, health economics, pharmacoeconomics, and public health policy as these apply to preclinical and clinical research on therapeutics.