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Systematic evaluation of urinary formic acid as a new potential biomarker for Alzheimer’s disease

INTRODUCTION: The accumulation of endogenous formaldehyde is considered a pathogenic factor in Alzheimer’s disease (AD). The purpose of this study was to investigate the relationship between urinary formic acid and plasma biomarkers in AD. MATERIALS AND METHODS: Five hundred and seventy-four partici...

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Autores principales: Wang, Yifan, Wang, Ying, Zhu, Jinhang, Guan, Yihui, Xie, Fang, Cai, Xiao, Deng, Jiale, Wei, Yan, He, Rongqiao, Fang, Zhuo, Guo, Qihao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747776/
https://www.ncbi.nlm.nih.gov/pubmed/36533170
http://dx.doi.org/10.3389/fnagi.2022.1046066
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author Wang, Yifan
Wang, Ying
Zhu, Jinhang
Guan, Yihui
Xie, Fang
Cai, Xiao
Deng, Jiale
Wei, Yan
He, Rongqiao
Fang, Zhuo
Guo, Qihao
author_facet Wang, Yifan
Wang, Ying
Zhu, Jinhang
Guan, Yihui
Xie, Fang
Cai, Xiao
Deng, Jiale
Wei, Yan
He, Rongqiao
Fang, Zhuo
Guo, Qihao
author_sort Wang, Yifan
collection PubMed
description INTRODUCTION: The accumulation of endogenous formaldehyde is considered a pathogenic factor in Alzheimer’s disease (AD). The purpose of this study was to investigate the relationship between urinary formic acid and plasma biomarkers in AD. MATERIALS AND METHODS: Five hundred and seventy-four participants were divided into five groups according to their diagnosis: 71 with normal cognitive (NC), 101 with subjective cognitive decline (SCD), 131 with cognitive impairment without mild cognitive impairment (CINM), 158 with mild cognitive impairment (MCI), and 113 with AD. RESULTS: With the progression of the disease, urinary formic acid levels showed an overall upward trend. Urinary formic acid was significantly correlated with Mini-Mental State Examination (MMSE) scores, the Chinese version of Addenbrooke’s Cognitive Examination III (ACE-III) scores, and Montreal Cognitive Assessment-Basic (MoCA-B) time. The areas under the receiver operating characteristic curves (AUC) of urinary formic acid in distinguishing NC from AD was 0.797, which was similar to that of plasma neurofilament light chain (NfL; AUC = 0.768) and better than other plasma biomarkers (Aβ40, Aβ42, Aβ42/Aβ40, T-tau, P-tau181, and P-tau181/T-tau). We also found that using urinary formic acid and formaldehyde levels could improve the accuracy of using plasma biomarkers to determine AD disease stage. DISCUSSION: Our study revealed the possibility of urinary formic acid as a potential novel biomarker for the early diagnosis of AD.
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spelling pubmed-97477762022-12-15 Systematic evaluation of urinary formic acid as a new potential biomarker for Alzheimer’s disease Wang, Yifan Wang, Ying Zhu, Jinhang Guan, Yihui Xie, Fang Cai, Xiao Deng, Jiale Wei, Yan He, Rongqiao Fang, Zhuo Guo, Qihao Front Aging Neurosci Neuroscience INTRODUCTION: The accumulation of endogenous formaldehyde is considered a pathogenic factor in Alzheimer’s disease (AD). The purpose of this study was to investigate the relationship between urinary formic acid and plasma biomarkers in AD. MATERIALS AND METHODS: Five hundred and seventy-four participants were divided into five groups according to their diagnosis: 71 with normal cognitive (NC), 101 with subjective cognitive decline (SCD), 131 with cognitive impairment without mild cognitive impairment (CINM), 158 with mild cognitive impairment (MCI), and 113 with AD. RESULTS: With the progression of the disease, urinary formic acid levels showed an overall upward trend. Urinary formic acid was significantly correlated with Mini-Mental State Examination (MMSE) scores, the Chinese version of Addenbrooke’s Cognitive Examination III (ACE-III) scores, and Montreal Cognitive Assessment-Basic (MoCA-B) time. The areas under the receiver operating characteristic curves (AUC) of urinary formic acid in distinguishing NC from AD was 0.797, which was similar to that of plasma neurofilament light chain (NfL; AUC = 0.768) and better than other plasma biomarkers (Aβ40, Aβ42, Aβ42/Aβ40, T-tau, P-tau181, and P-tau181/T-tau). We also found that using urinary formic acid and formaldehyde levels could improve the accuracy of using plasma biomarkers to determine AD disease stage. DISCUSSION: Our study revealed the possibility of urinary formic acid as a potential novel biomarker for the early diagnosis of AD. Frontiers Media S.A. 2022-11-30 /pmc/articles/PMC9747776/ /pubmed/36533170 http://dx.doi.org/10.3389/fnagi.2022.1046066 Text en Copyright © 2022 Wang, Wang, Zhu, Guan, Xie, Cai, Deng, Wei, He, Fang and Guo. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Wang, Yifan
Wang, Ying
Zhu, Jinhang
Guan, Yihui
Xie, Fang
Cai, Xiao
Deng, Jiale
Wei, Yan
He, Rongqiao
Fang, Zhuo
Guo, Qihao
Systematic evaluation of urinary formic acid as a new potential biomarker for Alzheimer’s disease
title Systematic evaluation of urinary formic acid as a new potential biomarker for Alzheimer’s disease
title_full Systematic evaluation of urinary formic acid as a new potential biomarker for Alzheimer’s disease
title_fullStr Systematic evaluation of urinary formic acid as a new potential biomarker for Alzheimer’s disease
title_full_unstemmed Systematic evaluation of urinary formic acid as a new potential biomarker for Alzheimer’s disease
title_short Systematic evaluation of urinary formic acid as a new potential biomarker for Alzheimer’s disease
title_sort systematic evaluation of urinary formic acid as a new potential biomarker for alzheimer’s disease
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747776/
https://www.ncbi.nlm.nih.gov/pubmed/36533170
http://dx.doi.org/10.3389/fnagi.2022.1046066
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