Correlation Between Urine Formaldehyde and Cognitive Abilities in the Clinical Spectrum of Alzheimer's Disease

被引:19
作者
Wang, Ying [1 ]
Pan, Fengfeng [1 ]
Xie, Fang [2 ]
He, Rongqiao [3 ,4 ]
Guo, Qihao [1 ]
机构
[1] Shanghai Jiao Tong Univ, Dept Gerontol, Affiliated Sixth Peoples Hosp, Shanghai, Peoples R China
[2] Fudan Univ, Huashan Hosp, PET Ctr, Shanghai, Peoples R China
[3] Chinese Acad Sci, Inst Biophys, State Key Lab Brain & Cognit Sci, Beijing, Peoples R China
[4] Chinese Acad Sci, Inst Psychol, Key Lab Mental Hlth, Beijing, Peoples R China
来源
FRONTIERS IN AGING NEUROSCIENCE | 2022年 / 14卷
基金
国家重点研发计划; 美国国家科学基金会;
关键词
Alzhaimer's disease; urine formaldehyde; biomarker; APOE; beta-amylaoid; ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; APOLIPOPROTEIN-E; NEUROFILAMENT LIGHT; THREAD PROTEIN; TAU; IMPAIRMENT; BIOMARKERS; HYPERPHOSPHORYLATION;
D O I
10.3389/fnagi.2022.820385
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Urine-based formaldehyde has been reported to be a potential biomarker for Alzheimer's disease (AD). However, there is a lack of research about the correlation between urine formaldehyde and cognitive abilities in the clinical spectrum of AD, especially the preclinical period. The relationship of urine formaldehyde with APOE genotype, brain A beta status and plasma pathological markers in AD are also not clear. This study intends to explore the correlation between urine formaldehyde and cognitive abilities throughout the AD continuum, to evaluate the role of APOE genotype and A beta accumulation on urine formaldehyde, and further to clarify the relationship between urine formaldehyde level and AD plasma pathological markers. We recruited 72 cognitively normal controls (NC), 110 subjective cognitive decline (SCD), 140 objectively defined subtle cognitive decline (Obj-SCD), 171 mild cognitive impairment (MCI) and 136 AD dementia participants. Next, we collected the data of clinical materials, neuropsychological examination, APOE genotyping, urine formaldehyde concentration, 18F-florbetapir PET imaging and plasma biomarkers. Compared with NC, Obj-SCD and MCI groups, the level of urine formaldehyde was found to be significantly upregulated in SCD group. In addition, the level of urine formaldehyde was significantly higher in AD group compared to both NC and MCI groups. Further subgroup analysis showed that, the level of urine formaldehyde was higher in APOE epsilon 4+ subgroup compared to APOE epsilon 4- subgroup in both NC and AD groups. There was no difference in urine formaldehyde level between the brain A beta+ subgroup and A beta- subgroup in each group. In addition, regression analysis showed urine formaldehyde level was correlated with gender, plasma A beta 42 and p-Tau181/T-tau. The dynamic change of urine formaldehyde in the AD continuum could be used as a potential biomarker, and combined with comprehensive cognitive evaluation could become a useful method to distinguish SCD from NC and Obj-SCD, and to distinguish MCI from AD.
引用
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页数:11
相关论文
共 57 条
[1]   On the path to 2025: understanding the Alzheimer's disease continuum [J].
Aisen, Paul S. ;
Cummings, Jeffrey ;
Jack, Clifford R., Jr. ;
Morris, John C. ;
Sperling, Reisa ;
Froelich, Lutz ;
Jones, Roy W. ;
Dowsett, Sherie A. ;
Matthews, Brandy R. ;
Raskin, Joel ;
Scheltens, Philip ;
Dubois, Bruno .
ALZHEIMERS RESEARCH & THERAPY, 2017, 9
[2]   The diagnosis of mild cognitive impairment due to Alzheimer's disease: Recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease [J].
Albert, Marilyn S. ;
DeKosky, Steven T. ;
Dickson, Dennis ;
Dubois, Bruno ;
Feldman, Howard H. ;
Fox, Nick C. ;
Gamst, Anthony ;
Holtzman, David M. ;
Jagust, William J. ;
Petersen, Ronald C. ;
Snyder, Peter J. ;
Carrillo, Maria C. ;
Thies, Bill ;
Phelps, Creighton H. .
ALZHEIMERS & DEMENTIA, 2011, 7 (03) :270-279
[4]   Urinary Biomarkers of Brain Diseases [J].
An, Manxia ;
Gao, Youhe .
GENOMICS PROTEOMICS & BIOINFORMATICS, 2015, 13 (06) :345-354
[5]   Body Fluid Biomarkers for Alzheimer's Disease-An Up-To-Date Overview [J].
Balasa, Adrian Florian ;
Chircov, Cristina ;
Grumezescu, Alexandru Mihai .
BIOMEDICINES, 2020, 8 (10) :1-21
[6]   Neuropsychological Criteria for Mild Cognitive Impairment Improves Diagnostic Precision, Biomarker Associations, and Progression Rates [J].
Bondi, Mark W. ;
Edmonds, Emily C. ;
Jak, Amy J. ;
Clark, Lindsay R. ;
Delano-Wood, Lisa ;
McDonald, Carrie R. ;
Nation, Daniel A. ;
Libon, David J. ;
Au, Rhoda ;
Galasko, Douglas ;
Salmon, David P. .
JOURNAL OF ALZHEIMERS DISEASE, 2014, 42 (01) :275-289
[7]   Potential implications of endogenous aldehydes in β-amyloid misfolding, oligomerization and fibrillogenesis [J].
Chen, Kun ;
Maley, Jason ;
Yu, Peter H. .
JOURNAL OF NEUROCHEMISTRY, 2006, 99 (05) :1413-1424
[8]   Plasma P-tau181 to Aβ42 ratio is associated with brain amyloid burden and hippocampal atrophy in an Asian cohort of Alzheimer's disease patients with concomitant cerebrovascular disease [J].
Chong, Joyce R. ;
Ashton, Nicholas J. ;
Karikari, Thomas K. ;
Tanaka, Tomotaka ;
Saridin, Francis N. ;
Reilhac, Anthonin ;
Robins, Edward G. ;
Nai, Ying-Hwey ;
Vrooman, Henri ;
Hilal, Saima ;
Zetterberg, Henrik ;
Blennow, Kaj ;
Lai, Mitchell K. P. ;
Chen, Christopher P. .
ALZHEIMERS & DEMENTIA, 2021, 17 (10) :1649-1662
[9]   GENE DOSE OF APOLIPOPROTEIN-E TYPE-4 ALLELE AND THE RISK OF ALZHEIMERS-DISEASE IN LATE-ONSET FAMILIES [J].
CORDER, EH ;
SAUNDERS, AM ;
STRITTMATTER, WJ ;
SCHMECHEL, DE ;
GASKELL, PC ;
SMALL, GW ;
ROSES, AD ;
HAINES, JL ;
PERICAKVANCE, MA .
SCIENCE, 1993, 261 (5123) :921-923
[10]   Local Functional MR Change Pattern and Its Association With Cognitive Function in Objectively-Defined Subtle Cognitive Decline [J].
Cui, Liang ;
Zhang, Zhen ;
Zac Lo, Chun-Yi ;
Guo, Qihao .
FRONTIERS IN AGING NEUROSCIENCE, 2021, 13