Urinary Amino Acid-Conjugated Acrolein and Taurine as New Biomarkers for Detection of Dementia.

Alzheimer’s disease Mini-Mental State Examination amino acid-conjugated acrolein (AC-Acro) taurine urinary biomarkers

Journal

Journal of Alzheimer's disease : JAD
ISSN: 1875-8908
Titre abrégé: J Alzheimers Dis
Pays: Netherlands
ID NLM: 9814863

Informations de publication

Date de publication:
2023
Historique:
pubmed: 7 2 2023
medline: 15 3 2023
entrez: 6 2 2023
Statut: ppublish

Résumé

Dementia, including Alzheimer's disease (AD), is one of the serious diseases at advanced age, and its early detection is important for maintaining quality of life (QOL). In this study, we sought novel biomarkers for dementia in urine. Samples of urine were collected from 57 control subjects without dementia, 62 mild cognitive impairment (MCI) patients, and 42 AD patients. Mini-Mental State Examination (MMSE) was evaluated when subjects were examined by medical doctors. Urinary amino acid (lysine)-conjugated acrolein (AC-Acro) was measured using N ɛ-(3-formyl-3, 4-dehydropiperidine) lysine (FDP-Lys) ELISA kit, and taurine content was measured using a taurine assay kit. Values were normalized by creatinine content which was measured with the colorimetric assay kit. We found that urinary amino acid (lysine)-conjugated acrolein (AC-Acro) and taurine negatively correlated with MMSE score and are significantly lower in dementia patients compared to the normal subjects. When AC-Acro and taurine were evaluated together with age using an artificial neural network model, median relative risk values for subjects with AD, subjects with mild cognitive impairment, and control subjects were 0.96, 0.53, and 0.06, respectively. Since urine is relatively easy to collect, our findings provide a novel biomarker for dementia without invasiveness.

Sections du résumé

BACKGROUND
Dementia, including Alzheimer's disease (AD), is one of the serious diseases at advanced age, and its early detection is important for maintaining quality of life (QOL).
OBJECTIVE
In this study, we sought novel biomarkers for dementia in urine.
METHODS
Samples of urine were collected from 57 control subjects without dementia, 62 mild cognitive impairment (MCI) patients, and 42 AD patients. Mini-Mental State Examination (MMSE) was evaluated when subjects were examined by medical doctors. Urinary amino acid (lysine)-conjugated acrolein (AC-Acro) was measured using N ɛ-(3-formyl-3, 4-dehydropiperidine) lysine (FDP-Lys) ELISA kit, and taurine content was measured using a taurine assay kit. Values were normalized by creatinine content which was measured with the colorimetric assay kit.
RESULTS
We found that urinary amino acid (lysine)-conjugated acrolein (AC-Acro) and taurine negatively correlated with MMSE score and are significantly lower in dementia patients compared to the normal subjects. When AC-Acro and taurine were evaluated together with age using an artificial neural network model, median relative risk values for subjects with AD, subjects with mild cognitive impairment, and control subjects were 0.96, 0.53, and 0.06, respectively.
CONCLUSION
Since urine is relatively easy to collect, our findings provide a novel biomarker for dementia without invasiveness.

Identifiants

pubmed: 36744340
pii: JAD220912
doi: 10.3233/JAD-220912
doi:

Substances chimiques

Acrolein 7864XYD3JJ
Lysine K3Z4F929H6
Biomarkers 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

361-369

Auteurs

Madoka Yoshida (M)

Amine Pharma Research Institute, Innovation Plaza at Chiba University, Chiba, Japan.

Takeshi Uemura (T)

Amine Pharma Research Institute, Innovation Plaza at Chiba University, Chiba, Japan.
Graduate School of Pharmaceutical Sciences, Chiba University, Chiba, Japan.

Mutsumi Mizoi (M)

Amine Pharma Research Institute, Innovation Plaza at Chiba University, Chiba, Japan.

Masaaki Waragai (M)

Higashi-Matsudo Municipal Hospital, Matsudo, Chiba, Japan.

Akihiko Sakamoto (A)

Faculty of Pharmacy, Chiba Institute of Science, Choshi, Chiba, Japan.

Yusuke Terui (Y)

Faculty of Pharmacy, Chiba Institute of Science, Choshi, Chiba, Japan.

Keiko Kashiwagi (K)

Faculty of Pharmacy, Chiba Institute of Science, Choshi, Chiba, Japan.

Kazuei Igarashi (K)

Amine Pharma Research Institute, Innovation Plaza at Chiba University, Chiba, Japan.
Graduate School of Pharmaceutical Sciences, Chiba University, Chiba, Japan.

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