Serum d-serine levels are altered in early phases of Alzheimer’s disease: towards a precocious biomarker
d -Serine acts as a co-agonist of N -methyl- d -aspartate receptors (NMDAR) which appear overactivated in AD, while d -aspartate is a modulatory molecule acting on NMDAR as a second agonist. The aim of this work is to clarify whether the levels of these d -amino acids in serum are deregulated in AD,...
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Published in | Translational psychiatry Vol. 11; no. 1; pp. 77 - 8 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
26.01.2021
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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Summary: | d
-Serine acts as a co-agonist of
N
-methyl-
d
-aspartate receptors (NMDAR) which appear overactivated in AD, while
d
-aspartate is a modulatory molecule acting on NMDAR as a second agonist. The aim of this work is to clarify whether the levels of these
d
-amino acids in serum are deregulated in AD, with the final goal to identify novel and precocious biomarkers in AD. Serum levels of
l
- and
d
-enantiomers of serine and aspartate were determined by HPLC using a pre-column derivatization procedure and a selective enzymatic degradation. Experimental data obtained from age-matched healthy subjects (HS) and AD patients were statistically evaluated by considering age, gender, and disease progression, and compared. Minor changes were apparent in the serum
l
- and
d
-aspartate levels in AD patients compared to HS. A positive correlation for the
d
-serine level and age was apparent in the AD cohort. Notably, the serum
d
-serine level and the
d
-/total serine ratio significantly increased with the progression of the disease. Gender seems to have a minor effect on the levels of all analytes tested. This work proposes that the serum
d
-serine level and
d
-/total serine ratio values as novel and valuable biomarkers for the progression of AD: the latter parameter allows to discriminate CDR 2 and CDR 1 patients from healthy (CDR 0) individuals. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 2158-3188 2158-3188 |
DOI: | 10.1038/s41398-021-01202-3 |