Intra-body dynamics of d-serine reflects the origin of kidney diseases
Introduction d -Serine, present only in trace amounts in humans, is now recognized as a biomarker of chronic kidney disease (CKD). CKD is heterogeneous in its original kidney diseases, whose diagnoses require kidney biopsy. In this study, we examined whether the intra-body dynamics of d- serine, ind...
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Published in | Clinical and experimental nephrology Vol. 25; no. 8; pp. 893 - 901 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Singapore
Springer Singapore
01.08.2021
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Introduction
d
-Serine, present only in trace amounts in humans, is now recognized as a biomarker of chronic kidney disease (CKD). CKD is heterogeneous in its original kidney diseases, whose diagnoses require kidney biopsy. In this study, we examined whether the intra-body dynamics of
d-
serine, indexed by its blood and urinary levels, reflects the origin of kidney diseases.
Methods
Patients with six kinds of kidney disease undergoing kidney biopsy were enrolled in a single center. Levels of
d-
and
l
-serine were measured using two-dimensional high-performance liquid chromatography. The associations between the origin of kidney diseases and the intra-body dynamics of
d-
serine were examined using multivariate cluster analyses.
Results
Unlike the non-CKD profile, patients with CKD showed broadly-distributed profiles of intra-body dynamics of
d-
serine. The plasma level of
d-
serine plays a key role in the detection of kidney diseases, whereas a combination of plasma and urinary levels of
d-
serine distinguished the origin of CKD, especially lupus nephritis.
Conclusion
Intra-body dynamics of
d-
serine have the potential to predict the origin of kidney diseases. Monitoring of
d-
serine may guide specific treatments for the origin of kidney diseases. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1342-1751 1437-7799 |
DOI: | 10.1007/s10157-021-02052-5 |