Serum amino acid alterations in hyperuricemia: potential targets for renal disease prevention

Abstract Observational studies have linked uric acid (UA) levels and kidney disease to amino acid homeostasis, but the causal relationship is unclear. This study aims to determine if elevated UA affects amino acid levels and whether amino acids mediate this relationship, focusing on the causal links...

Full description

Saved in:
Bibliographic Details
Main Authors: Qinglin Sheng, Yuqing Ma, Bingjie Geng, Jiahui Chen, Junfei Cheng, Su Liu, Rui Li, Xiangtong Li, Jing Wang, Hongtao Lu, Fangyuan Gao, Fu Gao
Format: Article
Language:English
Published: Springer 2025-02-01
Series:Amino Acids
Subjects:
Online Access:https://doi.org/10.1007/s00726-025-03444-7
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849724097199603712
author Qinglin Sheng
Yuqing Ma
Bingjie Geng
Jiahui Chen
Junfei Cheng
Su Liu
Rui Li
Xiangtong Li
Jing Wang
Hongtao Lu
Fangyuan Gao
Fu Gao
author_facet Qinglin Sheng
Yuqing Ma
Bingjie Geng
Jiahui Chen
Junfei Cheng
Su Liu
Rui Li
Xiangtong Li
Jing Wang
Hongtao Lu
Fangyuan Gao
Fu Gao
author_sort Qinglin Sheng
collection DOAJ
description Abstract Observational studies have linked uric acid (UA) levels and kidney disease to amino acid homeostasis, but the causal relationship is unclear. This study aims to determine if elevated UA affects amino acid levels and whether amino acids mediate this relationship, focusing on the causal links between UA, circulating amino acids, and kidney disease. Methods: This study utilized Uox-KO mice as a hyperuricemia model, assessed renal injury through blood biochemistry and pathology, analyzed serum amino acid changes via targeted amino acidomics, and employed Mendelian randomization to investigate the causal links between uric acid, amino acids, and renal disease. Results: Hyperuricemia Uox-KO mice have significantly higher serum UA and renal impairment markers, with histopathological analysis showing extensive renal tissue damage. Changes in amino acid balance were found in the mice's serum, with key metabolites like alanine, isoleucine, leucine, aspartic acid, cysteine, glutamate, and glycine potentially influencing UA pathophysiology. Genetically predicted UA was positively correlated with chronic renal failure (CRF) and blood urea nitrogen(BUN) levels and negatively with serum cystatin C (eGFRcys) and serum creatinine (eGFRcrea). Alanine (Ala) mediated the effect of UA on elevated CRF and BUN risk, accounting for 4.5% of the UA-CRF relationship and 14.4% of the UA-BUN association. Conclusion: In hyperuricemia mice, serum amino acids undergo metabolic changes. Genetically predicted UA levels are positively linked to CRF and BUN, but negatively linked to eGFRcys and eGFRcrea. Ala mediates UA's effect on CRF and BUN risk, indicating Ala could be a target for preventing renal diseases caused by hyperuricemia. Graphical abstract
format Article
id doaj-art-b58c33ea7b6948b7bb0d12cbbaceba5f
institution DOAJ
issn 1438-2199
language English
publishDate 2025-02-01
publisher Springer
record_format Article
series Amino Acids
spelling doaj-art-b58c33ea7b6948b7bb0d12cbbaceba5f2025-08-20T03:10:50ZengSpringerAmino Acids1438-21992025-02-0157111510.1007/s00726-025-03444-7Serum amino acid alterations in hyperuricemia: potential targets for renal disease preventionQinglin Sheng0Yuqing Ma1Bingjie Geng2Jiahui Chen3Junfei Cheng4Su Liu5Rui Li6Xiangtong Li7Jing Wang8Hongtao Lu9Fangyuan Gao10Fu Gao11University of Shanghai for Science and TechnologyDepartment of Naval Medicine, Naval Medical UniversityDepartment of Naval Medicine, Naval Medical UniversityDepartment of Naval Medicine, Naval Medical UniversityDepartment of Naval Medicine, Naval Medical UniversityDepartment of Naval Medicine, Naval Medical UniversityDepartment of Naval Medicine, Naval Medical UniversityDepartment of Naval Medicine, Naval Medical UniversityDepartment of Naval Medicine, Naval Medical UniversityDepartment of Naval Medicine, Naval Medical UniversityDepartment of Naval Medicine, Naval Medical UniversityUniversity of Shanghai for Science and TechnologyAbstract Observational studies have linked uric acid (UA) levels and kidney disease to amino acid homeostasis, but the causal relationship is unclear. This study aims to determine if elevated UA affects amino acid levels and whether amino acids mediate this relationship, focusing on the causal links between UA, circulating amino acids, and kidney disease. Methods: This study utilized Uox-KO mice as a hyperuricemia model, assessed renal injury through blood biochemistry and pathology, analyzed serum amino acid changes via targeted amino acidomics, and employed Mendelian randomization to investigate the causal links between uric acid, amino acids, and renal disease. Results: Hyperuricemia Uox-KO mice have significantly higher serum UA and renal impairment markers, with histopathological analysis showing extensive renal tissue damage. Changes in amino acid balance were found in the mice's serum, with key metabolites like alanine, isoleucine, leucine, aspartic acid, cysteine, glutamate, and glycine potentially influencing UA pathophysiology. Genetically predicted UA was positively correlated with chronic renal failure (CRF) and blood urea nitrogen(BUN) levels and negatively with serum cystatin C (eGFRcys) and serum creatinine (eGFRcrea). Alanine (Ala) mediated the effect of UA on elevated CRF and BUN risk, accounting for 4.5% of the UA-CRF relationship and 14.4% of the UA-BUN association. Conclusion: In hyperuricemia mice, serum amino acids undergo metabolic changes. Genetically predicted UA levels are positively linked to CRF and BUN, but negatively linked to eGFRcys and eGFRcrea. Ala mediates UA's effect on CRF and BUN risk, indicating Ala could be a target for preventing renal diseases caused by hyperuricemia. Graphical abstracthttps://doi.org/10.1007/s00726-025-03444-7Uric acidHyperuricemiaAmino acidomicsMendelian randomizationMediating effect
spellingShingle Qinglin Sheng
Yuqing Ma
Bingjie Geng
Jiahui Chen
Junfei Cheng
Su Liu
Rui Li
Xiangtong Li
Jing Wang
Hongtao Lu
Fangyuan Gao
Fu Gao
Serum amino acid alterations in hyperuricemia: potential targets for renal disease prevention
Amino Acids
Uric acid
Hyperuricemia
Amino acidomics
Mendelian randomization
Mediating effect
title Serum amino acid alterations in hyperuricemia: potential targets for renal disease prevention
title_full Serum amino acid alterations in hyperuricemia: potential targets for renal disease prevention
title_fullStr Serum amino acid alterations in hyperuricemia: potential targets for renal disease prevention
title_full_unstemmed Serum amino acid alterations in hyperuricemia: potential targets for renal disease prevention
title_short Serum amino acid alterations in hyperuricemia: potential targets for renal disease prevention
title_sort serum amino acid alterations in hyperuricemia potential targets for renal disease prevention
topic Uric acid
Hyperuricemia
Amino acidomics
Mendelian randomization
Mediating effect
url https://doi.org/10.1007/s00726-025-03444-7
work_keys_str_mv AT qinglinsheng serumaminoacidalterationsinhyperuricemiapotentialtargetsforrenaldiseaseprevention
AT yuqingma serumaminoacidalterationsinhyperuricemiapotentialtargetsforrenaldiseaseprevention
AT bingjiegeng serumaminoacidalterationsinhyperuricemiapotentialtargetsforrenaldiseaseprevention
AT jiahuichen serumaminoacidalterationsinhyperuricemiapotentialtargetsforrenaldiseaseprevention
AT junfeicheng serumaminoacidalterationsinhyperuricemiapotentialtargetsforrenaldiseaseprevention
AT suliu serumaminoacidalterationsinhyperuricemiapotentialtargetsforrenaldiseaseprevention
AT ruili serumaminoacidalterationsinhyperuricemiapotentialtargetsforrenaldiseaseprevention
AT xiangtongli serumaminoacidalterationsinhyperuricemiapotentialtargetsforrenaldiseaseprevention
AT jingwang serumaminoacidalterationsinhyperuricemiapotentialtargetsforrenaldiseaseprevention
AT hongtaolu serumaminoacidalterationsinhyperuricemiapotentialtargetsforrenaldiseaseprevention
AT fangyuangao serumaminoacidalterationsinhyperuricemiapotentialtargetsforrenaldiseaseprevention
AT fugao serumaminoacidalterationsinhyperuricemiapotentialtargetsforrenaldiseaseprevention