» Articles » PMID: 38171450

Amino Acid Metabolism and Atherosclerotic Cardiovascular Disease

Overview
Journal Am J Pathol
Publisher Elsevier
Specialty Pathology
Date 2024 Jan 3
PMID 38171450
Authors
Affiliations
Soon will be listed here.
Abstract

Despite significant advances in medical treatments and drug development, atherosclerotic cardiovascular disease (ASCVD) remains a leading cause of death worldwide. Dysregulated lipid metabolism is a well-established driver of ASCVD. Unfortunately, even with potent lipid-lowering therapies, ASCVD-related deaths have continued to increase over the past decade, highlighting an incomplete understanding of the underlying risk factors and mechanisms of ASCVD. Accumulating evidence over the past decades indicates a correlation between amino acids and disease state. This review explores the emerging role of amino acid metabolism in ASCVD, uncovering novel potential biomarkers, causative factors, and therapeutic targets. Specifically, the significance of arginine and its related metabolites, homoarginine and polyamines, branched-chain amino acids, glycine, and aromatic amino acids, in ASCVD are discussed. These amino acids and their metabolites have been implicated in various processes characteristic of ASCVD, including impaired lipid metabolism, endothelial dysfunction, increased inflammatory response, and necrotic core development. Understanding the complex interplay between dysregulated amino acid metabolism and ASCVD provides new insights that may lead to the development of novel diagnostic and therapeutic approaches. Although further research is needed to uncover the precise mechanisms involved, it is evident that amino acid metabolism plays a role in ASCVD.

Citing Articles

Identification of potential biomarkers for coronary slow flow using untargeted metabolomics.

Chen Y, Liang J, Chen S, Chen B, Guan F, Liu X Metabolomics. 2025; 21(1):23.

PMID: 39920375 DOI: 10.1007/s11306-025-02223-5.


Circulating amino acid signature features urea cycle alterations associated with coronary artery disease.

Prechtl L, Carrard J, Gallart-Ayala H, Borreggine R, Teav T, Konigstein K Sci Rep. 2024; 14(1):25848.

PMID: 39468229 PMC: 11519371. DOI: 10.1038/s41598-024-76835-7.


Association between tryptophan concentrations and the risk of developing cardiovascular diseases: a systematic review and meta-analysis.

Zhang J, Jiang X, Pang B, Li D, Kang L, Zhou T Nutr Metab (Lond). 2024; 21(1):82.

PMID: 39407297 PMC: 11476920. DOI: 10.1186/s12986-024-00857-1.


T-Cell Metabolic Reprogramming in Atherosclerosis.

Chang S, Wang Z, An T Biomedicines. 2024; 12(8).

PMID: 39200308 PMC: 11352190. DOI: 10.3390/biomedicines12081844.


Detailed Phytochemical Composition, Cyto-/Hepatotoxicity, and Antioxidant/Anti-Inflammatory Profile of Moroccan Spices: A Study on Coriander, Caraway, and Mystical Cumin.

Bouzaid H, Espirito Santo L, Ferreira D, Machado S, Costa A, Dias M Molecules. 2024; 29(15).

PMID: 39124890 PMC: 11313914. DOI: 10.3390/molecules29153485.


References
1.
Lynch C, Adams S . Branched-chain amino acids in metabolic signalling and insulin resistance. Nat Rev Endocrinol. 2014; 10(12):723-36. PMC: 4424797. DOI: 10.1038/nrendo.2014.171. View

2.
Wang W, Wu Z, Dai Z, Yang Y, Wang J, Wu G . Glycine metabolism in animals and humans: implications for nutrition and health. Amino Acids. 2013; 45(3):463-77. DOI: 10.1007/s00726-013-1493-1. View

3.
Metghalchi S, Ponnuswamy P, Simon T, Haddad Y, Laurans L, Clement M . Indoleamine 2,3-Dioxygenase Fine-Tunes Immune Homeostasis in Atherosclerosis and Colitis through Repression of Interleukin-10 Production. Cell Metab. 2015; 22(3):460-71. DOI: 10.1016/j.cmet.2015.07.004. View

4.
Ridaura V, Faith J, Rey F, Cheng J, Duncan A, Kau A . Gut microbiota from twins discordant for obesity modulate metabolism in mice. Science. 2013; 341(6150):1241214. PMC: 3829625. DOI: 10.1126/science.1241214. View

5.
de Mello V, Sehgal R, Mannisto V, Klavus A, Nilsson E, Perfilyev A . Serum aromatic and branched-chain amino acids associated with NASH demonstrate divergent associations with serum lipids. Liver Int. 2020; 41(4):754-763. PMC: 8048463. DOI: 10.1111/liv.14743. View