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Current HIV Research

Editor-in-Chief

ISSN (Print): 1570-162X
ISSN (Online): 1873-4251

Research Article

Impact of High Protein Intake on Viral Load and Hematological Parameters in HIV-infected Patients

Author(s): Evgeny Vlad. Butorov*

Volume 15, Issue 5, 2017

Page: [345 - 354] Pages: 10

DOI: 10.2174/1570162X15666171002121209

Price: $65

Abstract

Background: The impact of protein intake level leads to considerable alterations of the host essential amino acid profiles in the context of chronic viral infectious process. Amino acids play an important role in the pathogenesis of virus-related infections both as basic substrates for constant protein synthesis and as regulators in many metabolic pathways. The excess or deficiency of these host essential nutritional elements can play a limiting role in the life cycle of some viruses.

Objective: Our aim was to determine the changes of hematological parameters and viral load due to the high protein and L-lysine amino acid intake in HIV-infected patients.

Methods: Case-control study was performed in the Municipal Center of HIV/AIDS prophylaxis, Surgut, Russian Federation.

Results: The obtained data indicate that excess of dietary protein and L-lysine can increase the risk of high HIV replication, subsequent acceleration of immunosuppression and the disease progression. The present survey shows that HIV-infected Khanty indigenous people have the highest levels of plasma L-lysine and HIV-1 RNA and a more pronounced state of immunosuppression in comparison with the total patients' cohort.

Conclusion: There was evidence for an association between plasma L-lysine level and viral load. These findings are important for understanding the pathogenic impact of animal protein and Llysine consumption on the HIV-1 RNA levels and must be considered in further research for the development of new approaches in the treatment of HIV infection in era of HAART.

Keywords: HIV-infected Khanty indigenous people, viral load, L-lysine amino acid, animal protein intake, HIV replication, HIV-1 RNA.

Graphical Abstract


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