SARS-CoV-2 Infection: What Is Currently Known about Homocysteine Involvement?

Nina Filip1, Elena Cojocaru2, Oana Viola Badulescu3

  • 1Department of Morpho-Functional Sciences (II), Discipline of Biochemistry, Faculty of Medicine, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iasi, Romania.

Insights

This review examines homocysteine

Area of Science:

  • Biochemistry
  • Infectious Diseases
  • Cardiovascular Medicine

Background:

  • Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused global health and economic disruption since December 2019.
  • Comorbidities significantly impact SARS-CoV-2 infection severity and patient prognosis.
  • Thrombosis is a critical complication in COVID-19 patients.

Purpose of the Study:

  • To analyze current data on homocysteine's role in COVID-19.
  • To investigate the correlation between homocysteine levels and COVID-19 disease severity.
  • To explore potential mechanisms of homocysteine's involvement in COVID-19.

Main Methods:

  • Literature review of studies investigating homocysteine and COVID-19.
  • Analysis of data correlating homocysteine levels with clinical outcomes.
  • Synthesis of proposed pathophysiological mechanisms.

Main Results:

  • Elevated homocysteine levels are associated with increased COVID-19 severity.
  • Homocysteine may contribute to thrombosis in COVID-19 patients.
  • Potential mechanisms include endothelial dysfunction and inflammation.

Conclusions:

  • Homocysteine is implicated in the pathophysiology of severe COVID-19.
  • Homocysteine may serve as a biomarker for thrombotic risk in COVID-19.
  • Further research is needed to elucidate homocysteine's precise role and therapeutic implications.

Related Concept Videos

Conjugated Proteins02:50

Conjugated Proteins

Simple proteins and protein complexes contain only amino acids. In contrast, many other proteins, called conjugated proteins, covalently bond with non-protein moieties.
Nucleoproteins are protein complexes that contain nucleic acids, categorized as deoxyribonucleoproteins (DNPs) or ribonucleoproteins (RNPs) respectively. The nucleosome is a typical example of a DNP where nuclear DNA is associated with histone proteins. The major antigen for the Covid-19 virus SARS-CoV is an RNP that is critical...
18.4K
Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
15.5K
Blood Studies for Cardiovascular System II: CRP, Hcy, and Cardiac Natriuretic Peptide Markers01:19

Blood Studies for Cardiovascular System II: CRP, Hcy, and Cardiac Natriuretic Peptide Markers

Cardiac biomarkers are critical in diagnosing, prognosing, and managing cardiovascular diseases. Routine measurement of specific biomarkers such as B-type natriuretic peptide (BNP), C-reactive protein (CRP), and homocysteine (Hcy) is common practice in clinical settings to evaluate heart function and predict cardiovascular events.
These markers indicate stress or strain on the heart muscle:
Natriuretic Peptides (BNP)
Cardiac myocytes produce these hormones in response to ventricular stretching...
137
Rous Sarcoma Virus (RSV) and Cancer01:03

Rous Sarcoma Virus (RSV) and Cancer

Rous Sarcoma virus or RSV was discovered by F. Peyton Rous in the year 1911 as a filterable transmissible agent that could cause tumors in chickens. He won a Nobel Prize for this discovery in 1966. His experiments clearly demonstrated that some cancers could be caused by infectious agents and led to the discovery of many more cancer-causing viruses in animals as well as humans.
RSV is a retrovirus that contains two copies of a plus-strand  RNA genome. Its genome consists of four main open...
5.3K
Cystic Fibrosis: Pathogenesis01:23

Cystic Fibrosis: Pathogenesis

Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
324
Viral Mutations00:36

Viral Mutations

A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material...
32.7K