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Fast and Specific Assessment of the Halogenating Peroxidase Activity in Leukocyte-enriched Blood Samples
Published on: July 28, 2016
Serum myeloperoxidase concentration in a healthy population: biological variations, familial resemblance and new
A Hoy1, D Trégouët, B Leininger-Muller
1Faculté de Pharmacie, INSERM Unité 525, Nancy, France.
Abstract:
Myeloperoxidase (MPO) has been involved in the pathogenesis of several diseases through excessive production of reactive oxygen species (ROS) as well as through its genetic polymorphism. The aims of this study were to identify the factors affecting MPO serum concentration, to study the familial resemblance of MPO levels and to investigate the association between newly described MPO polymorphisms as well as the G-463A one and MPO levels in a healthy population. MPO serum concentrations were measured by an enzymatic immuno-assay (EIA) in 82 healthy families of the STANISLAS Cohort and MPO genotype, determination was performed using PCR-restriction fragment length polymorphism or allele specific oligonucleotide assay. MPO concentrations were significantly higher in parents than in offspring. The factors affecting MPO levels were age, the number of white cells, smoking in fathers and oral contraceptive intake in mothers. They explain from 12.4% up to 35.9% of MPO variability in men and women, respectively. Family correlations of MPO concentrations were of similar magnitude. The -129A allele of a newly described G-129A substitution was significantly associated with decreased MPO levels, whereas the -463A allele was suggested to be associated with increased levels of lipid variables. In this study, we identified factors affecting MPO serum concentrations and showed that molecular variations of the gene have only a weak influence on MPO variability. In contrast, the association between the G-463A polymorphism and lipid levels would suggest a possible implication of MPO in the risk of cardiovascular diseases. These results have to be confirmed and further investigations will be conducted in that way.
Insights
Myeloperoxidase (MPO) levels are influenced by age, lifestyle, and genetics. While MPO gene variations have a minor impact, the G-463A polymorphism may link MPO to cardiovascular disease risk.
Area of Science:
- Biochemistry
- Genetics
- Human Physiology
Background:
- Myeloperoxidase (MPO) contributes to disease pathogenesis via reactive oxygen species (ROS) and genetic variations.
- Understanding MPO serum concentration factors and genetic associations is crucial for disease risk assessment.
Purpose of the Study:
- Identify factors influencing MPO serum concentration in a healthy population.
- Examine familial resemblance of MPO levels.
- Investigate associations between MPO polymorphisms and MPO levels.
Main Methods:
- Enzymatic immuno-assay (EIA) for MPO serum concentrations in 82 families.
- PCR-restriction fragment length polymorphism and allele-specific oligonucleotide assays for MPO genotyping.
- Statistical analysis of MPO levels, genotypes, and influencing factors.
Main Results:
- MPO concentrations were higher in parents than offspring, indicating familial resemblance.
- Age, white blood cell count, smoking (fathers), and oral contraceptive use (mothers) affected MPO levels.
- The -129A MPO allele correlated with decreased MPO levels; the -463A allele suggested links to increased lipid variables.
Conclusions:
- MPO serum concentrations are influenced by demographic, lifestyle, and clinical factors.
- Genetic variations in MPO have a limited effect on MPO variability.
- The G-463A polymorphism's association with lipid levels warrants further investigation for cardiovascular disease implications.
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