Disclaimer: This article is for informational purposes only and is not intended for diagnostic use. LifeDNA does not provide diagnostic reports on any traits discussed. Genetics is just one piece of the puzzle; please consult a healthcare professional for comprehensive guidance on any health condition.
White blood cells (WBCs), or leukocytes, are crucial for the immune system. They circulate in the blood and defend the body against infections, foreign invaders, and diseases. There are several types of WBCs, including lymphocytes, monocytes, neutrophils, eosinophils, and basophils, each with specialized functions.Â
Neutrophils, for instance, are the most abundant and are first responders to infection sites, while lymphocytes, such as B and T cells, are central to the adaptive immune response. The presence and activity of WBCs are vital for maintaining overall health and preventing infections.
WBCs are essential for maintaining the immune defense system. They play a pivotal role in protecting the body from infections by identifying and destroying pathogens such as bacteria, viruses, and fungi. WBCs also help remove dead or damaged cells and respond to allergens and other foreign substances.Â
Their ability to move to infection sites and engulf or neutralize harmful invaders is crucial for preventing the spread of disease and aiding in the healing process. Without adequate WBCs, the body becomes susceptible to infections and diseases, highlighting their importance in overall health and immune function.
Low WBC counts, or leukopenia, implies a weak immune system and increased infection susceptibility. Causes of low WBC counts include bone marrow disorders, autoimmune diseases, severe illnesses, certain medications, and chemotherapy. Conversely, high WBC counts, known as leukocytosis, can suggest the presence of an infection, inflammation, stress, or other conditions such as leukemia. Elevated WBC levels might also result from intense physical activity or an immune response to trauma. Abnormally low and high WBC counts require further medical evaluation to determine the underlying cause and appropriate treatment.
A 2011 genome-wide association study (GWAS) involving 16,388 people from the African American population showed that members of this population typically have lower overall WBC and neutrophil counts due to the “null” variant of the Duffy Antigen Receptor for Chemokines (DARC) gene. Interestingly, this variant also protects against some forms of malaria. The DARC gene is significant for its impact on blood type classification and its role in immune function;,with variations in this gene influencing variations in WBC counts and susceptibility to diseases. The study further confirms that also the CXCL2, CDK6, and PSMD3-CSF3 gene regions are influential contributors to WBC counts across different populations, emphasizing their broader relevance.
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A 2012 GWAS involved 13,923 participants from both African ancestry and European ancestry. This study also found a significant association between WBC count and the DARC gene in the participants with African ancestry. It validated the association between WBC levels and the regulatory SNP variant rs2814778, which causes the Duffy negative phenotype (Fy-/-). Additionally, the study identified interaction effects of two variants, rs2814778 and rs12075, which are responsible for the differing antigens in the Duffy blood group system.
A 2019 GWAS involving 2064 discovery and 407 replication patients identified a new genetic locus at 14q24.3 to be associated with WBC counts. The 14q24.3 locus was also associated with acute stroke outcome and the expression of the ACOT1 and PTGR2 genes.
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A 2021 meta-analysis of GWAS involving 17,802 participants of African ancestry highlights the significant genetic influence on WBC and their subtype counts. The study identified five novel loci: LOC126987/MTCO3P14, LINC01525, GAPDHP32/HSD3BP3, FLG-AS1/HMGN3P1, and TRK-CTT13-1/MGST3.Â
Asthma is a chronic respiratory condition characterized by inflammation and narrowing of the airways, leading to difficulty in breathing. The genetic connection between WBC count and asthma is an area of significant research interest. Studies have shown that specific genetic variants associated with WBC count also influence the risk of developing asthma. Some genes, such as those located in the 17q21 region (e.g., GSDMA, MED24, PSMD3), have been associated with variations in WBC count and an increased risk of asthma. These genes are involved in immune system regulation and inflammation, important in WBC function and asthma pathogenesis.
The genetic variants that affect WBC count often impact inflammatory pathways. Since asthma is a chronic inflammatory disease of the airways, the overlap in genetic determinants suggests that individuals with specific genetic profiles may be predisposed to a certain inflammatory response type which influences WBC levels and asthma severity.
Non-genetic factors significantly influence WBC counts. Infections are a primary factor, typically causing an increase in WBCs as the body fights off pathogens. Chronic diseases, such as autoimmune disorders and cancer, can also alter WBC levels. Medications, including chemotherapy and certain antibiotics, can suppress WBC production.Â
Lifestyle factors like stress, smoking, diet, and physical activity also impact WBC count. Acute physical or emotional stress can cause temporary increases, while chronic stress can lead to longer-term changes. Nutritional deficiencies, particularly in vitamins like B12 and folate, can also affect WBC production and function.
WBCs play a crucial role in your immune system, defending your body against infections and diseases. Maintaining optimal WBC levels is essential for overall health. Here are some strategies to help you optimize your WBC levels:
By incorporating these strategies into your lifestyle, you can help maintain optimal WBC levels and support your immune system. Always consult with a healthcare professional before making significant changes to your diet or exercise routine, especially if you have existing health conditions.