The HLA DQ2/DQ8 lab test is a genetic analysis designed to assess an individual's risk for celiac disease, an autoimmune disorder triggered by gluten consumption that damages the small intestine. This test identifies specific genetic markers, particularly the HLA-DQ2 and HLA-DQ8 alleles, which are strongly associated with celiac disease. Approximately 90% of celiac patients carry the HLA-DQ2 haplotype, while 5-10% have the HLA-DQ8 haplotype. The test involves extracting DNA from a blood sample and using real-time PCR technology to detect the presence of these alleles. Results can indicate a genetic predisposition to celiac disease, with a significantly higher risk for those carrying these haplotypes. However, the presence of these genetic markers alone does not confirm the disease, as other genetic and environmental factors also contribute. The test is valuable for ruling out celiac disease in individuals without these haplotypes and aids in tailoring diagnostic and treatment strategies.
The HLA DQ2/DQ8 lab test is a genetic analysis designed to assess an individual's risk for celiac disease, an autoimmune disorder triggered by gluten consumption that damages the small intestine. This test identifies specific genetic markers, particularly the HLA-DQ2 and HLA-DQ8 alleles, which are strongly associated with celiac disease. Approximately 90% of celiac patients carry the HLA-DQ2 haplotype, while 5-10% have the HLA-DQ8 haplotype. The test involves extracting DNA from a blood sample and using real-time PCR technology to detect the presence of these alleles. Results can indicate a genetic predisposition to celiac disease, with a significantly higher risk for those carrying these haplotypes. However, the presence of these genetic markers alone does not confirm the disease, as other genetic and environmental factors also contribute. The test is valuable for ruling out celiac disease in individuals without these haplotypes and aids in tailoring diagnostic and treatment strategies.
The lowest price from the last 30 days: £388
Awaiting result:
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Blood
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The HLA DQ2/DQ8 lab test is a genetic analysis used to assess the risk of celiac disease by identifying specific genetic markers. This test focuses on detecting HLA-DQ2 and HLA-DQ8 alleles, which are strongly associated with celiac disease.
- DNA Extraction: Blood sample DNA is extracted.
- PCR Amplification: DNA is amplified to generate specific sequences.
- Probe Hybridization: TaqMan probes bind to DQA1 and DQB1 alleles.
- Detection: Presence of probes indicates specific alleles.
- Result Interpretation: Determines presence or absence of DQ2/DQ8 haplotypes.
Understanding these markers aids in managing celiac disease risk.
The HLA DQ2/DQ8 test is crucial for identifying individuals at risk for celiac disease, an autoimmune disorder triggered by gluten. This genetic test detects specific alleles linked to the disease. Key points include:
- Genetic Markers: HLA-DQ2 and HLA-DQ8 alleles are strongly associated with celiac disease.
- Testing Process: Involves DNA extraction, PCR amplification, probe hybridization, and result interpretation.
- Results:
- Absence of DQ2/DQ8: Low risk.
- Presence of DQ2/DQ8: Increased risk.
- Clinical Implications: Positive results indicate higher risk but not a definitive diagnosis.
Understanding test results from the HLA DQ2/DQ8 lab test is crucial for assessing genetic risk for celiac disease. Here's a brief guide:
- Negative Result: Absence of DQ2/DQ8 haplotypes suggests a low likelihood of developing celiac disease.
- Positive Result: Presence of DQ2 and/or DQ8 indicates a genetic predisposition, increasing risk significantly.
- Half DQ2: Detection of only one allele (HLA-DQA105 or HLA-DQB102) suggests a lower, yet elevated risk.
While these results highlight genetic risk, they don't confirm celiac disease, necessitating further clinical evaluation.
The lowest price from the last 30 days: £388
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