Evaluating for the following in an algorithmic process for the HAEV1 / Hemolytic Anemia Evaluation, Blood; HBEL1 / Hemoglobin Electrophoresis Evaluation, Blood; MEV1 / Methemoglobinemia Evaluation, Blood; REVE2 / Erythrocytosis Evaluation, Blood; THEV1 / Thalassemia and Hemoglobinopathy Evaluation, Blood and Serum:
-Diagnosing of beta thalassemia intermedia or major
-Identifying a specific beta thalassemia sequence variant (ie, unusually severe beta thalassemia trait)
-Evaluating an abnormal hemoglobin electrophoresis identifying a rare beta-globin variant
-Evaluating chronic hemolytic anemia of unknown etiology
-Evaluating hereditary erythrocytosis with left-shifted p50 oxygen dissociation results
-Preconception screening when there is a concern for a beta-hemoglobin disorder based on family history
Only orderable as a reflex. For more information see:
-HAEV1 / Hemolytic Anemia Evaluation, Blood
-HBEL1 / Hemoglobin Electrophoresis Evaluation, Blood
-MEV1 / Methemoglobinemia Evaluation, Blood
-REVE2 / Erythrocytosis Evaluation, Blood
-THEV1 / Thalassemia and Hemoglobinopathy Evaluation, Blood and Serum
Polymerase Chain Reaction (PCR)/Sanger Sequencing
Whole Blood EDTA
Only orderable as a reflex. For more information see:
-HAEV1 / Hemolytic Anemia Evaluation, Blood
-HBEL1 / Hemoglobin Electrophoresis Evaluation, Blood
-MEV1 / Methemoglobinemia Evaluation, Blood
-REVE2 / Erythrocytosis Evaluation, Blood
-THEV1 / Thalassemia and Hemoglobinopathy Evaluation, Blood and Serum
Specimen Type: Whole blood
Container/Tube:
Preferred: Lavender top (EDTA)
Acceptable: Yellow top (ACD)
Specimen Volume: 4 mL
1 mL
| Gross hemolysis | OK |
| Moderately to severely clotted | Reject |
| Specimen Type | Temperature | Time | Special Container |
|---|---|---|---|
| Whole Blood EDTA | Refrigerated | 14 days |
Evaluating for the following in an algorithmic process for the HAEV1 / Hemolytic Anemia Evaluation, Blood; HBEL1 / Hemoglobin Electrophoresis Evaluation, Blood; MEV1 / Methemoglobinemia Evaluation, Blood; REVE2 / Erythrocytosis Evaluation, Blood; THEV1 / Thalassemia and Hemoglobinopathy Evaluation, Blood and Serum:
-Diagnosing of beta thalassemia intermedia or major
-Identifying a specific beta thalassemia sequence variant (ie, unusually severe beta thalassemia trait)
-Evaluating an abnormal hemoglobin electrophoresis identifying a rare beta-globin variant
-Evaluating chronic hemolytic anemia of unknown etiology
-Evaluating hereditary erythrocytosis with left-shifted p50 oxygen dissociation results
-Preconception screening when there is a concern for a beta-hemoglobin disorder based on family history
Beta-globin gene sequencing is useful in the evaluation of beta-globin chain variants and beta thalassemia. It detects almost all beta-globin variants and the most common beta-thalassemia sequence variants, although prevalence is ethnicity dependent. Because these conditions are often complex, this test should always be interpreted in the context of protein studies, such as hemoglobin electrophoresis and red blood cell indices.
The majority of beta-globin chain variants are clinically and hematologically benign; however, some have important clinical consequences, such as erythrocytosis, cyanosis/hypoxia, chronic hemolysis, or unexplained microcytosis. Most of the common clinically significant hemoglobin (Hb) variants (ie, HbS, HbC, HbE, and others) are easily distinguished by hemoglobin electrophoresis and do not require molecular analysis. In addition, they are frequently found in complex hemoglobin disorders due to multiple genetic variants, and accurate classification requires sequencing data within the context of protein data. In some instances, beta-globin sequencing is necessary to identify or confirm the identity of rare variants, especially those associated with erythrocytosis and chronic hemolytic anemia. Rare hyper-unstable variants (also termed dominant beta thalassemia mutations) result in hemolytic anemia and do not create protein stable enough to be detectable by protein methods, including stability studies. They are not always associated with elevated HbA2 or microcytosis and, therefore, can be electrophoretically silent. These require a high degree of clinical suspicion as all electrophoretic testing as well as stability studies cannot exclude this condition.
Beta thalassemia is an autosomal recessive condition characterized by decreased or absent synthesis of beta-globin chains due to alterations in the beta-globin gene (HBB). No abnormal protein is present and diagnosis by electrophoresis relies on hemoglobin fraction percentage alterations (ie, HbA2 or HbF elevations).
Beta-thalassemia can be split into 3 broad classes (categorized by clinical features):
1. Beta thalassemia trait (also called beta thalassemia minor and beta thalassemia carrier) (B[A]B[+] or B[A]B[0]).
2. Beta thalassemia intermedia (B[+]B[+] or B[+]B[0])
3. Beta thalassemia major (B[+]B[0] or B[0]B[0])
Beta thalassemia trait is typically a harmless condition with varying degrees of microcytosis and hypochromia and sometimes mild anemia. Transfusions are not required. Beta thalassemia intermedia is a clinical distinction and is characterized by a more severe degree of anemia than beta thalassemia trait with few or intermittent transfusions required. Later in life, these individuals are at risk for iron overload even in the absence of chronic transfusion due to increased intestinal absorption of iron. Beta thalassemia major typically comes to medical attention early in life due to severe anemia, hepatosplenomegaly, and failure to thrive. Skeletal changes are also common due to expansion of the bone marrow. Without appropriate treatment these patients have a shortened lifespan.
The majority of beta-thalassemia variations (>90%) are point alterations, small deletions, or insertions, which are detected by beta-globin gene sequencing. The remaining beta-thalassemia sequence variants are either due to large genomic deletions of HBB or, very rarely, trans-acting beta thalassemia variations located outside of the beta-globin gene cluster. Some rare beta-chain variants can be clinically or electrophoretically indistinguishable from beta thalassemia and cannot be confirmed without molecular analysis.
Only orderable as a reflex. For more information see:
-HAEV1 / Hemolytic Anemia Evaluation, Blood
-HBEL1 / Hemoglobin Electrophoresis Evaluation, Blood
-MEV1 / Methemoglobinemia Evaluation, Blood
-REVE2 / Erythrocytosis Evaluation, Blood
-THEV1 / Thalassemia and Hemoglobinopathy Evaluation, Blood and Serum
An interpretive report will be provided.
The alteration will be provided with the classification, if known. Further interpretation requires correlation with protein studies and red blood cell indices.
This assay will not detect large deletions or duplications within the beta-globin gene. In addition, hybrid beta-globin variants (ie, Hb Lepore) will not be detected by this method. This method cannot distinguish between homozygous and compound heterozygous variants associated with large deletions. This method cannot distinguish between double substitution on single chromosome and a compound heterozygous state. Beta-globin sequencing alone is not able to distinguish between alterations that are found in the same copy of the HBB gene (ie, variants that are "linked" or "in cis") and alterations found on different HBB gene copies (ie, are "in trans"). This limitation of sequencing may complicate diagnosis and has implications for inheritance and proper genetic counseling. To resolve these cases, molecular results must be correlated with electrophoretic and protein data, other laboratory findings, clinical findings, and family studies. Misinterpretation of results may occur if the information provided is inaccurate or incomplete.
Rare genetic alterations exist that could lead to false-negative or false-positive results. If results obtained do not match the clinical findings, additional testing should be considered.
1. Hoyer JD, Hoffman DR: The thalassemia and hemoglobinopathy syndromes. In: McClatchey KD, ed. Clinical Laboratory Medicine. 2nd ed. Lippincott Williams and Wilkins; 2002;866-895
2. Thein SL: The molecular basis of beta-thalassemia. Cold Spring Harb Perspect Med. 2013 May 1;1;3(5):a011700
3. Hoyer JD, Kroft, SH: Color Atlas of Hemoglobin Disorders: A Compendium Based on Proficiency Testing. CAP; 2003
4. Merchant S, Oliveira JL, Hoyer JD, Viswanatha DS: Molecular diagnosis in hematopathology. In: Goldblum J, His E, eds. Hematopathology: A Volume in Foundations in Diagnostic Pathology Series. 2nd ed. Churchill Livingstone; 2012
Genomic DNA is extracted from whole blood. The HBB gene is amplified by polymerase chain reaction (PCR). The PCR product is then purified and sequenced in both directions using fluorescent dye-terminator chemistry. Sequencing products are separated on an automated sequencer and trace files analyzed for variations in all exons, introns with the exception of IVS-II-82 through IVS-II-650, the 5'UTR, the 3'UTR, and the promoter region. Results are correlated with routine studies to identify unusual beta globin variants.(Reddy PL, Bowie LJ: Sequence-based diagnosis of hemoglobinopathies in the clinical laboratory. Clin Lab Med. 1997;17[1]:85-96; Traeger-Synodinos J, Harteveld CL: Advances in technologies for screening and diagnosis of hemoglobinopathies. Biomarkers Med. 2014;8[1]:115-127)
Monday through Friday
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.
81364-HBB (hemoglobin, beta) full sequence
| Test Id | Test Order Name | Order LOINC Value |
|---|---|---|
| WBSQR | Beta Globin Gene Sequencing, B | 50996-8 |
| Result Id | Test Result Name |
Result LOINC Value
Applies only to results expressed in units of measure originally reported by the performing laboratory. These values do not apply to results that are converted to other units of measure.
|
|---|---|---|
| 47954 | Beta Globin Gene Sequencing Result | 50397-9 |
| 47955 | Interpretation | 59466-3 |