Test Code LAB9194 Glucose 6-Phosphate Dehydrogenase Enzyme Activity, Blood
Additional Codes
G6PD1
G6PD
Specimen Required
Collection Container/Tube:
Preferred: Yellow top (ACD solution B)
Acceptable: Lavender top (EDTA) or yellow top (ACD solution A)
Specimen Volume: 6 mL
Collection Instructions: Send specimen in original tube. Do not aliquot.
Secondary ID
607460G6PD
Useful For
Evaluation of individuals with episodic or chronic Coombs-negative nonspherocytic hemolytic anemia
Rapid testing to assess glucose 6-phosphate dehydrogenase (G6PD) enzyme capacity prior to rasburicase or other therapies that may cause hemolysis or methemoglobinemia in G6PD deficient patients
May aid in the creation of a comprehensive patient profile and can ensure appropriate patient monitoring for developing anemia
Testing Algorithm
The following are available:
-Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency Diagnostic Algorithm
-Glucose-6-Phosphate Dehydrogenase (G6PD) Genotyping Interpretive Algorithm
-Newborn Screen Follow-up for Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency
-Newborn Screening Act Sheet Glucose-6-Phosphate Dehydrogenase Deficiency
Special Instructions
- Newborn Screening Act Sheet Glucose-6-Phosphate Dehydrogenase Deficiency
- Newborn Screen Follow-up for Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency
- Glucose-6-Phosphate Dehydrogenase (G6PD) Genotyping Interpretive Algorithm
- Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency Diagnostic Algorithm
Method Name
Kinetic Spectrophotometry
Specimen Type
Whole Blood ACD-BSpecimen Minimum Volume
1 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Whole Blood ACD-B | Refrigerated | 20 days |
Reject Due To
Gross hemolysis | Reject |
Reference Values
≥12 months of age: 8.0-11.9 U/g Hb
Reference values have not been established for patients who are less than 12 months of age.
Interpretation
The World Health Organization (WHO) classification of glucose 6-phosphate dehydrogenase (G6PD) deficiency is historically based on enzyme activity level, and, in most cases, enzyme activity level is sufficient. Accurate classification requires correlation with clinical, and in certain cases, genetic data. The revised WHO classification (2022) has updated classification subtypes from classes I, II, III, IV and V to class A, B, C and U.
The Advisory Group panel concluded:(3)
"In future, G6PD variants should be classified based on the median residual enzyme activity expressed as a percentage of normal activity. It should be emphasized that this system is for classifying genetic variants of G6PD and should not be used to classify individual patients with G6PD deficiency. Currently, no variants have been identified in homozygous deficient females or hemizygous deficient males that have median G6PD enzyme activity falling between 45% and 60%. Therefore, a gap has been left between Classes B and C. If new variants are found with median G6PD enzyme activity in this range, these should be included in the "U" class and studied until solid evidence is found that they induce acute haemolytic anaemia (= Class B) or do not pose a haemolytic risk (= Class C). Based on new evidence, the thresholds may then need to be revisited."
Table. Updated (2022) and Legacy G6PD Variant WHO Classification and Associated G6PD Deficiency Phenotype
2022 WHO class |
Median* G6PD activity |
Hemolysis |
Legacy** WHO class |
Level of residual enzyme activity (% of normal) |
A |
<20% |
Chronic (CNSHA) |
I |
<10% |
B |
<45% |
Acute, triggered |
II |
<10% |
III |
10%-60% |
|||
C |
60-150% |
No hemolysis |
IV |
Normal |
U |
Any |
Uncertain clinical significance |
|
|
*The activity is per variant (ie, per allele) and most straightforward to assess in hemizygous male patients and homozygous female patients. Compound heterozygous female patients are more complex and rely on clinical and familial correlation. **Legacy WHO Class V: increased activity (enzyme activity >150%) has been discontinued in the 2022 recommendations. It was originally created due to a single variant that has not been corroborated and is not deemed clinically relevant. |
Although G6PD deficiency is an X-linked recessive disorder and most often seen in hemizygous male patients, some female patients are affected. In addition, older women who are heterozygous can develop deficiency due to differential X-skewing with age.(4) It is important to note that clinically significant G6PD deficiency can be masked in the setting of significant reticulocytosis, markedly elevated white blood cell count, or recent red blood cell transfusion. If any of these are present in the setting of a history of neonatal, chronic, or episodic jaundice or anemia, genotyping for G6PD genetic alterations is recommended. If desired, order G6PDZ / Glucose-6-Phosphate Dehydrogenase (G6PD) Full Gene Sequencing, Varies.
Method Description
Glucose 6-phosphate dehydrogenase in a hemolysate catalyzes the oxidation of glucose 6-phosphate to 6-phosphogluconate. Concomitantly, nicotinamide adenine dinucleotide phosphate (NADP[+]) is changed to its reduced form, NADPH, and the reaction is measured spectrophotometrically on an automated chemistry analyzer.(Beutler E. Red cell metabolism: A Manual of Biochemical Methods. 3rd ed. Grune and Stratton; 1984:68-71; van Solinge WW, van Wijk. Enzymes of the red blood cell. In: Rifai N, Horvath AR, Wittwer CT: eds. Tietz Textbook of Clinical Chemistry and Molecular Diagnostics. 6th ed. Elsevier; 2018:chap 30)
Specimen Retention Time
7 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterCPT Code Information
82955
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
G6PD1 | G6PD Enzyme Activity, B | 32546-4 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
G6PCL | G6PD Enzyme Activity, B | 32546-4 |
Day(s) Performed
Monday through Friday
Report Available
1 to 4 daysForms
If not ordering electronically, complete, print, and send a Benign Hematology Test Request (T755) with the specimen.