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Back to Test Catalogue
Test ID: ALAD

Aminolevulinic Acid (ALA) Dehydratase, Blood

Test Overview

Clinical Utility

This assay is not useful in evaluating lead intoxication as it re-activates ALAD that may have been inhibited by lead.

Method

Spectrofluorometry - enzymatic end point

Result Included

ALA Dehydratase; Interpretation

Aliases/Synonyms

Porphobilinogen Synthase; ALAD Deficiency Porphyria; Doss Porphyria; PBG Synthase

Specimen

Specimen Type

Whole Blood (Na Heparin)
Whole blood (Li Heparin)
Whole blood (EDTA)

Containers

Preferred Containers

Green top (sodium heparin)

Acceptable Containers

Lavender top (EDTA); Green top (lithium heparin)

Volume

Minimum Volume

3 mL

Patient Preparation

Patient should abstain from alcohol 24 hours prior to collection.

Collection & Handling

Collection Instructions

Avoid hemolysis

Handling Information

Refrigerate immediately. Submit full tube. Do not freeze. Due to limited stability, sample must be received at ICL from Mon – Wed within 3 days of collection.

Additional Information

Provide a list of current medications.

Stability

Refrigerated
4 days

Rejection Criteria

Criteria Specification
Hemolysis Visible
Other Ambient or frozen

Performance & Interpretation

Turnaround Time

7 days

Specimen Retention Time

14 days

Results

Name
Units
Reference Range
Conversion
  1. Aminolevulinic Acid (ALA) Dehydratase
    nmol/L/sec
    ≥4.0

    Indeterminate 3.5 - 3.9

    Diminished <3.5

    This assay is not useful in evaluating lead intoxication as it re-activates ALAD that may have been inhibited by lead.
  2. Interpretation
    Abnormal results are reported with a detailed interpretation including an overview of the results and their significance, a correlation to available clinical information provided with the specimen, differential diagnosis, and recommendations for additional testing when indicated and available

    Comment

    Abstinence from alcohol is essential for at least 24 hours prior to specimen collection as ethanol suppresses ALAD activity. False-positive values may result from enzyme degradation due to improper specimen handling. It is essential to adhere to collection and handling instructions.

Referral Location

Out-of-Country

Test Version

Last Updated

2019-09-30