Lab Guide
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Test ID: ALT
Alanine Aminotransferase
Useful For

Diagnosis and monitoring of liver disease associated with hepatic necrosis.

Method name and description

This assay follows the recommendations of the IFCC, but was optimized for performance and stability. ALT catalyzes the reaction between L‑alanine and 2‑oxoglutarate. The pyruvate formed is reduced by NADH in a reaction catalyzed by lactate dehydrogenase (LDH) to form L‑lactate and NAD + .
                                                                             ALT
L-Alanine + 2‑oxoglutarate pyruvate +                  L‑glutamate
                                                  LDH
Pyruvate + NADH + H +               L‑lactate + NAD +

The rate of the NADH oxidation is directly proportional to the catalytic ALT activity. It is determined by measuring the decrease in absorbance.

Reporting name

Alanine Aminotransferase

Clinical information

ALT has been widely reported to be present in a variety of tissues. The major source of ALT is the liver, which has led to the measurement of ALT activity for the diagnosis of hepatic diseases.

High ALT is found in Hepatitis, Cirrhosis, Obstructive jaundice, Carcinoma of the liver, chronic alcohol abuse, slightly elevated in patients who have an uncomplicated myocardial infarction. In patients with vitamin B6 deficiency, serum aminotransferase activity may be decreased.

Aliases

ALT

Specimen type / Specimen volume / Specimen container

Specimen type: Serum, Plasma

Minimum volume of sample: 1 mL

Serum: Plain tube (red or yellow top, free from hemolysis)

Plasma: Li‑heparin (free form hemolysis)

Collection instructions / Special Precautions / Timing of collection
Storage and transport instructions

Storage: 3 days at 15 – 25°C

                7 days at 2 – 8°C;

                > 7 days at ‑60 to -80 °C

Transport: 2-25°C 

Specimen Rejection Criteria

Grossly hemolyzed, icteric and lipemic, wrong collection container, insufficient sample.

Biological reference intervals and clinical decision values

 

Age

Reference Interval (U/L)

 

 From

To

 From

To

Male

0 minutes

1 month

1

25

Male

1 month

1 year

4

35

Male

1 year

3years

5

30

Male

3 years

6 years

5

20

Male

6 years

9 years

5

25

Male

9 years

18 years

5

30

Male

>18 year

 

0

41

Female

0 minutes

1 month

2

25

Female

1 month

1 year

3

30

Female

1 year

3 years

5

30

Female

3 years

9 years

5

25

Female

9 years

18 years

5

20

Female

>18 year

 

0

33

Factors affecting test performance and result interpretation

Lipemic samples may cause > Abs flagging. Choose diluted sample treatment for automatic rerun.

Calcium dobesilate and Isoniazid can cause artificially low and Furosemide artificially high ALT results at therapeutic concentrations. Cyanokit (Hydroxocobalamin) may cause interference with results

Physiological plasma concentrations of Sulfasalazine or Sulfapyridine may lead to false results.

Turnaround time / Days and times test performed / Specimen retention time

Daily (24/7)

Turn-around time:

STAT: 1 hour

Routine: One working day

Specimen retention:  4 days