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Test Code HCYSS Homocysteine, Total, Serum

Useful For

An aid for screening patients suspected of having an inherited disorder of methionine metabolism including:

-Cystathionine beta-synthase deficiency (homocystinuria)

-Methylenetetrahydrofolate reductase deficiency and its thermolabile variants:

-Methionine synthase deficiency

-Cobalamin (Cbl) metabolism

-Combined methyl-Cbl and adenosyl-Cbl deficiencies: Cbl C2, Cbl D2, and Cbl F3 deficiencies

-Methyl-Cbl specific deficiencies: Cbl D-Var1, Cbl E, and Cbl G deficiencies

-Transcobalamin II deficiency

-Adenosylhomocysteinase deficiency

-Glycine N-methyltransferase deficiency

-Methionine adenosyltransferase I/III deficiency

 

Screening and monitoring patients suspected of, or confirmed with, an inherited disorder of methionine metabolism

 

Evaluating individuals with suspected deficiency of vitamin B12 or folate

Disease States

  • Homocystinuria

Reporting Name

Homocysteine, Total, S

Specimen Type

Serum


Necessary Information


Patient's age and sex are required.



Specimen Required


Container/Tube:

Preferred: Serum gel

Acceptable: Red top

Specimen Volume: 1 mL

Collection Instructions: Centrifuge and aliquot serum into plastic vial within 4 hours of collection.


Specimen Minimum Volume

0.3 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Serum Refrigerated (preferred) 28 days
  Frozen  309 days
  Ambient  28 days

Reject Due To

Gross hemolysis OK
Gross lipemia OK
Gross icterus OK

Clinical Information

Homocysteine is an intermediary in the sulfur-amino acid metabolism pathways, linking the methionine cycle to the folate cycle. Inborn errors of metabolism that lead to homocysteinemia or homocystinuria include cystathionine beta-synthase deficiency (homocystinuria) and various defects of methionine remethylation. Genetic defects in vitamin cofactors (vitamins B6, B12, and folate) and nutritional deficiency of vitamin B12 and folate also lead to abnormal homocysteine accumulation.

 

Homocysteine concentration is an indicator of acquired folate or cobalamin deficiency and is a contributing factor in the pathogenesis of neural tube defects. Homocysteine was once thought to be an independent predictor of cardiovascular disease (atherosclerosis, heart disease, thromboembolism), as early observational studies prior to the year 2000 linked homocysteine to cardiovascular risk and morbidity and mortality. However, following U.S. Food and Drug Administration mandated folic acid supplementation in 1998, homocysteine concentrations decreased by approximately 10% without a similar change in cardiovascular or ischemic events. Currently, the use of homocysteine for assessment of cardiovascular risk is uncertain and controversial. Based on several meta-analyses, at present, homocysteine may be regarded as a weak risk factor for coronary heart disease, and there is a lack of direct causal relationship between hyperhomocysteinemia and cardiovascular disease. It is most likely an indicator of poor lifestyle and diet.

 

This test should be used in conjunction with plasma amino acids, quantitative acylcarnitines, methylmalonic acid, and urine organic acids to aid in the biochemical screening for primary and secondary disorders of methionine metabolism.

Reference Values

Age

Total Homocysteine (nmol/mL)

Female

Male

0-11 months

3.1-8.3

3.2-9.7

12-23 months

3.2-8.3

3.3-9.6

24-35 months

3.2-8.2

3.3-9.6

3 years

3.2-8.2

3.3-9.6

4 years

3.3-8.2

3.4-9.5

5 years

3.4-8.1

3.5-9.4

6 years

3.5-8.1

3.6-9.4

7 years

3.5-8.1

3.7-9.4

8 years

3.6-8.2

3.8-9.3

9 years

3.7-8.2

3.9-9.4

10 years

3.8-8.3

4.1-9.4

11 years

3.9-8.4

4.3-9.4

12 years

3.9-8.6

4.4-9.5

13 years

4.0-8.7

4.6-9.6

14 years

4.1-8.8

4.8-9.7

15 years

4.2-8.9

5.0-9.8

16 years

4.2-9.1

5.2-9.9

17 years

4.3-9.2

5.4-10.0

18 years

4.3-9.3

5.6-10.1

19 years

4.4-9.5

5.7-10.3

20 years

4.4-9.6

5.9-10.5

21 years

4.4-9.8

6.0-10.6

22 years

4.4-9.9

6.1-10.8

23 years

4.4-10.1

6.2-11.0

24 years

4.4-10.3

6.2-11.1

25 years

4.4-10.4

6.3-11.3

26 years

4.4-10.6

6.3-11.4

27 years

4.3-10.8

6.4-11.6

28 years

4.3-11.0

6.4-11.7

29 years

4.3-11.2

6.4-11.8

30 years

4.3-11.4

6.4-11.9

31 years

4.4-11.6

6.4-12.1

32 years

4.4-11.8

6.4-12.2

33 years

4.4-11.9

6.4-12.3

34 years

4.5-12.1

6.4-12.4

35 years

4.5-12.2

6.4-12.6

36 years

4.6-12.4

6.4-12.8

37 years

4.6-12.5

6.4-12.9

38 years

4.7-12.7

6.4-13.1

39 years

4.7-12.8

6.4-13.2

40 years

4.8-13.0

6.5-13.4

41 years

4.8-13.2

6.5-13.5

42 years

4.8-13.4

6.5-13.7

43 years

4.9-13.5

6.6-13.9

44 years

4.9-13.7

6.6-14.0

45 years

4.9-13.9

6.6-14.2

46 years

4.9-14.0

6.7-14.4

47 years

4.9-14.2

6.7-14.5

48 years

5.0-14.3

6.8-14.7

49 years

5.0-14.4

6.8-14.9

50 years

5.0-14.5

6.8-15.0

51 years

5.1-14.6

6.8-15.2

52 years

5.1-14.7

6.9-15.4

53 years

5.1-14.8

6.9-15.5

54 years

5.2-14.9

6.9-15.6

55 years

5.2-15.0

6.9-15.7

56 years

5.3-15.0

6.9-15.8

57 years

5.3-15.1

6.9-15.9

58 years

5.3-15.2

6.9-16.0

59 years

5.4-15.2

6.9-16.0

60 years

5.4-15.3

6.9-16.1

61 years

5.4-15.4

7.0-16.2

62 years

5.5-15.4

7.0-16.2

63 years

5.5-15.5

7.0-16.3

64 years

5.6-15.5

7.1-16.3

65 years

5.6-15.6

7.1-16.3

66 years

5.7-15.6

7.1-16.3

67 years

5.7-15.7

7.2-16.3

68 years

5.8-15.7

7.2-16.3

69 years

5.9-15.7

7.2-16.3

70 years

6.0-15.8

7.3-16.3

71 years

6.1-15.8

7.3-16.3

72 years

6.2-15.8

7.3-16.3

73 years

6.3-15.9

7.3-16.3

74 years

6.4-15.9

7.3-16.3

75 years

6.5-15.9

7.3-16.3

76 years

6.6-15.9

7.3-16.3

77 years

6.7-16.0

7.4-16.3

78 years

6.8-16.0

7.4-16.3

79 years

6.9-16.0

7.5-16.3

80 years

7.0-16.0

7.5-16.3

81 years

7.1-16.0

7.7-16.2

82 years

7.2-16.0

7.8-16.2

83 years

7.2-16.0

7.9-16.2

84 years

7.3-16.0

8.0-16.2

85 years

7.3-16.0

8.2-16.2

>85 years

7.4-16.0

8.3-16.2

Day(s) Performed

Monday through Friday

Report Available

3 to 5 days

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Test Classification

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.

CPT Code Information

83090

Method Name

Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS)

Forms

1. Biochemical Genetics Patient Information (T602)

2. If not ordering electronically, complete, print, and send 1 of the following forms with the specimen:

-Biochemical Genetics Test Request (T798)

-Cardiovascular Test Request (T724)