Evaluation of patients who present with signs or symptoms suggestive of disaccharidase disorders
This test is not intended for carrier detection.
Diagnostic testing for patients with clinical signs and symptoms suspicious of a disaccharidase deficiency.
Spectrophotometry
Disaccharidase Determination
Tissue
Freeze immediately after collection and ship frozen.
Source: Intestinal biopsy
Supplies: 15 mL Tissue Tube-DSAC (T993)
Container/Tube: 15 mL tissue tube
Specimen Volume: 5 mg
Collection Instructions:
1. Place specimen in tissue tube.
2. Specimen should not be placed on gauze, filter paper, or swabs/wooden sticks and should not have any saline, water, support, or embedding material added.
If not ordering electronically, complete, print, and send 1 of the following forms with the specimen:
See Specimen Required
Specimens sent in formaldehyde, saline, or any supportive media Specimens placed on gauze, filter paper, foil, or swabs/wooden sticks | Reject |
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Tissue | Frozen | 28 days | OTHER |
Evaluation of patients who present with signs or symptoms suggestive of disaccharidase disorders
This test is not intended for carrier detection.
Diagnostic testing for patients with clinical signs and symptoms suspicious of a disaccharidase deficiency.
Disaccharidases in the small intestines are responsible for the breakdown of disaccharides (double sugars) into monosaccharides (simple sugars). Patients with a deficiency of one or more disaccharidase can experience intolerance to foods containing complex sugars resulting in a range of gastrointestinal symptoms, including diarrhea or constipation, abdominal pain and cramping, gas, bloating, and nausea. In addition, patients may experience malnutrition, weight loss, or failure to thrive. Given the nonspecificity and frequency of abdominal symptoms, misdiagnosis or a diagnostic delay of disaccharide deficiencies may occur.
Primary and secondary causes of disaccharidase deficiencies exist, and age of onset may vary from birth through adulthood. Primary causes are rare and result from genetic alterations in a variety of genes. Secondary deficiencies typically result from small intestinal mucosal damage. Treatment of both primary and secondary disaccharidase deficiencies involves dietary management. While primary deficiencies require lifelong treatment, secondary disaccharidase deficiencies may require treatment only until the intestinal lining recovers.
Lactase: > or =14.0 nmol/min/mg protein
Sucrase: > or =19.0 nmol/min/mg protein
Maltase: > or =70.0 nmol/min/mg protein
Palatinase: > or =6.0 nmol/min/mg protein
Glucoamylase: > or =8.0 nmol/min/mg protein
Quantitative values of lactase, sucrase, maltase, palatinase, and glucoamylase are reported. Clinical interpretation of results is provided.
This test will not distinguish between primary and secondary causes of disaccharidase deficiencies.
1. Cohen SA, Oloyede H, Gold BD, Mohammed A, Elser HE. Clinical characteristics of disaccharidase deficiencies among children undergoing upper endoscopy. J Pediatr Gastroenterol Nutr. 2018;66 Suppl 3:S56-S60
2. Semenza G, Auricchio S, Mantei N. Small-intestinal disaccharidases. In: Valle DL, Antonarakis S, Ballabio A, Beaudet AL, Mitchell GA. eds. The Online Metabolic and Molecular Bases of Inherited Disease. McGraw Hill; 2019. Accessed October 10, 2024. Available at https://ommbid.mhmedical.com/content.aspx?bookid=2709§ionid=225081608
Disaccharidase activities are measured by incubating intestinal homogenates with an appropriate disaccharide substrate, which releases glucose. Glucose production is determined by a glucose oxidase reagent mixture that oxidizes glucose to produce peroxide, which reacts with phenol aminophenazone to form a red quinoneimine dye. The concentration of quinoneimine is determined spectrophotometrically, and the concentration of liberated glucose is calculated from a glucose standard curve. The amount of glucose produced is proportional to the disaccharidase activity in the intestinal homogenate. Disaccharidase activities are expressed as nanomoles of glucose per minute per milligram of protein (nmol/min/mg prot).(Unpublished Mayo method)
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.
82657
Test Id | Test Order Name | Order LOINC Value |
---|---|---|
DSAC | Disaccharidase Activity Panel, Ts | 57765-0 |
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.
|
---|---|---|
608237 | Lactase | 81315-4 |
608238 | Sucrase | 30372-7 |
608239 | Maltase | 30315-6 |
608240 | Palatinase | 81314-7 |
608241 | Glucoamylase | 81322-0 |
608242 | Interpretation | 57779-1 |
608243 | Reviewed By | 18771-6 |
Change Type | Effective Date |
---|---|
Test Changes - Specimen Information | 2024-10-08 |
Supply Item | 2024-10-08 |