CDG N-Glycan Profile
Congenital disorders of glycosylation (CDGs) are a group of inherited diseases characterized by abnormal protein and lipid glycosylation. To date, over 120 separate genetic deficiencies have been linked to a CDG and the breadth of causative genes leads to highly variable clinical presentation with multi-systemic involvement. The severity and long term outcome is dependent on the specific causative CDG, and shows significant inter- and intra-familial variability. While a common phenotype cannot be reported, the majority of CDGs may be associated with a significant neurologic component including hypotonia, seizures, cerebellar hypoplasia and developmental delay/intellectual disability. Additional common features may include abnormal fat distribution, coagulation defects, feeding difficulties, gastrointestinal abnormalities, ocular abnormalities and cardiac abnormalities including cardiomyopathy.
CDGs can be classified into two groups based on the pathway defect. Type I CDG (CDG-I) refers to defects in glycan assembly and transfer from the dolichol phosphate lipid to the asparagine residue on nascent proteins. Type II CDG (CDG-II) refers to defects in processing of the N-glycan to its mature form. CDG-II can also affect serine/threonine-linked glycosylation (O-glycosylation). Complete biochemical analyses for screening of CDGs include carbohydrate deficient transferrin (CDT), N-glycan profiling, and O-glycan profiling in serum or plasma.
N-glycan profiling: Plasma N-glycan profiling involves removal of N-glycans from proteins, purification, permethylation and MALDI-TOF/TOF analysis. A total of 42 glycans are monitored and their relative abundance provides a comprehensive view of N-glycan metabolism, particularly in regard to the processing after glycan transfer in the ER or Golgi-localized steps that are associated with type II CDGs. This assay can also reveal abnormalities associated with certain type I CDGs.
In patients suspected of having a CDG, N-Glycan profiling can be ordered in conjunction with Carbohydrate Deficient Transferrin (CDT) analysis and O-Glycan profiles in order to provide the most comprehensive view of the glycosylation status. These tests can also be utilized for monitoring patients on dietary treatment. Results should be correlated with the patient’s clinical findings. Positive biochemical findings should be confirmed with molecular analysis. Secondary glycosylation abnormalities have been reported in patients with alcoholism and other metabolic diseases such as fructose intolerance and galactosemia.
Please contact SEMA4 laboratory to discuss molecular testing options
- 1-2 mL in EDTA tube (lavender top) or sodium heparin tube (green top) or serum tube (red top). Minimum of 0.5 mL is required.
- 1 mL plasma or serum, minimum of 100 µL.
- Separate plasma immediately and ship frozen plasma on dry ice
- Plasma should be stored frozen until analysis
- 10-14 days
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New York, NY 10029
Tel: 800-298-6470, Fax: 646-859-6870
General Genetic Test Requisition