| Glycine | |
| CSFGLY | |
| CSF collected in a sterile 20ml universal and a paired plasma sample (orange bottle). Store refrigerated. | |
| This test is referred to another centre: Department of Clinical Chemistry Expected turnaround time: 6 weeks | |
| Used in the investigation of glycine encelopathy | |
| Contact referral laboratory | |
| Contact referral laboratory | |
| N/A | |
| N/A | 
Blood Science Test Repertoire
| Galactose-1-Phosphate Uridyl Transferase | |
| GAL-1-PUT | |
| Blood spot (Guthrie card) | |
| This test is referred to another centre: Department of Clinical Chemistry Expected turnaround time: 6 weeks | |
| Used in the investigation of abnormal liver function in neonates | |
| Contact referral laboratory | |
| Contact referral laboratory | |
| N/A | |
| N/A | 
| Gut Hormone Profile / Chromogranin A/B | |
| Chromogranin A, Chromogranin B, VIP, PP, PG, SRIF, NT, glucagon, gastrin, GHP, CGAB | |
| 1 x 7.5ml EDTA (Red Top) Tube + 1 x 4.7ml Gel (Brown Top) Tube. The red EDTA tube should be transported to the laboratory on ice. Upon arrival in the laboratory the EDTA sample is centrifuged at 4200 rpm for 12 min at +4oC within 15 minutes of venepuncture and the plasma stored frozen prior to referral. If sample is haemolysed, instruct phlebotomy to re-bleed patient. If sample is not haemolysed, instruct phlebotomy that patient may leave department. Urea and calcium should be requested and processed on the serum sample. | |
| Test referred to another centre for analysis: The SAS Laboratories Expected turnaround time: 6 weeks | |
| Used in the investigation of disorders of gut hormone secretion. Chromogranin A and B can be requested seperately for the investigation of neuroendocrine tumours. | |
| Blood must be collected with the patient at rest after a complete overnight fast. H2 anatgonists should be stopped for 72 hrs and omeprazole should be stopped for two weeks before blood is taken. Contact referral lab for more information | |
| Contact referral laboratory | |
| N/A | |
| N/A | 
| Glucosaminoglycans | |
| GAGU, | |
| Urine (universal). Store refrigerated prior to referral | |
| This test is referred to another centre: Department of Clinical Chemistry Expected turnaround time: 6 weeks | |
| Used in the investigation of mucopolysacchridosis disorders. Requests for Mucopolysaccharides should be processed for urine glucosaminoglycans | |
| Contact referral laboratory | |
| Contact referral laboratory | |
| N/A | |
| N/A | 
| Assay | Glomerular basement membrane (GBM) antibodies | 
| Key Words | Glomerular basement membrane antibodies, GBM | 
| Specimen Collection | Serum (brown) If this assay is needed URGENTLY please call the laboratory on x8454 to discuss | 
| Turnaround time | 7 days | 
| Test indications | Antibodies against type IV collagen are seen in Goodpasture’s syndrome, a pulmonary-renal form of vasculitis associated with rapidly progressing renal failure and haemoptysis. About 10% of patients with Wegener’s granulomatosis may also have GBM antibodies. | 
| Methodology | Enzyme immunoassay | 
| Interferences | No known methodological interferences | 
| Reference Range | Negative <7 U/mL Equivocal 7-10 U/mL Positive >10 U/mL | 
| Analytical error | Contact laboratory (x8454) | 
| Reference change value | N/A | 
| Growth Hormone | |
| GH | |
| Serum (brown top) tube) | |
| 24hrs | |
| Used in the investigation of hypo- and hyperpituitarism | |
| No known interferences | |
| Please contact laboratory for further information | |
| 2.1% | |
| N/A | 
| Assay | Glycated Haemoglobin | 
| Key Words | HbA1c | 
| Specimen Collection | Blood (red EDTA) | 
| Turnaround time | 72hrs | 
| Test indications | HbA1c is a measurement of the glycation of haemoglobin which occurs proportionally to both the average glucose concentration and the life span of the red blood cells in the circulation. The measurement of HbA1c has therefore been accepted as a monitoring tool for assessing blood glucose levels over the previous 120 days and is a vital tool in the clinical management for diabetes | 
| Interferences | HbA1c result are not reported in the presence of a number of haemoglobin variants. Results can be reported on patients with heterozygous HbS, HbC, HbD and HbE genotypes, however results on patients with haemoglobin variants are for monitoring only, and should not be used for diagnosis. 
 If a haemoglobin variant is detected during testing, further investigations can be performed. An EDTA sample will need to be sent to the Haematology department for a Haemoglobinopathy screen (RTS). 
 HbA1c is dependent on both the mean blood glucose concentration and turnover of red blood cells. An increased RBC turnover affects HbA1c, and should be considered when interpreting results. 
 **Please note, this information pertains to the analysis performed by the laboratory only** | 
| Reference Range | Non-diabetics: 20-42mmol/mol HbA1c of >48mmol/mol is used as a cut-off for the diagnosis of Type II Diabetes Mellitus | 
| Analytical error | 1.6% | 
| Reference change value | 5.5% | 
| Minimum retesting interval | Requests made within 7 days of a previous result on a patient are intervened | 
| Assay | G6PD Assay | 
| Key Words | Glucose-6-Phosphate Dehydrogenase, G6PD | 
| Specimen Collection | EDTA | 
| Referral | This test is referred to another centre for analysis: The Red cell centre Kings college Hospital trust Kings College Hospital Denmark Hill London 
 SE5 9RS | 
| Turnaround time | 14 days from receipt at reference laboratory | 
| Test indications | Abnormal/Equivocal G6PD screen or females with normal G6PD screen results; as a mild deficiency in females may not be detected by screening methods (Automatically actioned by the Haematology department) | 
| Interferences | Contact referral laboratory for information | 
| Reference Range | Contact referral laboratory for information | 
| Minimum retesting interval | N/A | 
| Assay | Gaucher’s Disease | 
| Key Words | Leucocyte β-glucocerebrosidase Activity, Plasma Chitriosidase Activity, Gaucher's disease | 
| Specimen Collection | 2 x 6ml-10ml EDTA (large EDTA) | 
| Referral | This test is referred to another centre for analysis: Willink Biochemical Genetics Laboratory 6th Floor, Pod 1 Saintt Mary's Hospital 
 Oxford Road Manchester M13 9WL | 
| turnaround time | 14 days from receipt at reference laboratory for enzyme investigations 28 days from receipt at reference laboratory for genetic investigations | 
| Test indications | Splenomegaly, thrombocytopaenia and raised ferritin, to exclude Gaucher’s Disease | 
| Interferences | Contact referral laboratory for information | 
| Reference Range | Contact referral laboratory for information | 
| Minimum retesting interval | N/A | 
| Assay | Glucose-6-Phosphate Dehydrogenase (G6PD) Screen | 
| Key Words | Glucose-6-Phosphate Dehydrogenase, G6PD, haemolysis, haemolytic anaemia | 
| Specimen Collection | 3.4ml EDTA (Red lid). 1.3ml EDTA for paediatric (Red lid), do not overfill. Carried out on FBC specimen. G6PD screens may be added on to samples that are up to 48 hours old. | 
| Turnaround time | Next working day | 
| Test indications | Haemolytic anaemia, and to assess potential primaquine sensitivity after positive malaria screen. 
 
 Please refer to the latest guidelines for Diagnosis of G6PD deficiency at: https://onlinelibrary.wiley.com/doi/10.1111/bjh.16366 | 
| Interferences | ‘A false normal result can occur in G6PD-deficient individuals with a high reticulocyte count due to an existing acute haemolytic episode.’ ‘A false abnormal result can occur in G6PD-normal individuals with severe anaemia. This G6PD screen cannot reliably detect G6PD deficiency in heterozygous women, therefore samples from females, with normal screening results, will be sent to the reference lab for G6PD assay to confirm | 
| Reference Range | N/A | 
| Minimum retesting interval | N/A | 
| Assay | Glandular Fever Screen | 
| Key Words | Paul Bunnell, Monospot, Glandular Fever, GF, Epstein Barr Virus, EBV, Heterophile antibody | 
| Specimen Collection | 3.4ml EDTA (Red lid). 1.3ml EDTA for paediatric (Red lid), do not overfill. Carried out on the Full Blood Count specimen. Paul Bunnell screens may be added on to samples that are up to 24 hours old, as long as they were stored at 2-8°C. | 
| Turnaround time | Next working day | 
| Test indications | Lymphadenopathy, atypical lymphocytosis. | 
| Interferences | A negative Paul Bunnell screen does not conclusively rule out infectious mononucleosis. | 
| Reference Range | N/A | 
| Minimum retesting interval | N/A | 
| Assay | Ganglioside antibodies | 
| Key Words | Ganglioside GM1 antibodies (GM1), Ganglioside GQ1B antibodies (GQ1B) | 
| Specimen Collection | Serum (brown) | 
| Turnaround time | 14 days This test is referred to another centre: Neuroimmunology & CSF laboratory (Box 76) 9th Floor UCL Queen Square Institute of Neurology Queen Square London WC1N 3BG Telephone : 020 3448 3812 
 | 
| Test indications | These antibodies are associated with the following neurological diseases: 
 | 
| Methodology | Contact referral centre | 
| Interferences | Contact referral centre | 
| Reference Range | N/A | 
| Analytical error | Contact referral centre | 
| Reference change value | N/A | 
| Assay | Gastric parietal cell antibodies (GPC) | 
| Key Words | Pernicious Anaemia Associated abs , GPC | 
| Specimen Collection | Serum (brown) | 
| Turnaround time | 7 days | 
| Test indications | These antibodies have a strong association with pernicious anaemia and autoimmune gastritis. Low titres are commonly found in normal elderly females. Positive results will automatically be referred for Intrinsic factor antibodies which are more specific, but less sensitive, for pernicious anaemia. GPC antibodies can also be found in patients with autoimmune thyroid disease and Sjogren's syndrome. | 
| Methodology | Indirect immunofluorescence | 
| Interferences | No known methodological interferences | 
| Reference Range | N/A | 
| Analytical error | N/A | 
| Reference change value | N/A | 
| Assay | Glutamic acid decarboxylase (GAD) antibodies | 
| Key Words | Glutamic acid decarboxylase antibodies, GAD | 
| Specimen Collection | Serum (brown) | 
| Turnaround time | 28 days | 
| Test indications | GAD antibodies are found in 60% of patients with Stiff man syndrome, usually with high titre. These antibodies are also found in up to 80% of patients with recent onset Type 1 Diabetes Mellitus. However these antibodies reduce with disease duration. In the assessment of first degree relatives for autoimmune diabetes, positive results in more than one of the marker antibodies (GAD, Islet cell, IA-2 or insulin) can be associated with the onset of autoimmune diabetes. GAD antibodies are not available as a routine test in established diabetes. | 
| Methodology | ELISA | 
| Interferences | No known methodological interferences | 
| Reference Range | Negative <10 IU/mL Positive ≥10 U/mL | 
| Analytical error | Contact laboratory (x8454) | 
| Reference change value | N/A | 
| Assay | Glycine Receptor antibodies | 
| Key Words | Glycine receptor abs, GLYA | 
| Specimen Collection | Serum (Brown) (CSF is not required but can be analysed if required) | 
| Turnaround time | 14 days 
 This test is referred to another centre: Churchill Hospital Old Road Headington Oxford OX3 7LE 0300 304 7777 
 | 
| Test indications | 
 These antibodies are particularly associated with PERM (Progressive encephalomyelitis with rigidity and myoclonus) and stiff person syndrome. Glycine receptor antibodies were associated with neoplasms in about 10% of a series of 52 patients (mainly thymoma and lymphoma). Carvajal-Gonzalez et al. Brain, Volume 137, Issue 8, August 2014, Pages 2178–2192, https://doi.org/10.1093/brain/awu142 
 | 
| Methodology | Cell based assay | 
| Interferences | Contact referral laboratory | 
| Reference Range | Contact referral laboratory | 
| Analytical error | Contact referral laboratory | 
| Reference change value | N/A | 




