Test Price
2,800 AEDโ Home Collection Available
Pancreatic Polypeptide (PP) Test in UAE | 2800 AED | DHA Licensed Lab
Executive Summary & Core Metrics
This page defines the advanced Pancreatic Polypeptide (PP) Test service provided by DNA Labs UAE under DHA License 1143. Utilizing a Chemiluminescent Immunoassay (CLIA), this assay delivers diagnostic-grade accuracy for neuroendocrine tumor evaluation and MEN1 syndrome monitoring.
Test Overview & Methodology
The Pancreatic Polypeptide (PP) Test quantifies fasting blood levels of this pancreatic islet hormone. It serves as a highly specific biomarker for pancreatic neuroendocrine tumors (pNETs) and is essential for monitoring Multiple Endocrine Neoplasia Type 1 (MEN1) kindreds. Our service employs a modern Chemiluminescent Immunoassay (CLIA), which offers superior analytical sensitivity and specificity compared to legacy Radioimmunoassay (RIA) methods, ensuring DHA-recognized results with reliable batch reporting.
Pre-Test Instructions
Overnight fasting (8โ12 hours) is strongly required. A completed Test Send Out Consent Form (Form 35) is mandatory prior to sample collection. A volume of 2 mL plasma (minimum 1 mL) is collected in a Lavender Top (EDTA) tube and must be shipped under refrigerated or frozen conditions to preserve analyte integrity.
| Feature | Our CLIA Platform | Standard RIA Method |
|---|---|---|
| Analytical Sensitivity | 0.1 pmol/L | Variable, up to 5 pmol/L |
| Clinical Specificity | >98% for pNETs | 85% (cross-reactivity) |
| Turnaround Time | Batch reporting within 2โ3 weeks | Similar, lacks ISO traceability |
| UAE Accreditation | ISO 9001:2015 & DHA Licensed (1143) | Often unregulated or non-clinical |
Physician Insight & Safety Protocols
โElevated fasting pancreatic polypeptide requires careful integration with cross-sectional imaging and a full neuroendocrine tumor biomarker panel. Isolated elevation does not confirm malignancy and must be contextualized within the patientโs clinical presentation and MEN1 risk profile. A comprehensive genetic evaluation is advised for patients with a family history of endocrine tumors.โ
โ Mr. Prabhakar Reddy Kalathoor, Specialist Diagnostic Radiology (DHA Registration ID: 61713011)
Medication Safety Advisory
Do not adjust or discontinue prescribed proton-pump inhibitors, somatostatin analogues, or any hormonal therapy without consulting your treating physician. Pancreatic polypeptide levels are directly influenced by medication adherence and fasting metabolic status. Self-manipulation of therapy based on a single laboratory value can lead to adverse clinical outcomes.
Exclusion Criteria & Emergency Red Flags
- Do not schedule the blood draw if you have an active febrile illness, acute pancreatitis, or have undergone major surgery within the last 4 weeks.
- Samples cannot be processed if the mandatory Form 35 (Test Send Out Consent) is missing, incomplete, or unsigned.
- Seek immediate emergency care if you experience sudden severe abdominal pain, jaundice, or unexplained weight loss โ do not wait for this test result to seek acute medical attention.
Patient FAQ & Clinical Guidance
1. What is the pancreatic polypeptide test and why is it ordered?
This fasting blood test measures the concentration of pancreatic polypeptide, a hormone secreted by the islet cells of the pancreas. It is primarily ordered to detect and monitor pancreatic neuroendocrine tumors (pNETs) and to screen individuals with a family history of MEN1 syndrome. It is frequently used alongside chromogranin A and endoscopic ultrasound for a comprehensive diagnostic evaluation.
2. How should I prepare for the sample collection procedure?
An overnight fasting period of 8 to 12 hours is mandatory. You must sign the Test Send Out Consent Form (Form 35) before the phlebotomy. A trained professional will draw blood from a vein in your arm into a specialized EDTA tube. The sample is immediately placed under cold-chain conditions for transport to our ISO-certified laboratory.
3. What do high PP levels indicate and what are the next steps?
Elevated levels indicate hypersecretion from pancreatic islet cells, commonly associated with neuroendocrine tumors but can also occur in renal impairment or chronic atrophic gastritis. Your specialist will correlate this result with MRI, CT, or endoscopic ultrasound findings. Further investigation may include a MEN1 genetic panel, somatostatin receptor imaging, or functional PET scans to localize the source of secretion.
UAE Regulatory & Data Privacy Adherence
DNA Labs UAE strictly operates in compliance with the following UAE federal legislations to ensure complete clinical safety, data confidentiality, and ethical medical practice:
- Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL): Governing the secure collection, processing, and storage of your personal health information.
- Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields: Regulating the digital infrastructure, telemedicine protocols, and electronic health record security used in this service.
- Federal Decree-Law No. 4 of 2016 on Medical Liability: Ensuring patient consent protocols, clinical safety standards, and physician accountability throughout the diagnostic pathway.
Our facility is licensed by the Dubai Health Authority (DHA License Number: 1143) and holds ISO 9001:2015 certification for quality management systems.
Clinical & Logistical Metadata
| Test Name | Pancreatic Polypeptide (PP) Test |
| Price (AED) | 2,800 AED |
| Turnaround Time | 2โ3 Weeks (Batch Reporting Cycle) |
| Sample Type / Matrix | Plasma (EDTA), 2 mL |
| Methodology Used | Chemiluminescent Immunoassay (CLIA) |
| ICD-10-CM Code | C25.4, D37.7, Z15.09 |
| LOINC Code | 2794-8 |
| DHA Facility License & Address | License Number: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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