Test Overview
Clinical Utility
Copeptin is a 39-amino acid glycopeptide, the C-terminal part of the AVP precursor (CT-proAVP), and is a stable and sensitive surrogate marker for Antidiuretic Hormone (ADH). Osmolality measurement is not performed as part of copeptin testing. To aid in interpretation of copeptin results, it is recommended that osmolality be ordered separately (separate specimen and billing) or tested at the laboratory where sample collection is performed.
Method
Fluorescence immunoassay (FIA)
Analytical Platform
Kryptor Compact Plus
Method Description
Kit: BRAHMS Copeptin proAVP KRYPTOR
Result Included
Copeptin
Aliases/Synonyms
ProAVP; ADH; Antidiuretic hormone; Vasopressin; Arginine Vasopressin; AVP; ADH
Specimen
Specimen Type
SerumPlasma
Containers
Preferred Containers
Plasma (Li heparin green top)
Acceptable Containers
Serum (Red top); Serum (Gold top); Plasma (Lavender top)
Volume
Sample Volume
0.5 mL
Pediatric
Minimum
0.25 mL
Collection & Handling
Handling Information
Store and send frozen.
Stability
| Ambient | Refrigerated | Frozen |
|---|---|---|
| 3 days | 3 days | 90 days |
Performance & Interpretation
Turnaround Time
7 days
Results
-
Copeptinpmol/LInterpretive guidelines effective 16-Oct-2023:
Adult (≥ 18 years):
Reference Interval (Non-Stimulated, Non-Fasting): < 13.1pmol/L (Keller T et al., JACC 2010; 55(19):2096-2106)
Nephrogenic Diabetes Insipidus (DI):
Baseline copeptin ≥21.4 pmol/L in adults with polyuria-polydipsia syndrome had 100% sensitivity (sens) and specificity (spec) (Timper K et al., JCEM 2015; 100(6):2268-2274)
Central DI:
- Following hypertonic saline infusion, copeptin ≤ 4.9 pmol/L identified complete/partial central DI (vs. primary polydipsia (PP)) with 93% sens and 100% spec (Fenske W et al., NEJM 2018; 379:428-439)
- At 60 min following arginine stimulation, copeptin ≤3.8 pmol/L identified complete/partial central DI (vs. PP) with 93% sens and 92% spec (Winzeler B et al., Lancet 2019; 394(10198):587-595)
Reference Intervals (Non-Stimulated, Non-Fasting): <14.5 pmol/L (Du J-M et al., Peptides 2013; 45:61-65)
Copeptin may be elevated at birth (< 3 days) with perinatal stress (Burckhardt M-A et al., JCEM 2014; 99(9):E1750-E1753)
Baseline Copeptin in Children with Polyuria-Polydipsia Syndrome:
Nephrogenic DI: > 20 pmol/L
Central DI: ≤ 3.5 pmol/L had 100% sens and 87% spec (so central DI excluded at > 3.5 pmol/L); ≤ 1.1 pmol/L had 29% sens and 100% spec (so PP excluded)(Bonnet L et al., ClinEndo 2022; 96:47-53)
Stimulated Copeptin in Children (e.g. Arginine, Water Deprivation, or Hypernatremia):
Complete Central DI: ≤ 3.5 pmol/L
Partial or Complete Central DI: ≤4.9 pmol/L
Sens 88-100%, spec 66-80% (Binder G et al., ClinEndo 2023; 98:548-553; Tuli G et al., ClinEndo 2018; 88:873-879; Al Nofal A et al., JPEM 2023; 36(5):492-499)
Sample Report
Copeptin (Adult)
Copeptin (Pediatric)
Copeptin (age not provided)
Referral Location
Canada
Interface & Setup
HL7 Interface Codes
| Order Code | Result Name | Result Codes | Units |
|---|---|---|---|
| COPEPTIN | COPEPTIN | 62877 | pmol/L |
| Copeptin Interpretation | 65174 |
Test Version
Last Updated
2023-10-27