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Back to Test Catalogue
Test ID: COPEPTIN

Copeptin, Serum/Plasma

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

Serum
Plasma

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

Name
Units
Reference Range
Conversion
  1. Copeptin
    pmol/L
    Interpretive 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)
    Pediatric (< 18 years):

    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)

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