Copeptin

From Wikipedia, the free encyclopedia
Jump to navigation Jump to search

Copeptin
Diagram of the pre-pro-vasopressin precursor showing position and size in amino acids of AVP, neurophysin II and copeptin
Identifiers
SymbolCT-proAVP
Alt. symbolscopeptine
OMIM192340
UniProtP01185
Other data
LocusChr. 20 p13
Search for
StructuresSwiss-model
DomainsInterPro

Copeptin (also known as CT-proAVP) is a 39-amino acid-long peptide derived from the C-terminus of pre-pro-hormone of arginine vasopressin, neurophysin II and copeptin. Arginine vasopressin (AVP), also known as the antidiuretic hormone (ADH), is encoded by the AVP gene and is involved in multiple cardiovascular and renal pathways and abnormal level of AVP are associated with various diseases. Hence measurement of AVP would be useful, but is not commonly carried out in clinical practice because of its very short half-life making it difficult to quantify. In contrast, copeptin can be immunologically tested with ease and therefore can be used as a vasopressin surrogate marker.

Synthesis and secretion

[edit | edit source]

Copeptin is a 39-amino acid-long, glycosylated peptide.[1] It is synthesized mainly in the paraventricular neurons of the hypothalamus and in the supraoptic nucleus.[2] During axonal transport, pre-pro-AVP is proteolytically cleaved into vasopressin, neurophysin II and copeptin.[3] These molecules are then stored in secretory granules in the posterior pituitary and released upon osmotic or non-osmotic (hemodynamical; stress-related) stimuli.[2]

Function

[edit | edit source]

Once secreted into the bloodstream, there is no known biological role for copeptin. However, when pre-pro-vasopressin is processed during the axonal transport, copeptin may contribute to the 3D folding of vasopressin.[2]

Surrogate vasopressin marker

[edit | edit source]

The size and half-life of copeptin permit an easier immunological testing, compared to vasopressin, and hence copeptin is proposed as a reliable AVP surrogate.[4][5] The clinical interest in copeptin testing is closely linked to the pathophysiological pathways in which vasopressin is involved: polydipsia-polyuria syndrome, hyponatremia, syndrome of inappropriate antidiuretic hormone secretion (SIADH) as well as heart failure and acute coronary syndrome.[6]

In blood

[edit | edit source]

The concentration of copeptin in the blood circulation ranges from 1 to 12 pmol/L in healthy individuals.[6] The levels of copeptin are slightly higher in men than in women[6] and are not influenced by age.[6] In response to serum osmolality fluctuations, the kinetics of copeptin are comparable to those of vasopressin.[6][7] For example, patients with an electrolyte disorders such as diabetes insipidus with very low vasopressin concentrations also show very low copeptin concentrations in blood plasma.[8] On the other hand, patients with syndrome of inappropriate antidiuretic hormone secretion show high concentrations of both vasopressin and copeptin.[9]

Acute myocardial infarction

[edit | edit source]

Several studies have shown that copeptin is released very early during the onset of an acute myocardial infarction (AMI),[10][11] raising the question of its potential value in the diagnosis of AMI and particularly in ruling-out AMI.[11][12][13] Indeed, copeptin is released much earlier than troponin, given that copeptin is actively released from the hypothalamus, while troponin occurs in the bloodstream as a breakdown product from dying cardiomyocytes,[14] making the interpretation of their complementary kinetics a useful tool to rule-out AMI.[11][12] It has been shown that the combination of a negative result of troponin together with a negative result of copeptin can rule out AMI at emergency department presentation with a negative predictive value ranging from 95% to 100%.[11][12][13] These results have been confirmed in a randomised controlled trial.[15][16][17]

Cardiogenic shock

[edit | edit source]

High concentrations of vasopressin during cardiogenic shock have been widely described.[18][19] It has been shown that the kinetics of copeptin are similar to vasopressin in that context.[20]

Heart failure

[edit | edit source]

The prognostic value of vasopressin for prediction of outcome in patients with heart failure has been known since the 1990s. Patients presenting with high levels of vasopressin have a worsened outcome.[21][22] Recently, a similar interest has been demonstrated for copeptin in heart failure.[10][23][24][25]

See also

[edit | edit source]

References

[edit | edit source]
  1. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  2. ^ a b c Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  3. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  4. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  5. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  6. ^ a b c d e Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  7. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  8. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  9. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  10. ^ a b Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  11. ^ a b c d Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  12. ^ a b c Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  13. ^ a b Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  14. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  15. ^ BIC-8 Archived 6 December 2013 at the Wayback Machine, on Site ESC2013 Archived 9 November 2013 at the Wayback Machine. On 10 September 2013
  16. ^ Results of BIC-8 Archived 3 March 2016 at the Wayback Machine, on Site biomarqueursinfos.fr Archived 10 January 2016 at the Wayback Machine. On 10 November 2013
  17. ^ Interview of principal investigator and ESC reviewer on BIC-8 Archived 4 March 2016 at the Wayback Machine, on Site biomarqueursinfos.fr Archived 10 January 2016 at the Wayback Machine. On 10 November 2013
  18. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  19. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  20. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  21. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  22. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  23. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  24. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  25. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).

Lua error in mw.title.lua at line 392: bad argument #2 to 'title.new' (unrecognized namespace name 'Portal').