Syndrome of inappropriate antidiuretic hormone classification: Difference between revisions

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==Classification==
==Classification==


[[SIADH]] may be classified in to several sub-types based on the pattern of[[ AVP]][[ secretion]] across a range of [[plasma]] osmolalities:
[[SIADH]] may be classified into several sub-types based on the pattern of [[AVP|arginine vasopressin (AVP)]] [[secretion]] across a range of [[Plasma osmolality|plasma osmolalities]]:<ref name="pmid20164214">{{cite journal |vauthors=Hannon MJ, Thompson CJ |title=The syndrome of inappropriate antidiuretic hormone: prevalence, causes and consequences |journal=Eur. J. Endocrinol. |volume=162 Suppl 1 |issue= |pages=S5–12 |year=2010 |pmid=20164214 |doi=10.1530/EJE-09-1063 |url=}}</ref>


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| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold; text-align:center;" |[[TypeA]]
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold; text-align:center;" |TypeA
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* Accounts for about 60-70% of [[SIADH]]
* Accounts for about 60-70% of [[SIADH]]
*Excessive secretion of ADH is noted  
*Excessive secretion of [[AVP]] is noted  
*Associated with [[lung cancer]] and nasopharyngeal tumors
*Associated with [[lung cancer]] and [[Nasopharyngeal Carcinoma|nasopharyngeal tumors]]
* Patients are more susceptible to development of severe [[hyponatremia]]
* Patients are more susceptible to development of severe [[hyponatremia]]
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*Accounts for (20–40%) of the cases
*Accounts for (20–40%) of the cases
*Secretion of [[AVP]] occurs at lower [[plasma]] [[osmolalities]] than normal 
*Secretion of [[AVP]] occurs at lower than normal [[Plasma osmolality|plasma osmolalities]]  
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| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold; text-align:center;" |[[TypeC]]
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold; text-align:center;" |Type C
| style="padding: 5px 5px; background: #F5F5F5;" |  
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* Failure to suppress AVP secretion at plasma osmolalities below the [[osmotic]] threshold
* Failure to suppress [[AVP]] secretion at [[Plasma osmolality|plasma osmolalities]]  below the [[osmotic]] threshold
* Occurs due to dysfunction of inhibitory neurons in the[[ hypothalamus]], leading to persistent low-grade basal AVP secretion
* Occurs due to dysfunction of [[inhibitory neurons]] in the [[hypothalamus]], leading to persistent low-grade basal [[AVP]] secretion


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| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold; text-align:center;" |[[Type D]]
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold; text-align:center;" |Type D
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* Low or undetectable[[ AVP]] levels and circulating AVP response is not defective   
* Low or undetectable [[AVP]] levels and circulating [[AVP]] response is not defective   
*Nephrogenic SIADH (NSIAD) may be attributed to this condition  
*Nephrogenic [[SIADH]] (NSIAD) may be attributed to this condition  
* Associated with Gain-of-function[[ mutations]] in the V2 receptor leading to a clinical picture of SIADH, with undetectable AVP levels  
*Associated with Gain-of-function [[mutations]] in the [[V2 receptor]] leading to a clinical picture of [[SIADH]], with undetectable [[AVP]] levels  
*The condition is inherited in an X-linked manner,although heterozygous females may have inappropriate antidiuresis of varying degrees. <ref name="pmid20164214">{{cite journal |vauthors=Hannon MJ, Thompson CJ |title=The syndrome of inappropriate antidiuretic hormone: prevalence, causes and consequences |journal=Eur. J. Endocrinol. |volume=162 Suppl 1 |issue= |pages=S5–12 |year=2010 |pmid=20164214 |doi=10.1530/EJE-09-1063 |url=}}</ref>
*The condition is inherited in an [[X-linked]] manner, although [[heterozygous]] females may have inappropriate antidiuresis of varying degrees.  


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Revision as of 15:10, 11 October 2017

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Vindhya BellamKonda, M.B.B.S [2]

Overview

SIADH may be classified into several sub-types based on the pattern of AVP (arginine vasopressin) secretion across a range of plasma osmolalities into type A, type B, type C and type D.

Classification

SIADH may be classified into several sub-types based on the pattern of arginine vasopressin (AVP) secretion across a range of plasma osmolalities:[1]

Classification Features
TypeA
Type B
Type C
Type D
  • Low or undetectable AVP levels and circulating AVP response is not defective
  • Nephrogenic SIADH (NSIAD) may be attributed to this condition
  • Associated with Gain-of-function mutations in the V2 receptor leading to a clinical picture of SIADH, with undetectable AVP levels
  • The condition is inherited in an X-linked manner, although heterozygous females may have inappropriate antidiuresis of varying degrees.

References

  1. Hannon MJ, Thompson CJ (2010). "The syndrome of inappropriate antidiuretic hormone: prevalence, causes and consequences". Eur. J. Endocrinol. 162 Suppl 1: S5–12. doi:10.1530/EJE-09-1063. PMID 20164214.

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