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{{CMG}}; {{AE}} {{Vbe}}
{{CMG}}; {{AE}} {{Vbe}}


Epidemiology and demographics
==SIADH==
 


{{CMG}} ; {{AE}} {{Vbe}}
SIADH


  Definition :The syndrome of inappropriate antidiuretic hormone (SIADH) is characterized by the excessive release of serum antidiuretic hormone (ADH) relative to serum osmolality. It typically results in excessive water reabsorption in the collecting ducts and hyponatremia
  Definition :The syndrome of inappropriate antidiuretic hormone (SIADH) is characterized by the excessive release of serum antidiuretic hormone (ADH) relative to serum osmolality. It typically results in excessive water reabsorption in the collecting ducts and hyponatremia
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*IFN-gamma
*IFN-gamma


Surgery: associated with hyper secretion of ADH, a response that is mediated by pain afferents.
*Surgery: associated with hyper secretion of ADH, a response that is mediated by pain afferents.


Pulmonary disease: particularly pneumonia (viral, bacterial, tuberculous), can lead to the SIADH, although the mechanism by which this occurs is not clear.A  
*Pulmonary disease: particularly pneumonia (viral, bacterial, tuberculous), can lead to the SIADH, although the mechanism by which this occurs is not clear.A  
similar response may infrequently be seen with asthma, atelectasis, acute respiratory failure, and pneumothorax.
similar response may infrequently be seen with asthma, atelectasis, acute respiratory failure, and pneumothorax.


Hormone deficiency: Hypopituitarism, hypothyroidism
*Hormone deficiency: Hypopituitarism, hypothyroidism
 
*HIV infection
 
* Malignancy- Ectopic production of ADH due to tumors can cause SIADH. Most often due to small cell carcinoma of the lung. Less common causes of malignancy-associated SIADH include head and neck cancer, olfactory neuroblastoma,GI cancers,breast cancers...
PMID:27142293
 


HIV infection
*Genetics:  clinical picture of SIADH may result from genetic disorders that result in antidiuresis. A mutation affecting the gene for the renal V2 receptor, which some investigators have named nephrogenic syndrome of inappropriate antidiuresis, has been found to cause clinically significant hyponatremia.
congenital nephrogenic diabetes insipidus is characterized by a resistance of the renal collecting duct to the action of the arginine vasopressin hormone responsible for the inability of the kidney to concentrate urine.He X-linked form is due to inactivating mutations of the vasopressin 2 receptor gene leading to a loss of function of the mutated receptors.conversely, the nephrogenic syndrome of inappropriate antidiuresis (NSIAD) is linked to a constitutive activation of the V(2)-receptor due to activating mutations with clinical and biological features of inappropriate antidiuresis but with low or undetectable plasma arginine vasopressin hormone levels.


Genetics: clinical picture of SIADH may result from genetic disorders that result in antidiuresis. A mutation affecting the gene for the renal V2 receptor, which some investigators have named nephrogenic syndrome of inappropriate antidiuresis, has been found to cause clinically significant hyponatremia.
PMID:25449762
ongenital nephrogenic diabetes insipidus is characterized by a resistance of the renal collecting duct to the action of the arginine vasopressin hormone responsible for the inability of the kidney to concentrate urine.he X-linked form is due to inactivating mutations of the vasopressin 2 receptor gene leading to a loss of function of the mutated receptors.onversely, the nephrogenic syndrome of inappropriate antidiuresis (NSIAD) is linked to a constitutive activation of the V(2)-receptor due to activating mutations with clinical and biological features of inappropriate antidiuresis but with low or undetectable plasma arginine vasopressin hormone levels.

Revision as of 16:50, 19 July 2017


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

SIADH

Definition :The syndrome of inappropriate antidiuretic hormone (SIADH) is characterized by the excessive release of serum antidiuretic hormone (ADH) relative to serum osmolality. It typically results in excessive water reabsorption in the collecting ducts and hyponatremia

Historical perspective:

Described by researchers from Boston, Massachusetts and Bethesda, Maryland (including Dr Frederic Bartter) in two patients with lung cancer.[1] Criteria were developed by Schwartz and Bartter in 1967,[2].

Pathogenesis:

Causes: CNS disturbances:

  • Stroke
  • trauma
  • infection
  • psychosis
  • hemorrhage


Drugs :

  • amiodarone
  • amitryptyline
  • bromocriptine
  • ciprpfloxacin
  • chlorpropamide
  • carbamazapine
  • cyclophosphamide
  • cisplatine
  • SSRI
  • Vincristine
  • Vinblastine
  • thioridazine
  • thiothixene
  • haloperidol
  • MAOI
  • melphalan
  • methotrexate
  • opiates
  • NSAID
  • IFN-alpha
  • IFN-gamma
*Surgery: associated with hyper secretion of ADH, a response that is mediated by pain afferents.
*Pulmonary disease: particularly pneumonia (viral, bacterial, tuberculous), can lead to the SIADH, although the mechanism by which this occurs is not clear.A 

similar response may infrequently be seen with asthma, atelectasis, acute respiratory failure, and pneumothorax.

*Hormone deficiency: Hypopituitarism, hypothyroidism
*HIV infection
  • Malignancy- Ectopic production of ADH due to tumors can cause SIADH. Most often due to small cell carcinoma of the lung. Less common causes of malignancy-associated SIADH include head and neck cancer, olfactory neuroblastoma,GI cancers,breast cancers...

PMID:27142293


*Genetics:  clinical picture of SIADH may result from genetic disorders that result in antidiuresis. A mutation affecting the gene for the renal V2 receptor, which some investigators have named nephrogenic syndrome of inappropriate antidiuresis, has been found to cause clinically significant hyponatremia.

congenital nephrogenic diabetes insipidus is characterized by a resistance of the renal collecting duct to the action of the arginine vasopressin hormone responsible for the inability of the kidney to concentrate urine.He X-linked form is due to inactivating mutations of the vasopressin 2 receptor gene leading to a loss of function of the mutated receptors.conversely, the nephrogenic syndrome of inappropriate antidiuresis (NSIAD) is linked to a constitutive activation of the V(2)-receptor due to activating mutations with clinical and biological features of inappropriate antidiuresis but with low or undetectable plasma arginine vasopressin hormone levels.

PMID:25449762