Showing posts with label Polycystic kidney disease. Show all posts
Showing posts with label Polycystic kidney disease. Show all posts

Monday, April 16, 2012

Low birth weight and polycystic kidney disease.

Getting the Post Birth Weight
Getting the Post Birth Weight (Photo credit: UhDuh)
Orskov and colleagues in a large danish autosomal polycystic kidney disease cohort believe that they have demonstrated what they think is a direct effect of birth weight on outcomes in polycystic kidney disease. In the previously mentioned study each kilogram of birth weight extended the mean age of ESRD onset by 1.7 years.

It is believed that this mechanism may be due to any or all of the following.


  • Placental insufficiency.
  • Activation of the Renin Angiotensin Aldosterone System.
  • Increased Fetal Vasopressin levels. 
  • Increased Insulin like growth factor levels. 
  • A reduction in total nephron number. 
It had been proposed many years earlier that what happens in utero to the developing child directly influences the adult, giving rise to a variety of adult chronic diseases such as diabetes mellitus and metabolic syndrome. 

ID#: 861 Description: Gross pathology of polyc...
ID#: 861 Description: Gross pathology of polycystic kidneys. Gross pathology of polycystic kidneys. Ureters are visible. Content Providers(s): CDC/Dr. Edwin P. Ewing, Jr. Creation Date: 1972 Copyright Restrictions: None - This image is in the public domain and thus free of any copyright restrictions. As a matter of courtesy we request that the content provider be credited and notified in any public or private usage of this image. (Photo credit: Wikipedia)


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Wednesday, April 11, 2012

Preventing Bleeding (hematuria) in Polycystic Kidney Disease

Tranexamic Acid


Image: by

Tranexamic acid is by no means a new drug it has been used routinely in surgery, for years particularlywhere there is a high risk of bleeding. Acting to prevent the breakdown of fibrin one of the key components of a blood clot, this drug has been found to decrease the risk of death from multiple trauma and is considered an essential medication by the World Health Organization.

Thursday, September 24, 2009

New and Upcoming Treatments for Polycystic Kidney Disease.

ID#: 861 Description: Gross pathology of polyc...
ID#: 861 Description: Gross pathology of polycystic kidneys. Gross pathology of polycystic kidneys. Ureters are visible. Content Providers(s): CDC/Dr. Edwin P. Ewing, Jr. Creation Date: 1972 Copyright Restrictions: None - This image is in the public domain and thus free of any copyright restrictions. As a matter of courtesy we request that the content provider be credited and notified in any public or private usage of this image. (Photo credit: Wikipedia)





Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic disease of the kidney. For many years the treatment of this condition has been at a relative standstill when compared to the advances in therapy in other kidney diseases. However exciting new developments are currently in the research pipeline. These may finally allow specific therapies aimed at reducing the progression of the underlying problem, which has always been the unrestricted almost exponential growth of cysts within the kidney leading to kidney failure.

The main approach to the treatment of autosomal dominant polycystic kidney disease has been good control of blood pressure. This has been shown to reduce the rate of progression of the disease to end stage. Patients with ADPKD have been shown to have elevated levels of a hormone known as renin. Renin is important in regulating the balance of fluid and salts within the body and under normal circumstances renin signals the kidney to retain salt and water in order to maintain a normal volume of blood within the body. In ADPKD renin levels are increased, this may be due to the compression of sensitive areas within the kidney by enlarging cysts, compression of these areas may stimulate the production of renin. Renin and other substances directly produced because of high levels of renin result in increased cyst growth in ADPKD. This produces a viscous cycle of events that leads to ESRD.

Aliskerin is a novel drug which is now available, it functions as an inhibitor of renin. This drug has been shown to significantly lower the levels of renin in patients with ADPKD as well as providing better control of hypertension. This may be become a mainstay of the treatment of hypertension in ADPKD and should definitely be a drug to watch.

A very old drug that has been hypothesized to have a preventative role in ADPKD is colchicine. It is better known for its role in the management of gout. It is a potent anti inflammatory agent and has effects which may be useful in delaying cyst growth.

Cyst growth in ADPKD is based on the accumulation of fluids within the cyst by the action of a complex pump known as CFTR which is the same protein which is abnormal in cystic fibrosis. Inhibtors of CFTR have been available for some time. Recently they have been shown to be of efficacy in reducing cyst growth in mouse models of APKD.

The drug sirolimus which has been used for many years for immunosuppression post renal transplant has been shown in mammalian models of ADPKD to reduce the growth of cysts and is now the target of a study which will determine its role in the treatment of ADPKD in humans. The results of this study will be available in 2010.
Deutsch: Schema der beiden Proteine PKD1 und P...
Deutsch: Schema der beiden Proteine PKD1 und PKD2. Nach einer Vorlage von http://www.bio.davidson.edu/Courses/Molbio/MolStudents/spring2003/MaloneyH/Polycystins.html (Photo credit: Wikipedia)

The focus thus far has been on possible therapies aimed at reducing the growth of cysts in order to reduce progression to ESRD. However other new therapies are available currently for the treatment of symptoms associated with ADPKD such as recurrent hematuria and pain.

Techniques aimed at reducing the number of existing cysts in the kidney have been shown to reduce symptoms. Options for this kind of therapy range from open surgery with direct decompression and decortication of cysts, laparoscopic procedures to reduce cyst volume and more recently ultrasound guided techniques where substances that destroy the structure of the cysts are injected under guidance. All these techniques have been proved beneficial in terms of symptom relief but have not been shown to delay progression of the kidney disease.

That  particular goal remains elusive but we are closer now than ever before.

Adult Polycystic Kidney
Creative Commons License photo credit: euthman





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Monday, August 17, 2009

Gene for severe Polycystic Kidney Disease can be predicted.

Polycystic kidney disease is the third single most common cause of ESRD in the dialysis population based on US data. It is a disease charachterised by the development of cysts within the kidney which expand over time and damage the structure and function of the organ giving rise to chronic kidney disease then chronic renal failure. The rate of progression varies between patients, however sophisticated genetic tools are capable of distinguishing those who are likely to progress more slowly from those who are likely to need dialysis at a younger age.

The current study by Moumita et. al. published in the Journal of the association of nephrology (JASN) demonstrates that while sophisticated genetic tests are quite well and good, simply taking certain historical details from the patient at interview had a positive predictive value of 100% and sensitivity of 75% to detect the presence of the more severe type of polycystic kidney disease.

When interviewed, if patients had even one relative who had to be dialysed because of chronic kidney disease they were almost guaranteed to have the PKD1 gene. The PKD1 gene is the gene responsible for polycystic kidney disease in 85% of cases and has a median age of onset of kidney disease requiring dialysis at 53 years of age as opposed to PKD2 gene which has a median age of kidney disease requiring dialysis at 72.7 years of age.

This is a simple option for gaining prognostic information which is cheap and easily applied to all patients. However if there is insufficient clinical history then this criteria cannot be applied and gene testing is the way to go.
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