About PKD
PKD Polycystic Kidney Disease alters our kidneys' inner structure, eventually filling with multiples of cysts. Cystic cells replace normal functioning kidney tissue. These kidney cells die and are not capable of being replaced. Some with polycystic kidneys experience a decrease in kidney functioning. Almost all have a rise in blood pressure and spill protein in their urine. Oftentimes blood pressure spikes or an infection can alert doctors to an underlying illness such as ADPKD. In some, cystic cells replace liver cells. This is PLD or Polycystic Liver Disease. Both conditions are inherited.40% of people with Polycystic Kidneys never require dialysis or transplant. Many of us are striving to be included among these healthy individuals; through diet and lifestyle changes, some have succeeded. Among our personal choices are: which foods do we eat? Do we smoke? Do we exercise? Do we drink sufficient water? Do we limit salt? Do we eat whole fresh unprocessed foods? With guided attention from our personal physicians, we have found a positive influence on our state of well-being. Perhaps eventually, more individuals will experience having healthy PKD polycystic kidneys throughout a lifetime.
We have no control over whether we inherit PKD2, or the more common aggressive PKD1 gene (earlier onset of symptoms). We have no influence if born male or female. PKD males have a higher incidence of cardiac problems with an earlier progression to left ventricular heart failure. Females with liver cysts, have an increased chance of developing severe Polycystic Liver Disease or PLD. In both instances symptoms are hormonally related. With PKD'ers, it is our hearts, not our kidneys, that leads to our demise. A medical paper suggests that if we eat a low salt diet and maintain a high value for good cholesterol, these have a positive influence over the expression of PKD symptoms A 2010 alkaline clinical trial shows maintaining alkalinity can improve kidney functioning, even with chronic kidney disease. Preventing enlargement of the kidneys will lessen the effects of late-stage PKD kidney insufficiency.
How is ADPKD Passed Onto Children?
Each child of a parent with ADPKD has a 50% chance of inheriting the disease, because the gene for ADPKD is dominant. The prospects are similar to a flip of a coin. So, although 1 in every 2 children has a chance of inheriting ADPKD, sometimes both or neither will be affected. This form of inheritance is called Autosomal Dominant inheritance.
Definition of ADPKD
- At least 2 cysts in one kidney or a single cyst in each kidney (less than 30).
- At least 2 cysts in each kidney in individuals between 30-59.
- At least 4 cysts in each kidney in individuals 60 years or older.
There are two genes known to be associated with ADKPD. PKD1 is found in approximately 85 percent of individuals who have ADPKD. This is the more aggressive gene; diminished kidney functioning can occur in the 40's. PKD2 is found in about 15 percent of individuals who have ADPKD. Symptoms do not usually appear until the 60's.
ADPKD autosomal dominant polycystic kidney disease is inherited. Some extra renal manifestations are liver cysts, pancreatic cysts, epididymus cysts, aneurysms.