Kidneys - polycystic kidney disease (PKD)
Kidneys - polycystic kidney disease (PKD)
Polycystic kidney disease (PKD) is group of chronic
kidney diseases
where thousands of
cysts
(fluid filled sacs) grow in the
kidneys
. PKD is the most common inherited kidney disease and is a common cause of Chronic Kidney Disease.
If you have PKD both of your kidneys will be affected but one kidney may develop the cysts earlier than the other. The cysts gradually grow which makes your kidneys larger and reduces the healthy kidney tissue. This makes it harder for your kidneys to work properly.
Some people develop
high blood pressure
and kidney failure as a result of PKD. PKD affects males and females in equal numbers, and the cysts can appear at any age, depending on the type of PKD.
It is not uncommon for people to develop simple kidney cysts as they become older. Around 50% of people over the age of 50 develop simple cysts. These cysts are not inherited and do not usually require treatment. This fact sheet will discuss PKD which is the inherited type of cyst disease.
Different types of PKD
PKD is an inherited disease. This means it is passed from parents to their children. However not all people with PKD will have a family history.
Autosomal dominant PKD
Autosomal dominant PKD (ADPKD) is the most common inherited form of polycystic kidney disease. A parent with autosomal dominant PKD has a 50 per cent chance of passing the altered gene (PKD1 or PKD2) and associated condition to each of their children. If a person doesn’t inherit the gene, there is no chance of their children inheriting the gene because it never ‘skips’ a generation.
Occasionally, a person develops the condition when there is no family history. It is thought that a different inheritance pattern or perhaps a genetic change may be responsible. Like inherited PKD, the affected person has a 50 per cent chance of passing the altered gene and associated disease to each of their children. Autosomal dominant PKD can lead to kidney failure.
Symptoms of autosomal dominant PKD
There may be no symptoms of autosomal dominant PKD in the early stages. The cysts usually start growing during the teenage years. As the cysts replace healthy tissue, the outline of the kidneys looks irregular or ‘moth-eaten’.
Symptoms usually develop between the ages of 30 and 40 (but can begin earlier), and may include:
high blood pressure
(may occur before cysts appear)
pain in the
back
or sides
headaches
enlarged and painful abdomen
blood in the urine (haematuria)
urinary tract infections
kidney stones
liver
, intestine,
brain
and
pancreatic
cysts
abnormal heart valves
abdominal wall hernias
reduced kidney function or
kidney failure
.
Autosomal recessive PKD
Autosomal recessive PKD is a less common inherited form of polycystic kidney disease. Signs begin in the early months of life or even while the baby is still developing in the uterus (womb).
Autosomal recessive PKD is sometimes called ‘infantile PKD’. Children born with autosomal recessive PKD often develop kidney failure within a few years of birth and experience liver problems as they grow into adults.
Symptoms of autosomal recessive PKD
Symptoms and signs in severely affected babies can include:
reduced amniotic fluid surrounding the baby in the uterus
an unusual shape to the face due to the lack of amniotic fluid (Potter’s facies)
enlargement of the child’s abdomen due to enlarged kidneys, liver or spleen
heart defects
underdeveloped lungs
kidney failure at birth or in the first few weeks of life.
Diagnosis of polycystic kidney disease
The severe symptoms of autosomal recessive PKD usually result in a prompt diagnosis. However, in most cases of autosomal dominant PKD, for many years there are no signs that a person has the condition.
Physical check-ups or blood and urine tests may not always identify the disease. It is often detected during medical investigations for other health problems, such as urinary tract infections. At other times, the disease isn’t discovered until the kidneys begin to fail.
Diagnosis of PKD may involve a number of tests including:
physical examination
– can detect symptoms such as high blood pressure or enlarged kidneys
blood tests
– to assess kidney function
urine tests
– blood or protein (or both) may be found in the urine
ultrasound
– a simple, non-invasive test that can identify even quite small cysts
genetic testing
– this is not a routine test but may be used for family testing. The presence of the abnormal genetic material can be detected with special blood tests. Genetic counselling is available for affected couples.
Genetic counselling for polycystic kidney disease
If you or a family member have been diagnosed with PKD, or if PKD runs in your family, it can be helpful to speak to a genetic counsellor.
Genetic counsellors
are health professionals qualified in both counselling and genetics. As well as providing emotional support, they can help you to understand PKD and what causes it, how it is inherited, and what a diagnosis means for your health, lifestyle, and plans for the future. Genetic counsellors are trained to provide information and support that is sensitive to your family circumstances, culture and beliefs.
If PKD runs in your family, a genetic counsellor can explain what genetic testing options are available to you and other family members. You may choose to visit a genetic counsellor if you are planning a family, to find out your risk of passing that condition on to your child, or to arrange for prenatal tests.
PKD
Australia
External Link
brings the community of PKD families together across the country for support and education and to advocate for the many families that are affected by this disease that currently has no cure.
Treatment of polycystic kidney disease
Currently there is no cure for PKD. However, early detection and treatment can reduce or prevent some of the complications of PKD.
Common complications and their treatments include:
high blood pressure
– controlling high blood pressure is very important. Antihypertensive medication may be prescribed
pain
– may be due to
kidney stones
,
bleeding
or infection. Treatment will depend on the cause. Talk to your doctor if you are getting repeated or severe
back
and
kidney pain
or
headaches
.
Cysts
can sometimes be drained to relieve extreme back and leg pain
blood in the urine
– fluids, pain-relieving medication, antibiotics and bed rest may be recommended
urinary tract infections
– symptoms may include frequent urination, painful urination and fever. Consult with your doctor immediately about treatment with antibiotics. An untreated urinary tract infection can spread to the kidneys
kidney failure
– this is treated by dialysis, which is a procedure to remove waste products and extra water from the body by filtering the blood through a special membrane. A kidney transplant is another treatment option. PKD does not redevelop in the transplanted kidney.
Self-care for polycystic kidney disease
Your doctor or healthcare professional will discuss best healthcare choices in managing this condition. Be guided by your doctor. Self-care suggestions for PKD generally include:
changing your diet
– this may help to manage some symptoms. Dietary changes may include reducing
salt
,
protein
,
cholesterol (fats)
and
caffeine
. Only make dietary changes after discussion with your
doctor
or
dietitian
. Dietary recommendations will depend on your test results
making healthier lifestyle choices
– for example, participate in regular and moderate physical activity and maintain an appropriate weight for your height and build. It is strongly advised that you do not
smoke
avoiding non-steroidal anti-inflammatory drugs (NSAIDs)
– do not take NSAIDs without medical advice as they can worsen kidney function
considering avoiding contact sports
if your kidneys, liver, spleen or abdomen are enlarged. A strong blow to the belly could injure affected organs.
Where to get help
Your
GP (doctor)
Polycystic Kidney Disease (PKD)
Australia
External Link
Kidney
Helpline
External Link
Tel.
1800 454 363
Genetic Support Network of Victoria
(GSNV)
External Link
Tel.
(03) 8341 6315
Victorian Clinical Genetics
Services
External Link
Tel.
1300 118 247