Polycystic Kidney Disease: Symptoms, Causes, Diagnosis & Treatment Guide

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Polycystic Kidney Disease: Symptoms, Causes, Diagnosis & Treatment Guide

Are you ignoring your kidney health? Have you heard about  Polycystic Kidney Disease?

Polycystic Kidney Disease is a genetic condition where clusters of fluid-filled sacs, or cysts, take over your kidneys. 

They are not normal blemishes. They can slowly crowd out healthy tissue, turning your kidneys into a giant cluster of grapes. This can lead to a gradual loss of the kidneys' incredible ability to filter waste.  

This can eventually cause kidney failure.

But don't worry! PKD can be managed effectively. At NU Hospitals, Bangalore, a leading nephrology and urology hospital, we help you manage and fight such complex conditions. 

Follow this guide to learn more about Polycystic Kidney Disease, PKD symptoms, types, and PKD treatment. 

What is Polycystic Kidney Disease?

Polycystic Kidney Disease is the most common genetic kidney disorder. It’s caused by a faulty gene that can trigger the growth of multiple cysts. 

When the cysts grow, your kidneys get much larger. Sometimes it can weigh several pounds each. This disease also causes your kidneys' function to decline. 

What are the causes of Polycystic Kidney Disease?

PKD is usually inherited. It is your genetics, not your lifestyle choices.

  • Genetic Mutation: A mutation in specific genes is usually the cause.

  • Inheritance: The disease is passed down through families. Sometimes, it can be a new mutation, but it is rare.

Polycystic Kidney Disease Types

There are two major types of Polycystic Kidney Disease:

Autosomal Dominant Polycystic Kidney Disease (ADPKD):

  • Common: This is the most common form of PKD. It accounts for about 90% of all cases.

  • Onset: Symptoms appear in your adulthood between the ages of 30 and 40. However, cysts start developing much earlier.

  • Inheritance: Only one parent needs to carry the gene for the child to have a 50% chance of inheriting it. This type is also known as "Polycystic kidney, adult type". 

Autosomal Recessive Polycystic Kidney Disease (ARPKD):

  • Rare: Less common and usually more severe.

  • Onset: Symptoms begin in the womb of the mother or during the first few months of life.

  • Inheritance: Both parents must carry the gene, but they may not have the disease themselves. The child must inherit two copies of the faulty gene to develop the condition.

Feature

Autosomal Dominant PKD (ADPKD)

Autosomal Recessive PKD (ARPKD)

Prevalence

Most common
Rare

Found in 

Adulthood (30s to 40s),
Infancy or childhood, sometimes even before birth

What to expect

  • Slower progression
  • End-stage kidney failure usually occurs by age 60-70
  • Rapid progression
  • Usually, kidney failure can happen in the first decade of life

Associated Organ Cysts

Liver, pancreas, and brain aneurysms
Liver scarring is common

Key Treatment

  • Blood pressure control
  • Managing cyst growth
  • Managing respiratory failure
  • Growth
  • Liver disease

 

PKD Symptoms and How to Diagnose 

In the early stages, ADPKD hides in plain sight, showing few or no symptoms. You can catch this disease early with the help of careful monitoring. 

What are the early PKD symptoms?

  • High Blood Pressure (Hypertension)

High BP is usually the first sign. It appears even before your kidney function declines.

  • Pain

Chronic pain in your back, side, or abdomen. This is usually due to the enlarged cysts or kidney stones.

  • Headaches

You may experience frequent and severe headaches.

  • Blood in Urine (Hematuria)

Blood in urine can happen if your cyst ruptures.

How is PKD Diagnosed?

Diagnosis is simple and usually involves imaging.

Family History:

A family history of this condition is usually the first clue.

Imaging Tests:

  • Polycystic kidney disease ultrasound

This is the most common and first tool. It shows the number and size of the cysts in your kidneys.

  • CT or MRI Scans

Used for a detailed view of your kidney size and the full extent of cysts.

Blood Tests:

  • Kidney function test (KFTs):

KFT helps to check how well your kidneys are filtering waste. It also shows your creatinine levels.

PKD Treatment 

There is no cure for Polycystic Kidney Disease yet. However, with proper treatment, you can slow the disease progression and improve the quality of your life.

1. Blood Pressure Control

Controlling your BP is the most important step. High BP can damage your kidneys faster.

2. Pain Management

Your doctors may prescribe medication, fluid drainage, or surgery in rare cases to deal with any cyst pain.

3. Treating Infections

UTIs are quite common. Early treatment can prevent kidney damage.

4. Tolvaptan

It is a medicine that helps to slow down your cyst growth in ADPKD. It requires close monitoring of serum electrolytes and liver function while on this medication.

5. Lifestyle Changes

  • Low-salt diet

  • Drink an adequate amount of water

  • Avoid smoking

  • Do moderate exercise

  • Healthy weight

6. Dialysis

If your kidneys fail, you might have to go through dialysis.

7. Kidney Transplant

A kidney transplant is the best option for long-term survival after kidney failure.

How PKD Can Affect Daily Life

Polycystic Kidney Disease is a life-changing condition.

  • Fatigue is quite common, especially as your kidney function test results get worse. Prioritise rest and gentle, regular exercise is everyday.

  • You may have severe restrictions in your diet. Monitoring your salt and fluid intake can become a part of your life.

  • Dealing with a chronic condition can be emotionally tiring. 

  • You might have to go for frequent doctor visits due to your condition. 

Managing life with PKD can be quite difficult. However, with proper care, lifestyle adjustments, and regular follow-up, many people live an active and fulfilling life.

Living Life with PKD

Life with Polycystic Kidney Disease is quite challenging. It will require continuous monitoring and care. If you or your loved one is dealing with PKD, you will need expert care.

At NU Hospitals, we understand the difficult journey you are on. From proper diagnosis to personalized medical treatment, we take care of all. We help you manage your condition effectively. 

Frequently Asked Questions On Polycystic Kidney Disease (PKD):

1. Can you live a long life with polycystic kidney disease?

Yes, with proper medical care, proper management of blood pressure, and treatments such as Tolvaptan, people with ADPKD can usually live a long life. 

2. What is the life expectancy of someone with polycystic kidney disease?

Life expectancy with Polycystic Kidney Disease varies. ADPKD has a good outlook with proper treatment. However, ARPKD needs early and aggressive care.

3. How do you manage polycystic kidney disease in adults?

PKD can be managed with the help of:

  • Blood pressure control with the help of ACE inhibitors or ARBs.

  • Slowing cyst growth with Tolvaptan.

  • Dietary and lifestyle modifications, such as low salt, adequate hydration, and avoiding NSAIDs.

  • Regular monitoring of Creatinine levels and kidney function test results.

  • Proper treatment of pain and infections.

4. What is the role of ultrasound in PKD?

Ultrasound helps to detect and track your cysts safely and easily in PKD.

Dr. Ramprasad Ramalingam

Medically Reviewed By:

Dr. Ramprasad Ramalingam

Sr. Consultant Nephrologist & Transplant Physician

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