There is no cure for Gilbert’s syndrome as it is caused by a specific gene in DNA, and this makes it a lifelong condition.
It’s not a threat to your health and won’t increase your risk of liver disease, however there are ways to improve and manage your symptoms.
For example, you need to avoid medication or drugs that inhibit the UGT enzyme or impair the breakdown of red blood cells, such as:
- Atazanavir (Reyataz®) and indinavir (Crixivan®) used to treat HIV infection
- Gemfibrozil (Lopid®), that lowers cholesterol
- Irinotecan (Camptosar®), that treats advanced bowel cancer
- Paracetamol, which is partly metabolised by UGT so you may want to try a different painkiller
Statins are only partly metabolised by the UGT so they are safe in most people with Gilbert’s syndrome.
Speak to your specialist about any medications you’re taking to ensure they don’t require the UGT enzyme to help clear them from your body, and that they don’t impair the breakdown of red blood cells.
Reducing how much alcohol you drink may be something you want to consider, as people who have Gilbert’s syndrome tend to experience hangovers that are more severe than people who don’t.
Living with Gilbert’s syndrome
Jaundice and Gilbert’s syndrome do not damage the liver or cause complications so there’s no specific treatment for it.
Most people manage the condition by taking extra care of themselves when they are ill or under stress so their body can recover more quickly.
Episodes of jaundice are usually short lived and don’t increase the risk of other serious conditions.
You can talk to your hepatologist about any concerns you may have and undergo any tests to gain peace of mind.