Crohn’s disease is a long-term condition that causes inflammation of the lining of the digestive system.
Inflammation can affect any part of the digestive system, from the mouth to the back passage, but most commonly occurs in the last section of the small intestine (ileum) or the large intestine (colon).
Common symptoms can include:
- abdominal pain
- fatigue (extreme tiredness)
- unintended weight loss
- blood and mucus in your faeces (stools)
People with Crohn’s disease sometimes go for long periods without symptoms or with very mild symptoms. This is known as remission. Remission can be followed by periods where symptoms flare up and become particularly troublesome.
Why it happens
The exact cause of Crohn’s disease is unknown. However, research suggests a combination of factors may be responsible. These include:
- genetics – genes you inherit from your parents may increase your risk of developing Crohn’s disease
- the immune system – the inflammation may be caused by a problem with the immune system (the body’s defence against infection and illness) that causes it to attack healthy bacteria in the gut
- previous infection – a previous infection may trigger an abnormal response from the immune system
- smoking – smokers with Crohn’s disease usually have more severe symptoms than non-smokers
- environmental factors – Crohn’s disease is most common in westernised countries such as the UK, and least common in poorer parts of the world such as Africa, which suggests the environment (particularly sanitation) has a part to play
Read more about the possible causes of Crohn’s disease.
Treating Crohn’s disease
There’s currently no cure for Crohn’s disease, so the aim of treatment is to stop the inflammatory process, relieve symptoms (induce and maintain remission) and avoid surgery wherever possible.
The first treatment offered to reduce symptoms is usually steroid medication (corticosteroids). If this doesn’t help, medication to suppress the immune system (immunosuppressants) and medication to reduce inflammation may be used.
In some cases, surgery may be needed to remove the inflamed section of intestine.
Once your symptoms are under control (in remission), further medication may be needed to help maintain this.
Who is affected?
Crohn’s disease is a relatively uncommon condition. There are currently at least 115,000 people living with the condition in the UK.
Crohn’s disease can affect people of all ages, including children. However, most cases first develop between the ages of 16 and 30.
A large number of cases also develop between the ages of 60 and 80.
It affects slightly more women than men, but in children more boys are affected than girls.
The condition is more common in white people than in black or Asian people. It’s most prevalent among Jewish people of European descent.
Read more about treating Crohn’s disease.
Over time, inflammation can damage sections of the digestive system, resulting in complications such as narrowing of the intestine (stricture), or a channel developing between the end of the bowel and the skin near the anus or vagina (fistula). These problems usually require surgical treatment.
Read more about the possible complications of Crohn’s disease.
Symptoms of Crohn’s disease
The symptoms of Crohn’s disease vary, depending on which part of the digestive system is inflamed.
Common symptoms include:
- recurring diarrhoea
- abdominal pain and cramping, which is usually worse after eating
- extreme tiredness (fatigue)
- unintended weight loss
- blood and mucus in your faeces (stools)
You may experience all or only one of the above. Some people experience severe symptoms, but others only have mild problems.
There may be long periods, lasting for weeks or months, where you have very mild or no symptoms (known as remission), followed by periods where the symptoms are particularly troublesome (known as flare-ups or relapses).
Less common symptoms include:
- a high temperature (fever) of 38C (100F) or above
- feeling sick (nausea)
- being sick (vomiting)
- joint pain and swelling (arthritis)
- inflammation and irritation of the eyes (uveitis)
- areas of painful, red and swollen skin – most often the legs
- mouth ulcers
Children with Crohn’s disease may grow at a slower rate than expected, because the inflammation can prevent the body absorbing nutrients from food.
When to seek medical advice
You should contact your GP if you have:
- persistent diarrhoea
- persistent abdominal pain
- unexplained weight loss
- blood in your stools
You should also see your GP if you’re concerned about your child’s development.
Causes of Crohn’s disease
The exact cause of Crohn’s disease is unknown. Most researchers think it’s caused by a combination of factors.
These are thought to be:
- the immune system
- previous infection
- environmental factors
There’s no evidence to suggest a particular diet can cause Crohn’s disease, although dietary changes can control certain symptoms and may be recommended by your specialist or dietitian.
Read about treatment for Crohn’s disease for more information.
There’s evidence to suggest genetics plays a role in the development of Crohn’s disease.
Researchers have identified more than 200 different genes that are more common in people with Crohn’s disease than in the general population.
There’s also evidence that Crohn’s disease can run in families. About 3 in 20 people with the condition have a close relative (mother, father, sister or brother) who also has Crohn’s disease. For example, if you have an identical twin with the condition, you have a 70% chance of developing it.
The fact that Crohn’s disease is more common in some ethnic groups than in others also suggests that genetics plays an important role.
The immune system
The immune system provides protection against harmful bacteria that could potentially find their way into the digestive system.
The digestive system is also home to many different types of so-called “friendly bacteria” that help to digest food. The immune system usually recognises these bacteria and lets them do their job without attacking them.
However, in Crohn’s disease, it seems that something disrupts the immune system, which sends a special protein known as tumour necrosis factor-alpha (TNF-alpha) to kill all bacteria, regardless of whether they’re friendly or not. This causes most of the inflammation associated with Crohn’s disease.
In certain genetically susceptible individuals, a previous childhood infection may lead to an abnormal immune response, causing the symptoms of Crohn’s disease.
Aside from family history and ethnic background, smoking is the most important risk factor for Crohn’s disease. Smokers are twice as likely to develop the condition than non-smokers.
Furthermore, people with Crohn’s disease who smoke usually experience more severe symptoms and are much more likely to require surgery.
Read about how to get help to stop smoking.
There are two unusual aspects of Crohn’s disease that have led many researchers to believe that environmental factors may play a role. These are explained below:
- Crohn’s disease is a “disease of the rich”. The highest number of cases occurs in developed parts of the world, such as the UK and the US, and the lowest number occur in developing parts of the world, such as Africa and Asia.
- Crohn’s disease became much more widespread from the 1950s onwards.
This suggests there is something associated with modern Western lifestyles that increases a person’s risk of developing the condition.
One theory to explain this is known as the hygiene hypothesis. It suggests that as children grow up in increasingly germ-free environments, their immune system doesn’t fully develop because of a lack of exposure to childhood infections. However, there’s little in the way of hard scientific evidence to support this theory.
An alternative theory is the cold-chain hypothesis, which suggests that the increase in Crohn’s disease cases might be linked to the increased use of refrigerators after the Second World War.
Diagnosing Crohn’s disease
A number of different tests may be needed to diagnose Crohn’s disease, as it has similar symptoms to several other conditions.
During your initial assessment, your GP will usually ask you about the pattern of your symptoms and check whether there may be any contributing causes, such as:
- recent travel – for example, you may have developed travellers’ diarrhoea while travelling abroad
- whether you’re taking any medication, including any over-the-counter medicines
- whether you have a family history of Crohn’s disease
Your GP may also carry out a series of standard tests to assess your general state of health. For example, they may:
- check your pulse
- check your blood pressure
- measure your height and weight
- measure your temperature
- examine your abdomen (tummy)
Your GP may then arrange a series of blood tests. These can be used to assess:
- the levels of inflammation in your body
- whether you have an infection
- whether you’re anaemic, which could suggest you’re malnourished or losing blood from your bowel
You may be asked to provide a stool sample, which can be checked for blood and mucus. It can also be used to determine whether your symptoms are being caused by a parasitic infection such as roundworm, or other infections.
A faecal calprotectin test may be offered to adults who have recently developed symptoms such as abdominal pain, diarrhoea or constipation and are being considered for specialist treatment. This test helps clinicians to distinguish between irritable bowel syndrome (IBS) and inflammatory bowel disease (IBD).
After you’ve provided a stool and blood sample, you’ll probably be referred to a gastroenterologist (a specialist in conditions of the digestive system). They’ll discuss the results with you and carry out the tests described below if they’re necessary.
A colonoscopy is a test used to examine the inside of your colon. It involves inserting a long, flexible tube called an endoscope into your colon through your back passage (rectum).
The endoscope has a light and a camera on the end. The camera can be used to send images to a television screen. These show the level and extent of inflammation inside your colon.
The endoscope can also be fitted with surgical tools that can be used to take a number of small tissue samples from different sections of your digestive system. This is known as a biopsy. The procedure may feel uncomfortable, but it’s not painful.
These tissue samples will be examined under a microscope for the cell changes known to occur in cases of Crohn’s disease.
Wireless capsule endoscopy
A wireless capsule endoscopy is a new type of test that involves swallowing a small capsule (about the size of a large vitamin tablet). The capsule works its way down to your small intestines, where it transmits images to a recording device worn on a belt or in a small shoulder bag.
A few days after the test, the capsule passes out of your body in the stool. The capsule is disposable, so you don’t have to worry about retrieving it from your stools.
As this is a relatively new test, availability may be limited. In some cases, MRE or CTE scans may be used instead of capsule endoscopy.
MRE and CTE scans
Scans called magnetic resonance enterography/enteroclysis (MRE) or computerised tomography enterography/enteroclysis (CTE) may be used to examine the small intestine in people with suspected Crohn’s disease.
Before having these scans, you’ll either need to drink a harmless liquid called a contrast agent (enterography), or contrast agent may be placed through a tube in your nose that leads to your small intestine (enteroclysis). These contrast agents allow your small intestine to show up more clearly during the scans.
During an MRE scan, magnetic fields and radio waves are used to produce detailed images of your small intestines. During CTE scans, several X-rays are taken and assembled by computer to create a detailed image.
These tests are increasingly used instead of a small bowel enema or small bowel follow-through, because they allow more detailed examination of the small intestine. MRE scans also avoid any exposure to X-ray radiation.
Small bowel enema or small bowel follow-through
A small bowel enema (SBE) and small bowel follow-through (SBFT) are two similar tests that have traditionally been used to examine the whole of the inside of the small intestine, usually at the point where it meets the colon. They’re sometimes used because only about the last 20cm of the small intestine is usually seen during colonoscopy.
During an SBE/SBFT, a local anaesthetic spray is used to numb the inside of your nose and throat. A tube is passed down your nose and into your throat before being threaded into your small intestine. This can feel unpleasant at first, but most people find they get used to the sensation after a few minutes.
A harmless liquid called barium is passed down the tube. The barium coats the lining of your small intestines, so they show up clearly on X-ray. A series of X-ray images will then be taken. The images can often highlight the areas of narrowing and inflammation caused by Crohn’s disease.
After the test, you’ll be advised to drink plenty of fluid to help wash the barium out of your body. You may notice that your stools look white for the first few days after having an SBE or SBFT. This is perfectly normal and nothing to worry about.
Treating Crohn’s disease
There’s currently no cure for Crohn’s disease, but treatment can improve the symptoms.
The main aims of treatment are to:
- reduce symptoms – known as inducing remission (remission is a period without symptoms)
- maintain remission
In children, treatment also aims to promote healthy growth and development.
Your treatment will usually be provided by a range of healthcare professionals, including specialist doctors (such as gastroenterologists or surgeons), GPs and specialist nurses.
If you have Crohn’s disease and it’s causing moderate or severe symptoms, this is known as an “active disease”. Treatment for active Crohn’s disease usually involves medication, but surgery is sometimes the best option.
In most cases, the first treatment offered is steroid medication (corticosteroids) to reduce the inflammation. Examples of corticosteroids used for Crohn’s disease include prednisolone tablets or hydrocortisone injections.
These medications are often effective in reducing the symptoms of Crohn’s disease, but they can have significant side effects, such as:
- weight gain
- swelling of the face
- increased vulnerability to infections
- thinning and weakening of the bones (osteopenia and osteoporosis)
Because of these possible side effects, your dose will be gradually reduced when your symptoms start to improve.
If you prefer, you may be able to choose to have a milder steroid called budesonide, or a type of medication called a 5-aminosalicylate (such as mesalazine), as an alternative initial treatment. These medications have fewer side effects, but they’re less effective.
In children or young people, where there are concerns about growth and development, a special liquid diet may be recommended as an initial treatment. This is known as an elemental or polymeric diet, and it can reduce inflammation by allowing your digestive system to recover while ensuring you get all the nutrients you need.
If your symptoms flare up twice or more during 12 months, or return when your steroid dose is reduced, further treatment may be necessary.
In these cases, medicines to suppress your immune system (immunosuppressants) may be combined with your initial medication. Medicines called azathioprine or mercaptopurine are most commonly used.
These medicines aren’t suitable for everyone, so a blood test should be carried out to check if you can use them. If they’re not suitable, an alternative immunosuppressant medication called methotrexate may be used.
Side effects of these immunosuppressants can include:
- nausea and vomiting
- increased vulnerability to infection
- feeling tired, breathless and weak, which is caused by anaemia
- liver problems
During the course of medication, you’ll have regular blood tests to check for serious side effects.
The immunosuppressants azathioprine and mercaptopurine are considered safe in pregnancy and breastfeeding. Women can continue to use these drugs when trying to start a family and during pregnancy.
However, methotrexate must not be taken for at least six months before trying for a baby, as this drug is known to cause birth defects. This applies to both men and women. It must also be avoided while you’re breastfeeding.
It’s important to speak to your doctor if you’re planning a pregnancy or if you become pregnant during your course of treatment for Crohn’s disease.
Severe Crohn’s disease
For people in poor general health with severe symptoms of Crohn’s disease, medicines called biological therapies may be used to reduce your symptoms if corticosteroids and immunosuppressants are unsuitable or ineffective.
Biological therapies are a type of powerful immunosuppressant medication created using naturally occurring biological substances, such as antibodies and enzymes.
The two medicines used to treat Crohn’s disease in the UK are called infliximab and adalimumab. They work by targeting a protein called tumour necrosis factor-alpha (TNF-alpha), which is believed to be responsible for the inflammation associated with Crohn’s disease. Infliximab can be used for children over six years old and adults, but adalimumab should only be used by adults.
Infliximab is given as a drip into a vein in your arm (known as an infusion) in hospital. Adalimumab is given as an injection, and it may be possible for you, a family member or a friend to be taught how to give it, so you don’t need to visit hospital for every treatment.
Treatment usually lasts at least 12 months, unless these drugs stop being effective sooner than this. After this time, your condition will be assessed to determine if further treatment is necessary.
There’s a risk of these medicines causing an allergic reaction, which can cause symptoms such as:
- itchy skin
- a high temperature
- joint and muscle pain
- swelling of the hands or lips
- problems swallowing
You should seek immediate medical assistance if you experience these symptoms. Reactions can occur immediately after treatment, although they have been known to occur months later, even after treatment stops.
Surgery may be recommended to reduce your symptoms if your healthcare team feel the benefits outweigh the risks.
In many cases, a type of surgery called a resection is used. This involves removing the inflamed area of the intestine and stitching the healthy sections together.
In some cases, your doctor may recommend a procedure called an ileostomy to temporarily divert digestive waste away from the inflamed colon (large intestine) to give it a chance to heal.
During this operation, the end of the small intestine (the ileum) is disconnected from the colon and re-routed through a hole made in the abdomen, which is known as a stoma. An external bag is attached to the opening to collect waste products.
Once the colon has sufficiently recovered – usually after several months – a second operation will be needed to close the stoma and re-attach the small intestine to the colon.
Remission is a period when you don’t have any symptoms or your symptoms are mild. During these periods, you can choose whether or not to use medication to help maintain this.
If you decide not to have further treatment, you should be advised about attending regular follow-up appointments and which symptoms to look out for. These symptoms include unintended weight loss, abdominal pain and diarrhoea.
If you choose to have treatment, this will usually involve immunosuppressants. Corticosteroids aren’t recommended for maintaining remission.
If you develop complications of Crohn’s disease, such as anal fistulas or intestinal narrowing (stricture), these will also need to be treated. Surgery is necessary in most of these cases.
See complications of Crohn’s disease for more information.
Diet and smoking
Although there’s no evidence to suggest diet plays a role in Crohn’s disease, some people have found certain foods aggravate their symptoms. It may be useful to keep a food diary to make a note of the foods you eat and to record the effects they have on your symptoms.
If you notice certain foods make your symptoms worse, avoiding these may reduce your symptoms. However, the total elimination of entire food types, such as grains or sugars, isn’t usually recommended.
Some people find that eating six smaller meals a day, rather than three larger meals, improves their symptoms.
If you smoke, stopping can also reduce your symptoms and maintain remission.
Read about treatments to help you quit smoking.
Complications of Crohn’s disease
People with Crohn’s disease are at risk of developing a number of complications.
The two most common problems associated with Crohn’s disease are discussed in more detail below.
The inflammation of the bowel (intestines) in Crohn’s disease can cause scar tissue to form, leading to the affected areas becoming narrowed. This is known as stricture.
If this happens, there’s a risk of digestive waste causing an obstruction. This means you won’t be able to pass any stools or you’ll only be able to pass watery stools.
Other symptoms of bowel obstruction include:
- abdominal pain and cramping
- being sick (vomiting)
- an uncomfortable feeling of fullness in your abdomen
Left untreated, there’s a risk the bowel could split (perforate). This creates a hole that the contents of the bowel can leak from. You should contact your GP as soon as possible if you suspect your bowel is obstructed. If this isn’t possible, call NHS 111.
Intestinal stricture is usually treated with surgery to widen the affected section of intestine. In some cases this may be achieved without surgery, using a procedure called balloon dilation, which is performed during colonoscopy.
During balloon dilation, a colonoscope is passed up your back passage (rectum) and a balloon is inserted through the colonoscope. This is then inflated to open up the affected area.
Read diagnosing Crohn’s disease for more information on colonoscopy.
If this doesn’t work or is unsuitable, a surgical procedure known as a stricturoplasty may be needed to widen the affected area. During this operation, the surgeon widens the narrowed part of the intestine by opening it, reshaping it and sewing it back together.
If your digestive system becomes scarred as a result of excessive inflammation, ulcers can develop.
Over time, the ulcers develop into tunnels that run from one part of your digestive system to another or, in some cases, to the bladder, vagina, anus or skin. These passageways are known as fistulas.
Small fistulas don’t usually cause symptoms. However, larger fistulas can become infected and cause symptoms, such as:
- a constant, throbbing pain
- a high temperature (fever) of 38C (100F) or above
- blood or pus in your stools
- leakage of stools or mucus into your underwear
If a fistula develops on your skin (usually on or near the anus) it may release a foul-smelling discharge.
Biological medication is usually used to treat fistulas. Surgery is usually required if these aren’t effective.
Read more about treating a fistula.
People with Crohn’s disease are also at an increased risk of other complications, such as:
- osteoporosis – weakening of the bones caused by the intestines not absorbing nutrients and the use of steroid medication to treat Crohn’s disease
- iron deficiency anaemia – a condition that can occur in people with Crohn’s disease because of bleeding in the digestive tract; common symptoms include tiredness, shortness of breath and a pale complexion
- vitamin B12 or folate deficiency anaemia – a condition caused by a lack of vitamin B12 or folate being absorbed by the body; common symptoms include tiredness and lack of energy
- pyoderma gangrenosum – a rare skin reaction that causes painful skin ulcers
Children with Crohn’s disease may also experience problems with their growth and development because their bodies aren’t absorbing enough nutrients.
Some people with Crohn’s disease have a slightly increased risk of developing colorectal cancer in later life.
You should be offered regular check-ups to look for colon cancer if your healthcare team feels you may be at an increased risk.
This usually involves a colonoscopy and a biopsy. See diagnosing Crohn’s disease for more information about these tests.
‘Crohn’s disease grinds on and on. It zaps you of vigour and energy’
Author William Fiennes has lived with Crohn’s disease since he was a teenager. Despite debilitating symptoms, he has written two bestselling books and co-founded the charity First Story, which promotes writing in secondary schools. He reflects on his experience of the disease and how it affects him now.
“I first knew something was wrong when I was 18 years old. I was having a year out in Brazil working as a teacher, and started getting unexplained abdominal pain and persistent diarrhoea.
“I was reluctant to talk about it or seek help, so I didn’t see a GP until about six months later, when I was back in England. It was then that I was diagnosed with Crohn’s disease. The treatment options around that time were quite limited. There were no biologics and I was put straight on steroid medication.
“Being on steroid medication during my time at university wasn’t easy. The side effects were unpredictable and really affected my emotions. Sometimes they gave me a boost and I was full of energy, and sometimes I felt very low. Also, although steroids can be incredibly effective and helpful, they only keep you in remission for so long. As soon as I came off them, the symptoms would return.
“I started pretty much every other kind of treatment that was available, including complementary medicines, and tried changing my diet, but nothing really got to the symptoms.
“This cycle of flare-ups and remission continued for the next few years until, at the age of 24, I was offered the option of surgery. I had a loop ileostomy, where the surgeon diverts your bowel to a stoma to give your colon (the part of my bowel affected by Crohn’s) a chance to rest.
“I lived with a bag for 18 months. It was not an easy time. After that, they reversed the surgery and my colon was reconnected.
“I felt pretty good for the following year, before my symptoms returned.”
Living with the condition now
“At the moment, I feel pretty stable. I’m currently taking a mixture of infliximab (one of the biologics) and an immunosuppressant called 6-MP (mercaptopurine). This combination therapy is effective and the big advantage for me is that I can avoid steroids. I’ve been taking 6-MP for the past year and am so glad I decided to go on it.
“If I’m in remission, I can eat pretty much anything, although there are certain foods that I avoid because they make me feel uncomfortable. If I’m having a relapse, everything is hypersensitive.
“Crohn’s disease does interfere a lot with my work. It’s very hard to write a book when you’ve got constant pain in your abdomen and you’re running to the bathroom all the time.
“When I’m not writing, I’m teaching and helping to run First Story. I also like to run, swim and play cricket. But if I’m in a bad state, it’s incredibly hard to do those things. It can be hard to muster up the strength, and I just want to flop and lie down.
“Crohn’s disease grinds on and on. It zaps you of vigour and energy – both physically and psychologically.
“Crohn’s is a hard condition for people to understand. Everyone’s familiar with diarrhoea, but normally for just 24 hours. What they’ve got to imagine is diarrhoea for 24 hours every day for months, with pain and weakness.
“Also, people make the assumption (as Crohn’s is a bowel condition) that it’s to do with food allergy and you can just cut out certain foods like dairy or wheat and that will solve everything. While this might be helpful in some patients to an extent, it’s not in any way a treatment for such an organic disease.
“I’m not sure why I developed Crohn’s disease. I’ve never been a smoker and no-one in my family has it. It’s possible that I had a genetic predisposition and the disease was triggered by the bacteria and viruses I was constantly exposed to in Brazil, where I first started getting symptoms.”
‘My life is now back on track’
Joseph Barr talks about managing Crohn’s disease with medication and how he can still play the sports he loves.
“I had diarrhoea, weight loss and was unable to keep my food down. I threw up three or four times a day. Eventually, I ended up in hospital for two weeks, where doctors carried out tests, including stomach X-rays, a colonoscopy and a barium meal test.
“For the barium meal test, I had to swallow a liquid and 20 minutes later my stomach was X-rayed. Under the X-ray, the liquid highlights everything that’s going on in the stomach.
“A colonoscopy isn’t the greatest experience. A camera is attached to a microscope and inserted into the back passage. It goes quite far up into the colon and everything is recorded on video, which I was able to watch on a screen beside me.
“I was finally diagnosed with Crohn’s disease, an inflammatory disease of the gut. It affects the small and large intestine, and can lead to internal bleeding.
“Initially, I was given steroids. It made a big difference straight away and reduced the inflammation a lot. I now take anti-inflammatory drugs every day, and I’ll have to take them for the rest of my life. There’s no cure for Crohn’s disease, so the treatment I’ve been given helps me to manage my condition. My life is now back on track.
“I still do a lot of the things I used to do. I still go out with my friends, I can drink alcohol and I don’t need to avoid any types of food. I’m still quite active. I can play football and cricket, and go to the gym as often as I can.”