Our cookies

We use cookies, which are small text files, to improve your experience on our website.
You can allow or reject non essential cookies or manage them individually.

Manage cookiesAllow all

Cookie policy

Our cookies

Allow all

We use cookies, which are small text files, to improve your experience on our website. You can allow all or manage them individually.

You can find out more on our cookie page at any time.

EssentialThese cookies are needed for essential functions such as logging in and making payments. Standard cookies can't be switched off and they don't store any of your information.
AnalyticsThese cookies help us collect information such as how many people are using our site or which pages are popular to help us improve customer experience. Switching off these cookies will reduce our ability to gather information to improve the experience.
FunctionalThese cookies are related to features that make your experience better. They enable basic functions such as social media sharing. Switching off these cookies will mean that areas of our website can't work properly.
AdvertisingThese cookies help us to learn what you're interested in so we can show you relevant adverts on other websites and track the effectiveness of our advertising.
PersonalisationThese cookies help us to learn what you're interested in so we can show you relevant content.

Save preferences

What are the diagnostic criteria for FH?

 

How does your doctor make a diagnosis of FH?

Once your doctor has asked about your family history, taken blood tests and checked for physical signs of FH, they will use the Simon Broome criteria to see if you have it. You might be diagnosed as having definite FH or possible FH. Alternatively, they might use the Dutch Clinical.

Read more about the tests for FH

Are You a Healthcare Professional? Visit our HCP section.

Find Out More

 The Simon Broome Criteria

A: Definite familial hypercholesterolaemia is defined as:

Total cholesterol greater than 6.7mmol/L or low density lipoprotein cholesterol (LDL-C) greater than 4.0mmol/L in a child aged younger than 16 years or total cholesterol greater than 7.5mmol/L or LDL-C greater than 4.9mmol/L in an adult (levels either pre-treatment or highest on treatment).

Plus:

Tendon xanthomas in patient or in 1st degree relative (parent, sibling, child) or in 2nd degree relative (grandparent, uncle, aunt)

Or:

DNA-based evidence of an LDL receptor mutation or familial defective apo B-100 or a PCSK9 mutation

B: Possible Familial Hypercholesterolaemia is defined as:

Total cholesterol greater than 6.7mmol/L or low density lipoprotein cholesterol (LDL-C) greater than 4.0mmol/L in a child aged younger than 16 years or total cholesterol greater than 7.5mmol/L or LDL-C greater than 4.9mmol/L in an adult (levels either pre-treatment or highest on treatment)

and at least one of the following:

Family history of myocardial infarction: younger than 50 years of age in a 2nd degree relative or younger than 60 in a 1st degree relative

Or:

Family history of raised cholesterol greater than 7.5mmol/L in adult 1st or 2nd degree relative or greater than 6.7mmol/L in child or sibling aged younger than 16 years

The Dutch Lipid Clinics Network Criteria

The Dutch Lipid Clinical Network criteria is used in the Netherlands to diagnose FH, but it’s sometimes used by doctors in Britain too. It works on a points system, where a set number of points are given to certain signs and symptoms, your cholesterol levels and illnesses in your family.

  • a total point score of greater than 8 is considered "definite FH"
  • a total point score of 6-8 is considered "probable FH"
  • a total point score of 3-5 is considered "possible FH"

The Wales FH Service Criteria

There is also a Wales FH Service criteria which is a version of the Dutch criteria used in Wales.

 

Read more about how FH is diagnosed