Table 3.

Clinical scores of patients with or without FH mutation

	FH mutation (n = 40)	No FH mutation (n = 65)	p value
Simon Broome criteria
Unlikely FH	25 (62.5%)	62 (95.4%)
Possible FH	7 (17.5%)	1 (1.5%)
Definite FH	8 (20.0%)	2 (3.1%)
(Possible and definite)	15 (37.5%)	3 (4.6%)	< 0.001
Dutch Lipid Clinic criteria
Unlikely FH	3 (7.5%)	25 (38.5%)
Possible FH	14 (35.0%)	35 (53.8%)
Probable FH	11 (27.5%)	1 (1.5%)
Definite FH	12 (30.0%)	4 (6.2%)
(Probable and definite)	23 (57.5%)	5 (7.7%)	< 0.001

Data are expressed as n (%). FH familial hypercholesterolemia