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. 2013 Jul;229(1):161–168. doi: 10.1016/j.atherosclerosis.2013.04.011

Table 3.

FH mutation detection rate by quartile of pre-treatment TC and pre-treatment TG.

Oxford FH study
Quartile of pre-treatment TC (mmol/l) N Mutation + ve (%) Quartile of pre-treatment TG (mmol/l) N Mutation + ve (%)
Q1 ≤8.0 40 10 (25) Q1 ≤1.0 42 25 (60)
Q2 8.1–8.7 41 12 (29) Q2 1.10–1.32 38 15 (40)
Q3 8.8–9.9 44 15 (34) Q3 1.33–2.15 39 14 (36)
Q4 >10.0 34 25 (74) Q4 2.16–4.30 40 8 (20)
P value (trend) p = 9.83 × 10−5 0.000458
Replication SBBHF study
Quartile of pre-treatment TC (mmol/l) N Mutation + ve (%) Quartile of post-treatment TG (mmol/l)a N Mutation + ve (%)
Q1 ≤8.7 76 52 (68.4) Q1 <1 105 92 (87.6)
Q2 8.8–10.1 82 66 (80.5) Q2 1–1.3 123 109 (88.6)
Q3 10.2–11.6 69 62 (89.9) Q3 1.4–1.8 90 70 (77.8)
Q4 >11.6 72 65 (90.3) Q4 >1.8 91 57 (62.6)
P value (trend) 0.0001 P = 1.80 × 10−6
a

Pre-treatment TG were not available for SBBHF study.