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. 2017 Jun 13;8:372. doi: 10.3389/fphar.2017.00372

Table 1.

Summary of population studies investigating onset of DM in FH patients with statins treatment.

Author and Published year Country Study design Population and the cause of FH DM-related findings
Vohl et al., 1997 Canada Case control study 102 patients without FH, 102 hFH patients; a defective allele at LDLR or LDLR mutation. The prevalence of DM was significantly higher in the non-FH group than in the two FH groups (P < 0.05).
Skoumas et al., 2007 Greece Cross-sectional study. A total 1306 subjects: 600 individuals with hFH, and 706 individuals with FCH; LDLR mutation or plasma levels of LDL cholesterol above the 95th percentile. FCH had a significantly increased prevalence of DM (13 vs. 2%, P < 0.001) vs FH group, whereas total cholesterol, LDL-cholesterol, and apolipoprotein B levels were higher (all P < 0.001) in FH subjects.
Skoumas et al., 2014 Greece Ambispective cohort study. A total of 523 adult patients (314 hFH and 209 FCH patients); LDL-receptor mutation or plasma levels of LDL cholesterol above the 95th percentile. 14% of FCH and only 1% of hFH patients developed DM during follow up.
Kusters et al., 2014 Netherland Retrospective cohort study 2144 children with hFH; LDR mutation. Statin treatment was not associated with an increased risk of new-onset DM in these patients.
Besseling et al., 2015 Netherland Cross-sectional study All individuals (n = 63 320) who underwent DNA testing for FH; 3475 were ApoB mutation carriers, 21 606 had the LDLR mutation, and 56 had PCSK9 mutation. The prevalence of T2DM was 1.75% in FH patients (n = 440/25 137) vs 2.93% in unaffected relatives (P < 0.001). The adjusted prevalence of type 2 DM by APOB vs LDL receptor gene was 1.91% vs 1.33%.
Fuentes et al., 2015 Spain Cross-sectional and prospective cohort study 2558 FH and 1265 unaffected relatives with a mean follow-up of 5.9 years; LDLR mutation. Finally, in the adjusted Kaplan–Meier curve, there are no differences between FH group vs control group in the incidence of T2DM according the duration of treatment with statins.

hFH, heterozygous Familial Hypercholesterolemia; FCH, familial combined hyperlipidemia; LDLR, low density lipoprotein receptor; T2DM, type 2 diabetes mellitus; PCSK9, proprotein convertase subtilisin/kexin type 9; ApoB, apolipoprotein B.