Background:
Statins are the most prescribed lipid-lowering drugs worldwide. The associated
adverse events, especially muscle symptoms, have been frequently reported despite their perceived
safety. Three pharmacogenes, the solute carrier organic anion transporter family member 1B1
(SLCO1B1), ATP-binding cassette subfamily G member 2 (ABCG2), and cytochrome P450 9C9
(CYP2C9) are suggested as safety biomarkers for statins. The Clinical Pharmacogenomic Implementation
Consortium (CPIC) issued clinical guidelines for statin use based on these three genes.
Objectives:
The present study aimed to examine variants in these pharmacogenes to predict the safety
of statin use among the Emirati population.
Methods:
Analyzing 242 whole exome sequencing data at the three genes enabled the determination
of the frequencies of the single nucleotide polymorphisms (SNPs), annotating the haplotypes and the
predicted functions of their proteins.
Results:
In our cohort, 29.8% and 5.4% had SLCO1B1 decreased and poor function, respectively. The
high frequency warns of the possibility of significant side effects of some statins and the importance
of pharmacogenomic testing. We found a low frequency (6%) of the ABCG2:rs2231142 variant,
which indicates the low probability of Emirati patients being recommended against higher rosuvastatin
doses compared with other populations with higher frequencies of this variant. In contrast, we
found high frequencies of the functionally impaired CYP2C9 alleles, which makes fluvastatin a less
favorable choice.
Conclusion:
Among the sparse studies available, the present one demonstrates all SLCO1B1 and
CYP2C9 function-impairing alleles among Emiratis. We highlighted how population-specific pharmacogenomic
data can predict safer choices of statins, especially in understudied populations.