Impact of genetic variation in the 5-HT transporter and receptor on platelet function in patients with stable CAD taking aspirin. Issue 146 (October 2016)

• Record Type: Journal Article
• Authors: Bajrangee, Amrit; Ryan, Nicola; Vangjeli, Ciara; Brennan, Marian; Cox, Dermot; Shields, Denis C.; Fitzgerald, Desmond; Maree, Andrew
• Is Part Of: Thrombosis research. Issue 146(2016)
• Page Start: 51
• Page End: 55
• Publication Date: 2016-10
• Subjects: CAD Coronary artery disease -- MI Myocardial infraction -- CABG Coronary artery bypass grafting -- TXB2 Thromboxane B2; Aspirin -- Genetic -- Serotonin -- Coronary disease; Thrombosis -- Periodicals; 616.135
• DOI: 10.1016/j.thromres.2016.08.019
• Languages: English
• ISSNs: 0049-3848

Abstract

Abstract: Background: Serotonin (5-HT) induces platelet aggregation by activating its 5-HT2A receptor. Platelet uptake is mediated by the 5-HT transporter (5-HTT). A common 5-HTT promoter (5-HTTLPR) splice variant results in long (L) and short (S) alleles. 5-HTTLPR genotype has been associated with increased platelet activation and risk of MI. Variation within HTR2A gene (C1354T) that encodes the 5-HT2A receptor has also been associated with enhanced platelet aggregation. We hypothesised that 5-HTT and/or HTR2A variation may influence platelet response to aspirin in patients with stable CAD. Methods: Patients ( n = 144) with stable cardiovascular disease taking aspirin were genotyped for the 5-HTTLPR and HTR2A variants. Platelet inhibition was assessed by serum thromboxane and arachidonic acid-induced platelet aggregation assay. Results: 5-HTT genotype (LL vs *S) was a significant determinant of serum TX level (8.9 ± 2.6 ng/ml vs 6.0 ± 1.6 ng/ml respectively; p < 0.02) and 5-HTT LL genotype predicted an incomplete aspirin response (serum TXB2 > 2.2 ng/ml) ( p = 0.04; OR = 2.22, CI = 1.03–4.79). Odds ratio of the effect of LL genotype on TX elevation was 3.8 (95% CI 1.2–11.6) in younger patients (under 64) compared to 1.0 (95% CI = 0.3–3.8) in older subjects. LL genotype did not influence AA aggregation ( p = 0.83, OR = 1.2, CI = 0.3–4.1). The HTR2A variant had no effect on TX generation ( p = 0.70; OR = 1.22, CI = 0.45–3.26) nor AA aggregation ( p = 0.99; OR = 1.0, CI = 0.2–4.9). Conclusions: In younger patients with stable CAD 5HTT LL genotype carried by almost one third of our cohort is associated with a diminished response to aspirin that may increase cardiovascular risk. Genotypic variation in platelet activation may be a contributing mechanism. Highlights: 5-HTT genotype (LL vs *S) was a significant determinant of serum TX level. 5-HTT LL genotype predicted an incomplete aspirin response. The HTR2A variant had no effect on TX generation.