Why the study?
Do antidepressants with high serotonin reuptake transporter affinity increase serum lipid levels in older adults?
Do antidepressants with high serotonin reuptake transporter affinity increase serum lipid levels in older adults?
Antidepressants with high serotonin transporter affinity may be associated with elevated LDL cholesterol in older adults, highlighting a potential metabolic side effect influenced by genetics.
High-affinity antidepressants were associated with higher LDL in older adults; leaves open whether monitoring or risk modification is warranted.
OBJECTIVE: We aimed to investigate the association between antidepressants and serum lipid levels in a population-based study in older adults. METHODS: We included participants from the prospective Rotterdam Study with data on lipid levels (total, low-density lipoprotein (LDL) and high-density lipoprotein cholesterol, and triglycerides). We classified antidepressants based on binding affinity to the serotonin transporter (low/intermediate- and high-affinity antidepressants). We compared lipid levels in users of these groups of antidepressants with lipid levels in non-users. Furthermore, we studied effect modification by the 102 C>T polymorphism (HTR2A gene), which is associated with antidepressant drug response and metabolic outcomes. RESULTS: Compared with non-users (N = 6438), LDL cholesterol level was higher (2.9 versus 3.1 mmol/L, respectively; p = 0.05) in users of high-affinity antidepressants (N = 89). Similar levels of the other lipids were observed between the groups for the other lipids. The mean difference in serum LDL cholesterol level between non-users and users of high-affinity antidepressants was largest in participants with the CC genotype compared with the other genotypes (notably 0.47 mmol/L), indicative of effect modification (p-value for interaction = 0.03). CONCLUSION: Antidepressants with a high serotonin reuptake transporter affinity were associated with higher LDL cholesterol levels, which were modified by a common genetic variation in the HTR2A gene.
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Noordam et al. (2015) studied this question.
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