Key result
The 5-HTTLPR s/s genotype linked to ~123% greater odds of hopelessness vs l/l in stable CHD.
Why the study?
Hopelessness is associated with mortality in cardiac disease patients independent of depression severity, but genetic associations with hopelessness are unclear.
Is the 5-HTTLPR polymorphism associated with increased hopelessness in patients with stable coronary heart disease?
Cross-Sectional (n=870)
Yes
Is the 5-HTTLPR polymorphism associated with increased hopelessness in patients with stable coronary heart disease?
Odds Ratio: 2.23 (95% CI 1.5–3.4)
p-value: p=<0.001
The 5-HTTLPR polymorphism is independently associated with increased hopelessness among men with stable coronary heart disease.
5-HTTLPR variants may refine hopelessness assessment in CHD; leaves open prospective validation before any clinical application.
BACKGROUND: Hopelessness is associated with mortality in patients with cardiac disease even after accounting for severity of depression. We sought to determine whether a polymorphism in the promoter region of the serotonin transporter gene (5-HTTLPR) is associated with increased hopelessness, and whether this effect is modified by sex, age, antidepressant use or depression in patients with coronary heart disease. METHODS: We conducted a cross-sectional study of 870 patients with stable coronary heart disease. Our primary outcomes were hopelessness score (range 0-8) and hopeless category (low, moderate and high) as measured by the Everson hopelessness scale. Analysis of covariance and ordinal logistic regression were used to examine the independent association of genotype with hopelessness. RESULTS: Compared to patients with l/l genotype, adjusted odds of a higher hopeless category increased by 35% for the l/s genotype and 80% for s/s genotype (p-value for trend = 0.004). Analysis of covariance demonstrated that the effect of 5-HTTLPR genotype on hopelessness was modified by sex (.04), but not by racial group (p = 0.63). Among men, odds of higher hopeless category increased by 40% for the l/s genotype and by 2.3-fold for s/s genotype (p-value p < 0.001), compared to no effect in the smaller female sample (p = 0.42). Results stratified by race demonstrated a similar dose-response effect of the s allele on hopelessness across racial groups. CONCLUSIONS: We found that the 5-HTTLPR is independently associated with hopelessness among men with cardiovascular disease.
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Kangelaris et al. (2010) conducted a cross-sectional in Stable coronary heart disease (n=870). 5-HTTLPR s allele (s/s genotype) vs. l/l genotype was evaluated on Higher hopeless category (low, moderate, high) (OR 2.23, 95% CI 1.5-3.4, p=<0.001). Among men with stable coronary heart disease, the 5-HTTLPR s/s genotype was associated with a 2.23-fold increased odds of a higher hopelessness category compared to the l/l genotype.
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