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. Author manuscript; available in PMC: 2015 Oct 1.
Published in final edited form as: Am J Geriatr Psychiatry. 2013 Sep 8;22(10):971–979. doi: 10.1016/j.jagp.2013.07.003

Table 4.

Serotonin transporter, 1A and 2A receptors by low- and high-expressing genotype groupings for significant drug effects. Highlighted pairs represent ‘pharmacogenetic effects’ where there is a significant difference in regression coefficients between the expression-based groupings for a side-effect.

UKU 5-HTTLPR triallelic haplotype HTR1A rs6295 HTR2A rs6311
genotype (expression- level) LA− (low) LA+ (high) CC (low) GG/CG (high) GG (low) AA/AG (high)
n 49 102 35 116 53 97
Increased sleep β (SE) .70 (.59) 1.32 (.47) 1.70 (.69) 1.12 (.47) 1.39 (.51) 1.10 (.53)
Dry mouth β (SE) 1.20 (.41)* .17 (.30)* .41 (.61) .54 (.27) .89 (.38) .30 (.32)
Diarrhea β (SE) .66 (.43) .57 (.28) 1.37 (.45)* .30 (.27)* 1.15 (.40) .42 (.30)
Diminished Sexual Desire β (SE) .16 (.55)* 2.39 (.73)* 1.09 (.76)* 1.58 (.64)* .89 (.66)* 2.25 (.85)*
*

p<.05 between GEE regression coefficients for low- and high-expressing genotypes

A Z test was used to test for the equality of regression coefficients (30).