Background: Melanopsin, a non-visual photopigment [found in specialized cells in the retina of the eye that are sensitive to non-visible light] may play a role in aberrant responses to low winter light levels in Seasonal Affective Disorder (SAD).
We hypothesize that functional sequence variation in the melanopsin gene could contribute to increasing the light needed for normal functioning during winter in SAD.
Methods: Associations between alleles, genotypes, and haplotypes of melanopsin in SAD participants (n = 130) were performed relative to controls with no history of psychopathology (n = 90).
Results: SAD participants had a higher frequency of the homozygous minor genotype (T/T) for the missense variant rs2675703 (P10L) than controls, compared to the combined frequencies of C/C and C/T. Individuals with the T/T genotype were 5.6 times more likely to be in the SAD group than the control group, and all 7 (5%) of individuals with the T/T genotype at P10L were in the SAD group.
Limitations: The study examined only one molecular component of the non-visual light input pathway, and recruitment methods for the comparison groups differed.
Conclusion: These findings support the hypothesis that melanopsin variants may predispose some individuals to SAD. Characterizing the genetic basis for deficits in the non-visual light input pathway has the potential to define mechanisms underlying the pathological response to light in SAD, which may improve treatment.
Source: Journal of Affective Disorders, Sep 18, 2008. E-pub ahead of print. Roecklein KA, Rohan KJ, Duncan WC, Rollag MD, Rosenthal NE, Lipsky RH, Provencio I. Graduate Program in Medical Psychology, Uniformed Services University of the Health Sciences, Bethesda, MD, United States. [E-mail: firstname.lastname@example.org]