Literature DB >> 27821359

Pupillary response abnormalities in depressive disorders.

Scott A Laurenzo1, Randy Kardon2, Johannes Ledolter3, Pieter Poolman2, Ashley M Schumacher1, James B Potash1, Jan M Full2, Olivia Rice2, Anna Ketcham2, Cole Starkey2, Jess G Fiedorowicz4.   

Abstract

Depressive disorders lack objective physiological measurements to characterize the affected population and facilitate study of relevant mechanisms. The melanopsin-mediated light signaling pathway may contribute to seasonal variation and can be measured non-invasively by pupillometry. We prospectively studied changes in melanopsin-mediated pupillary constriction in 19 participants with major depressive disorder (MDD) and 10 control across the summer and winter solstices. The melanopsin-mediated response, as measured by the pupil's sustained constriction six s after a high intensity blue light stimulus, was marginally attenuated in those with MDD relative to controls (p=0.071). The participants with MDD unexpectedly showed a significantly reduced transient pupillary response to low intensity red (p=0.011) and blue light (p=0.013), but not high intensity red and blue light. Sustained pupillary constriction in response to high intensity blue light was more pronounced with increasing daylight hours (p=0.037) and was more strongly related to objectively measured versus estimated light exposure. Melanopsin-mediated impairments in pupil response may serve as a biological marker for vulnerability to depression in low light conditions. Assessment of these and other responses to light stimuli, such as response to low intensity light, may be useful for the study of the neurobiology of MDD and related mood disorders. Published by Elsevier Ireland Ltd.

Entities:  

Keywords:  Bipolar disorder; Major depressive disorder; Pupillometry; Seasonality

Mesh:

Year:  2016        PMID: 27821359      PMCID: PMC5161673          DOI: 10.1016/j.psychres.2016.10.039

Source DB:  PubMed          Journal:  Psychiatry Res        ISSN: 0165-1781            Impact factor:   3.222


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