Salivary melatonin onset in youth at familial risk for bipolar disorder

dc.contributor.authorGhaziuddin, Neera
dc.contributor.authorShamseddeen, Wael A.
dc.contributor.authorBertram, Holli S.
dc.contributor.authorMcInnis, Melvin G.
dc.contributor.authorWilcox, Holly C.
dc.contributor.authorMitchell, Philip B.
dc.contributor.authorFullerton, Janice M.
dc.contributor.authorRoberts, Gloria M.P.
dc.contributor.authorGlowinski, Anne L.
dc.contributor.authorKamali, Masoud P.
dc.contributor.authorStapp, Emma K.
dc.contributor.authorHulvershorn, Leslie A.
dc.contributor.authorNurnberger, John I.
dc.contributor.authorArmitage, Roseanne
dc.contributor.departmentPsychiatry
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T12:11:54Z
dc.date.available2025-01-24T12:11:54Z
dc.date.issued2019
dc.description.abstractMelatonin secretion and polysomnography (PSG) were compared among a group of healthy adolescents who were at high familial risk for bipolar disorder (HR) and a second group at low familial risk (LR). Adolescent participants (n = 12) were a mean age 14 ± 2.3 years and included 8 females and 4 males. Saliva samples were collected under standardized condition light (red light) and following a 200 lux light exposure over two consecutive nights in a sleep laboratory. Red Light Melatonin onset (RLMO) was defined as saliva melatonin level exceeding the mean of the first 3 readings plus 2 standard deviations. Polysomnography was also completed during each night. HR youth, relative to LR, experienced a significantly earlier melatonin onset following 200 lux light exposure. Polysomnography revealed that LR youth, relative to HR, spent significantly more time in combined stages 3 and 4 (deep sleep) following red light exposure. Additionally, regardless of the group status (HR or LR), there was no significant difference in Red Light Melatonin Onset recorded at home or in the laboratory, implying its feasibility and reliability. © 2019
dc.identifier.doihttps://doi.org/10.1016/j.psychres.2019.02.013
dc.identifier.eid2-s2.0-85061546501
dc.identifier.pmid30780062
dc.identifier.urihttp://hdl.handle.net/10938/32611
dc.language.isoen
dc.publisherElsevier Ireland Ltd
dc.relation.ispartofPsychiatry Research
dc.sourceScopus
dc.subjectAdolescent
dc.subjectBipolar
dc.subjectMelatonin
dc.subjectPolysomnography
dc.subjectRisk
dc.subjectAdult
dc.subjectBiomarkers
dc.subjectBipolar disorder
dc.subjectChild
dc.subjectCircadian rhythm
dc.subjectFemale
dc.subjectGenetic predisposition to disease
dc.subjectHumans
dc.subjectMale
dc.subjectPhotic stimulation
dc.subjectReproducibility of results
dc.subjectSaliva
dc.subjectSleep
dc.subjectSleep disorders, circadian rhythm
dc.subjectBiological marker
dc.subjectAdolescence
dc.subjectArticle
dc.subjectHigh risk population
dc.subjectHuman
dc.subjectHuman experiment
dc.subjectLow risk population
dc.subjectNormal human
dc.subjectPriority journal
dc.subjectRed light
dc.subjectSaliva level
dc.subjectSleep time
dc.subjectChemistry
dc.subjectCircadian rhythm sleep disorder
dc.subjectGenetic predisposition
dc.subjectGenetics
dc.subjectMetabolism
dc.subjectPhotostimulation
dc.subjectPhysiology
dc.subjectProcedures
dc.subjectReproducibility
dc.subjectTrends
dc.titleSalivary melatonin onset in youth at familial risk for bipolar disorder
dc.typeArticle

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