TY - JOUR
T1 - Eveningness chronotype preference among individuals at clinical high risk for psychosis
AU - Lunsford-Avery, Jessica R.
AU - Pelletier-Baldelli, Andrea
AU - Korenic, Stephanie A.
AU - Schiffman, Jason
AU - Ellman, Lauren M.
AU - Jackson, Leah
AU - Mittal, Vijay A.
N1 - Funding Information:
This work was supported by the National Institutes of Health : K23108704 to J.R.L.A., R01MH112613 and R01MH120091 to L.M.E, R01MH116039 , R01MH112545 , and R01MH120088 to V.A.M., R01MH112612 and R34MH110506 J.S., and T32MH106440 and T32HD007376 to A.P. This work was further supported by National Science Foundation Graduate Research Fellowship Program award number 2038235 to S.A.K. We are grateful to the participants for their contributions to research.
Publisher Copyright:
© 2021
PY - 2021/10
Y1 - 2021/10
N2 - Background: Circadian rhythm disturbances are frequently implicated in psychosis. Indeed, research has suggested several avenues by which circadian rhythms may play a mechanistic role as well as contribute to clinical outcomes. Despite its potential role as a risk factor, little is known about circadian rhythm disruption among individuals at clinical high risk (CHR) for psychosis, clinical correlates, or specificity to the psychosis risk syndrome. Methods: Eighty-four CHR, 74 individuals with depressive disorders (DD), and 101 non-psychiatric controls (NPC) participated in structured clinical interviews and provided self-reports of chronotype preference. Clinical (positive, negative, anxious, and depressive symptoms) and social functioning outcomes were self-reported and/or clinician-rated. Analyses of covariance controlling for demographics examined group differences in chronotype preference, and partial Pearson correlations evaluated associations with clinical/functional outcomes. Results: Group differences were observed (F(11, 246) = 8.05, p < .001) with CHR and DD individuals indicating greater eveningness preference compared to NPC. A follow-up sensitivity analysis examining CHR participants with (n = 25) and without (n = 59) depressive disorders indicated no difference in chronotype preference (F(10,72) = 0.00, p = .99). Greater eveningness preference was related to greater negative symptoms (i.e., avolition; r = −0.25) and anxiety (r = −0.34) among CHR individuals. Conclusions: CHR and DD display greater preference for eveningness chronotype compared to NPC indicating the disruption is associated with a range of mental health concerns, and not specific to the psychosis-risk syndrome. However, comorbidity with DD did not appear to be driving the finding in the CHR group. Further research may examine shared versus non-shared underlying mechanisms contributing to chronotype preference across psychiatric presentations.
AB - Background: Circadian rhythm disturbances are frequently implicated in psychosis. Indeed, research has suggested several avenues by which circadian rhythms may play a mechanistic role as well as contribute to clinical outcomes. Despite its potential role as a risk factor, little is known about circadian rhythm disruption among individuals at clinical high risk (CHR) for psychosis, clinical correlates, or specificity to the psychosis risk syndrome. Methods: Eighty-four CHR, 74 individuals with depressive disorders (DD), and 101 non-psychiatric controls (NPC) participated in structured clinical interviews and provided self-reports of chronotype preference. Clinical (positive, negative, anxious, and depressive symptoms) and social functioning outcomes were self-reported and/or clinician-rated. Analyses of covariance controlling for demographics examined group differences in chronotype preference, and partial Pearson correlations evaluated associations with clinical/functional outcomes. Results: Group differences were observed (F(11, 246) = 8.05, p < .001) with CHR and DD individuals indicating greater eveningness preference compared to NPC. A follow-up sensitivity analysis examining CHR participants with (n = 25) and without (n = 59) depressive disorders indicated no difference in chronotype preference (F(10,72) = 0.00, p = .99). Greater eveningness preference was related to greater negative symptoms (i.e., avolition; r = −0.25) and anxiety (r = −0.34) among CHR individuals. Conclusions: CHR and DD display greater preference for eveningness chronotype compared to NPC indicating the disruption is associated with a range of mental health concerns, and not specific to the psychosis-risk syndrome. However, comorbidity with DD did not appear to be driving the finding in the CHR group. Further research may examine shared versus non-shared underlying mechanisms contributing to chronotype preference across psychiatric presentations.
KW - Chronotype
KW - Circadian rhythms
KW - Clinical high risk
KW - Diurnal preference
KW - Psychosis
KW - Schizophrenia
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U2 - 10.1016/j.schres.2021.07.034
DO - 10.1016/j.schres.2021.07.034
M3 - Article
C2 - 34358763
AN - SCOPUS:85111841683
SN - 0920-9964
VL - 236
SP - 3
EP - 8
JO - Schizophrenia Research
JF - Schizophrenia Research
ER -