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Chronotype and cellular circadian rhythms predict the clinical response to lithium maintenance treatment in patients with bipolar disorder.


ABSTRACT: Bipolar disorder (BD) is a serious mood disorder associated with circadian rhythm abnormalities. Risk for BD is genetically encoded and overlaps with systems that maintain circadian rhythms. Lithium is an effective mood stabilizer treatment for BD, but only a minority of patients fully respond to monotherapy. Presently, we hypothesized that lithium-responsive BD patients (Li-R) would show characteristic differences in chronotype and cellular circadian rhythms compared to lithium non-responders (Li-NR). Selecting patients from a prospective, multi-center, clinical trial of lithium monotherapy, we examined morning vs. evening preference (chronotype) as a dimension of circadian rhythm function in 193 Li-R and Li-NR BD patients. From a subset of 59 patient donors, we measured circadian rhythms in skin fibroblasts longitudinally over 5 days using a bioluminescent reporter (Per2-luc). We then estimated circadian rhythm parameters (amplitude, period, phase) and the pharmacological effects of lithium on rhythms in cells from Li-R and Li-NR donors. Compared to Li-NRs, Li-Rs showed a difference in chronotype, with higher levels of morningness. Evening chronotype was associated with increased mood symptoms at baseline, including depression, mania, and insomnia. Cells from Li-Rs were more likely to exhibit a short circadian period, a linear relationship between period and phase, and period shortening effects of lithium. Common genetic variation in the IP3 signaling pathway may account for some of the individual differences in the effects of lithium on cellular rhythms. We conclude that circadian rhythms may influence response to lithium in maintenance treatment of BD.

SUBMITTER: McCarthy MJ 

PROVIDER: S-EPMC6333516 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature

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Chronotype and cellular circadian rhythms predict the clinical response to lithium maintenance treatment in patients with bipolar disorder.

McCarthy Michael J MJ   Wei Heather H   Nievergelt Caroline M CM   Stautland Andrea A   Maihofer Adam X AX   Welsh David K DK   Shilling Paul P   Alda Martin M   Alliey-Rodriguez Ney N   Anand Amit A   Andreasson Ole A OA   Balaraman Yokesh Y   Berrettini Wade H WH   Bertram Holli H   Brennand Kristen J KJ   Calabrese Joseph R JR   Calkin Cynthia V CV   Claasen Ana A   Conroy Clara C   Coryell William H WH   Craig David W DW   D'Arcangelo Nicole N   Demodena Anna A   Djurovic Srdjan S   Feeder Scott S   Fisher Carrie C   Frazier Nicole N   Frye Mark A MA   Gage Fred H FH   Gao Keming K   Garnham Julie J   Gershon Elliot S ES   Glazer Kara K   Goes Fernando F   Goto Toyomi T   Harrington Gloria G   Jakobsen Petter P   Kamali Masoud M   Karberg Elizabeth E   Kelly Marisa M   Leckband Susan G SG   Lohoff Falk F   McInnis Melvin G MG   Mondimore Francis F   Morken Gunnar G   Nurnberger John I JI   Obral Sarah S   Oedegaard Ketil J KJ   Ortiz Abigail A   Ritchey Megan M   Ryan Kelly K   Schinagle Martha M   Schoeyen Helle H   Schwebel Candice C   Shaw Martha M   Shekhtman Tatyana T   Slaney Claire C   Stapp Emma E   Szelinger Szabolcs S   Tarwater Bruce B   Zandi Peter P PP   Kelsoe John R JR  

Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 20181116 3


Bipolar disorder (BD) is a serious mood disorder associated with circadian rhythm abnormalities. Risk for BD is genetically encoded and overlaps with systems that maintain circadian rhythms. Lithium is an effective mood stabilizer treatment for BD, but only a minority of patients fully respond to monotherapy. Presently, we hypothesized that lithium-responsive BD patients (Li-R) would show characteristic differences in chronotype and cellular circadian rhythms compared to lithium non-responders (  ...[more]

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