Evidence map›Paper›PMID 30172210›Full record

ArticleJournal of affective disorders2018

Daytime midpoint as a digital biomarker for chronotype in bipolar disorder.

Christopher N Kaufmann, Anda Gershon, Colin A Depp, Shefali Miller, Jamie M Zeitzer, Terence A Ketter

Abstract read
In one paragraph

Article in Journal of affective disorders, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
1.3field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 18 citations in OpenAlex.

  1. Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Christopher N KaufmannDivision of Geriatrics and Gerontology, Department of Medicine, University of California San Diego School of Medicine, La Jolla, CA, USA; Sam and Rose Stein Institute for Research on Aging, University of California San Diego, La Jolla, CA, USA. Electronic address: cnkaufmann@ucsd.edu.
Anda GershonDepartment of Psychiatry and Behavioral Sciences, Stanford University, Palo Alto, CA, USA.
Colin A DeppSam and Rose Stein Institute for Research on Aging, University of California San Diego, La Jolla, CA, USA; Department of Psychiatry, University of California San Diego School of Medicine, La Jolla, CA, USA.
Shefali MillerDepartment of Psychiatry and Behavioral Sciences, Stanford University, Palo Alto, CA, USA.
Jamie M ZeitzerDepartment of Psychiatry and Behavioral Sciences, Stanford University, Palo Alto, CA, USA.
Terence A KetterDepartment of Psychiatry and Behavioral Sciences, Stanford University, Palo Alto, CA, USA.
Stanford University · USUniversity of California San Diego · US

Funding

FELLOWSHIP IN GERIATRIC MENTAL HEALTHT32MH019934 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Elizabeth W Twamley · 1994 to 2026
$9.5M
Sleep and Circadian Dysregulation in Pediatric Bipolar DisorderK01MH100433 · NIMH · STANFORD UNIVERSITY · PI GERSHON, ANDA · 2014 to 2017
$723k
A mechanism of sleep disturbance in bipolar disorderF32MH076339 · NIMH · UNIVERSITY OF CALIFORNIA BERKELEY · PI GERSHON, ANDA · 2007 to 2009
$148k
NIMH NIH HHS F32 MH076339NIMH NIH HHS K01 MH100433NIMH NIH HHS T32 MH019934
6 · The paper itself

Abstract

backgroundBipolar disorder (BD) is associated with later sleep and daily activity (evening rather than morning chronotype). Objective chronotype identification (e.g., based on actigraphs/smartphones) has potential utility, but to date, chronotype has mostly been assessed by questionnaires. Given the ubiquity of accelerometer-based devices (e.g. actigraphs/smartphones) worn/used during daytime and tendency to recharge rather than wear at night, we assessed chronotype using daytime (rather than sleep) interval midpoints.

methodsSixty-one participants with BD type I (BD-I) or II (BD-II) and 61 healthy controls completed 25-50 days of continuous actigraphy. The Composite Scale of Morningness (CSM) was completed by a subset of this group. Daytime activity midpoint was calculated for each daytime interval, excluding naps. Evening chronotype was defined as having a daytime interval midpoint at or after 16:15:00 (4:15:00 PM).

resultsBD versus controls had delayed daytime midpoint (mean ± standard deviation) (16:49:07 ± 01:26:19 versus 16:12:51 ± 01:02:14, p < 0.01), and greater midpoint variability (73.3 ± 33.9 min versus 58.1 ± 18.3 min, p < 0.01). Stratifying by gender and age, females and adolescents with BD had delayed and more variable daytime midpoints versus controls. Adults with BD had greater midpoint variability than controls. Within-person mean and standard deviations of daytime midpoints were highly correlated with sleep midpoints (r = 0.99, p < 0.01 and r = 0.86, p < 0.01, respectively). Daytime midpoint mean was also significantly correlated with the CSM (r = -0.56, p < 0.01). LIMITATIONS: Small sample size; analyses not fully accounting for daytime napping.

conclusionsWrist actigraphy for determination of daytime midpoints is a potential tool to identify objective chronotype. Exploration of the use of consumer devices (wearables/smartphones) is needed.

Indexed as

BiomarkersCircadian RhythmActigraphyAdolescentAdultBipolar DisorderChronobiology DisordersFemaleHumansMaleMiddle AgedSleepSurveys and QuestionnairesYoung AdultBiomarkersActigraphyBipolar disorderChronotypeDaytime

Identifiers

PMID30172210
PMCPMC6436809
OpenAlexW2886472795

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.