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1.
J Clin Sleep Med ; 14(11): 1911-1919, 2018 11 15.
Article in English | MEDLINE | ID: mdl-30373685

ABSTRACT

STUDY OBJECTIVES: Individuals with primary insomnia often have poorer self-reported sleep than objectively measured sleep, a phenomenon termed negative sleep discrepancy. Recent studies suggest that this phenomenon might differ depending on comorbidities. This study examined sleep discrepancy, its night-to-night variability, and its correlates in comorbid insomnia and fibromyalgia. METHODS: Sleep diaries and actigraphy data were obtained from 223 adults with fibromyalgia and insomnia (age = 51.53 [standard deviation = 11.90] years; 93% women) for 14 days. Sleep discrepancy was calculated by subtracting diary from actigraphy estimates of sleep onset latency (SOL-D), wake after sleep onset (WASO-D), and total sleep time (TST-D) for each night. Night-to-night variability in sleep discrepancy was calculated by taking the within-individual standard deviations over 14 days. Participants completed measures of mood, pain, fatigue, sleep/pain medications, nap duration, and caffeine consumption. RESULTS: Average sleep discrepancies across 14 days were small for all sleep parameters (< 10 minutes). There was no consistent positive or negative discrepancy. However, sleep discrepancy for any single night was large, with average absolute discrepancies greater than 30 minutes for all sleep parameters. Greater morning pain was associated with larger previous-night WASO-D, although diary and actigraphy estimates of WASO remained fairly concordant. Taking prescribed pain medications, primarily opioids, was associated with greater night-to-night variability in WASO-D and TST-D. CONCLUSIONS: Unlike patients with primary insomnia, patients with comorbid fibromyalgia do not exhibit consistent negative sleep discrepancy; however, there are both substantial positive and negative discrepancies in all sleep parameters at the daily level. Future research is needed to investigate the clinical significance and implications of high night-to-night variability of sleep discrepancy, and the role of prescribed opioid medications in sleep perception.


Subject(s)
Fibromyalgia/complications , Sleep Initiation and Maintenance Disorders/complications , Sleep Initiation and Maintenance Disorders/epidemiology , Actigraphy , Adult , Aged , Comorbidity , Correlation of Data , Cross-Sectional Studies , Female , Fibromyalgia/epidemiology , Fibromyalgia/psychology , Health Records, Personal , Humans , Male , Middle Aged , Pain Measurement , Risk Factors , Self Report , Sleep Initiation and Maintenance Disorders/psychology
2.
Cogn Affect Behav Neurosci ; 18(6): 1283-1297, 2018 12.
Article in English | MEDLINE | ID: mdl-30225599

ABSTRACT

Affect regulation plays a key role in several theories of racial bias reduction. Here, we tested whether engaging in emotion regulation strategies while performing an implicit racial bias task (Weapons Identification Task; WIT) would alter neural and behavioral manifestations of bias. Participants either suppressed or reappraised in a positive light the distress associated with making errors during the WIT, while an electroencephalogram (EEG) was recorded. We hypothesized that engaging in emotion regulation strategies would reduce the distress associated with making errors indicative of bias, resulting in smaller error-related negativity (ERN) amplitude during errors and increased expression of racial bias. Results of within-subjects comparisons (Experiment 1) generally supported these predictions. However, when emotion regulation strategies were manipulated between subjects (Experiment 2) there was no effect of suppression or reappraisal on bias expression. Across both experiments, engaging in emotion regulation led to larger ERNs for errors occurring on Black- relative to White-primed trials. In addition, a number of significant order effects were observed, indicating important differences in the effects of engaging in emotion regulation strategies when those strategies are attempted in participants' first versus second block of trials. No such order effects were evident when a second trial block was completed with no emotion regulation instructions. Findings are discussed in terms of the need for greater specificity in experimental tests of emotion regulation on error processing and cognitive performance.


Subject(s)
Brain/physiology , Emotions/physiology , Racism/psychology , Stress, Psychological/physiopathology , Adolescent , Cognition/physiology , Electroencephalography , Female , Humans , Male , Reaction Time/physiology , Stress, Psychological/psychology , Young Adult
3.
Sleep Med Rev ; 40: 170-182, 2018 08.
Article in English | MEDLINE | ID: mdl-29366543

ABSTRACT

Recent research suggests that sleep plays an important role in obesity (OB). No systematic reviews have investigated the association between OB and insomnia specifically. The present study reviewed the past 10 y of findings on the association between insomnia diagnosis (IND) and insomnia symptoms (INS) with OB. A total of 67 studies were included in the meta-analyses. Multilevel random effects models showed that the odds of having OB among those who had IND was not significantly greater than the odds of having OB among those who did not have IND (odds ratio (OR) = .80, p = .61). A small, significant cross-sectional correlation (r = .06, p = .03) was found between INS and body mass index. Longitudinal data were limited. Based on three studies, the odds of developing future INS among those who had OB were not significantly greater than those who were normal-weight (NW) (OR = 1.07, p = .40). Longitudinal data on the association between INS and future incidence of OB are inconclusive. We found no indication of systematic publication biases and high heterogeneity in the effect sizes across studies. Meta-regressions showed that some of the heterogeneity was explained by the types of measures of insomnia symptoms, publication year, and regions where a study was conducted.


Subject(s)
Obesity/epidemiology , Sleep Initiation and Maintenance Disorders/epidemiology , Body Mass Index , Humans , Risk Factors
4.
Psychol Sci ; 29(1): 83-94, 2018 01.
Article in English | MEDLINE | ID: mdl-29160742

ABSTRACT

We tested whether affiliating beer brands with universities enhances the incentive salience of those brands for underage drinkers. In Study 1, 128 undergraduates viewed beer cues while event-related potentials (ERPs) were recorded. Results showed that beer cues paired with in-group backgrounds (logos for students' universities) evoked an enhanced P3 ERP component, a neural index of incentive salience. This effect varied according to students' levels of identification with their university, and the amplitude of the P3 response prospectively predicted alcohol use over 1 month. In Study 2 ( N = 104), we used a naturalistic advertisement exposure to experimentally create in-group brand associations and found that this manipulation caused an increase in the incentive salience of the beer brand. These data provide the first evidence that marketing beer via affiliating it with students' universities enhances the incentive salience of the brand for underage students and that this effect has implications for their alcohol involvement.


Subject(s)
Direct-to-Consumer Advertising , Evoked Potentials , Motivation , Students/psychology , Underage Drinking/psychology , Adolescent , Beer , Cues , Electroencephalography , Female , Humans , Male , Universities/economics , Young Adult
5.
Psychophysiology ; 55(5): e13044, 2018 05.
Article in English | MEDLINE | ID: mdl-29226966

ABSTRACT

EEG data, and specifically the ERP, provide psychologists with the power to examine quickly occurring cognitive processes at the native temporal resolution at which they occur. Despite the advantages conferred by ERPs to examine processes at different points in time, ERP researchers commonly ignore the trial-to-trial temporal dimension by collapsing across trials of similar types (i.e., the signal averaging approach) because of constraints imposed by repeated measures ANOVA. Here, we present the advantages of using multilevel modeling (MLM) to examine trial-level data to investigate change in neurocognitive processes across the course of an experiment. Two examples are presented to illustrate the usefulness of this technique. The first demonstrates decreasing differentiation in N170 amplitude to faces of different races across the course of a race categorization task. The second demonstrates attenuation of the ERN as participants commit more errors within a task designed to measure implicit racial bias. Although the examples presented here are within the realm of social psychology, the use of MLM to analyze trial-level EEG data has the potential to contribute to a number of different theoretical domains within psychology.


Subject(s)
Brain/physiology , Evoked Potentials/physiology , Adolescent , Adult , Brain Mapping , Electroencephalography , Female , Humans , Male , Middle Aged , Multilevel Analysis , Reaction Time/physiology , Signal Processing, Computer-Assisted , Young Adult
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