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Broad Street Scientific Journal 2020

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emotional one-back task, the influence of the emotional

valence (i.e. whether a stimulus is neutral or negative) on

WM can be calculated.

The influence of emotion on cognition is an essential

topic to research, but research on this topic has received

less attention than others in schizophrenia literature. In

controls, it has been shown that emotional stimuli can

garner more attention than neutral stimuli. This extra attention

may facilitate the processing of emotional stimuli.

In patients with schizophrenia, there may be reduced activation

and worsened performance due to the addition

of emotional valence to the WM task. DLPFC has an important

role in the integration of emotional and cognitive

information [7]. Studies of negative valence and cognition

tend to produce more robust results due to the arousing

nature of the images used. Other studies [4] also explore

the interaction between EP and WM, but only with control

and schizophrenia patient groups. By including HR

participants, which have been found to show similar

working memory deficits as those with schizophrenia [2],

in our study of the interaction of WM and EP, we address a

new set of questions in how high-risk participants perform

compared to controls and RO and if they exhibit deficits

similar to RO participants.

The overarching goal of this study is to identify how

WM and emotional processes interact, particularly in the

context of schizophrenia. In order to achieve this aim, we

administered an emotional n-back task to 76 participants

(35 control, 20 HR, 21 RO) to determine group differences

in regional activation and WM performance associated

with psychotic illness. We hypothesized that RO participants

would perform consistently across neutral and negative

conditions (because emotional blunting may result in

less expressed performance differences between valences),

while control participants would have more impaired performance

in the negative condition compared to the neutral

condition. Moreover, we hypothesized that changes in

performance between conditions will differ between subject

groups. When looking at brain activation, we hypothesized

that the control participants would exhibit a greater

change in ventral regions when comparing between the

neutral and negative conditions and that control participants

would have a greater change in activation in WM

regions between neutral to negative. We also hypothesized

that genetic high-risk participants would exhibit brain activation

and task performance intermediate between CON

and RO. Finally, we investigated links between activation

and behavior to see if changes in activation correlated with

changes in task performance.

2. Methods

2.1 – Participants

Twenty-one patients with recent-onset schizophrenia

and twenty genetic high-risk patients were recruited from

the UNC Healthcare System. Thirty-five healthy control

subjects were also included. All participants provided

written consent to the study approved by the University

of North Carolina- Chapel Hill IRB. All participants were

between the ages of 16-45, of any ethnicities or gender,

had no presence of metallic implants or devices interfering

with MRI, and were not pregnant. Inclusion criteria for

recent-onset schizophrenia (RO) patients were: (1) Meet

DSM-IV criteria for SZ or schizophreniform disorder, (2)

No history of major central nervous system disorder or intellectual

disability (IQ<65), (3) Must have illness for <5

years, (4) No current diagnosis of substance dependence,

and no substance abuse for 6 weeks. RO patients were also

instructed to refrain from taking benzodiazepine medications

on the morning of testing but instead to bring their

medication with them to take after scanning. Inclusion

criteria for genetic high risk (HR) patients were: (1) Must

have first degree relative with psychotic disorder, (2) Must

not meet DSM-IV criteria for past or current Axis I psychotic

disorder on bipolar affective disorder, (3) No history

of major central nervous system disorder or intellectual

disability (IQ<65), (4) No current treatment with antipsychotic

medication. Healthy controls (CON) were excluded

if they had history of a DSM-IV axis I psychiatric disorder,

family history of psychosis, history of current substance

abuse/dependence, history or current medical illness that

could affect brain morphology, or clinically significant

neurological or medical problems that could influence the

diagnosis or the assessment of the biological variables in

the study. All participants gave written informed consent

consistent with the IRB of UNC if over 18 or assent and

parent/guardian provided consent for minors prior to

their participation in the study.

2.2 – Emotional One-back Task and Procedure

Each participant completed an emotional one-back task

with an auditory component during a functional magnetic

imaging (fMRI) session with 8 runs. The emotional oneback

task consists of a visual tracking task, using images

with either Positive, Neutral, or Negative valence, as defined

by the International Affective Picture System (IAPS)

[8]. Further analysis was performed with only Neutral and

Negative Valences. Patients with schizophrenia report

feeling negative emotion strongly but are less outwardly

expressive of this negative emotion [9]. By focusing on the

Negative valence, we want to observe if RO exhibit similar

activation to CON during negative emotional situations,

as the contexts in which RO patients experience negative

emotion is different than those without SZ. All images in

the run were of the same valence, and subjects were asked

to press a button when they saw the same image two times

in a row (Fig. 1). A control condition with no n-back

task was also included. The auditory component, which

occurred simultaneously with the visual component, involved

subjects hearing irrelevant standard and pitch devi-

26 | 2019-2020 | Broad Street Scientific BIOLOGY

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