scholarly journals Elevated reward-related neural activation as a unique biological marker of bipolar disorder: Assessment and treatment implications

2014 ◽  
Vol 62 ◽  
pp. 74-87 ◽  
Author(s):  
Robin Nusslock ◽  
Christina B. Young ◽  
Katherine S.F. Damme
Author(s):  
Robin Nusslock ◽  
James Glazer ◽  
Tommy H. Ng ◽  
Madison K. Titone ◽  
Lauren B. Alloy

The behavioral approach system (BAS)/reward hypersensitivity model of bipolar disorder proposes that risk for bipolar disorder, in particular hypo/manic episodes, is characterized by a hypersensitivity to goal- and reward-relevant cues. This hypersensitivity can lead to an excessive increase in approach-related affect and motivation to positive or rewarding life events, which, in the extreme, is reflected in hypo/manic symptoms. By contrast, multiple other psychiatric disorders, including major depressive disorder, attention deficit hyperactivity disorder, schizophrenia, and anxiety, appear to be characterized by reduced or unaffected reward processing. This suggests that elevated reward processing may be unique to bipolar disorder and thus important for understanding the differential risk for bipolar symptoms and the pathophysiology of hypo/manic episodes. The objective of the present chapter is four-fold. First, the literature on reward processing and reward-related neural activation in bipolar disorder is reviewed, in particular risk for hypomania/mania. Second, it is proposed that reward-related neural activation reflects a unique biological marker of risk for bipolar disorder that may help facilitate psychiatric assessment and differential diagnosis. Third, the pharmacological and psychosocial treatment implications of research on reward-processing and reward-related neural activation in bipolar disorder are addressed. Finally, new and novel directions of research on reward processing in bipolar disorder are discussed, including an integrated reward and circadian rhythm dysregulation model of bipolar symptoms and our neuroimmune network hypothesis of abnormalities in reward processing across mood-related disorders.


2017 ◽  
Vol 81 (10) ◽  
pp. S353-S354
Author(s):  
Isabelle Bauer ◽  
Nithya Ramakrishnan ◽  
Stefan Ursu ◽  
Kirti Saxena ◽  
Giovana Zunta-Soares ◽  
...  

2018 ◽  
Vol 9 ◽  
Author(s):  
Xue Han ◽  
Xiaowu Liu ◽  
Linling Li ◽  
Bo Xie ◽  
Beifang Fan ◽  
...  

2009 ◽  
Vol 24 (S1) ◽  
pp. 1-1
Author(s):  
F. Pompei ◽  
M. Haldane ◽  
M. Kempton ◽  
J. Jogia ◽  
P. Girardi ◽  
...  

Aims:To examine potential similarities in neural activation during the STROOP colour word test (SCWT) in patients with Bipolar Disorder (BD) and their unaffected first degree relatives of BD patients as an expression of genetic predisposition.Methods:39 remitted BD patients were compared to 46 of their healthy relatives and to 42 controls. fMRI data were collected on a 1.5 T GE Signa MR system using a blocked periodic design and analysed in SPM5.Results:There was no statistically significant group difference in the behavioural performance. At the corrected cluster level threshold of p< 0.001 controls showed more activation than:a.BD patients in the caudate, the inferior (BA 47), middle and superior frontal gyri (BA 8, 6, 46), the parietal cortices (BA 7, 40), the precuneus and occipital cortices (BA 7, 19).b.Relatives in the caudate and cingulate cortex (BA 24, 31!). No other contrasts were significant.Conclusion:These findings suggest that changes in neural activation during response inhibition may reflect genetic predisposition to BD.


2012 ◽  
Vol 2 (7) ◽  
pp. e130-e130 ◽  
Author(s):  
H C Whalley ◽  
M Papmeyer ◽  
E Sprooten ◽  
L Romaniuk ◽  
D H Blackwood ◽  
...  

1997 ◽  
Vol 12 (1) ◽  
pp. 11-15 ◽  
Author(s):  
E Vieta ◽  
C Gastó ◽  
MJ Martínez de Osaba ◽  
A Otero ◽  
E Nieto ◽  
...  

SummaryCortisol-binding globulin (CBG) is an alpha-1-glycoprotein with high affinity for cortiso that could be a potential biological marker of chronic stress, according to several previous studies. In order to examine CBG concentrations in bipolar disorder, we determined serum CBG levels by radioimmunoassay with monoclonal antibodies in a sample of 39 RDC bipolar I patients in remission and 21 healthy age-, sex- and weight-matched control subjects. Only lithium treatment was permitted. Plasma cortisol and serum lithium levels were also determined. Bipolar males showed statistically significant lower serum CBG levels than controls, whereas women showed very similar values. No correlation was found between CBG levels and cortisol or lithium concentrations. It is concluded that CBG levels are affected by chronic affective illness, even during remission periods, at least in bipolar males.


2020 ◽  
Author(s):  
Olav Nielssen ◽  
Lauren Staples ◽  
Eyal Karin ◽  
Rony Kayrouz ◽  
Blake Dear ◽  
...  

Abstract BackgroundMindSpot is a national digital mental health service providing free assessment and treatment for anxiety and depression. Mindspot services have been accessed by people with a broad range of psychiatric conditions, including people who report a diagnosis of bipolar disorder (BD). There is comparatively little research reporting the outcome of internet delivered cognitive behaviour therapy (iCBT) for the depressed phase of BD (BDd), including as part of routine care. MethodDemographic characteristics, baseline scores and treatment outcomes were examined for patients who reported taking Lithium and had entries in their clinic records confirming the diagnosis of BD. Results were compared to the clinic benchmarks. Outcomes were completion rates, patient satisfaction and changes in measures of psychological distress, depression and anxiety as measured by the Kessler-10 item (K-10), Patient Health Questionnaire 9 Item (PHQ-9), and Generalized Anxiety Disorder Scale 7 Item (GAD-7), respectively. ResultsA total of 21,745 people completed a MindSpot assessment between January 2013 and December 2019 and enrolled in a MindSpot treatment course. Of these, 124 reported that they were currently taking Lithium, of whom 83 had entries in their clinic records confirming a diagnosis of BD. Mean age of patients with confirmed BD was 43.8 years, compared to the clinic mean of 39.8 years. Their baseline symptom scores were higher than the benchmark. However, reductions in symptoms on the K-10, PHQ-9, and GAD-7 were large (effect sizes > 1.0 on all measures, percentage change between 32.4% and 40%), and lesson completion and satisfaction with the course were also high. ConclusionsMindSpot treatments were effective in treating anxiety and depression in people diagnosed with BD, and the outcomes were comparable to clinic benchmarks. Results suggest that the routine provision of iCBT can help overcome the under-use of evidence based psychological treatments of people with BDd.


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