Abstract

Bipolar disorder (BPD) is a mood disorder, which is characterized by alternating affective states, namely (hypo)mania, depression, and euthymia. Evidence is growing that BPD has indeed a biologic substrate characterized by chronic inflammation, oxidative stress, and disturbed energy metabolism. Apart from this, there is obviously a hereditary component of this disease with multi-genetic factors. Most probably a susceptibility threshold favors the outbreak of clinical disease after a cascade of stress events that remain to be elucidated in more detail. Evidence is also growing that weak points in brain energy metabolism contribute to outbreak and severity of BPD. Conventional psychopharmacologic therapy must be reassessed under the aspects of weight cycling and development of central obesity as a deterioration factor for a worse clinical course leading to early cardiovascular events in BPD subgroups.

Highlights

  • Frontiers in NutritionBipolar disorder (BPD) is a mood disorder, which is characterized by alternating affective states, namely (hypo)mania, depression, and euthymia

  • Bipolar disorder (BD) is a mood disease, which is characterized by alternating affective states between the poles of euphoria or dysphoria, euthymia, and depression [1, 2]

  • In the “BIPFAT study” we found significantly reduced total antioxidative capacity (TAC) and lipid oxidation [Malondialdehyde (MDA)] in fasting blood of euthymic patients with BD compared to controls

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Summary

Frontiers in Nutrition

Bipolar disorder (BPD) is a mood disorder, which is characterized by alternating affective states, namely (hypo)mania, depression, and euthymia. Evidence is growing that BPD has a biologic substrate characterized by chronic inflammation, oxidative stress, and disturbed energy metabolism. Apart from this, there is obviously a hereditary component of this disease with multi-genetic factors. Most probably a susceptibility threshold favors the outbreak of clinical disease after a cascade of stress events that remain to be elucidated in more detail. Evidence is growing that weak points in brain energy metabolism contribute to outbreak and severity of BPD. Conventional psychopharmacologic therapy must be reassessed under the aspects of weight cycling and development of central obesity as a deterioration factor for a worse clinical course leading to early cardiovascular events in BPD subgroups

INTRODUCTION
Weight Gain as Psychopharmacological Side Effect
Obesity as a Trait Marker for BD Itself
Nutrition and Microbiome
The Influence of Obesity on Course of BD and Cognitive Function
Chronic Inflammation and KYN Pathways
Obesity and Circadian Rhythms
The Effect of Weight Management on Therapeutic Success in BD
Findings
CONCLUSIONS
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