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Reduced gamma-aminobutyric acid is associated with emotional and behavioral problems in Prader-Willi syndrome
Lauren J Rice1,2, Jim Lagopoulos1,3, Michael Brammer4
1Brain and Mind Centre, University of Sydney, Sydney, New South Wales, Australia.
Insights
Individuals with Prader-Willi syndrome (PWS) and significant behavioral issues show lower brain gamma-aminobutyric acid (GABA) levels. Reduced GABA is linked to behavioral problems, suggesting a role for the GABAergic system in PWS pathophysiology.
Area of Science:
- Neuroscience
- Genetics
- Psychiatry
Background:
- Prader-Willi syndrome (PWS) presents with hypotonia, hypogonadism, distinct facial features, and intellectual impairment.
- Severe behavioral disturbances, including hyperphagia, temper outbursts, and compulsive behaviors, are common in PWS.
- These behaviors suggest impaired neural inhibition, potentially implicating gamma-aminobutyric acid (GABA), the primary inhibitory neurotransmitter.
Purpose of the Study:
- To investigate in vivo brain GABA levels in individuals with PWS.
- To explore the relationship between GABA levels and emotional and behavioral disturbances in PWS.
- To determine if GABAergic system alterations contribute to PWS pathophysiology.
Main Methods:
- Single voxel proton magnetic resonance spectroscopy (1H-MRS) was used.
- 15 individuals with PWS and 15 age- and gender-matched controls participated.
- GABA was measured in the parieto-occipital lobe; other metabolites in the anterior cingulate cortex.
Main Results:
- Participants with PWS and significant behavioral problems exhibited lower GABA levels compared to controls and PWS individuals without such problems.
- GABA levels were negatively correlated with total behavioral problem scores, temper outbursts, skin-picking, depression, and social difficulties.
- Alterations in the GABAergic system were observed in individuals with PWS exhibiting behavioral issues.
Conclusions:
- Reduced brain GABA levels are associated with behavioral and emotional disturbances in Prader-Willi syndrome.
- The GABAergic system may play a significant role in the pathophysiology of PWS.
- Findings may offer insights into controlling similar behaviors in the general population.
Abstract:
Prader-Willi syndrome (PWS) is characterized by infantile hypotonia, hypogonadism, small hands and feet, distinct facial features and usually intellectual impairment. The disorder is associated with severe behavioral disturbances which include hyperphagia leading to morbid obesity, temper outbursts, skin-picking, and compulsive behaviors. While the brain mechanisms that underpin these disturbances are unknown these behaviors suggest a lack of inhibition and thus gamma-aminobutyric acid (GABA), the main inhibitory neurotransmitter may be implicated. In the present study, we investigated in vivo brain GABA and its relationship with emotion and behavior in individuals with PWS. Single voxel proton magnetic resonance spectroscopy (1H-MRS) was performed on 15 individuals with PWS and 15 age- and gender-matched typically developing controls. GABA levels were measured in the parieto-occipital lobe. All other metabolite levels (N-acetyl aspartate, myo-Inositol, glutathione, glutamate, and glutamine + glutamate) were measured in the anterior cingulate cortex (ACC). GABA levels were significantly lower in the participants with PWS who had clinically significant emotional and behavioral problems relative to typically developing control participants and participants with PWS who did not have emotional and behavioral problems within the clinically significant range. GABA levels were negatively correlated with total behavioral problem scores as well as temper outbursts, skin-picking, depression, social relating difficulties, and a tendency to be self-absorbed. Our data suggests that alterations of the GABAergic system may play an important role in aspects of the pathophysiology of PWS. Pathological mechanism found in PWS may be relevant to understanding the control of similar behaviors in the general population. © 2016 Wiley Periodicals, Inc.
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