Abstract:Obesity is a growing health concern, as it increases risk for heart disease, hypertension, type 2 diabetes, cancer, COVID-19 related hospitalizations and mortality. However, current weight loss therapies are often associated with psychiatric or cardiovascular side effects or poor tolerability that limit their long-term use. The hypothalamic neuropeptide, oxytocin (OT), mediates a wide range of physiologic actions, which include reproductive behavior, formation of prosocial behaviors and control of body weight.… Show more
“…Previous studies suggest that OXT may have anti-depressant, anxiolytic and appetite suppressing effects [12][13][14][15][16]42]. Also, available data suggest that rs2254298 G/ A and rs53576 A/A alleles may be related with neuroticism and various psychopathologies [12][13][14][15][16]. Partially supporting those results, we found that OXT levels were signi cantly reduced among obese youth while rs53576 G/ G allele was signi cantly elevated and rs2254298 allele displayed no signi cant difference.…”
Section: Discussionsupporting
confidence: 86%
“…The rs53576 and rs2254298 polymorphisms in oxytocin receptor may be especially important in this regard [14]. Previous studies suggest that OXT may have anti-depressant, anxiolytic and appetite suppressing effects [12][13][14][15][16]42]. Also, available data suggest that rs2254298 G/ A and rs53576 A/A alleles may be related with neuroticism and various psychopathologies [12][13][14][15][16].…”
Section: Discussionmentioning
confidence: 99%
“…Oxytocin (OXT) is a hypothalamic neuropeptide mediating reproduction, prosocial behaviors, and control of body weight [12,13]. It may reduce both food intake and energy expenditure and is being investigated as a potential anti-obesity agent [12,13].…”
Section: Introductionmentioning
confidence: 99%
“…Oxytocin (OXT) is a hypothalamic neuropeptide mediating reproduction, prosocial behaviors, and control of body weight [12,13]. It may reduce both food intake and energy expenditure and is being investigated as a potential anti-obesity agent [12,13]. Variations in oxytocin levels and polymorphisms of its receptors have been linked with stress, stress-related psychopathology, anxiety, depression and eating disorders [14][15][16].…”
Objectives
We aimed to investigate the relation of oxytocin receptor (OXTR) gene variants (rs53576 and rs2254298) and serum oxytocin (OXT) levels with psychiatric symptoms in healthy Turkish adolescents and matched adolescents with obesity.
Methods
A total of 250 adolescents with obesity and age and gender-matched 250 healthy adolescents were included in this study. Attachment properties, anxiety, and depression were evaluated with self-reports while diagnoses were ascertained with KIDDIE-SADS-PL Turkish version. Serum OXT level was studied with the ELISA method, OXTR gene variants were studied by quantitative polymerase chain reaction(rs53576) and restriction fragment length polymorphism (RFLP) (rs2254298) methods.
Results
Serum OXT level was significantly lower in adolescents with obesity than in healthy controls. Self-reported symptoms of anxiety and depression were significantly elevated, especially for female adolescents with obesity while parent/ peer attachment was significantly lower. rs53576 A/A genotype was found to be significantly higher amog obese youth. 29.2% of obese youth were diagnosed with psychopathology, especially anxiety and depression. OXT levels and receptor polymorphisms were not related with self-reported symptoms, attachment and presence of psychopathology.
Conclusions
Further studies should evaluate the roles of other constructs (e.g., early adversity, parenting, social supports, coping, temperament etc.) and discern the roles of parent-child synchrony in elucidating relationships between OXT, pediatric obesity and psychopathology.
“…Previous studies suggest that OXT may have anti-depressant, anxiolytic and appetite suppressing effects [12][13][14][15][16]42]. Also, available data suggest that rs2254298 G/ A and rs53576 A/A alleles may be related with neuroticism and various psychopathologies [12][13][14][15][16]. Partially supporting those results, we found that OXT levels were signi cantly reduced among obese youth while rs53576 G/ G allele was signi cantly elevated and rs2254298 allele displayed no signi cant difference.…”
Section: Discussionsupporting
confidence: 86%
“…The rs53576 and rs2254298 polymorphisms in oxytocin receptor may be especially important in this regard [14]. Previous studies suggest that OXT may have anti-depressant, anxiolytic and appetite suppressing effects [12][13][14][15][16]42]. Also, available data suggest that rs2254298 G/ A and rs53576 A/A alleles may be related with neuroticism and various psychopathologies [12][13][14][15][16].…”
Section: Discussionmentioning
confidence: 99%
“…Oxytocin (OXT) is a hypothalamic neuropeptide mediating reproduction, prosocial behaviors, and control of body weight [12,13]. It may reduce both food intake and energy expenditure and is being investigated as a potential anti-obesity agent [12,13].…”
Section: Introductionmentioning
confidence: 99%
“…Oxytocin (OXT) is a hypothalamic neuropeptide mediating reproduction, prosocial behaviors, and control of body weight [12,13]. It may reduce both food intake and energy expenditure and is being investigated as a potential anti-obesity agent [12,13]. Variations in oxytocin levels and polymorphisms of its receptors have been linked with stress, stress-related psychopathology, anxiety, depression and eating disorders [14][15][16].…”
Objectives
We aimed to investigate the relation of oxytocin receptor (OXTR) gene variants (rs53576 and rs2254298) and serum oxytocin (OXT) levels with psychiatric symptoms in healthy Turkish adolescents and matched adolescents with obesity.
Methods
A total of 250 adolescents with obesity and age and gender-matched 250 healthy adolescents were included in this study. Attachment properties, anxiety, and depression were evaluated with self-reports while diagnoses were ascertained with KIDDIE-SADS-PL Turkish version. Serum OXT level was studied with the ELISA method, OXTR gene variants were studied by quantitative polymerase chain reaction(rs53576) and restriction fragment length polymorphism (RFLP) (rs2254298) methods.
Results
Serum OXT level was significantly lower in adolescents with obesity than in healthy controls. Self-reported symptoms of anxiety and depression were significantly elevated, especially for female adolescents with obesity while parent/ peer attachment was significantly lower. rs53576 A/A genotype was found to be significantly higher amog obese youth. 29.2% of obese youth were diagnosed with psychopathology, especially anxiety and depression. OXT levels and receptor polymorphisms were not related with self-reported symptoms, attachment and presence of psychopathology.
Conclusions
Further studies should evaluate the roles of other constructs (e.g., early adversity, parenting, social supports, coping, temperament etc.) and discern the roles of parent-child synchrony in elucidating relationships between OXT, pediatric obesity and psychopathology.
“…Importantly, a hybrid intervention with OXT and psychotherapy has been shown to have a potent effect on PTSD severity ( Flanagan et al, 2018 ), though these effects reportedly vary across the sexes ( Frijling et al, 2015 ). Likewise, OXT, being anorectic, functions as a “nutrient status sensor” ( McCormack et al, 2020 , p. 122), and is found to reduce obesity across humans, rodents, and non-human primates ( Niu et al, 2021 ), through its effect on consumptive behaviors by simultaneously regulating cognitive control as well as food reward processing ( Spetter et al, 2018 ). Importantly, increased OXT signaling and secretion are known to regulate both energy intake and energy expenditure which result in weight loss by its effect on fat mass loss (as opposed to lean mass loss) ( McCormack et al, 2020 ).…”
The co-occurrence of stress-induced posttraumatic stress disorder (PTSD) and obesity is common, particularly among military personnel but the link between these conditions is unclear. Individuals with comorbid PTSD and obesity manifest other physical and psychological problems, which significantly diminish their quality of life. Current understanding of the pathways connecting stress to PTSD and obesity is focused largely on behavioral mediators alone with little consideration of the biological regulatory mechanisms that underlie their co-occurrence. In this work, we leverage prior knowledge to systematically highlight such bio-behavioral mechanisms and inform on the design of confirmatory pilot studies. We use natural language processing (NLP) to extract documented regulatory interactions involved in the metabolic response to stress and its impact on obesity and PTSD from over 8 million peer-reviewed papers. The resulting network describes the propagation of stress to PTSD and obesity through 34 metabolic mediators using 302 documented regulatory interactions supported by over 10,000 citations. Stress jointly affected both conditions through 21 distinct pathways involving only two intermediate metabolic mediators out of a total of 76 available paths through this network. Moreover, oxytocin (OXT), Neuropeptide-Y (NPY), and cortisol supported an almost direct propagation of stress to PTSD and obesity with different net effects. Although stress upregulated both NPY and cortisol, the downstream effects of both markers are reported to relieve PTSD severity but exacerbate obesity. The stress-mediated release of oxytocin, however, was found to concurrently downregulate the severity of both conditions. These findings highlight how a network-informed approach that leverages prior knowledge might be used effectively in identifying key mediators like OXT though experimental verification of signal transmission dynamics through each path will be needed to determine the actual likelihood and extent of each marker’s participation.
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