Reward Deficiency Syndrome (RDS) Surprisingly Is Evolutionary and Found Everywhere: Is It "Blowin' in the Wind"?
Kenneth BlumThomas McLaughlinAbdalla BowirratEdward J ModestinoDavid BaronLuis Llanos GomezMauro CeccantiEric R BravermanPanayotis K ThanosJean-Lud CadetIgor ElmanRajendra D BadgaiyanRehan JalaliRichard GreenThomas A SimpaticoAshim GuptaMark S GoldPublished in: Journal of personalized medicine (2022)
Reward Deficiency Syndrome (RDS) encompasses many mental health disorders, including a wide range of addictions and compulsive and impulsive behaviors. Described as an octopus of behavioral dysfunction, RDS refers to abnormal behavior caused by a breakdown of the cascade of reward in neurotransmission due to genetic and epigenetic influences. The resultant reward neurotransmission deficiencies interfere with the pleasure derived from satisfying powerful human physiological drives. Epigenetic repair may be possible with precision gene-guided therapy using formulations of KB220, a nutraceutical that has demonstrated pro-dopamine regulatory function in animal and human neuroimaging and clinical trials. Recently, large GWAS studies have revealed a significant dopaminergic gene risk polymorphic allele overlap between depressed and schizophrenic cohorts. A large volume of literature has also identified ADHD, PTSD, and spectrum disorders as having the known neurogenetic and psychological underpinnings of RDS. The hypothesis is that the true phenotype is RDS, and behavioral disorders are endophenotypes. Is it logical to wonder if RDS exists everywhere? Although complex, "the answer is blowin' in the wind," and rather than intangible, RDS may be foundational in species evolution and survival, with an array of many neurotransmitters and polymorphic loci influencing behavioral functionality.
Keyphrases
- genome wide
- dna methylation
- mental health
- endothelial cells
- clinical trial
- copy number
- gene expression
- systematic review
- induced pluripotent stem cells
- attention deficit hyperactivity disorder
- pluripotent stem cells
- oxidative stress
- randomized controlled trial
- working memory
- metabolic syndrome
- mass spectrometry
- obsessive compulsive disorder
- depressive symptoms
- social support
- posttraumatic stress disorder
- uric acid
- genome wide association study
- double blind