cortistatin-14 and Feeding-and-Eating-Disorders

Copy number variations (CNV) have become an important source of human genome variability noteworthy to consider when studying genetic susceptibility to complex diseases. As recent studies have found evidences for the potential involvement of CNVs in psychiatric disorders, we have studied the dosage effect of structural genome variants as a possible susceptibility factor for different psychiatric disorders in a candidate gene approach.. After selection of 68 psychiatric disorders' candidate genes overlapping with CNVs, MLPA assays were designed to determine changes in copy number of these genes. The studied sample consisted of 724 patients with psychiatric disorders (accounting for anxiety disorders, mood disorders, eating disorders and schizophrenia) and 341 control individuals.. CNVs were detected in 30 out of the 68 genes screened, indicating that a considerable proportion of neuronal pathways genes contain CNVs. When testing the overall burden of rare structural genomic variants in the different psychiatric disorders compared to control individuals, there was no statistically significant difference in the total amount of gains and losses. However, 14 out of the 30 changes were only found in psychiatric disorder patients but not in control individuals. These genes include GRM7, previously associated to major depression disorder and bipolar disorder, SLC6A13, in anxiety disorders, and S100B, SSTR5 and COMT in schizophrenia.. Although we have not been able to found a clear association between the studied CNVs and psychiatric disorders, the rare variants found only within the patients could account for a step further towards understanding the pathophysiology of psychiatric disorders.

Topics: Adult; Aged; Anxiety Disorders; Bipolar Disorder; Catechol O-Methyltransferase; Diagnostic and Statistical Manual of Mental Disorders; DNA Copy Number Variations; Feeding and Eating Disorders; Female; GABA Plasma Membrane Transport Proteins; Genetic Predisposition to Disease; Genome, Human; Humans; Male; Mental Disorders; Middle Aged; Mood Disorders; Nerve Growth Factors; Neural Pathways; Neuropeptides; Polymerase Chain Reaction; Receptors, Metabotropic Glutamate; Receptors, Somatostatin; S100 Calcium Binding Protein beta Subunit; S100 Proteins; Schizophrenia