The CACNA1C risk allele rs1006737 is associated with age-related prefrontal cortical thinning in bipolar I disorder

• Published in: Translational psychiatry 2017-04, Vol.7 (4), p.e1086-e1086
• Main Authors: Soeiro-de-Souza, M G, Lafer, B, Moreno, R A, Nery, F G, Chile, T, Chaim, K, da Costa Leite, C, Machado-Vieira, R, Otaduy, M C G, Vallada, H
• Format: Article
• Language: English
• Subjects: 692/53/2423; Adolescent; Adult; Age Factors; Alleles; Behavioral Sciences; Biological Psychology; Bipolar Disorder - diagnostic imaging; Bipolar Disorder - genetics; Bipolar Disorder - pathology; Calcium Channels, L-Type - genetics; Dominance, Cerebral - genetics; Dominance, Cerebral - physiology; Female; Genetic Carrier Screening; Genetic Predisposition to Disease - genetics; Humans; Imaging, Three-Dimensional; Magnetic Resonance Imaging; Male; Medicin och hälsovetenskap; Medicine; Medicine & Public Health; Neurosciences; Original; original-article; Pharmacotherapy; Polymorphism, Genetic - genetics; Prefrontal Cortex - diagnostic imaging; Prefrontal Cortex - pathology; Psychiatry; Statistics as Topic; Young Adult
• ISSN: 2158-3188; 2158-3188
• DOI: 10.1038/tp.2017.57

Calcium channels control the inflow of calcium ions into cells and are involved in diverse cellular functions. The CACNA1C gene polymorphism rs1006737 A allele has been strongly associated with increased risk for bipolar disorder (BD) and with modulation of brain morphology. The medial prefrontal cortex (mPFC) has been widely associated with mood regulation in BD, but the role of this CACNA1C polymorphism in mPFC morphology and brain aging has yet to be elucidated. One hundred seventeen euthymic BD type I subjects were genotyped for CACNA1C rs1006737 and underwent 3 T three-dimensional structural magnetic resonance imaging scans to determine cortical thickness of mPFC components (superior frontal cortex (sFC), medial orbitofrontal cortex (mOFC), caudal anterior cingulate cortex (cACC) and rostral anterior cingulate cortex (rACC)). Carriers of the CACNA1C allele A exhibited greater left mOFC thickness compared to non-carriers. Moreover, CACNA1C A carriers showed age-related cortical thinning of the left cACC, whereas among A non-carriers there was not an effect of age on left cACC cortical thinning. In the sFC, mOFC and rACC (left or right), a negative correlation was observed between age and cortical thickness, regardless of CACNA1C rs1006737 A status. Further studies investigating the direct link between cortical thickness, calcium channel function, apoptosis mechanism and their underlying relationship with aging-associated cognitive decline in BD are warranted.