BDNF Levels According to Variations in the CACNA1C Gene: Sex-Based Disparity

• Published in: Cellular and molecular neurobiology 2023, Vol.43 (1), p.357-366
• Main Authors: Bastos, Clarissa Ribeiro, Xavier, Janaina, Camerini, Laísa, Dewes, Samantha Seibt, Moreira, Fernanda Pedrotti, Wiener, Carolina David, Jansen, Karen, Kaster, Manuella Pinto, de Mattos Souza, Luciano Dias, da Silva, Ricardo Azevedo, Oses, Jean Pierre, Portela, Luis Valmor, Lara, Diogo Rizzato, Tovo-Rodrigues, Luciana, Ghisleni, Gabriele
• Format: Article
• Language: English
• Subjects: Biomedical and Life Sciences; Biomedicine; Brain-derived neurotrophic factor; Brain-Derived Neurotrophic Factor - genetics; Calcium channels; Calcium channels (L-type); Calcium channels (voltage-gated); Calcium Channels, L-Type - genetics; Calcium influx; Cell Biology; Channel gating; Cross-Sectional Studies; Female; Fetuses; Genetic Predisposition to Disease; Haplotypes; Humans; Male; Mental disorders; Neurobiology; Neurosciences; Original Research; Polymorphism, Single Nucleotide - genetics; Single-nucleotide polymorphism; Women; Young Adult; Young adults
• ISSN: 0272-4340; 1573-6830
• DOI: 10.1007/s10571-022-01189-5

The CACNA1C gene encodes the pore-forming alpha-1c subunit of L-type voltage-gated calcium channels. The calcium influx through these channels regulates the transcription of the brain-derived neurotrophic factor (BDNF). Polymorphisms in this gene have been consistently associated with psychiatric disorders, and alterations in BDNF levels are a possible biological mechanism to explain such associations. Here, we sought to investigate the effect of the CACNA1C rs1006737 and rs4765913 polymorphisms and their haplotypes on serum BDNF concentration. We further aim to investigate the regulatory function of these SNPs and the ones linked to them. The study enrolled 641 young adults (362 women and 279 men) in a cross-sectional population-based survey. Linear regression was used to test the effects of polymorphisms and haplotypes on BDNF levels adjusted for potential confounders. Moreover, regulatory putative functional roles were assessed using in silico approach. BDNF levels were not associated with CACNA1C polymorphisms/haplotype in the total sample. When the sample was stratified by sex, checking the effect of polymorphisms on men and women separately, the A-allele of rs4765913 was associated with lower BDNF levels in women compared with the TT genotype ( p  = 0.010). The AA (rs1006737–rs4765913) haplotype was associated with BDNF levels in opposite directions regarding sex, with lower levels of BDNF in women ( p  = 0.040) compared to those without this haplotype, while with higher levels in men ( p  = 0.027). These findings were supported by the presence of regulatory marks only on the male fetal brain. Our results suggest that the BDNF levels regulation may be a potential mechanism underpinning the association between CACNA1C and psychiatric disorders, with a differential role in women and men.