4.7 Article

BDNF Val66Met gene polymorphism modulates brain activity following rTMS-induced memory impairment

Journal

SCIENTIFIC REPORTS
Volume 12, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41598-021-04175-x

Keywords

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Funding

  1. European Commission
  2. Innovative Medicine Initiative's (IMI) 'PharmaCog' project
  3. Spanish Ministry of Science, Innovation and Universities (MICIU/FEDER) [RTI2018-095181-B-C21]
  4. ICREA Academia 2019 grant award
  5. Spanish Ministry of Education, Culture and Sport (MECD) [12135072325-79]
  6. Spanish Ministry of Economy and Competitiveness (MINECO/FEDER) [PSI2015-64227-R, BES-2016077620]
  7. H2020 Marie S. Curie ITN-ETN project
  8. Italian Ministry of Health
  9. Sidney R. Baer Jr. Foundation
  10. National Institutes of Health [NIH R01 MH100186, R01 NS073601, R01 HD069776, R21 MH099196, R21 NS082870, R21 NS085491, R21 HD07616]
  11. Harvard Catalyst \ The Harvard Clinical and Translational Science Center (NCRR)
  12. DARPA [HR001117S0030]
  13. Football Players Health Study at Harvard University
  14. Government of Catalonia [2017SGR748]
  15. MICIU/FEDER [RTI2018-095181-B-C21]
  16. Harvard Catalyst \ The Harvard Clinical and Translational Science Center (NCATS NIH) [UL1 RR025758]

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The BDNF Val66Met gene polymorphism influences individual responses to TMS in memory tasks, particularly in Val/Val genotype carriers, who show reduced memory performance with rTMS over the left frontal cortex. This genetic variation is also associated with increased brain activity during memory recognition, specifically in frontal regions, which correlates positively with cognitive performance.
The BDNF Val66Met gene polymorphism is a relevant factor explaining inter-individual differences to TMS responses in studies of the motor system. However, whether this variant also contributes to TMS-induced memory effects, as well as their underlying brain mechanisms, remains unexplored. In this investigation, we applied rTMS during encoding of a visual memory task either over the left frontal cortex (LFC; experimental condition) or the cranial vertex (control condition). Subsequently, individuals underwent a recognition memory phase during a functional MRI acquisition. We included 43 young volunteers and classified them as 19 Met allele carriers and 24 as Val/Val individuals. The results revealed that rTMS delivered over LFC compared to vertex stimulation resulted in reduced memory performance only amongst Val/Val allele carriers. This genetic group also exhibited greater fMRI brain activity during memory recognition, mainly over frontal regions, which was positively associated with cognitive performance. We concluded that BDNF Val66Met gene polymorphism, known to exert a significant effect on neuroplasticity, modulates the impact of rTMS both at the cognitive as well as at the associated brain networks expression levels. This data provides new insights on the brain mechanisms explaining cognitive inter-individual differences to TMS, and may inform future, more individually-tailored rTMS interventions.

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