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"Genetic polymorphism"

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"Genetic polymorphism"

Original Articles
Reduction of Continuous Theta Burst Stimulation-Induced Motor Plasticity in Healthy Elderly With COMT Val158Met Polymorphism
Nam Jae Lee, Hyun Jung Ahn, Kwang-Ik Jung, Suk Hoon Ohn, Jeonghoon Hong, Yun Joong Kim, Woo-Kyoung Yoo
Ann Rehabil Med 2014;38(5):658-664.   Published online October 30, 2014
DOI: https://doi.org/10.5535/arm.2014.38.5.658
Objective

To delineate whether cortical plasticity induced by continuous theta burst stimulation (cTBS) differed according to catechol-O-methyltransferase (COMT) gene polymorphism in healthy older adults.

Methods

Eighteen healthy older volunteers (mean age 73.78±5.04; 12 females and 6 males) were recruited. Volunteers randomly assigned in either a sham-first or real cTBS first group participated in two separate TMS visits with at least a 2-day wash-out period. Genotyping was carried out at baseline by a separate researcher who was blinded. cTBS was delivered in a hot spot over M1 at an active motor threshold of 80%. Motor evoked potentials (MEPs) were obtained at 120% of the resting motor threshold before and after sham/cTBS.

Results

The relative MEP to baseline was significantly decreased 0 and 10 minutes post-stimulation and increased 40 minutes post-stimulation, as compared with the sham condition. Immediately after cTBS, the Val/Val group had a significantly reduced relative MEP value, as compared with the MET carrier group.

Conclusion

In healthy older persons, cTBS-induced motor plasticity was reduced in the COMT Val/Val group as compared with the 158Met carrier group.

Citations

Citations to this article as recorded by  
  • Age-related changes in responsiveness to non-invasive brain stimulation neuroplasticity paradigms: A systematic review with meta-analysis
    Mahima Shah, Suraj Suresh, Johanna Paddick, Maddison L. Mellow, Amy Rees, Carolyn Berryman, Tasha R. Stanton, Ashleigh E. Smith
    Clinical Neurophysiology.2024; 162: 53.     CrossRef
  • Assessing the mechanisms of brain plasticity by transcranial magnetic stimulation
    Ali Jannati, Lindsay M. Oberman, Alexander Rotenberg, Alvaro Pascual-Leone
    Neuropsychopharmacology.2023; 48(1): 191.     CrossRef
  • Correlations between COMT polymorphism and brain structure and cognition in elderly subjects
    Eunsil Cha, Hyun Jung Ahn, Wonil Kang, Kwang-Ik Jung, Suk Hoon Ohn, Shahid Bashir, Woo-Kyoung Yoo
    Medicine.2022; 101(18): e29214.     CrossRef
  • Identifying novel biomarkers with TMS-EEG – Methodological possibilities and challenges
    Elisa Kallioniemi, Zafiris J. Daskalakis
    Journal of Neuroscience Methods.2022; 377: 109631.     CrossRef
  • Cortical hyperexcitability and plasticity in Alzheimer’s disease: developments in understanding and management
    Mehdi A. J van den Bos, Parvathi Menon, Steve Vucic
    Expert Review of Neurotherapeutics.2022; 22(11-12): 981.     CrossRef
  • Determining the optimal pulse number for theta burst induced change in cortical excitability
    Daniel M. McCalley, Daniel H. Lench, Jade D. Doolittle, Julia P. Imperatore, Michaela Hoffman, Colleen A. Hanlon
    Scientific Reports.2021;[Epub]     CrossRef
  • Modulation of motor cortical excitability by continuous theta-burst stimulation in adults with autism spectrum disorder
    Ali Jannati, Mary A. Ryan, Gabrielle Block, Fae B. Kayarian, Lindsay M. Oberman, Alexander Rotenberg, Alvaro Pascual-Leone
    Clinical Neurophysiology.2021; 132(7): 1647.     CrossRef
  • Large-scale analysis of interindividual variability in single and paired-pulse TMS data
    Daniel T. Corp, Hannah G.K. Bereznicki, Gillian M. Clark, George J. Youssef, Peter J. Fried, Ali Jannati, Charlotte B. Davies, Joyce Gomes-Osman, Melissa Kirkovski, Natalia Albein-Urios, Paul B. Fitzgerald, Giacomo Koch, Vincenzo Di Lazzaro, Alvaro Pascua
    Clinical Neurophysiology.2021; 132(10): 2639.     CrossRef
  • A Checklist to Reduce Response Variability in Studies Using Transcranial Magnetic Stimulation for Assessment of Corticospinal Excitability: A Systematic Review of the Literature
    Michael Pellegrini, Maryam Zoghi, Shapour Jaberzadeh
    Brain Connectivity.2020; 10(2): 53.     CrossRef
  • Cognitive Enhancement via Neuromodulation and Video Games: Synergistic Effects?
    Marc Palaus, Raquel Viejo-Sobera, Diego Redolar-Ripoll, Elena M. Marrón
    Frontiers in Human Neuroscience.2020;[Epub]     CrossRef
  • Large-scale analysis of interindividual variability in theta-burst stimulation data: Results from the ‘Big TMS Data Collaboration’
    Daniel T. Corp, Hannah G.K. Bereznicki, Gillian M. Clark, George J. Youssef, Peter J. Fried, Ali Jannati, Charlotte B. Davies, Joyce Gomes-Osman, Julie Stamm, Sung Wook Chung, Steven J. Bowe, Nigel C. Rogasch, Paul B. Fitzgerald, Giacomo Koch, Vincenzo Di
    Brain Stimulation.2020; 13(5): 1476.     CrossRef
  • Age-related differences of motor cortex plasticity in adults: A transcranial direct current stimulation study
    Ensiyeh Ghasemian-Shirvan, Leila Farnad, Mohsen Mosayebi-Samani, Stefanie Verstraelen, Raf L.J. Meesen, Min-Fang Kuo, Michael A. Nitsche
    Brain Stimulation.2020; 13(6): 1588.     CrossRef
  • Genetic influences on the variability of response to repetitive transcranial magnetic stimulation in human pharyngeal motor cortex
    Alicja Raginis‐Zborowska, Ivy Cheng, Neil Pendleton, Antony Payton, William Ollier, Emilia Michou, Shaheen Hamdy
    Neurogastroenterology & Motility.2019;[Epub]     CrossRef
  • Variability and Predictors of Response to Continuous Theta Burst Stimulation: A TMS-EEG Study
    Lorenzo Rocchi, Jaime Ibáñez, Alberto Benussi, Ricci Hannah, Vishal Rawji, Elias Casula, John Rothwell
    Frontiers in Neuroscience.2018;[Epub]     CrossRef
  • Interindividual variability in response to continuous theta-burst stimulation in healthy adults
    Ali Jannati, Gabrielle Block, Lindsay M. Oberman, Alexander Rotenberg, Alvaro Pascual-Leone
    Clinical Neurophysiology.2017; 128(11): 2268.     CrossRef
  • Genetic polymorphisms and the adequacy of brain stimulation: state of the art
    Amene Saghazadeh, Shadi A. Esfahani, Nima Rezaei
    Expert Review of Neurotherapeutics.2016; 16(9): 1043.     CrossRef
  • Ten Years of Theta Burst Stimulation in Humans: Established Knowledge, Unknowns and Prospects
    A. Suppa, Y.-Z. Huang, K. Funke, M.C. Ridding, B. Cheeran, V. Di Lazzaro, U. Ziemann, J.C. Rothwell
    Brain Stimulation.2016; 9(3): 323.     CrossRef
  • 6,406 View
  • 55 Download
  • 18 Web of Science
  • 17 Crossref
The Insertion/Deletion Polymorphism of Angiotensin I Converting Enzyme Gene is Associated With Ossification of the Posterior Longitudinal Ligament in the Korean Population
Dong Hwan Kim, Dong Hwan Yun, Hee-Sang Kim, Seong Ki Min, Seung Don Yoo, Kyu Hoon Lee, Ki-Tack Kim, Dae Jean Jo, Su Kang Kim, Joo-Ho Chung, Ju Yeon Ban, Sung Yong Lee
Ann Rehabil Med 2014;38(1):1-5.   Published online February 25, 2014
DOI: https://doi.org/10.5535/arm.2014.38.1.1
Objective

To determine whether ACE insertion/deletion (I/D) polymorphism is associated with the ossification of the posterior longitudinal ligament (OPLL) of the spine in the Korean population.

Methods

A case-control study was conducted to investigate the association between I/D polymorphism of the angiotensin I converting enzyme (peptidyl-dipeptidase A) 1 (ACE) gene and OPLL. The 95 OPLL patients and 274 control subjects were recruited. Polymerase chain reaction for the genotyping of ACE I/D polymorphism was performed. The difference between the OPLL patients and the control subjects was compared using the contingency χ2 test and the logistic regression analysis. For statistical analysis, SPSS, SNPStats, SNPAnalyzer, and Helixtree programs were used.

Results

The genotype and allele frequencies of ACE I/D polymorphism showed significant differences between the OPLL patients and the control subjects (genotype, p<0.001; allele, p=0.009). The frequencies of D/D genotype and D allele in the OPLL group were higher than those in the control group. In logistic regression analysis, ACE I/D polymorphism was associated with OPLL (dominant model; p=0.002; odd ratio, 2.20; 95% confidence interval, 1.33-3.65).

Conclusion

These results suggest that the deletion polymorphism of the ACE gene may be a risk factor for the development of OPLL in the Korean population.

Citations

Citations to this article as recorded by  
  • Evaluation of Genetic and Nongenetic Risk Factors for Degenerative Cervical Myelopathy
    Maksim A. Shlykov, Erica M. Giles, Michael P. Kelly, Shiow J. Lin, Vy T. Pham, Nancy L. Saccone, Elizabeth L. Yanik
    Spine.2023; 48(16): 1117.     CrossRef
  • Genetics of Diffuse Idiopathic Skeletal Hyperostosis and Ossification of the Spinal Ligaments
    Hajime Kato, Demetrios T. Braddock, Nobuaki Ito
    Current Osteoporosis Reports.2023; 21(5): 552.     CrossRef
  • Evidence for a genetic contribution to the ossification of spinal ligaments in Ossification of Posterior Longitudinal Ligament and Diffuse idiopathic skeletal hyperostosis: A narrative review
    Ana Rita Couto, Bruna Parreira, Deborah M. Power, Luís Pinheiro, João Madruga Dias, Irina Novofastovski, Iris Eshed, Piercarlo Sarzi-Puttini, Nicola Pappone, Fabiola Atzeni, Jorrit-Jan Verlaan, Jonneke Kuperus, Amir Bieber, Pasquale Ambrosino, David Kiefe
    Frontiers in Genetics.2022;[Epub]     CrossRef
  • Genetics of Degenerative Cervical Myelopathy: A Systematic Review and Meta-Analysis of Candidate Gene Studies
    Daniel H. Pope, Benjamin M. Davies, Oliver D. Mowforth, A. Ramsay Bowden, Mark R. N. Kotter
    Journal of Clinical Medicine.2020; 9(1): 282.     CrossRef
  • Quantification of Risk Factors for Cervical Ossification of the Posterior Longitudinal Ligament in Korean Populations
    Jaeyong Shin, Ja Young Choi, Yong Wook Kim, Jee Suk Chang, Seo Yeon Yoon
    Spine.2019; 44(16): E957.     CrossRef
  • Genetic polymorphisms in bone morphogenetic protein receptor type IA gene predisposes individuals to ossification of the posterior longitudinal ligament of the cervical spine via the smad signaling pathway
    Hao Wang, Weitao Jin, Haibin Li
    BMC Musculoskeletal Disorders.2018;[Epub]     CrossRef
  • Cohort study of cervical ossification of posterior longitudinal ligament in a Korean populations: Demographics of prevalence, surgical treatment, and disability
    Jaeyong Shin, Yong Wook Kim, Sang Gyu Lee, Eun-Cheol Park, Seo Yeon Yoon
    Clinical Neurology and Neurosurgery.2018; 166: 4.     CrossRef
  • The Pathogenesis of Ossification of the Posterior Longitudinal Ligament
    Liang Yan, Rui Gao, Yang Liu, Baorong He, Shemin Lv, Dingjun Hao
    Aging and disease.2017; 8(5): 570.     CrossRef
  • 6,500 View
  • 53 Download
  • 7 Web of Science
  • 8 Crossref
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