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Neuropsychiatric Disease and Treatment Volume 14, 2018 - Issue
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Original Research

The role of COMT gene Val108/158Met polymorphism in suicidal behavior: systematic review and updated meta-analysis

Thelma Beatriz González-Castro1 Multidisciplinary Academic Division of Jalpa de Méndez, Juarez Autonomous University of Tabasco, Jalpa de Méndez, Tabasco, Mexico
,
Yazmín Hernández-Díaz1 Multidisciplinary Academic Division of Jalpa de Méndez, Juarez Autonomous University of Tabasco, Jalpa de Méndez, Tabasco, Mexico
,
Isela Esther Juárez-Rojop2 Multidisciplinary Academic Division of Health Sciences, Juarez Autonomous University of Tabasco, Villahermosa, Tabasco, Mexico
,
María Lilia López-Narváez3 General Hospital of Yajalon, Ministry of Health, Yajalon, Chiapas, Mexico
,
Carlos Alfonso Tovilla-Zárate4 Multidisciplinary Academic Division of Comalcalco, Juarez Autonomous University of Tabasco, Comalcalco, Tabasco, Mexico, [email protected]Correspondence[email protected]
,
Julian Ramírez-Bello5 Research Unit, Juárez Hospital of Mexico, Ministry of Health, Mexico City, Mexico
,
Nonanzit Pérez-Hernández6 Department of Molecular Biology, National Institute of Cardiology, Mexico City, Mexico
,
Alma Delia Genis-Mendoza7 Psychiatric Care Services, National Institute of Genomic Medicine (INMEGEN), Health Secretary, Ministry of Health, Mexico City, Mexico
,
Ana Fresan8 Sub-direction of Clinical Research, Children’s Psychiatric Hospital “Dr. Juan N. Navarro”, Mexico City, Mexico
&
Crystell Guadalupe Guzmán-Priego2 Multidisciplinary Academic Division of Health Sciences, Juarez Autonomous University of Tabasco, Villahermosa, Tabasco, Mexico
 show all
Pages 2485-2496 | Published online: 28 Sep 2018

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Juan Angel Garcia-Quiñones, Celia Nohemí Sánchez-Domínguez, María Fernanda Serna-Rodríguez, Iván Alberto Marino-Martínez, Ana María Rivas-Estilla & Antonio Alí Pérez-Maya. (2023) Genetic Variants Associated with Suicide Risk in the Mexican Population: A Systematic Literature Review. Archives of Suicide Research 0:0, pages 1-19.
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Martina Focardi, Barbara Gualco, Vilma Pinchi, Norelli Gian-Aristide, Regina Rensi, Elisabetta Pelo, Ilaria Carboni & Ugo Ricci. (2022) Genetic analysis of suicide: a sample study in Tuscany (Central Italy). Forensic Sciences Research 7:4, pages 790-797.
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Selin Kurnaz, Ahmet Bulent Yazici, Ayse Feyda Nursal, Pinar Cetinay Aydin, Ayca Ongel Atar, Nazan Aydin, Zeliha Kincir & Sacide Pehlivan. (2019) CNR2 rs2229579 and COMT Val158Met variants, but not CNR2 rs2501432, IL-17 rs763780 and UCP2 rs659366, contribute to susceptibility to substance use disorder in the Turkish population. Psychiatry and Clinical Psychopharmacology 29:4, pages 847-853.
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Articles from other publishers (6)

Matthew T. Tull, Margaret M. Baer, Tara L. Spitzen, Aaron A. Lee, Eric J. Vallender, Michael R. Garrett, Michael D. Anestis & Kim L. Gratz. (2021) The roles of borderline personality disorder symptoms and dispositional capability for suicide in suicidal ideation and suicide attempts: Examination of the COMT Val158Met polymorphism. Psychiatry Research 302, pages 114011.
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Jiaojiao Li, Chunxiao Sun, Wenwen Cai, Jing Li, Barry P. Rosen & Jian Chen. (2021) Insights into S-adenosyl-l-methionine (SAM)-dependent methyltransferase related diseases and genetic polymorphisms. Mutation Research/Reviews in Mutation Research 788, pages 108396.
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Ekaterina Rafikova, Maria Shadrina, Peter Slominsky, Alla Guekht, Alexey Ryskov, Dmitry Shibalev & Vasiliy Vasilyev. (2021) SLC6A3 (DAT1) as a Novel Candidate Biomarker Gene for Suicidal Behavior. Genes 12:6, pages 861.
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Shirley Y. Hill, Bobby L. Jones & Gretchen L. Haas. (2020) Suicidal ideation and aggression in childhood, genetic variation and young adult depression. Journal of Affective Disorders 276, pages 954-962.
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Zhen Tang, Shumin Zhang, Dongmei Guo & Hanyan Wang. (2020) Association between COMT gene Val108/158Met and antidepressive treatment response: A meta-analysis. Gene 734, pages 144333.
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Kathryn T Hall, Joseph Loscalzo & Ted J Kaptchuk. (2019) Systems pharmacogenomics – gene, disease, drug and placebo interactions: a case study in COMT. Pharmacogenomics 20:7, pages 529-551.
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