A Systematic Review of Genetic Polymorphisms Associated with Bipolar Disorder Comorbid to Substance Abuse

被引:4
作者
de Marco, Adriano [1 ]
Scozia, Gabriele [1 ,2 ]
Manfredi, Lucia [1 ]
Conversi, David [1 ]
机构
[1] Univ Roma La Sapienza, Dept Psychol, I-00185 Rome, Italy
[2] Univ Roma La Sapienza, PhD Program Behav Neurosci, I-00185 Rome, Italy
关键词
bipolar disorder; substance use disorder; polymorphisms; GENOME-WIDE ASSOCIATION; ALCOHOL DEPENDENCE; PSYCHIATRIC-DISORDERS; EUROPEAN-AMERICANS; MAJOR DEPRESSION; I DISORDER; ANK3; SUSCEPTIBILITY; RISK; LOCI;
D O I
10.3390/genes13081303
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
It is currently unknown which genetic polymorphisms are involved in substance use disorder (SUD) comorbid with bipolar disorder (BD). The research on polymorphisms in BD comorbid with SUD (BD + SUD) is summarized in this systematic review. We looked for case-control studies that genetically compared adults and adolescents with BD and SUD, healthy controls, and BD without SUD. PRISMA was used to create our protocol, which is PROSPERO-registered (identification: CRD4221270818). The following bibliographic databases were searched indefinitely until December 2021 to identify potentially relevant articles: PubMed, PsycINFO, Scopus, and Web of Science. This systematic review, after the qualitative analysis of the study selection, included 17 eligible articles. In the selected studies, 66 polymorphisms in 29 genes were investigated. The present work delivers a group of potentially valuable genetic polymorphisms associated with BD + SUD: rs11600996 (ARNTL), rs228642/rs228682/rs2640909 (PER3), PONQ192R (PON1), rs945032 (BDKRB2), rs1131339 (NR4A3), and rs6971 (TSPO). It is important to note that none of those findings have been confirmed by two or more studies; thus, we believe that all the polymorphisms identified in this review require additional evidence to be confirmed.
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共 74 条
[1]  
APA, 1980, Diagnostic and statistical manual of mental disorders
[2]   Clock genes polymorphisms in male bipolar patients with comorbid alcohol abuse [J].
Banach, Ewa ;
Pawlak, Joanna ;
Kapelski, Pawel ;
Szczepankiewicz, Aleksandra ;
Rajewska-Rager, Aleksandra ;
Skibinska, Maria ;
Czerski, Piotr ;
Twarowska-Hauser, Joanna ;
Dmitrzak-Weglarz, Monika .
JOURNAL OF AFFECTIVE DISORDERS, 2018, 241 :142-146
[3]   Paraoxonase 1 status and interactions between Q192R functional genotypes by smoking contribute significantly to total plasma radical trapping antioxidant potential [J].
Bortolasci, Chiara Cristina ;
Maes, Michael ;
Vargas, Heber Odebrecht ;
Souza-Nogueira, Andre ;
Moreira, Estefania Gastaldello ;
Vargas Nunes, Sandra Odebrecht ;
Berk, Michael ;
Dodd, Seetal ;
Barbosa, Decio Sabbatini .
NEUROSCIENCE LETTERS, 2014, 581 :46-51
[4]   Lowered plasma paraoxonase (PON)1 activity is a trait marker of major depression and PON1 Q192R gene polymorphism-smoking interactions differentially predict the odds of major depression and bipolar disorder [J].
Bortolasci, Chiara Cristina ;
Vargas, Heber Odebrecht ;
Souza-Nogueira, Andre ;
Barbosa, Decio Sabbatini ;
Moreira, Estefania Gastaldello ;
Vargas Nunes, Sandra Odebrecht ;
Berk, Michael ;
Dodd, Seetal ;
Maes, Michael .
JOURNAL OF AFFECTIVE DISORDERS, 2014, 159 :23-30
[5]   Genome-wide association meta-analysis of cocaine dependence: Shared genetics with comorbid conditions [J].
Cabana-Dominguez, Judit ;
Shivalikanjli, Anu ;
Fernandez-Castillo, Noelia ;
Gormand, Bru .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2019, 94
[6]   Comorbid alcohol dependence disorder may be related to aldehyde dehydrogenase 2 (ALDH2) and alcohol dehydrogenase 1B (ADH1B) in bipolar II disorder, but only to ALDH2 in bipolar I disorder, in Han Chinese [J].
Chang, Yun-Hsuan ;
Lee, Sheng-Yu ;
Wang, Tzu-Yun ;
Chen, Shiou-Lan ;
Tzeng, Nian-Sheng ;
Chen, Po See ;
Lee, I. Hui ;
Chen, Kao Chin ;
Huang, San-Yuan ;
Yang, Yen Kuang ;
Ko, Hui-Chen ;
Lu, Ru-Band .
BIPOLAR DISORDERS, 2015, 17 (05) :536-542
[7]   Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder [J].
Chen, D. T. ;
Jiang, X. ;
Akula, N. ;
Shugart, Y. Y. ;
Wendland, J. R. ;
Steele, C. J. M. ;
Kassem, L. ;
Park, J-H ;
Chatterjee, N. ;
Jamain, S. ;
Cheng, A. ;
Leboyer, M. ;
Muglia, P. ;
Schulze, T. G. ;
Cichon, S. ;
Noethen, M. M. ;
Rietschel, M. ;
McMahon, F. .
MOLECULAR PSYCHIATRY, 2013, 18 (02) :195-205
[8]   Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112117) [J].
Clarke, T-K ;
Adams, M. J. ;
Davies, G. ;
Howard, D. M. ;
Hall, L. S. ;
Padmanabhan, S. ;
Murray, A. D. ;
Smith, B. H. ;
Campbell, A. ;
Hayward, C. ;
Porteous, D. J. ;
Deary, I. J. ;
McIntosh, A. M. .
MOLECULAR PSYCHIATRY, 2017, 22 (10) :1376-1384
[9]  
Colom F., 2006, MANUALE PSICOEDUCAZI
[10]   Variation in NGFB Is Associated With Primary Affective Disorders in Women [J].
Cui, Donghong ;
Zhang, Huiping ;
Yang, Bao-Zhu ;
Listman, Jennifer B. ;
Li, Dawei ;
Price, Lawrence H. ;
Carpenter, Linda L. ;
Tyrka, Audrey R. ;
Anton, Raymond F. ;
Kranzler, Henry R. ;
Gelernter, Joel .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2011, 156B (04) :401-412