Lack of association of DRD3 and CNR1 polymorphisms with premenstrual dysphoric disorders

被引:0
|
作者
Yildiz, Mesut [1 ]
Vural, Mehmet [2 ]
Erdal, Mehmet Emin [3 ]
Ay, Ozlem Izci [3 ]
Yilmaz, Senay Gorucu [3 ]
Karababa, Ibrahim Fatih [4 ]
Selek, Salih [5 ]
机构
[1] Gaziosmanpasa Univ, Fac Med, Dept Psychiat, Tokat, Turkey
[2] Harran Univ, Fac Med, Dept Obstet & Gynecol, Sanliurfa, Turkey
[3] Mersin Univ, Fac Med, Dept Med Biol & Genet, Mersin, Turkey
[4] Harran Univ, Fac Med, Dept Psychiat, Sanliurfa, Turkey
[5] Univ Texas Hlth Sci Ctr Houston, Dept Psychiat & Behav Sci, Houston, TX 77030 USA
关键词
Cannabinoid receptor; Dopamine D3 receptor; Premenstrual syndrome; Genetic polymorphism;
D O I
暂无
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Background: Premenstrual dysphoric disorder (PMDD) is a mood disorder characterized with physical and affective symptoms during the luteal phase of susceptible women. Objective: The aim of this study was to investigate the association of Dopamine D3 receptor (DRD3) polymorphism, and Cannabinoid receptor Type 1 (CNR1) polymorphism with PMDD. Materials and Methods: Fifty one participants with documented PMDD according to the DSM IV criteria and 51 healthy controls were included in this cross sectional study. Symptom severity was measured with daily self-rating, monthly premenstrual assessment forms and psychiatric interviews. The genotyping of DRD3 receptor and Cannabinoid type 1 receptors were performed using Taqmanfluorogenic assay method. Results: Distribution of DRD3 and CNR1 polymorphism was not different between patients and controls. Conclusion: These findings do not support a major role of DRD3, and CNR1 polymorphisms in contributing to susceptibility to premenstrual dysphoric disorder.
引用
收藏
页码:221 / 226
页数:6
相关论文
共 29 条
  • [21] Lack of association between human longevity and genetic polymorphisms in drug-metabolizing enzymes at the NAT2, GSTM1 and CYP2D6 loci
    M.-L. Muiras
    Patrick Verasdonck
    Florence Cottet
    François Schächter
    Human Genetics, 1998, 102 : 526 - 532
  • [22] New polymorphisms in the human poly(ADP-ribose) polymerase-1 coding sequence: Lack of association with longevity or with increased cellular poly(ADP-ribosyl)ation capacity
    Cottet F.
    Blanché H.
    Verasdonck P.
    Le Gall I.
    Schächter F.
    Bürkle A.
    Muiras M.-L.
    Journal of Molecular Medicine, 2000, 78 (8) : 431 - 440
  • [23] Analysis of the association of ANO3/MUC15, COL4A4, RRBP1, and KLK1 polymorphisms with COPD susceptibility in the Kashi population
    Tang, Lifeng
    Zhong, Xuemei
    Gong, Hui
    Tuerxun, Maimaitiaili
    Ma, Tao
    Ren, Jie
    Xie, Chengxin
    Zheng, Aifang
    Abudureheman, Zulipikaer
    Abudukadeer, Ayiguzali
    Aini, Paierda
    Yilamujiang, Subinuer
    Li, Li
    BMC PULMONARY MEDICINE, 2022, 22 (01)
  • [24] Analysis of the association of ANO3/MUC15, COL4A4, RRBP1, and KLK1 polymorphisms with COPD susceptibility in the Kashi population
    Lifeng Tang
    Xuemei Zhong
    Hui Gong
    Maimaitiaili Tuerxun
    Tao Ma
    Jie Ren
    Chengxin Xie
    Aifang Zheng
    Zulipikaer Abudureheman
    Ayiguzali Abudukadeer
    Paierda Aini
    Subinuer Yilamujiang
    Li Li
    BMC Pulmonary Medicine, 22
  • [25] Maternal polymorphisms in the FADS1 and FADS2 genes modify the association between PUFA ingestion and plasma concentrations of omega-3 polyunsaturated fatty acids
    Carvalho, G. Q.
    Pereira-Santos, M.
    Marcon, L. D.
    Louro, I. D.
    Peluzio, M. C. G.
    Santos, D. B.
    PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 2019, 150 : 38 - 46
  • [26] Lack of association between 4-base pair insertion/deletion (rs3783553) polymorphism within the 3′UTR of IL1A and breast cancer: A preliminary report
    Karami, Shima
    Sarabandi, Sahel
    Pourzand, Pouria
    Tabasi, Farhad
    Hashemi, Mohammad
    Bahari, Gholamreza
    GENE REPORTS, 2021, 23
  • [27] Genetic Polymorphisms in Genes Involved in the Type I Interferon System (IFIH1/MDA-5, TNFAIP3/A20, and STAT4): Association with SLE Risk in Egyptian Children and Adolescents
    Zedan, Mohamed M.
    Attia, Zeinab Rizk
    Abd El Azeem, Rania A.
    Mutawi, Thuraya M.
    El Shehawy, Amora S.
    Bakr, Ashraf
    JOURNAL OF INFLAMMATION RESEARCH, 2021, 14 : 3349 - 3358
  • [28] Interactive Association of XRCC1, XRCC2, XRCC3, and TP53 Gene Polymorphisms With Gastrointestinal Cancer Risk: Insights From a Hospital-Based Case-Control Study
    Datkhile, Kailas D.
    Gudur, Rashmi
    Patil, Madhavi N.
    Gudur, Anand
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2024, 16 (06)
  • [29] Association of genetic polymorphisms in DNA repair genes ERCC2 Asp312Asn (rs1799793), ERCC2 Lys 751 Gln (rs13181), XRCC1 Arg399 Gln (rs25487) and XRCC3 Thr 241Met (rs861539) with the susceptibility of lung cancer in Saudi population
    Alsagaby, Suliman
    Ahmed, Ahmed A.
    Rasheed, Zafar
    Althwab, Sami A.
    Aljohani, Abdullah S. M.
    Alhumaydhi, Fahad A.
    Alhomaidan, Homaidan T.
    Alkhamiss, Abdullah S.
    Alkhowailed, Mohammad
    Alaqeel, Aqeel
    Alblihed, Mohamd A.
    Alrehaili, Jihad
    Fernandez, Nelson
    Al Abdulmonem, Waleed
    NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS, 2022, 41 (5-6) : 530 - 554