The catechol-O-methyltransferase (COMT) gene polymorphism and prevalence of uterine fibroids

被引:15
|
作者
de Oliveira, Emerson [1 ]
Castro, Rodrigo de Aquino [1 ]
Vieira Gomes, Mariano Tamura [1 ]
Cotrim Guerreiro da Silva, Ismael Dale [1 ]
Baracat, Edmund Chada [1 ]
de Lima, Geraldo Rodrigues [1 ]
Ferreira Sartori, Marair Gracio [1 ]
Batista Castello Girao, Manoel Joao [1 ]
机构
[1] Univ Fed Sao Paulo UNIFESP, Dept Gynecol, BR-04062500 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Uterine fibroids; Uterine leiomyoma; Risk factors; Catechol-O-methyltransferase; Polymorphism;
D O I
10.1016/j.maturitas.2008.07.001
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Objective: To assess the possible association between the catechol-O-methyltransferase (COMT) polymorphism and uterine fibroids in Brazilian women. Design: Case-control study. Patient(s): One hundred twenty-four premenopausal women with fibroids, and 193 postmenopausal controls not presenting the disease. Intervention(s): The subjects were classified as white or non-white (black and mulatto), and COMT genotypes were determined. DNA was extracted from the uterus of cases and from peripheral blood of controls and submitted to polymerase chain reaction (PCR) and agarose gel electrophoresis. Main outcome measure(s): The presence of the COMT polymorphism was recorded for all patients, and the frequency and distribution among cases and controls were compared according to race. Binomial log regression models were used to estimate odds-ratios (OR) for uterine volumes of <290 cm(3) (small fibroids) vs. those >290 cm(3) (large fibroids). Potential confounding variables (age, race and parity) were added to the model. Results: Genotypes positive for the COMT polymorphism (heterozygous or mutant homozygous) were found in 45% of white and 28.9% of non-white women (p =.013) and the polymorphic allele frequencies in these groups were 27.2% and 16.3%, respectively (p=.006). However, there were no clear differences between patients and controls within the white subgroup with regard to the presence of COMT polymorphism-containing genotypes (41.5% vs. 46.0%, respectively) (p =.60), or for the polymorphic allele frequency (26.8% vs. 27.3%, respectively) (p =.92). For non-white women, there were also no differences between cases and controls for the frequency of polymorphic genotypes (28.9% vs. 28.9%, respectively) (p =.995), or for the polymorphic allele frequency (17.8 vs. 14.5, respectively) (p =.565). Estimated OR for small or large fibroids in association with the polymorphic allele revealed a positive association between the allele with lower activity and large fibroids (vs. small) (OR = 3.3; 95% confidence interval [CI] = 1.31-8.46). The adjusted OR was 4.35 (95% confidence interval [CI] = 1.58-11.9). Conclusions: The catechol-O-methyltransferase polymorphism is a risk factor for the development of large uterine fibroids in Brazilian women suffering from fibroids. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:235 / 238
页数:4
相关论文
共 50 条
  • [1] Polymorphism of catechol-o-methyltransferase and uterine leiomyoma
    Ates, Omer
    Demirturk, Fazli
    Toprak, Muhammet
    Sezer, Saime
    [J]. MOLECULAR AND CELLULAR BIOCHEMISTRY, 2013, 375 (1-2) : 179 - 183
  • [2] Polymorphism of catechol-o-methyltransferase and uterine leiomyoma
    Omer Ates
    Fazli Demirturk
    Muhammet Toprak
    Saime Sezer
    [J]. Molecular and Cellular Biochemistry, 2013, 375 : 179 - 183
  • [3] Investigation of the catechol-O-methyltransferase (COMT) gene polymorphism in a sample of cocaine dependents
    Cunha, N
    Cordeiro, Q
    Guindalini, C
    Messas, GP
    Castelo, A
    Laranjeira, R
    Vallada, H
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2004, 130B (01): : 110 - 110
  • [4] Catechol-O-methyltransferase (COMT) genetic polymorphism in a Turkish population
    Kocabas, NA
    Karakaya, AE
    Cholerton, S
    Sardas, S
    [J]. ARCHIVES OF TOXICOLOGY, 2001, 75 (07) : 407 - 409
  • [5] Catechol-O-methyltransferase (COMT) genetic polymorphism in a Turkish population
    Neslihan Kocabaş
    Ali Karakaya
    Suzanne Cholerton
    Şemra Şardaş
    [J]. Archives of Toxicology, 2001, 75 : 407 - 409
  • [6] Association Between Hypnotizability and the Catechol-O-Methyltransferase (COMT) Polymorphism
    Szekely, Anna
    Kovacs-Nagy, Reka
    Banyai, Eva I.
    Gosi-Greguss, Anna C.
    Varga, Katalin
    Halmai, Zsuzsa
    Ronai, Zsolt
    Sasvari-Szekely, Maria
    [J]. INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL HYPNOSIS, 2010, 58 (03) : 301 - 315
  • [7] G/A(1947) polymorphism in catechol-O-methyltransferase (COMT) gene in Parkinson's disease
    Xie, T
    Ho, SL
    Li, LSW
    Ma, OCK
    [J]. MOVEMENT DISORDERS, 1997, 12 (03) : 426 - 427
  • [8] Catechol-O-Methyltransferase (COMT) gene polymorphism and breast cancer risk in young women
    Bergman-Jungeström, M
    Wingren, S
    [J]. BRITISH JOURNAL OF CANCER, 2001, 85 (06) : 859 - 862
  • [9] Catechol-O-Methyltransferase (COMT) gene polymorphism and breast cancer risk in young women
    M Bergman-Jungeström
    S Wingren
    [J]. British Journal of Cancer, 2001, 85 : 859 - 862
  • [10] Identification of a BglI polymorphism of catechol-O-methyltransferase (COMT) gene, and association study with schizophrenia
    Chen, CH
    Lee, YR
    Liu, MY
    Wei, FC
    Koong, FJ
    Hwu, HG
    Hsiao, KJ
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1996, 67 (06): : 556 - 559