Programa de Pós-Graduação em Ciências Farmacêuticas, Departamento de Análises Clínicas, Escola de Farmácia, Universidade Federal de Ouro Preto, Ouro Preto, Minas Gerais, Brazil.
Serviço de patologia do trato genital inferior da Maternidade Odete Valadares - Fundação Hospitalar do Estado de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Nutr Cancer. 2022;74(8):2779-2788. doi: 10.1080/01635581.2021.2022723. Epub 2021 Dec 28.
To analyze the association of cervical cytological abnormalities with genetic polymorphisms of enzymes involved in folate metabolism, and the effect of micronutrients on association of polymorphisms with cervical carcinogenesis. Our samples were divided in Control (120 women with normal cytology), and Cases: 37 women with Atypical Squamous Cells of Undetermined Significance(ASC-US), 33 participants presenting Low-Grade Squamous Intraepithelial Lesion(LSIL), and 24 women presenting High-Grade cervical lesions(HSIL/ASC-H). We obtained cervical samples for cytological analysis, HPV detection, and analysis of polymorphisms and cervical cell folate. Blood samples were obtained for serum folate and vitamin B12 evaluation. To analyze all polymorphisms simultaneously, we calculated Genetic Risk Score(GRS). Median concentrations were used as cutoff for determination of micronutrient levels. We observed no differences of genotype or allelic frequencies of polymorphisms according to cervical lesions. However, high levels of cervical cell folate and high number of genetic alterations increased risk of High-Grade lesions [OR(IC95%):1.85(0.42-8.11)]. Instead, women with vitamin B12 ≤ 274 pg/ml and GRS ≥ 3 presented even greater risk of HSIL/ASC-H [OR(IC95%):2.91(0.46-18.62)]. High frequency of genetic polymorphisms involved in one-carbon metabolism associated with high levels of cell folate or low levels of serum vitamin B12, increased the risk of High-Grade lesion in uterine cervix.
为了分析与叶酸代谢相关酶的遗传多态性与宫颈细胞学异常的关联,以及微量营养素对多态性与宫颈癌发生关联的影响。我们的样本分为对照组(120 名细胞学正常的女性)和病例组:37 名非典型鳞状细胞不能明确意义(ASC-US)患者,33 名低度鳞状上皮内病变(LSIL)患者,以及 24 名高度宫颈病变(HSIL/ASC-H)患者。我们获得了宫颈细胞学分析、HPV 检测以及多态性和宫颈细胞叶酸分析的样本。采集血样用于评估血清叶酸和维生素 B12。为了同时分析所有多态性,我们计算了遗传风险评分(GRS)。中位数浓度用作确定微量营养素水平的截止值。我们没有观察到多态性的基因型或等位基因频率根据宫颈病变而有所不同。然而,高浓度的宫颈细胞叶酸和大量遗传改变增加了发生高级别病变的风险[比值比(95%置信区间):1.85(0.42-8.11)]。相反,维生素 B12≤274pg/ml 和 GRS≥3 的女性发生 HSIL/ASC-H 的风险更高[比值比(95%置信区间):2.91(0.46-18.62)]。参与一碳代谢的遗传多态性频率较高,与细胞叶酸水平较高或血清维生素 B12 水平较低相关,增加了子宫颈高级别病变的风险。