Soares Nayara Pereira, Santos Ana Celly Souza dos, Costa Eduardo Caldas, Azevedo George Dantas, Damasceno Débora Cristina, Fayh Ana Paula Trussardi, Lemos Telma Maria Araújo Moura
Department of Clinical and Toxicological, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Ann Nutr Metab. 2016;68(3):220-7. doi: 10.1159/000444130. Epub 2016 Apr 14.
We aimed to investigate the impact of following a diet to induce weight loss (500 kcal deficit per day) over DNA damage and cardiometabolic risk factors in women with overweight/obesity diagnosed with polycystic ovary syndrome (PCOS).
A study was conducted in Natal, RN, Brazil selecting overweight/obese (body mass index ≥25 and <39 kg/m2) women (18-35 years). The levels of DNA damage were assessed by a single cell gel electrophoresis. Repeated 24 h dietary recall questionnaires, anthropometry, biochemical profile and sex hormones were collected at baseline and after 12 weeks of intervention.
Women exhibiting a decrease in the markers of DNA damage: tail intensity (24.35 ± 5.86 - pre diet vs. 17.15 ± 5.04 - post-diet; p < 0.001) and tail moment (20.47 ± 7.85 - pre diet vs. 14.13 ± 6.29 - post-diet; p < 0.002). Reduction of calorie intake, weight loss, decreased sexual hormone and cardiometabolic markers such as insulin, homeostasis model assessment of insulin resistance and low-density lipoprotein cholesterol were verified In the multivariate regression analysis, quantitative insulin sensitivity check index and progesterone were responsible for the variation markers in DNA damage before the diet, losing its influence upon diet.
DNA damage and the impact of cardiometabolic risk factors decreased after the intervention in women with PCOS, indicating the relevance of a nutritional approach in this group of patients.
我们旨在研究遵循一种导致体重减轻(每天500千卡热量缺口)的饮食对诊断为多囊卵巢综合征(PCOS)的超重/肥胖女性的DNA损伤和心血管代谢危险因素的影响。
在巴西纳塔尔进行了一项研究,选择超重/肥胖(体重指数≥25且<39kg/m²)的18 - 35岁女性。通过单细胞凝胶电泳评估DNA损伤水平。在基线和干预12周后收集重复的24小时饮食回忆问卷、人体测量数据、生化指标和性激素。
女性的DNA损伤标志物有所下降:尾强度(饮食前24.35±5.86 vs. 饮食后17.15±五.04;p<0.001)和尾矩(饮食前20.47±7.85 vs. 饮食后14.13±6.29;p<0.002)。热量摄入减少、体重减轻、性激素和心血管代谢标志物如胰岛素、胰岛素抵抗稳态模型评估和低密度脂蛋白胆固醇降低。在多变量回归分析中,定量胰岛素敏感性检查指数和孕酮在饮食前是DNA损伤变异标志物的原因,饮食后失去其影响。
PCOS女性干预后DNA损伤和心血管代谢危险因素的影响降低,表明营养方法在该组患者中的相关性。