Jiménez-Ortega Rogelio F, Aparicio-Bautista Diana I, Becerra-Cervera Adriana, López-Montoya Priscilla, León-Reyes Guadalupe, Flores-Morales Jeny, Castillejos-López Manuel, Hidalgo-Bravo Alberto, Salmerón Jorge, Rivera-Paredez Berenice, Velázquez-Cruz Rafael
Laboratorio de Genómica del Metabolismo Óseo, Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City 14610, Mexico.
Consejo Nacional de Humanidades, Ciencias y Tecnologías (CONAHCYT), Mexico City 03940, Mexico.
Antioxidants (Basel). 2023 Dec 8;12(12):2089. doi: 10.3390/antiox12122089.
Oxidative stress is essential in developing multiple bone metabolism diseases, including osteoporosis. Single-nucleotide variants (SNVs) have been associated with oxidative stress, promoting an imbalance between the production of reactive oxygen species and the ability to neutralize them, and it has been reported that antioxidant nutrient intake can influence bone mineral density (BMD). This work reports the association between oxidative stress-related SNVs (-rs1050450, rs17650792, -rs4880, and -rs769217), BMD, and antioxidant nutrient intake. The study included 1269 Mexican women from the Health Workers Cohort Study. Genotyping was performed using predesigned TaqMan assays. Dietary data were collected using a 116-item semi-quantitative food frequency questionnaire. A dietary antioxidant quality score (DAQS) was used to estimate antioxidant-nutrient intake. Association analysis was estimated via linear, logistic, or quantile regression models. The results showed an association of the rs1050450-A and rs17650792-A alleles with femoral neck BMD ( = 0.038 and = 0.017, respectively) and the SNV rs4880-A allele with total hip BMD ( = 0.026) in respondents aged 45 years or older. In addition, antioxidant-nutrient intake was associated with the rs4880-GG genotype, being significant for fiber ( = 0.007), riboflavin ( = 0.005), vitamin B6 ( = 0.034), and vitamin D ( = 0.002). The study showed an association between oxidative stress-related SNVs, BMD, and antioxidant-nutrient intake in Mexican women. Therefore, treatments for low BMD could be developed based on antioxidant supplementation.
氧化应激在包括骨质疏松症在内的多种骨代谢疾病的发生发展中至关重要。单核苷酸变异(SNV)与氧化应激相关,会促使活性氧生成与中和能力之间失衡,并且据报道抗氧化营养素的摄入会影响骨矿物质密度(BMD)。本研究报告了氧化应激相关单核苷酸变异(-rs1050450、rs17650792、-rs4880和-rs769217)、骨矿物质密度和抗氧化营养素摄入之间的关联。该研究纳入了来自健康工作者队列研究的1269名墨西哥女性。使用预先设计的TaqMan分析进行基因分型。通过一份包含116项的半定量食物频率问卷收集饮食数据。采用饮食抗氧化质量评分(DAQS)来估算抗氧化营养素的摄入量。通过线性、逻辑或分位数回归模型进行关联分析。结果显示,在45岁及以上的受访者中,rs1050450 - A和rs17650792 - A等位基因与股骨颈骨密度相关(分别为P = 0.038和P = 0.017),SNV rs4880 - A等位基因与全髋骨密度相关(P = 0.026)。此外,抗氧化营养素的摄入与rs4880 - GG基因型相关,对纤维(P = 0.007)、核黄素(P = 0.005)、维生素B6(P = 0.034)和维生素D(P = 0.002)而言具有显著性。该研究表明了氧化应激相关单核苷酸变异、骨矿物质密度和抗氧化营养素摄入在墨西哥女性中的关联。因此,可以基于抗氧化剂补充来开发针对低骨矿物质密度的治疗方法。